A big enhance of bile acid (BA) ranges has been acknowledged as a basic metabolic phenotype of numerous liver illnesses. Monitoring of BA profiles has been proposed for etiology differentiation on liver damage. Right here, we quantitatively profiled serum BAs of wholesome controls and 719 sufferers with persistent liver illness of 5 etiologies, hepatitis B virus (HBV), hepatitis C virus (HCV), nonalcoholic steatohepatitis (NASH), alcohol-induced liver illness (ALD), and first biliary cirrhosis (PBC), and investigated the generality and specificity of various etiologies. The uncooked knowledge have been deposited into MetaboLights (ID: MTBLS2459). We discovered that sufferers with HBV, HCV, and NASH seemed to be extra comparable, and ALD and PBC sufferers clustered collectively.
BA profiles, consisting of a complete focus of the 21 quantified BAs [total BAs (TBAs)], 21 BA proportions, and 24 BA related variables, have been extremely completely different among the many etiologies. Particularly, the full BAs was larger in ALD and PBC sufferers in contrast with the opposite three teams. The proportion of conjugated deoxycholates was the very best in HBV-infected sufferers. The ratio of 12α-hydroxylated (12α-OH) to non-12α-OH BAs was the very best in NASH sufferers. The proportion of taurine-conjugated BAs was the very best in ALD sufferers. For PBC sufferers, the proportion of ursodeoxycholate species was the very best, and the ratio of major to secondary BAs was the bottom.
Comparatively, the distinction of BA profiles amongst cirrhosis sufferers was constant however weaker than that of all sufferers. The correlations between BA profiles and scientific indices have been additionally fairly completely different in several pathological teams, each in all sufferers and in sufferers with cirrhosis. Total, our findings prompt that BA compositions are distinct amongst sufferers with completely different etiologies of persistent liver illness, and a few BA-relevant variables are of scientific potentials for liver damage kind differentiation, though additional validations on extra etiologies and populations are wanted.
Circulatory cadmium positively correlates with epithelial-mesenchymal transition in sufferers with persistent obstructive pulmonary illness
Environmental cadmium (Cd) publicity may cause a number of pulmonary illnesses. Epithelial-mesenchymal transition (EMT) concerned within the technique of persistent obstructive pulmonary illness (COPD). Nonetheless, the affiliation between environmental Cd publicity and EMT was unclear in COPD sufferers. This examine aimed to research the associations amongst circulatory Cd, EMT and COPD primarily based on case-control examine. 4 hundred COPD sufferers and 400 management topics have been recruited. Circulatory Cd was detected utilizing atomic adsorption spectrometer. MicroRNA-30 (miR-30) was measured by RT-PCR and the markers of pulmonary EMT have been evaluated by way of western blotting.
Circulatory Cd focus was elevated and serum miR-30 was decreased in COPD sufferers. Circulatory Cd was inversely related to pulmonary perform in COPD sufferers. Furthermore, serum miR-30 was regularly decreased in parallel with FEV1 in COPD sufferers. In the meantime, there was a unfavourable affiliation between serum miR-30 and circulatory Cd in COPD sufferers. Additional evaluation discovered that E-cadherin, certainly one of epithelial biomarkers, was diminished in lung tissues of COPD sufferers with larger circulatory Cd. Our outcomes present proof that miR-30 discount contributing to pulmonary EMT might contain within the technique of Cd-induced COPD.
Nationwide developments and outcomes of genetically inherited non-alcoholic persistent liver illness within the USA: estimates from the Nationwide Inpatient Pattern (NIS) database
Medical literature on the prevalence of genetic liver illness is missing. On this examine, we investigated the in-hospital healthcare and financial burden from genetic causes of non-alcoholic persistent liver illness (NACLD) and non-alcoholic liver cirrhosis (NALC) within the USA. Knowledge have been abstracted from the Nationwide Inpatient Pattern database between 2002 and 2014 utilizing ICD9 codes for sufferers discharged with NACLD and NALC secondary to genetic illnesses together with alpha-1 antitrypsin deficiency (A1ATd), cystic fibrosis (CF), Wilson illness (WD), hereditary hemochromatosis (HHC), glycogen storage illness, and issues of fragrant amino-acid metabolism (DAAAM).
All through the examine interval, there have been 19,332 discharges for NACLD related to the six genetic illnesses together with 14,368 for NALC. There have been $1.09 billion in hospital fees, 790 in-hospital deaths, and 955 liver transplants carried out. Total, A1ATd was related to 8,983 (62.52%) hospitalizations for NALC adopted by WD, CF, and HHC. The best in-hospital mortality was seen with HHC. The best frequency of liver transplants was seen with DAAAM. The variety of hospitalizations for genetic liver illnesses continues to extend. With elevated funding and directed analysis efforts, we are able to goal to enhance medical remedies and the standard of life for sufferers in danger for liver deterioration.
Mini Samples Mouse Pulmonary Activation Regulated Chemokine (PARC) ELISA Kit |
MEB522Mu-1x96wellstestplate |
Cloud-Clone |
1x96-wells test plate |
EUR 878.6 |
|
Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Mini Samples Mouse Pulmonary Activation Regulated Chemokine (PARC). |
Mini Samples Mouse Pulmonary Activation Regulated Chemokine (PARC) ELISA Kit |
MEB522Mu-5x96wellstestplate |
Cloud-Clone |
5x96-wells test plate |
EUR 3593.72 |
|
Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Mini Samples Mouse Pulmonary Activation Regulated Chemokine (PARC). |
Mini Samples Mouse Pulmonary Activation Regulated Chemokine (PARC) ELISA Kit |
4-MEB522Mu |
Cloud-Clone |
-
Ask for price
-
Ask for price
-
Ask for price
|
- 10 plates of 96 wells
- 5 plates of 96 wells
- 1 plate of 96 wells
|
|
Description: Enzyme-linked immunosorbent assay based on the Double-antibody Sandwich method for detection of Mini Samples Mouse Pulmonary Activation Regulated Chemokine (PARC) in samples from n/a with no significant corss-reactivity with analogues from other species. |
Human Chronic Kidney Disease Peripheral Blood Mononuclear Cells |
ABC-TC4342 |
AcceGen |
1 vial |
Ask for price |
|
Description: Clinical data may include: Medication (current and historical), Disease Severity, Creatine Clearance Value, GFR, standard blood chemistry results, BNP. |
Single Donor Human Pulmonary Fibrosis Plasma |
IPLASPF |
Innovative research |
each |
EUR 209 |
|
Description: Single Donor Human Pulmonary Fibrosis Plasma |
Diseased Human Lung Fibroblasts, Idiopathic Pulmonary Fibrosis |
ABC-TC5520 |
AcceGen |
1 vial |
Ask for price |
|
Description: IPF (Idiopathic Pulmonary Fibrosis) is a fatal disease that usually affects adults between the ages of 50-70. The disease is characterized by progressive decline in lung function resulting from scarring of lung tissue.IPF varies from person to person where in some, fibrosis happens quickly, while the process can be much slower in others. IPF has no cure yet and both geneticand environmental factors are attributed to the development of the disease. Genetics may play a role in causing IPF, and cigarette smoking is the most accepted risk factor in increasing the chances of developing IPF. Recent research has helped doctors understand the disease more closely so they can more quickly diagnose it than in the past. Efforts are still underway in the research community to understand the pathways of disease progression and subsequently develop cures for IPF. IPF was once thought to be a chronic inflammatory process but recent evidence suggests that the abnormal activation of alveolar epithelial cells (AECs) induce over-activation of fibrotic response. The fibroblast and myofibroblast foci secrete excessive amounts of collagens, leading to scarringand destruction of the lung architecture. The mechanisms that link IPF with ageing and aberrant epithelial activation are unknown. |
Human Chronic Myeloid Leukemia PB Plasma (Chronic Phase) |
ABC-TC3364 |
AcceGen |
1 vial |
Ask for price |
|
Description: Chronic Myeloid Leukemia-PB Plasma is obtained by centrifuging Chronic Myeloid Leukemia peripheral blood. Plasma has a diminished number of cells and platelets. Chronic Myeloid Leukemia plasma is available in the chronic phase and accelerated or blast crisis phase. |
Human Chronic Myeloid Leukemia Bone Marrow Plasma (Chronic Phase) |
ABC-TC3361 |
AcceGen |
1 vial |
Ask for price |
|
Description: Chronic Myeloid Leukemia-Bone Marrow plasma is obtained by centrifugation of the Chronic Myeloid Leukemia bone marrow. Plasma has a diminished number of cells and platelets. Chronic Myeloid Leukemia-Bone Marrow plasma is available in chronic phase and accelerated or blast crisis phase. |
Plasma Membrane GFP Tagged Human Pulmonary Microvascular Endothelial Cells |
cAP-0032GFP-PM |
Angio Proteomie |
1Frozen Vial |
EUR 782.1 |
Human Crohn's Disease PB Plasma |
ABC-TC3392 |
AcceGen |
1 vial |
Ask for price |
|
Description: Crohn's Disease peripheral blood plasma is obtained by centrifugation of the PB. This product has a diminished number of cells and platelets. Fresh Crohn's PB plasma is available upon request. |
Low Sample Volume Mouse Pulmonary Activation Regulated Chemokine / PARC (CCL18) ELISA Kit |
abx585726-100g |
Abbexa |
100 µg |
EUR 7087.5 |
Low Sample Volume Mouse Pulmonary Activation Regulated Chemokine / PARC (CCL18) ELISA Kit |
abx585726-10g |
Abbexa |
10 µg |
EUR 787.5 |
Low Sample Volume Mouse Pulmonary Activation Regulated Chemokine / PARC (CCL18) ELISA Kit |
abx585726-50g |
Abbexa |
50 µg |
EUR 3750 |
Single Donor Human Crohn's Disease Plasma |
IPLASCRHN |
Innovative research |
each |
EUR 209 |
|
Description: Single Donor Human Crohn's Disease Plasma |
Single Donor Human Heart Disease Plasma |
IPLASHDS1 |
Innovative research |
each |
EUR 247 |
|
Description: Single Donor Human Heart Disease Plasma |
Single Donor Human Heart Disease Plasma |
IPLASHDS10 |
Innovative research |
each |
EUR 2352 |
|
Description: Single Donor Human Heart Disease Plasma |
Human Chronic Lymphoid Leukemia PB Plasma(Relapsed/Refractory) |
ABC-TC3351 |
AcceGen |
1 vial |
Ask for price |
|
Description: Chronic Lymphoid Leukemia-PB Plasma is obtained by centrifugation of the Chronic Lymphoid Leukemia-PB-Mononuclear Cells. Plasma has a diminished number of cells and platelets. Chronic Lymphoid Leukemia plasma is available in untreated and relapsed/refractory stages. |
Human Chronic Myeloid Leukemia PB Plasma (Accelerated/Blast Crisis) |
ABC-TC3363 |
AcceGen |
1 vial |
Ask for price |
|
Description: Chronic Myeloid Leukemia-PB Plasma is obtained by centrifuging Chronic Myeloid Leukemia peripheral blood. Plasma has a diminished number of cells and platelets. Chronic Myeloid Leukemia plasma is available in the chronic phase and accelerated or blast crisis phase. |
Human Chronic Lymphoid Leukemia PB Plasma (Newly Diagnosed/Untreated) |
ABC-TC3350 |
AcceGen |
1 vial |
Ask for price |
|
Description: Chronic Lymphoid Leukemia-PB Plasma is obtained by centrifugation of the Chronic Lymphoid Leukemia-PB-Mononuclear Cells. Plasma has a diminished number of cells and platelets. Chronic Lymphoid Leukemia plasma is available in untreated and relapsed/refractory stages. |
Human Chronic Lymphoid Leukemia Bone Marrow Plasma (Relapsed/Refractory) |
ABC-TC3345 |
AcceGen |
1 vial |
Ask for price |
|
Description: Chronic Lymphoid Leukemia Bone Marrow-Plasma is obtained by centrifugation of the Chronic Lymphoid Leukemia bone marrow. Plasma has a diminished number of cells and platelets. Chronic Lymphoid Leukemia plasma is available in untreated and relapsed/refractory stages. |
Human Chronic Myeloid Leukemia Bone Marrow Plasma (Accelerated/Blast Crisis) |
ABC-TC3360 |
AcceGen |
1 vial |
Ask for price |
|
Description: Chronic Myeloid Leukemia-Bone Marrow plasma is obtained by centrifugation of the Chronic Myeloid Leukemia bone marrow. Plasma has a diminished number of cells and platelets. Chronic Myeloid Leukemia-Bone Marrow plasma is available in chronic phase and accelerated or blast crisis phase. |
Human Chronic Lymphoid Leukemia Bone Marrow Plasma (Newly Diagnosed/Untreated) |
ABC-TC3344 |
AcceGen |
1 vial |
Ask for price |
|
Description: Chronic Lymphoid Leukemia Bone Marrow-Plasma is obtained by centrifugation of the Chronic Lymphoid Leukemia bone marrow. Plasma has a diminished number of cells and platelets. Chronic Lymphoid Leukemia plasma is available in untreated and relapsed/refractory stages. |
Rat Pulmonary Fibroblasts |
ABC-TC4204 |
AcceGen |
1 vial |
Ask for price |
|
Description: The most abundant cell type in lung interstitium is fibroblasts. They resemble ordinary fibroblasts but have some distinguishing features, for example, they have long branching processes and gap junctions. |
Human Pulmonary Fibroblasts |
ABC-TC3776 |
AcceGen |
1 vial |
Ask for price |
|
Description: The most abundant cell type in lung interstitium is fibroblasts. They resemble ordinary fibroblasts but have some distinguishing features, for example, they have long branching processes and gap junctions. Their principle function is production of type III collagen, elastin, and proteoglycans of the extracellular matrix of the alveolar septa. Pulmonary fibroblasts (PF) play an important role in the repair and remodeling processes following injury. The controlled accumulation of fibroblasts to sites of inflammation is crucial to effective tissue repair after injury. Either inadequate or excessive accumulation of fibroblasts could result in abnormal tissue function. For example, the excess proliferation of fibroblasts contributes to the adventitial thickening observed during the development of hypoxia-induced pulmonary hypertension. HPF from Gentaur Research Laboratories are isolated from human lung tissue. HPF are cryopreserved at primary culture and delivered frozen. Each vial contains 5×10^5 cells in 1 ml volume. HPF are characterized by immunofluorescent method with antibody to fibronectin. HPF are negative for HIV-1, HBV, HCV, mycoplasma, bacteria, yeast and fungi. HPF are guaranteed to further expand for 15 population doublings at the condition provided by Gentaur Research Laboratories. |
cDNA - Pulmonary Embolism: Lung |
C1236152Ld-5 |
Biochain |
40 reactions |
EUR 989 |
2019-nCoV IgG/IgM RapiCard InstaTest for Whole Blood/Serum/Plasma samples |
GEN-176552-25tests |
Cusabio |
25 tests |
EUR 331.2 |
Description: A rapid test for detection of antibodies (IgG and IgM) for 2019-nCoV, the novel Coronavirus from the Wuhan strain. The test is easy to perform, takes 10 minutes to provide reliable results and is higly specific to the 2019-nCoV Coronavirus. |
2019-nCoV IgG/IgM RapiCard InstaTest for Whole Blood/Serum/Plasma samples |
GEN-176552-50tests |
Cortez Diagnostic |
50 tests |
EUR 566.4 |
Description: A rapid test for detection of antibodies (IgG and IgM) for 2019-nCoV, the novel Coronavirus from the Wuhan strain. The test is easy to perform, takes 10 minutes to provide reliable results and is higly specific to the 2019-nCoV Coronavirus. |
Rat Pulmonary Vein Fibroblasts |
ABC-TC4206 |
AcceGen |
1 vial |
Ask for price |
|
Description: Rat Primary Pulmonary Vein Fibroblasts from Gentaur are isolated from tissue of neonatal Sprague-Dawley Rats. Rat Primary Pulmonary Vein Fibroblasts are grown in T75 tissue culture flasks pre-coated with gelatin-based solution for 0.5 hour and incubated in Gentaur's Cell Culture Medium for 3-7 days. Cultures are then expanded. Prior to shipping, cells are detached from flasks and immediately cryo-preserved in vials. Each vial contains at least 1x10^6 cells per ml and is delivered frozen.Cells are negative for bacteria, yeast, fungi, and mycoplasma. Rat Primary Pulmonary Vein Fibroblasts are tested for expression of marker using the antibody of anti-FSP1/S100A4 by immunofluorescence staining and can be expanded by 2-4 passages at a split ratio of 1:2 under the cell culture conditions specified by Gentaur. Repeated freezing and thawing of cells is not recommended.Standard biochemical procedures performed with fibroblast cultures include the assays of cell to cell interaction, PCR, Western blotting, immunoprecipitation, immunofluorescent staining, immunofluorescent flow cytometry or generating cell derivatives for desired research applications. |
Lung (Pulmonary embolism) Lysate |
XBL-10364 |
ProSci |
0.1 mg |
EUR 796.2 |
Description: Human lung tissue lysate was prepared by homogenization using a proprietary technique. The tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The human lung tissue total protein is provided in a buffer including HEPES (pH7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, Sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the lung tissue pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The lung tissue is then Western analyzed by either GAPDH or β-actin antibody, and the expression level is consistent with each lot. |
Rat Pulmonary Artery Fibroblasts |
ABC-TC4202 |
AcceGen |
1 vial |
Ask for price |
|
Description: Rat Primary Pulmonary Artery Fibroblasts from Gentaur are isolated from tissue of neonatal Sprague-Dawley Rats. Rat Primary Pulmonary Artery Fibroblasts are grown in T75 tissue culture flasks pre-coated with gelatin-based solution for 0.5 hour and incubated in Gentaur's Cell Culture Medium for 3-7 days. Cultures are then expanded. Prior to shipping, cells are detached from flasks and immediately cryo-preserved in vials. Each vial contains at least 1x10^6 cells per ml and is delivered frozen.Cells are negative for bacteria, yeast, fungi, and mycoplasma. Rat Primary Pulmonary Artery Fibroblasts are tested for expression of marker using the antibody of anti-FSP1/S100A4 by immunofluorescence staining and can be expanded by 2-4 passages at a split ratio of 1:2 under the cell culture conditions specified by Gentaur. Repeated freezing and thawing of cells is not recommended.Standard biochemical procedures performed with fibroblast cultures include the assays of cell to cell interaction, PCR, Western blotting, immunoprecipitation, immunofluorescent staining, immunofluorescent flow cytometry or generating cell derivatives for desired research applications. |
Rat Primary Pulmonary Fibroblasts |
T4801 |
ABM |
5x10^5 cells / 1.0 ml |
Ask for price |
Rabbit Pulmonary Artery Fibroblast |
CP-Rb010 |
Elabscience Biotech |
5×105 cells/vial |
EUR 610 |
|
Description: Rabbit |
Human Primary Pulmonary Fibroblasts |
T4009 |
ABM |
5x10^5 cells / 1.0 ml |
EUR 975 |
Mouse Primary Pulmonary Fibroblasts |
T4504 |
ABM |
5x10^5 cells / 1.0 ml |
Ask for price |
Primary Rat Pulmonary Fibroblasts (PF) |
CSI034Ra01 |
Cloud-Clone |
5X10^5 |
EUR 780 |
|
Rat Pulmonary Vein Endothelial Cells |
ABC-TC4205 |
AcceGen |
1 vial |
Ask for price |
|
Description: Rat Pulmonary Vein Endothelial Cells from Gentaur are isolated from tissue of adult Sprague-Dawley Rats. Rat Pulmonary Vein Endothelial Cells are grown in T75 tissue culture flasks pre-coated with gelatin-based solution for 0.5 hour and incubated in Gentaur's Cell Culture Medium generally for 3-7 days. Cultures are then expanded. Prior to shipping, cells are detached from flasks and immediately cryo-preserved in vials. Each vial contains at least 1x10^6 cells per ml and are delivered frozen.Rat Pulmonary Vein Endothelial Cells can be used in assays of cell to cell adhesion, migration, vascular tube formation, or transendothelial resistance (TER). Standard biochemical procedures performed with endothelial cell cultures include PCR, Western blotting, immunoprecipitation, immunofluorescent staining or immunofluorescent flow cytometry or generating cell derivatives for desired research applications. |
Total Protein - Pulmonary embolism: Lung |
P1236152Ld-5 |
Biochain |
1 mg |
EUR 542 |
Primary Mouse Pulmonary Fibroblasts (PF) |
CSI034Mu01 |
Cloud-Clone |
5X10^5 |
EUR 720 |
|
Rat Pulmonary Artery Endothelial Cells |
ABC-TC4201 |
AcceGen |
1 vial |
Ask for price |
|
Description: Rat Pulmonary Artery Endothelial Cells from Gentaur are isolated from tissue of adult Sprague-Dawley Rats. Rat Pulmonary Artery Endothelial Cells are grown in T25 tissue culture flasks pre-coated with gelatin-based solution for 0.5 hour and incubated in Gentaur's Cell Culture Medium generally for 3-7 days. Cultures are then expanded. Prior to shipping, cells are detached from flasks and immediately cryo-preserved in vials. Each vial contains at least 1x10^6 cells per ml and are delivered frozen.Rat Pulmonary Artery Endothelial Cells can be used in assays of cell to cell adhesion, migration, vascular tube formation, or transendothelial resistance (TER). Standard biochemical procedures performed with endothelial cell cultures include PCR, Western blotting, immunoprecipitation, immunofluorescent staining or immunofluorescent flow cytometry or generating cell derivatives for desired research applications. |
Primary Canine Pulmonary Fibroblasts (PF) |
CSI034Ca01 |
Cloud-Clone |
5X10^5 |
EUR 1200 |
|
Primary Rabbit Pulmonary Fibroblasts (PF) |
CSI034Rb01 |
Cloud-Clone |
5X10^5 |
EUR 820 |
|
Rat Pulmonary Alveolar Epithelial Cells |
ABC-TC4200 |
AcceGen |
1 vial |
Ask for price |
|
Description: Pulmonary alveolar epithelial cells (PAEpiC) comprised of alveolar type I and type II epithelial cells, line more than 99% of the internal surface area of the lung. Type I cells are large squamous cells whose thin cytoplasmic extensions cover 95%.Rat Pulmonary alveolar epithelial cells are isolated from tissue of pathogen-free laboratory Sprague–Dawley (SD). They are grown in T75 tissue culture flasks pre-coated with 0.2% gelatin for 1 hour and incubated in Culture Complete Growth Medium. |
Rat Pulmonary Vein Smooth Muscle Cells |
ABC-TC4207 |
AcceGen |
1 vial |
Ask for price |
|
Description: Rat Pulmonary Vein Smooth Muscle Cells from Gentaur are isolated from tissue of Sprague-Dawley Rats. Rat Pulmonary Vein Smooth Muscle Cells are grown in T75 tissue culture flasks pre-coated with gelatin-based coating solution for 0.5 hour and incubated in Gentaur's Cell Culture Medium for 3-7 days. Cultures are then expanded. Prior to shipping, cells are detached from flasks and immediately cryo-preserved in vials. Each vial contains at least 1x10^6 cells per ml and is delivered frozen.Cells are negative for bacteria, yeast, fungi, and mycoplasma and are characterized by immunofluorescent staining with antibodies to α-smooth muscle actin. Cells can be expanded on a multiwell culture plate ready for experiments under the cell culture conditions specified by Gentaur.Repeated freezing and thawing of cells is not recommended.Standard biochemical procedures performed with smooth muscle cell cultures include the assays of cell to cell interaction, PCR, Western blotting, immunoprecipitation, immunofluorescent staining, immunofluorescent flow cytometry or generating cell derivatives for desired research applications. |
Primary Caprine Pulmonary Fibroblasts (PF) |
CSI034Cp01 |
Cloud-Clone |
5X10^5 |
EUR 950 |
|
Human Pulmonary Artery Endothelial Cells |
ABC-TC3774 |
AcceGen |
1 vial |
Ask for price |
|
Description: Human Pulmonary Artery Endothelial Cells (HPAEC), when grown in LIVas Medium, provide an ideal low-serum culture model, with or without human VEGF, for the study of angiogenesis, atherosclerosis or vascular biology.Cell Features:HUVEC are isolated from human umbilical cords, cultured on plastic and cryopreserved as primary cells.HAoEC and HUVEC 10-Donor Pool are isolated from human aorta or umbilical cord, cultured on plastic and cryopreserved as secondary cells.HPAEC are isolated from human pulmonary artery, cultured on plastic and cryopreserved as secondary cells.HCAEC are isolated from human coronary arteries, cultured on plastic and cryopreserved as tertiary cells.Human endothelial cells can be grown in low serum (2%) medium without phenol red or antimicrobials when cultured in VascuLife medium.Culture human endothelial cells with or without VEGF. human endothelial cells are extensively tested to meet quality standards and exhibit optimal performance.Gentaur guarantees performance and quality. |
Porcine Pulmonary Vein Endothelial Cells |
ABC-TC4037 |
AcceGen |
1 vial |
Ask for price |
|
Description: Porcine Pulmonary Vein Endothelial Cells are derived from healthly porcinine pulmonary vein tissue. Porcine Pulmonary Vein Endothelial Cells are grown in T25 tissue culture flasks pre-coated with gelatin-based solution for 0.5 hour and incubated in Gentaur's Culture Complete Growth Medium generally for 3-7 days. Cultures are then expanded. Prior to shipping, cells are detached from flasks and immediately cryo-preserved in vials. Each vial contains at least 1x10^6 cells per ml and are delivered frozen.Porcine Pulmonary Vein Endothelial Cells can be used in assays of cell to cell adhesion, migration, vascular tube formation, or transendothelial resistance (TER). Standard biochemical procedures performed with endothelial cell cultures include RT-PCR, Western blotting, immunoprecipitation, immunofluorescent staining or immunofluorescent flow cytometry or generating cell derivatives for desired research applications. |
Human Pulmonary Artery Endothelial Cells |
ABC-TC4046 |
AcceGen |
1 vial |
Ask for price |
|
Description: Cardiac Endothelial Cells include cells isolated from the aorta (HAEC), coronary artery (HCAEC), pulmonary artery (HPAEC), iliac artery (HIAEC), and microvascular cardiac cells (HMVEC-C). Cells are isolated from normal donors. |
Rat Pulmonary Aorta Smooth Muscle Cells |
CP-R010 |
Elabscience Biotech |
5×105 cells/vial |
EUR 610 |
|
Description: Rat |
Human Pulmonary Alveolar Epithelial Cells |
ABC-TC3770 |
AcceGen |
1 vial |
Ask for price |
|
Description: Pulmonary alveolar epithelial cells (PAEpiC) are comprised of alveolar type I and type II epithelial cells, line more than 99% of the internal surface area of the lung. Type I cells are large squamous cells whose thin cytoplasmic extensions cover 95% of the internal surface area. They contain aquaporins and exhibit the highest osmotic water permeability of among all mammalian cells. Type II cells, which cover 2-5% of the surface area, produce, secrete, and recycle pulmonary surfactant. The currently accepted hypothesis is that Type II cells maintain pulmonary fluid homeostasis by regulating active Na+ transport in the lungs, whereas Type I cells are "inert" cells that provide solely a barrier function, rather than having active functions. Recent study indicates that Type I cells are also important in regulating ion and fluid transport. HPAEpiC from Gentaur Research Laboratories are isolated from human lung tissue. HPAEpiC are cryopreserved at primary culture and shipped with dry ice. Each vial contains 1 x 10^6 cells in 1 ml volume. HPAEpiC are characterized by immunofluorescent method with antibodies CK-18, -19, and vimentin. HPAEpiC are negative for HIV-1, HBV, HCV, mycoplasma, bacteria, yeast and fungi. HPAEpiC are guaranteed to further culture at the conditions provided by Gentaur Research Laboratories. However, this cell type is not recommended for expanding or long term cultures since the cells would differentiate into type I alveolar epithelial cells immediately after plating and type I alveolar epithelial cells do not proliferate in culture. |
Bovine Pulmonary Artery Endothelial Cells |
ABC-TC3133 |
AcceGen |
1 vial |
Ask for price |
|
Description: Bovine large artery endothelial cells are derived from the arteries of USDA-inspected cattle. They are cryopreserved at second passage (BCAEC at third passage) and can be cultured and propagated at least 16 population doublings. |
Bovine Pulmonary Artery Endothelial Cells |
cAP-b0002 |
Angio Proteomie |
1Frozen Vial |
EUR 742.5 |
Bovine Pulmonary Artery Endothelial Cells |
B1020 |
Alphabioregen |
1ml frozen Vial |
EUR 0.2 |
Rat Pulmonary Artery Smooth Muscle Cells |
ABC-TC4203 |
AcceGen |
1 vial |
Ask for price |
|
Description: Rat Pulmonary Artery Smooth Muscle Cells from Gentaur are isolated from tissue of Sprague-Dawley Rats. Rat Pulmonary Artery Smooth Muscle Cells are grown in T75 tissue culture flasks pre-coated with gelatin-based coating solution for 0.5 hour and incubated in Gentaur's Cell Culture Medium for 3-7 days. Cultures are then expanded. Prior to shipping, cells are detached from flasks and immediately cryo-preserved in vials. Each vial contains at least 1x10^6 cells per ml and is delivered frozen.Cells are negative for bacteria, yeast, fungi, and mycoplasma and are characterized by immunofluorescent staining with antibodies to α-smooth muscle actin. Cells can be expanded on a multiwell culture plate ready for experiments under the cell culture conditions specified by Gentaur.Repeated freezing and thawing of cells is not recommended.Standard biochemical procedures performed with smooth muscle cell cultures include the assays of cell to cell interaction, PCR, Western blotting, immunoprecipitation, immunofluorescent staining, immunofluorescent flow cytometry or generating cell derivatives for desired research applications. |
Porcine Pulmonary Artery Endothelial Cells |
ABC-TC4035 |
AcceGen |
1 vial |
Ask for price |
|
Description: Porcine Pulmonary Artery Endothelial Cells are derived from healthly porcinine pulmonary vascular tissue. Porcine Pulmonary Artery Endothelial Cells are grown in T25 tissue culture flasks pre-coated with gelatin-based solution for 0.5 hour and incubated in Gentaur's Culture Complete Growth Medium generally for 3-7 days. Cultures are then expanded. Prior to shipping, cells are detached from flasks and immediately cryo-preserved in vials. Each vial contains at least 1x10^6 cells per ml and are delivered frozen.Porcine Pulmonary Artery Endothelial Cells can be used in assays of cell to cell adhesion, migration, vascular tube formation, or transendothelial resistance (TER). Standard biochemical procedures performed with endothelial cell cultures include RT-PCR, Western blotting, immunoprecipitation, immunofluorescent staining or immunofluorescent flow cytometry or generating cell derivatives for desired research applications. |
Human Pulmonary Artery Smooth Muscle Cells |
ABC-TC3775 |
AcceGen |
1 vial |
Ask for price |
|
Description: Human Pulmonary Artery Smooth Muscle Cells (HPASMC), when grown in LIVas SMC Medium, provide an ideal culture model for the study of angiogenesis, atherosclerosis, diabetes or vascular/pulmonary biology.Cell Features:HSMC are cryopreserved as secondary cells, e.g. cells are isolated from the stated tissue and expanded in culture vessels twice before cryopreservation.HAoSMC are isolated from human aorta (ascending and/or descending).HPASMC are isolated from human pulmonary artery.HCASMC are isolated from human coronary arteries.HLMSC are isolated from the lobes of the lungs.HBTSMC are isolated from the trachea and primary bronchi.HSMC can be grown without phenol red or antimicrobials when cultured in VascuLife SMC Medium.HSMC are extensively tested to meet quality standards and exhibit optimal performance.Gentaur guarantees performance and quality. |
Rabbit Pulmonary Aorta Smooth Muscle Cells |
CP-Rb009 |
Elabscience Biotech |
5×105 cells/vial |
EUR 640 |
|
Description: Rabbit |
Human Pulmonary Artery Smooth Muscle Cells |
CSC-7718W |
Creative Bioarray |
One Frozen vial |
Ask for price |
Human Pulmonary Artery Smooth Muscle Cells |
cAP-0101 |
Angio Proteomie |
1Frozen Vial |
EUR 594 |
Pulmonary sarcomatoid carcinoma Tissue block |
55 |
BioCoreUSA |
1 unit |
Ask for price |
Pulmonary surfactant-associated protein B |
AP79146 |
SAB |
1mg |
EUR 2640 |
|
Pulmonary surfactant-associated protein C |
AP79147 |
SAB |
1mg |
EUR 2640 |
|
Pulmonary surfactant-associated protein B |
AP79756 |
SAB |
1mg |
EUR 2640 |
|
Pulmonary surfactant-associated protein C |
AP86782 |
SAB |
1mg |
EUR 2640 |
|
Pulmonary surfactant-associated protein B |
AP86797 |
SAB |
1mg |
EUR 2640 |
|
Pulmonary surfactant-associated protein B |
AP86911 |
SAB |
1mg |
EUR 2640 |
|
Pulmonary surfactant-associated protein C |
AP86912 |
SAB |
1mg |
EUR 2640 |
|
Pulmonary surfactant-associated protein B |
AP87084 |
SAB |
1mg |
EUR 2640 |
|
Pulmonary surfactant-associated protein C |
AP87101 |
SAB |
1mg |
EUR 2640 |
|
Pulmonary surfactant-associated protein B |
AP87203 |
SAB |
1mg |
EUR 2640 |
|
Pulmonary surfactant-associated protein C |
AP87303 |
SAB |
1mg |
EUR 2640 |
|
Pulmonary surfactant-associated protein C |
AP87462 |
SAB |
1mg |
EUR 2640 |
|
Pulmonary surfactant-associated protein A1 |
AP87589 |
SAB |
1mg |
EUR 2640 |
|
Pulmonary surfactant-associated protein D |
AP87590 |
SAB |
1mg |
EUR 2640 |
|
Pulmonary surfactant-associated protein D |
AP87783 |
SAB |
1mg |
EUR 2640 |
|
Pulmonary surfactant-associated protein A |
AP87820 |
SAB |
1mg |
EUR 2640 |
|
Pulmonary surfactant-associated protein D |
AP88214 |
SAB |
1mg |
EUR 2640 |
|
Pulmonary surfactant-associated protein A |
AP88233 |
SAB |
1mg |
EUR 2640 |
|
Pulmonary surfactant-associated protein A |
AP88247 |
SAB |
1mg |
EUR 2640 |
|
Pulmonary surfactant-associated protein A |
AP88313 |
SAB |
1mg |
EUR 2640 |
|
Pulmonary surfactant-associated protein A |
AP88448 |
SAB |
1mg |
EUR 2640 |
|
Pulmonary surfactant-associated protein D |
AP78765 |
SAB |
1mg |
EUR 2640 |
|
Pulmonary surfactant-associated protein D |
AP78766 |
SAB |
1mg |
EUR 2640 |
|
Pulmonary interstitial fibrosis tissue array |
LC561 |
TissueArray |
each |
EUR 270 |
Description: Pulmonary interstitial fibrosis tissue array, 28 cases/56 cores |
C57BL/6 Mouse Pulmonary Artery Fibroblasts |
ABC-TC3234 |
AcceGen |
1 vial |
Ask for price |
|
Description: C57BL/6 Mouse Primary Pulmonary Artery Fibroblasts from Gentaur are isolated from tissue of pathogen-free laboratory mice. Mouse Primary Pulmonary Artery Fibroblasts are grown in T25 tissue culture flasks pre-coated with gelatin-based solution for 0.5 hour and incubated in Gentaur Culture Complete Growth Medium generally for 3-7 days. Cultures are then expanded. Prior to shipping, cells are detached from flasks and immediately cryo-preserved in vials. Each vial contains at least 1x10^6 cells per ml and is delivered frozen.Mouse Primary Pulmonary Artery Fibroblasts are negative for bacteria, yeast, fungi, and mycoplasma. Cells are tested for expression of marker using the antibody of anti-FSP1/S100A4 by immunofluorescence staining. Cells can be expanded for 2-4 passages at a split ratio of 1:2 under the cell culture conditions specified by Gentaur. Repeated freezing and thawing of cells is not recommended.Standard biochemical procedures performed with cell cultures include the assay of cell to cell interaction, RT-PCR, Western blotting, immunoprecipitation, immunofluorescent staining, flow cytometry or generating cell derivatives for desired research applications. |
Canine Pulmonary Artery Smooth Muscle Cells |
ABC-TC3267 |
AcceGen |
1 vial |
Ask for price |
|
Description: Canine Pulmonary Artery Smooth Muscle Cells (CnPASMC) are derived from the tunica intima and tunica media of canine pulmonary arteries and are cryopreserved at second passage. CnAOEC can be passaged at least 16 population doublings. |
Bovine Pulmonary Artery Smooth Muscle Cells |
ABC-TC3134 |
AcceGen |
1 vial |
Ask for price |
|
Description: Bovine large artery smooth muscle cells are derived from tunica intima and tunica media of healthy, fibrous, plaque-free bovine large arteries. They are cryopreserved at second passage and can be cultured and propagated at least 16 population doublings. |
Single Donor Human Pulmonary Fibrosis Serum |
ISERSPF |
Innovative research |
each |
EUR 209 |
|
Description: Single Donor Human Pulmonary Fibrosis Serum |
Human Pulmonary Artery Adventitia Fibroblasts |
ABC-TC3773 |
AcceGen |
1 vial |
Ask for price |
|
Description: Fibroblasts are mesenchymal cells which derived from the embryonic mesoderm. They have been extensively used for a wide range of cellular and molecular studies. This is mainly because they are one of easiest types of cells to grow in culture, and their durability makes them amenable to a wide variety of manipulations ranging from studies employing gene transfection to microinjection. There is good evidence that fibroblasts in different parts of the body are intrinsically different. The pulmonary arterial vesculature responds to various insults with a characteristic pattern of remodeling that includes an increase in connective tissue in the medial layer of the vessel wall. One of the pathogenetic mechanisms involved is the functional derangements of vascular fibroblasts. Their proliferative response contributes to the adventitial thickening observed during the development of hypoxia-induced pulmonary hypertension. HPAAF from Gentaur Research Laboratories are isolated from human pulmonary artery. HPAAF are cryopreserved at passage one and delivered frozen. Each vial contains 5×10^5 cells in 1 ml volume. HPAAF are characterized by spindle morphology and by immunofluorescent method with antibody to fibronectin. HPAAF are negative for HIV-1, HBV, HCV, mycoplasma, bacteria, yeast and fungi. HPAAF are guaranteed to further expand for 15 population doublings at the condition provided by Gentaur Research Laboratories. |
Human Pulmonary Artery Adventitia Fibroblasts |
CSC-C4028X |
Creative Bioarray |
One Frozen vial |
Ask for price |
Rat Pulmonary Microvascular Endothelial Cells |
cAP-r0004 |
Angio Proteomie |
1Frozen Vial |
EUR 544.5 |
S-adenosylmethionine ELISA kit for plasma, serum, or tissue/cell homogenate samples |
IK00201s |
Arthus |
96 tests |
EUR 699 |
Description: S-adenosylmethionine ELISA kit for plasma, serum, or tissue/cell homogenate samples |
Porcine Pulmonary Artery Smooth Muscle Cells |
ABC-TC4036 |
AcceGen |
1 vial |
Ask for price |
|
Description: Porcine large artery smooth muscle cells are derived from tunica intima and tunica media of healthy, fibrous plaque-free porcine arteries. They are cryopreserved at first passage (PCASMC at second passage) and can be cultured and propagated at least 16 passages. |
Lewis Rat Pulmonary Artery Endothelial Cells |
ABC-HP025X |
AcceGen |
1 vial |
Ask for price |
|
Description: Lewis Rat Pulmonary Artery Endothelial Cells from are isolated from pulmonary artery of 6-8 week old Lewis rat. Lewis Rat Pulmonary Artery Endothelial Cells are cryopreserved at passage 3 and delivered frozen. |
Immortalized Human Pulmonary Fibroblasts Cells |
T0490 |
ABM |
1x106 cells / 1.0 ml |
EUR 2750 |
Immortalized Human Pulmonary Fibroblasts Cells |
CSC-I9127L |
Creative Bioarray |
One Frozen vial |
Ask for price |
Frozen Tissue Section - Pulmonary embolism: Lung |
T1236152Ld-5 |
Biochain |
5 slides |
EUR 523 |
Human Pulmonary Small Airway Epithelial Cells |
cAP-0122 |
Angio Proteomie |
1Frozen Vial |
EUR 594 |
Human Pulmonary Microvascular Endothelial Cells |
ABC-TC3779 |
AcceGen |
1 vial |
Ask for price |
|
Description: Primary Human Lung Microvascular Endothelial Cells(Human Pulmonary Microvascular Endothelial Cells) are initiated from normal human peripheral lung tissue.These cells were originated using Complete Serum-Free Medium Kit With AcceSup™, are available at <12 Cumulative Population Doublings (CPD) in vitro [Passage 3] and were cryopreserved in aliquots of ~1.5×10^6 cells. This vial will initiate a Passage 4 cell culture in a 75cm1 flask. |
Human Pulmonary Microvascular Endothelial Cells |
cAP-0032 |
Angio Proteomie |
1Frozen Vial |
EUR 643.5 |
Mouse Pulmonary Microvascular Endothelial Cells |
cAP-m0003 |
Angio Proteomie |
1Frozen Vial |
EUR 594 |
Human Pulmonary Microvascular Endothelial Cells |
ALHE44 |
Alphabioregen |
1ml frozen Vial |
EUR 620 |
S-adenosylhomocysteine ELISA kit for plasma, serum, or tissue/cell homogenate samples |
IK00301s |
Arthus |
96 tests |
EUR 1349 |
Description: S-adenosylhomocysteine ELISA kit for plasma, serum, or tissue/cell homogenate samples |
BKS DB Mouse Pulmonary Vein Endothelial Cells |
ABC-TC5492 |
AcceGen |
1 vial |
Ask for price |
|
Description: BKS db Mouse Pulmonary Vein Endothelial Cells are isolated from the pulmonary vein of Mice homozygous for the diabetes spontaneous mutation (Lepr/db) manifest morbid obesity, chronic hyperglycemia, pancreatic beta cell atrophy and become hypoRIemic. BKS db Mouse Pulmonary Vein Endothelial Cells are grown in T25 tissue culture flasks pre-coated with gelatin-based solution for 2 min and incubated in Gentaur's Culture Complete Growth Medium generally for 3-7 days. Cultures are then expanded. Prior to shipping, cells at passage 3 are detached from flasks and immediately cryopreserved in vials. Each vial contains at least 0.5×106 cells per ml. The method we use to isolate primary endothelial cells was developed based on a combination of established and our proprietary methods. These cells are pre-coated with PECAM-1 antibody, following the application of magnetic beads pre-coated with secondary antibody. |
Rat Primary Pulmonary Artery Endothelial Cells |
T4810 |
ABM |
5x10^5 cells / 1.0 ml |
Ask for price |
Human Primary Pulmonary Vein Endothelial Cells |
T5411 |
ABM |
5x10^5 cells / 1.0 ml |
EUR 975 |
Custom Testing of Samples for Antibodies (IgA/IgG/IgM) to Mumps/Parotitis Virus vaccines bVaccine ELISAs for human diseases ELISA |
520-100-CUX |
Alpha Diagnostics |
Custom |
Ask for price |
Paraffin Tissue Section - Pulmonary embolism: Lung |
T2236152Ld-5 |
Biochain |
5 slides |
EUR 523 |
BALB/c Mouse Pulmonary Vein Endothelial Cells |
ABC-TC3099 |
AcceGen |
1 vial |
Ask for price |
|
Description: BALB/c Mouse Pulmonary Vein Endothelial Cells from Gentaur are isolated from tissue of pathogen-free laboratory mice. Mouse Pulmonary Vein Endothelial Cells are grown in T25 tissue culture flasks pre-coated with gelatin-based solution for 0.5 hour and incubated in Gentaur's Culture Complete Growth Medium generally for 3-7 days. Cultures are then expanded. Prior to shipping, cells are detached from flasks and immediately cryo-preserved in vials. Each vial contains at least 1x10^6 cells per ml and are delivered frozen.Mouse Pulmonary Vein Endothelial Cells can be used in assays of cell to cell adhesion, migration, vascular tube formation, or transendothelial resistance (TER). Standard biochemical procedures performed with endothelial cell cultures include RT-PCR, Western blotting, immunoprecipitation, immunofluorescent staining or immunofluorescent flow cytometry or generating cell derivatives for desired research applications. |
Porcine Pulmonary Microvascular Endothelial Cells |
cAP-p0002 |
Angio Proteomie |
1Frozen Vial |
EUR 643.5 |
Human Primary Pulmonary Artery Endothelial Cells |
T4040 |
ABM |
5x10^5 cells / 1.0 ml |
Ask for price |
Mouse Primary Pulmonary Artery Endothelial Cells |
T4510 |
ABM |
5x10^5 cells / 1.0 ml |
Ask for price |
Human Pulmonary Artery Endothelial Cells (HPuAECs) |
cAP-0120 |
Angio Proteomie |
1Frozen Vial |
EUR 643.5 |
Human Pulmonary Lobar Bronchial Epithelial Cells |
cAP-0123 |
Angio Proteomie |
1Frozen Vial |
EUR 594 |
C57BL/6 Mouse Pulmonary Vein Endothelial Cells |
ABC-TC3236 |
AcceGen |
1 vial |
Ask for price |
|
Description: C57BL/6 Mouse Pulmonary Vein Endothelial Cells from Gentaur are isolated from tissue of pathogen-free laboratory mice. Mouse Pulmonary Vein Endothelial Cells are grown in T25 tissue culture flasks pre-coated with gelatin-based solution for 0.5 hour and incubated in Gentaur's Culture Complete Growth Medium generally for 3-7 days. Cultures are then expanded. Prior to shipping, cells are detached from flasks and immediately cryo-preserved in vials. Each vial contains at least 1x10^6 cells per ml and are delivered frozen.Mouse Pulmonary Vein Endothelial Cells can be used in assays of cell to cell adhesion, migration, vascular tube formation, or transendothelial resistance (TER). Standard biochemical procedures performed with endothelial cell cultures include RT-PCR, Western blotting, immunoprecipitation, immunofluorescent staining or immunofluorescent flow cytometry or generating cell derivatives for desired research applications. |
HighQC™ Human Pulmonary Mesenchymal Stem Cell |
ABC-TC3778 |
AcceGen |
1 vial |
Ask for price |
Description: Mesenchymal stem cells (MSC) are a well-characterized population of adult stem cells. MSC have the potential to develop into mature cells that produce fat, cartilage, bone, tendons, and muscle. This property, in combination with MSC's developmental plasticity, has generated tremendous interest in the potential use of MSC to replace damaged tissues. Fetal lung has been identified as a rich source of MSCs and has been reported that MSCs can differentiate into neural cells in addition to their mesenchymal differentiation potential; enhance the engraftment of human umbilical cord blood-derived CD34 hematopoietic cells in nonobese diabetic-severe combined immunodeficiency mice. Flow cytometric analysis showed that fetal lung MSCs expressed CD13, CD29, CD44, CD90, CD105, CD166, and HLA-ABC.HPMSC from Gentaur Research Laboratories are isolated from lung tissue. HPMSC are cryopreserved at passage one culture and delivered frozen. Each vial contains andgt;5 x 10^5 cells in 1 ml volume. HPMSC are characterized by immunofluorescent method with antibodies to CD73, CD90 and CD105. HPMSC are negative for HIV-1, HBV, HCV, mycoplasma, bacteria, yeast and fungi. HPMSC are guaranteed to further culture at the conditions provided by Gentaur Research Laboratories. |
BKS DB Mouse Pulmonary Artery Endothelial Cells |
ABC-TC5491 |
AcceGen |
1 vial |
Ask for price |
|
Description: BKS db Mouse Pulmonary Artery Endothelial Cells are isolated from the pulmonary artery of Mice homozygous for the diabetes spontaneous mutation (Lepr/db) manifest morbid obesity, chronic hyperglycemia, pancreatic beta cell atrophy and become hypoRIemic. BKS db Mouse Pulmonary Artery Endothelial Cells are grown in T25 tissue culture flasks pre-coated with gelatin-based solution for 2 min and incubated in Gentaur's Culture Complete Growth Medium generally for 3-7 days. Cultures are then expanded. Prior to shipping, cells at passage 3 are detached from flasks and immediately cryopreserved in vials. Each vial contains at least 0.5×106 cells per ml. The method we use to isolate primary endothelial cells was developed based on a combination of established and our proprietary methods. These cells are pre-coated with PECAM-1 antibody, following the application of magnetic beads pre-coated with secondary antibody. |
BALB/c Mouse Pulmonary Artery Endothelial Cells |
ABC-TC3098 |
AcceGen |
1 vial |
Ask for price |
|
Description: BALB/c Mouse Pulmonary Artery Endothelial Cells from Gentaur are isolated from tissue of pathogen-free laboratory mice. Mouse Pulmonary Artery Endothelial Cells are grown in T25 tissue culture flasks pre-coated with gelatin-based solution for 0.5 hour and incubated in Gentaur's Culture Complete Growth Medium generally for 3-7 days. Cultures are then expanded. Prior to shipping, cells are detached from flasks and immediately cryo-preserved in vials. Each vial contains at least 1x10^6 cells per ml and are delivered frozen.Mouse Pulmonary Artery Endothelial Cells can be used in assays of cell to cell adhesion, migration, vascular tube formation, or transendothelial resistance (TER). Standard biochemical procedures performed with endothelial cell cultures include RT-PCR, Western blotting, immunoprecipitation, immunofluorescent staining or immunofluorescent flow cytometry or generating cell derivatives for desired research applications. |
Rat Primary Pulmonary Artery Smooth Muscle Cells |
T4821 |
ABM |
5x10^5 cells / 1.0 ml |
Ask for price |
GFP-Human Pulmonary Artery Smooth Muscle Cells |
cAP-0101GFP |
Angio Proteomie |
1Frozen Vial |
EUR 782.1 |
Rabbit Pulmonary Artery Fibroblast Complete Medium |
CM-Rb010-100mL |
Elabscience Biotech |
100 mL |
EUR 75 |
Description: Complete Growth Medium |
Rabbit Pulmonary Artery Fibroblast Complete Medium |
CM-Rb010-125mL4 |
Elabscience Biotech |
125 mL×4 |
EUR 338 |
Description: Complete Growth Medium |
Rabbit Pulmonary Artery Fibroblast Complete Medium |
CM-Rb010 |
Elabscience Biotech |
100mL |
EUR 75 |
|
Description: Primary cells complete growth medium |
C57BL/6 Mouse Pulmonary Artery Endothelial Cells |
ABC-TC3233 |
AcceGen |
1 vial |
Ask for price |
|
Description: C57BL/6 Mouse Pulmonary Artery Endothelial Cells from Gentaur are isolated from tissue of pathogen-free laboratory mice. Mouse Pulmonary Artery Endothelial Cells are grown in T25 tissue culture flasks pre-coated with gelatin-based solution for 0.5 hour and incubated in Gentaur's Culture Complete Growth Medium generally for 3-7 days. Cultures are then expanded. Prior to shipping, cells are detached from flasks and immediately cryo-preserved in vials. Each vial contains at least 1x10^6 cells per ml and are delivered frozen.Mouse Pulmonary Artery Endothelial Cells can be used in assays of cell to cell adhesion, migration, vascular tube formation, or transendothelial resistance (TER). Standard biochemical procedures performed with endothelial cell cultures include RT-PCR, Western blotting, immunoprecipitation, immunofluorescent staining or immunofluorescent flow cytometry or generating cell derivatives for desired research applications. |
Innovative Grade US Origin Bovine Valve Pulmonary |
IGBOVLPMF |
Innovative research |
each |
EUR 133 |
|
Description: Innovative Grade US Origin Bovine Valve Pulmonary |
Innovative Grade US Origin Bovine Valve Pulmonary |
IGBOVLPMP |
Innovative research |
each |
EUR 210 |
|
Description: Innovative Grade US Origin Bovine Valve Pulmonary |
Innovative Grade US Origin Bovine Valve Pulmonary |
IGBOVLPMS |
Innovative research |
each |
EUR 210 |
|
Description: Innovative Grade US Origin Bovine Valve Pulmonary |
Innovative Grade US Origin Bovine Valve Pulmonary |
IGBOVLPMZ |
Innovative research |
each |
EUR 133 |
|
Description: Innovative Grade US Origin Bovine Valve Pulmonary |
C57BL/6 Mouse Pulmonary Vein Smooth Muscle Cells |
ABC-TC3237 |
AcceGen |
1 vial |
Ask for price |
|
Description: Mouse Pulmonary Vein Vascular Smooth Muscle Cells from Gentaur are isolated from tissue of pathogen-free laboratory mice. Mouse Pulmonary Vein Vascular Smooth Muscle Cells are grown in T25 tissue culture flasks pre-coated with gelatin-based solution for 0.5 hour and incubated in Gentaur's Cell Culture Medium generally for 3-7 days. Cultures are then expanded. Prior to shipping, cells are detached from flasks and immediately cryo-preserved in vials. Each vial contains at least 1x10^6 cells per ml and is delivered frozen.Mouse Pulmonary Vein Vascular Smooth Muscle Cells are characterized by immunofluorescent cell staining with antibodies of α-smooth muscle actin and are negative for bacteria, yeast, fungi, and mycoplasma.Cells can be expanded on a multiwell culture plate ready for experiments under the cell culture conditions specified by Gentaur.Repeated freezing and thawing of cells is not recommended.Standard biochemical procedures performed with cell cultures include RT-PCR, Western blotting, immunoprecipitation, immunofluorescent staining, flow cytometry or generating cell derivatives for desired research applications. |
Pulmonary Surfactant Associated Protein C Antibody |
20-abx110527 |
Abbexa |
-
Ask for price
-
Ask for price
-
Ask for price
-
Ask for price
-
Ask for price
|
- 100 ug
- 1 mg
- 200 ug
- 20 ug
- 50 ug
|
|
Pulmonary Surfactant Associated Protein B Antibody |
20-abx110638 |
Abbexa |
-
Ask for price
-
Ask for price
-
Ask for price
-
Ask for price
-
Ask for price
|
- 100 ug
- 1 mg
- 200 ug
- 20 ug
- 50 ug
|
|
Human Pulmonary Bronchial/Tracheal Epithelial Cells |
cAP-0124 |
Angio Proteomie |
1Frozen Vial |
EUR 594 |
Polycystic ovary syndrome (PCOS) is likely one of the commonest ovarian illnesses amongst ladies of reproductive age. The reproductive and metabolic traits of PCOS are underpinned by adipocyte dysfunction, particularly diminished adiponectin secretion. Based mostly on proof that niacin stimulates adiponectin secretion, this examine evaluated the results of niacin on adiponectin concentrations and reproductive traits in a rat mannequin of PCOS. PCOS was induced by single injection of 4mg kg-1 oestradiol valerate (i.m.), and PCOS teams have been administered orally with saline or niacin (10 or 25mg kg-1) every day for 30 days after PCOS induction.