Human Endometriotic Stromal Cells
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AcceGen provides high-quality Human Endometriotic Stromal Cells from Endometriosis Tissue, which are cryopreserved at passage 1 with 0.5 million cells in each vial. Human Endometriotic Stromal Cells express Vimentin and can be further expanded for 6-8 passages under the conditions suggested by AcceGen.
Species | Human |
Cat.No | ABC-TC069G |
Quality Control | All cells test negative for HIV-1, HBV, HCV, mycoplasma, bacteria, yeast, and fungi. |
Product Category | Primary Cells |
Size/Quantity | 1 vial |
Cell Type | Stromal Cell |
Shipping Info | Dry Ice |
Growth Conditions | 37 ℃, 5% CO2 |
Source Organ | Endometriosis Tissue |
Disease | Endometriosis |
Biosafety Level | 1 |
Storage | Liquid Nitrogen |
Product Type | Female Reproductive Cells |
When you publish your research, please cite our product as “AcceGen Biotech Cat.# XXX-0000”. In return, we’ll give you a $100 coupon. Simply click here and submit your paper’s PubMed ID (PMID).
For research use only
Human Endometriotic Stromal Cells are derived from the stromal tissue of endometriotic lesions. These cells are isolated from surgically obtained endometriotic tissue samples, ensuring high purity and viability for research applications.
These cells are extensively used in studies focusing on endometriosis pathogenesis, drug screening, and the development of novel therapeutic strategies. They are also valuable for investigating the cellular and molecular mechanisms underlying endometriotic lesion formation and progression.
Human Endometriotic Stromal Cells require a specialized growth medium designed for stromal cells, typically supplemented with fetal bovine serum, growth factors, and other essential nutrients. Cells should be cultured at 37°C in a humidified atmosphere with 5% CO2.
These cells exhibit fibroblast-like morphology and express specific markers such as vimentin, CD10, and estrogen receptors. They are also characterized by their ability to respond to hormonal stimuli, which is crucial for studying endometriosis.
When passaging these cells, it is important to avoid over-confluency, as it can affect their growth and viability. Typically, cells should be passaged at 70-80% confluency using standard trypsinization protocols. Ensuring gentle handling and using appropriate cell culture reagents will help maintain cell integrity and functionality.