For research use only
| Cat No. | ABC-SC044G |
| Product Type | Animal Embryonic Stem Cells |
| Cell Type | Stem Cell |
| Species | Mouse |
| Growth Conditions | 37 ℃, 5% CO2 |
| Source Organ | Embryonic |
| Disease | Normal |
| Storage | Liquid Nitrogen |
Explore HighQC™ C57BL/6 Mouse Embryonic Stem Cells with GFP for visual tracking in developmental studies, gene function analysis, and transgenic modeling.
AcceGen’s HighQC™C57BL/6 Mouse ESCs/GFP are derived from the inner cell mass
of strain C57BL/6 Mouse blastocysts (at 3.5 dpc) and cultured on γ-ray irradiated
mouse embryonic fibroblasts as feeder cells in AcceGen’s Mouse ESC Growth Medium,
Cells have been transfected with a lentiviral construct with GFP.
| Product Code | HighQC™ C57BL/6 Mouse Embryonic Stem Cells with GFP, C57BL/6 mESCs GFP, B6 Mouse ES Cells GFP, GFP-labeled C57BL/6 ESCs, Green Fluorescent B6 ESCs |
| Species | Mouse |
| Cat.No | ABC-SC044G |
| Product Category | Stem Cells |
| Size/Quantity | 1 vial |
| Cell Type | Stem Cell |
| Growth Mode | Adherent |
| Shipping Info | Dry Ice |
| Growth Conditions | 37 ℃, 5% CO2 |
| Source Organ | Embryonic |
| Disease | Normal |
| Biosafety Level | 1 |
| Storage | Liquid Nitrogen |
| Product Type | Animal Embryonic Stem Cells |
| Quality Control | All cells test negative for mycoplasma, bacteria, yeast, and fungi. |
When you publish your research, please cite our product as “AcceGen Biotech Cat.# XXX-0000”. In return, we’ll give you a $200 coupon. Simply click here and submit your paper’s PubMed ID (PMID).
GFP expression in HighQC™ C57BL/6 Mouse Embryonic Stem Cells with GFP is driven by the cytomegalovirus (CMV) promoter. The GFP expression cassette was introduced by random genomic integration via electroporation, followed by hygromycin selection to establish a stable cell line.
GFP expression is stable during routine maintenance and expansion of the undifferentiated cells. However, GFP expression during differentiation may vary depending on the differentiated cell type and the activity of the CMV promoter, which can be influenced by lineage-specific regulatory mechanisms and transgene integration sites. Therefore, GFP expression should be evaluated in differentiated cells rather than assumed to remain unchanged.
For best results, GFP expression should be monitored at different stages of culture and differentiation using flow cytometry (FACS) or fluorescence microscopy.