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MORC4（p.S734A, c.2200T>G） Point Mutation in SW480 Cell Line
Cat.No.:
EDC90606
Species:
Human
Cell Name:
SW480
Gene:
MORC4
Gene ID:
79710
Size:
1×10⁶cells
The MORC4（p.S734A, c.2200T>G） Point Mutation in SW480 Cell Line generated using a well-established RNA interference-based stable transfection method. The cell line has undergone rigorous quality control, including STR authentication and mycoplasma testing, ensuring a stable and reliable model suitable for long-term culture.
| Cat.No. | EDC90606 |
|---|---|
| Product Name | MORC4（p.S734A, c.2200T>G） Point Mutation in SW480 Cell Line |
| Cell Line | SW480 |
| Gene | |
| NCBI Gene ID | |
| Mutation Site | p.S734A, c.2200T>G |
| Morphology | Adherent |
| Passage Ratio | 1 : 3，1-2 days |
| Complete Culture Medium | DMEM + 10% FBS |
| Freezing Medium | 95% Complete medium + 5% DMSO |
* For research use only. Not intended for use in humans or animals, including clinical, therapeutic, or diagnostic purposes.
| Loci | STR Info (Sample Cell) Sample Cell Line: SW480 | STR Info (Cell bank) Cell Line: SW480 | ||
| Allele1 | Allele2 | Allele1 | Allele2 | |
| Amelogenin | X | X | ||
| CSF1PO | 13 | 14 | 13 | 14 |
| D2S1338 | 17 | 24 | 17 | 24 |
| D3S1358 | 15 | 15 | ||
| D5S818 | 13 | 13 | ||
| D7S820 | 8 | 8 | ||
| D8S1179 | 13 | 13 | ||
| D13S317 | 12 | 12 | ||
| D16S539 | 13 | 13 | ||
| D18S51 | 13 | 13 | ||
| D19S433 | 13 | 13 | ||
| D21S11 | 30 | 30.2 | 30 | 30.2 |
| FGA | 24 | 24 | ||
| Penta D | 9 | 15 | 9 | 15 |
| Penta E | 10 | 10 | ||
| TH01 | 8 | 8 | ||
| TPOX | 11 | 11 | ||
| vWA | 16 | 16 | ||
| D6S1043 | 11 | 12 | ||
| D12S391 | 17 | 17 | ||
| D2S441 | 10 | 15 | 10 | 15 |
* STR authentication data of this cell line matches with that of cell lines sourced from ATCC, DSMZ, JCRB, and RIKEN databases.
Conclusion: The STR identification of this cell is correct.
Conclusion: The STR identification of this cell is correct.
* Research Use Disclaimer: Content is generated from publicly available research data, bioinformatic resources, and computational analyses for research reference only.
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