HSPD1(p.K133E) Point Mutation in HeLa Cell Line
Cat.No.:
EDC03010
Species:
Human
Cell Name:
HeLa
Gene:
HSPD1
Gene ID:
3329
The HSPD1(p.K133E) Point Mutation in HeLa 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. | EDC03010 |
|---|---|
| Product Name | HSPD1(p.K133E) Point Mutation in HeLa Cell Line |
| Cell Line | HeLa |
| Gene | HSPD1 |
| Gene ID | |
| Mutation Site | p.K133E, c.397A>G |
| Morphology | Adherent |
| Passage Ratio | 1:5-1:4,2 days |
| Complete Culture Medium | MEM + 10% FBS |
| Freezing Medium | 70% Complete medium + 20% FBS + 10% 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: HeLa | STR Info (Cell bank) Cell Line: HeLa | ||
| Allele1 | Allele2 | Allele1 | Allele2 | |
| Amelogenin | X | X | ||
| CSF1PO | 9 | 10 | 9 | 10 |
| D1S1656 | 12 | 15 | 12 | 15 |
| D2S1338 | 17 | 17 | ||
| D3S1358 | 15 | 18 | 15 | 18 |
| D5S818 | 11 | 12 | 11 | 12 |
| D6S1043 | 18 | 18 | ||
| D7S820 | 8 | 12 | 8 | 12 |
| D8S1179 | 12 | 13 | 12 | 13 |
| D12S391 | 20 | 25 | 20 | 25 |
| D13S317 | 12 | 14 | 12 | 14 |
| D16S539 | 9 | 10 | 9 | 10 |
| D18S51 | 16 | 16 | ||
| D19S433 | 13 | 14 | 13 | 14 |
| D21S11 | 27 | 28 | 27 | 28 |
| FGA | 18 | 21 | 18 | 21 |
| Penta D | 8 | 15 | 8 | 15 |
| Penta E | 7 | 17 | 7 | 17 |
| TPOX | 8 | 12 | 8 | 12 |
| VWA | 16 | 18 | 16 | 18 |
* 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.