EGFR（p.C797S, c.2390G>C and p.Q787Q） Point Mutation in HCT 116 Cell Line
Cat.No.:
EDC03164
Species:
Human
Cell Name:
HCT 116
Gene:
EGFR
Gene ID:
1956
The EGFR（p.C797S, c.2390G>C and p.Q787Q） Point Mutation in HCT 116 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. | EDC03164 |
|---|---|
| Product Name | EGFR（p.C797S, c.2390G>C and p.Q787Q） Point Mutation in HCT 116 Cell Line |
| Cell Line | HCT 116 |
| Gene ID | |
| Mutation Site | p.C797S, c.2390G>C and p.Q787Q, c.2361G>A |
| Gene | EGFR |
| Morphology | Adherent |
| Passage Ratio | 1:5-1:4，2 days |
| Complete Culture Medium | McCoy's 5A + 10% FBS |
| Freezing Medium | 90% FBS/Complete medium + 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: HCT 116 | STR Info (Cell bank) Cell Line: HCT 116 | ||||||
| Allele1 | Allele2 | Allele3 | Allele4 | Allele1 | Allele2 | Allele3 | Allele4 | |
| Amelogenin | X | X | ||||||
| CSF1PO | 7 | 10 | 7 | 9 | 10 | 11 | ||
| D2S1338 | 16 | 16 | ||||||
| D3S1358 | 12 | 17 | 18 | 19 | 12 | 18 | 19 | |
| D5S818 | 10 | 11 | 10 | 11 | ||||
| D7S820 | 11 | 12 | 11 | 12 | ||||
| D8S1179 | 10 | 12 | 14 | 15 | 10 | 12 | 14 | 15 |
| D13S317 | 10 | 12 | 10 | 12 | ||||
| D16S539 | 11 | 13 | 11 | 12 | 13 | 14 | ||
| D18S51 | 16 | 17 | 16 | 17 | ||||
| D19S433 | 12 | 13 | 12 | |||||
| D21S11 | 29 | 30 | 29 | 30 | ||||
| FGA | 18 | 23 | 18 | 23 | ||||
| Penta D | 9 | 13 | 9 | 13 | ||||
| Penta E | 12 | 13 | 14 | 12 | 13 | 14 | ||
| TH01 | 8 | 9 | 8 | 9 | ||||
| TPOX | 8 | 8 | ||||||
| vWA | 17 | 21 | 22 | 23 | 17 | 21 | 22 | 23 |
| D6S1043 | 13 | |||||||
| D12S391 | 17 | 21 | 22 | |||||
| D2S441 | 11 | 12 | ||||||
* 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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EGFR（p.C797S, c.2389T>A and p.Q787Q） Point Mutation in HCT 116 Cell LineEGFR（p.C797S, c.2389T>A and p.Q787Q） Point Mutation in HCT 116 Cell Line
