| 名稱 | EGFR S768_V769delinsIL(S768I/V769L)/BaF3 |
| 型號(hào) | CBP73181 |
| 報(bào)價(jià) | ![]() |
| 特點(diǎn) | EGFR S768_V769delinsIL(S768I/V769L)/BaF3,母細(xì)胞:BaF3,凍存條件:90% FBS+10% DMSO |
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藥靶細(xì)胞株 > kinase激酶細(xì)胞株 > CBP73181EGFR S768_V769delinsIL(S768I/V769L)/BaF3
- 詳細(xì)內(nèi)容
| CBP73181 | |
| I. Introduction | |
Cell Line Name: | EGFR S768_V769delinsIL(S768I&V769L)/BaF3 |
Host Cell: | Ba/F3 |
| Stability: | 16 passages (in-house test, that not means the cell line will be instable beyond the passages we tested.) |
Application: | Useful for the study of enzyme kinetics, screening inhibitors, and selectivity profiling. |
Freeze Medium: | 90% FBS+10% DMSO |
Complete Culture Medium: | RPMI-1640+10%FBS+2ug/ml puromycin |
Mycoplasma Status: | Negative |
| II.Background | |
EGFR is the receptor for members of the EGF family and is a transmembrane glycoprotein that has tyrosine kinase activity. EGFR S768_V769delinsIL results in a deletion of two amino acids in the protein kinase domain of the Egfr protein from aa 768 to aa 769, combined with the insertion of an isoleucine (I) and a leucine (L) at the same site (UniProt.org). S768_V769delinsIL has been identified in the scientific literature (PMID: 17045698, PMID: 27304188), but has not been biochemically characterized and therefore, its effect on Egfr protein function is unknown (PubMed, Jul 2019). | |
| III. Representative Data | |
1. WB of EGFR S768_V769delinsIL(S768I&V769L)/BaF3
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2. Anti-proliferation assay | |





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