| 名稱 | LMNA-NTRK1/BaF3 |
| 型號(hào) | CBP73202 |
| 報(bào)價(jià) | ![]() |
| 特點(diǎn) | LMNA-NTRK1/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 > CBP73202LMNA-NTRK1/BaF3
- 詳細(xì)內(nèi)容
CBP73202 | |
| I. Introduction | |
Cell Line Name: | LMNA-NTRK1/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: | Anti-proliferation assay and PD assay |
Freeze Medium: | 90% FBS+10% DMSO |
Complete Culture Medium: | RPMI-1640+10%FBS+2ug/ml puromycin |
Mycoplasma Status: | Negative |
| II.Background | |
NTRK1 rearrangements involve the kinase domain of the NTRK1 gene which includes 17 exons located on chromosome 1q21-22 (Alberti et al. 2003). The frequency of NTRK1 fusions in patients with adenocarcinoma histology is 3.3% of cases (3 out of 91 patients; Vaishnavi et al. 2013). a In preclinical studies, cell lines expressing MPRIP-NTRK1 or CD74-NTRK1 were inhibited by ARRY-470, a TRKA/B/C inhibitor (Vaishnavi et al. 2013). b In preclinical studies, cell lines expressing MPRIP-NTRK1 or CD74-NTRK1 were inhibited by lestaurtinib, a FLT3/TRKA inhibitor (Vaishnavi et al. 2013). c A patient with non-small cell lung cancer harboring an MPRIP-NTRK1 fusion mutation was treated with crizotinib, which has activity against TRKA in addition to ALK, MET and ROS1 (Vaishnavi et al. 2013). The patient demonstrated a small radiographic decrease in tumor size but experienced disease progression after three months (Vaishnavi et al. 2013) | |
| III. Representative Data | |
1. WB of LMNA-NTRK1/BaF3 expression | |
| |
2. Sanger of LMNA-NTRK1/BaF3 expression
Figure 2. Sanger Sequencing of LMNA-NTRK1/BaF3 | |
3. Anti-proliferation assay | |
| |
Figure 3. Anti-proliferation assay of two reference compounds on the LMNA-NTRK1/BaF3 Stable Cell Line | |







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