| 名稱 | LMNA-NTRK1/BaF3 | 
| 型號 | CBP73202 | 
| 報價 | ![]()  | 
								
| 特點 | LMNA-NTRK1/BaF3,母細胞:BaF3,凍存條件:90% FBS+10% DMSO | 
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						藥靶細胞株 > kinase激酶細胞株  >  CBP73202LMNA-NTRK1/BaF3
            
              
					
				
				
						- 詳細內(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  | |
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2. Sanger of LMNA-NTRK1/BaF3 expression 
 Figure 2. Sanger Sequencing of LMNA-NTRK1/BaF3  | |
3. Anti-proliferation assay  | |
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Figure 3. Anti-proliferation assay of two reference compounds on the LMNA-NTRK1/BaF3 Stable Cell Line  | |







