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药靶细胞株 > kinase激酶细胞株 > CBP73200EML4-ALK V1 G1202R/BaF3

EML4-ALK V1 G1202R/BaF3
名称 EML4-ALK V1 G1202R/BaF3
型号 CBP73200
报价
特点 EML4-ALK V1 [G1202R]/BaF3,母细胞:BaF3,冻存条件:90% FBS+10% DMSO
  • 详细内容


CBP73200
I. Introduction

Cell Line Name:

EML4-ALK V1 [G1202R]/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

Mycoplasma Status:

Negative


II.Background
Approximately 3–7% of lung tumors harbor ALK fusions (Koivunen et al. 2008; Kwak et al. 2010; Shinmura et al. 2008; Soda et al. 2007; Takeuchi et al. 2008; Wong et al. 2009). ALK fusions are more commonly found in light smokers (< 10 pack years) and/or never-smokers (Inamura et al. 2009; Koivunen et al. 2008; Kwak et al. 2010; Soda et al. 2007; Wong et al. 2009). ALK fusions are also associated with younger age (Inamura et al. 2009; Kwak et al. 2010; Wong et al. 2009) and adenocarcinomas with acinar histology (Inamura et al. 2009; Wong et al. 2009) or signet-ring cells (Kwak et al. 2010). Clinically, the presence of EML4-ALK fusions is associated with EGFR tyrosine kinase inhibitor (TKI) resistance (Shaw et al. 2009).
Multiple different ALK rearrangements have been described in NSCLC. The majority of these ALK fusion variants are comprised of portions of the echinoderm microtubule-associated protein-like 4 (EML4) gene with the ALK gene. At least nine different EML4-ALK fusion variants have been identified in NSCLC (Figure 1; Choi et al. 2008; Horn and Pao 2009; Koivunen et al. 2008; Soda et al. 2007; Takeuchi et al. 2008; Takeuchi et al. 2009; Wong et al. 2009). In addition, non-EML4 fusion partners have also been identified, including KIF5B-ALK (Takeuchi et al. 2009) and TFG-ALK (Rikova et al. 2007). Clinically, the presence of an ALK rearrangement is detected by fluorescence in situ hybridization (FISH) with an ALK break apart probe. FISH testing is not able to discern which particular ALK fusion is found in a clinical sample.

III. Representative Data

1.WB of  EML4-ALK V1 G1202R/BaF3

CBP73200 WB.png

Figure 1. Protein Expression of ALK detected by antibody


2. Sanger Sequencing of EML4-ALK v1 Fusion


Figure 2. Sanger sequencing of EML4-ALK v1 Fusion


CBP73200 sanger2.png

Figure 3. Sanger sequencing of ALK v1 G1202R (c.3604G>A)


3. Anti-proliferation assay

CBP73200 fig.png


Figure 4. Anti-proliferation assay of three reference compounds on the EML4-ALK v1 [G1202R]/BaF3 Stable Cell Line.




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