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      當前位置:首頁 > 產品展示 > 藥靶細胞株 > 激酶細胞株 > EML4-ALK V1 C1156Y/G1202R/BaF3 Kinase
      EML4-ALK V1 C1156Y/G1202R/BaF3 Kinase

      EML4-ALK V1 C1156Y/G1202R/BaF3 Kinase

      型    號: CBP73364
      報    價:
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      EML4-ALK V1 [C1156Y/G1202R]/BaF3

      CBP73364EML4-ALK V1 C1156Y/G1202R/BaF3 Kinase的詳細資料:

      CBP73364
      I. Introduction

      Cell Line Name:

      EML4-ALK V1 [C1156Y/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. Sanger of EML4-ALK V1 [C1156Y/G1202R]/BaF3

      CBP73364 sanger-C1156Y.png


      Figure 1. EML4-ALK V1 [C1156Y/G1202R]/BaF3 C1156Y

      CBP73364 sanger-G1202R.png

      Figure 2.  EML4-ALK V1 [C1156Y/G1202R]/BaF3 G1202R 

      CBP73364 sanger-Fusion.png


      Figure 3. EML4-ALK V1 [C1156Y/G1202R]/BaF3 Fusion

       

      2. Anti-proliferation assay

      CBP73364 數據圖.png

      Figure 4. CTG Proliferation Assay of BaF3 EML4-ALK V1 [C1156Y/G1202R] (C1).

       

       

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