名稱 | EML4-ALK V3b/BaF3 |
型號 | CBP73186 |
報(bào)價(jià) | ![]() |
特點(diǎn) | EML4-ALK V3b/BaF3,母細(xì)胞:BaF3,凍存條件:90% FBS+10% DMSO |
產(chǎn)品搜索
相關(guān)文章
- 老靶點(diǎn)迭代突破創(chuàng)新:Her2靶點(diǎn)細(xì)胞模型
- NKG2A細(xì)胞篩選模型
- GLP1R藥靶篩選模型應(yīng)用展示
- 【產(chǎn)品推介】TIGIT靶點(diǎn)細(xì)胞篩選模型
- 從人結(jié)腸癌細(xì)胞株延伸出早期結(jié)腸癌治療方法
- 科學(xué)家發(fā)現(xiàn)10個(gè)新的智力障礙易感基因
- PIK3CA診斷標(biāo)準(zhǔn)品
- eLife:為何肺癌靶向治療會(huì)失???看看科學(xué)家們怎么說
- 黃金賽道——CDH17靶點(diǎn)
- TROP2靶點(diǎn)藥物爆發(fā),診斷質(zhì)控緊跟步伐--科佰TROP2 IHC質(zhì)控品上新
聯(lián)系我們
電話:4008750250
號碼:
手機(jī):18066071954
地址:南京市棲霞區(qū)緯地路9號
Email: zhangxiangwen@cobioer.com
產(chǎn)品展示 / PRODUCTS
藥靶細(xì)胞株 > kinase激酶細(xì)胞株 > CBP73186EML4-ALK V3b/BaF3

- 詳細(xì)內(nèi)容
CBP73186 | |
I. Introduction | |
Cell Line Name: | EML4-ALK V3b/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 | |
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 V3b/BaF3 expression | |
![]() | |
Figure 1. WB of ALK expression | |
2. Anti-proliferation assay | |
Figure 2. Anti-proliferation assay of three reference compounds on the EML4-ALK V3b/BaF3 Stable Cell Line |