CBP73197 KIF5B（E15）-RET（E12） V804E/BaF3

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公司名稱 南京科佰生物科技有限公司
品牌 cobioer/科佰生物
型號(hào) CBP73197
產(chǎn)地
廠商性質(zhì) 代理商
更新時(shí)間 2025/1/10 10:33:31
訪問(wèn)次數(shù) 651

產(chǎn)品標(biāo)簽

JAK2 藥靶細(xì)胞株 BaF3 激酶細(xì)胞株細(xì)胞株

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公司介紹 主營(yíng)產(chǎn)品

南京科佰生物科技有限公司成立于2013年，是一家專業(yè)提供自主生物產(chǎn)品，提供生命醫(yī)學(xué)研究外包服務(wù)，生物大數(shù)據(jù)庫(kù)的綜合型公司。公司在多年的發(fā)展歷程中，整合資源，悉心研發(fā)逐步建立起“腫瘤細(xì)胞庫(kù)”，“STR鑒定比對(duì)信息庫(kù)”，“DNA/RNA標(biāo)準(zhǔn)品庫(kù)”，“藥靶細(xì)胞庫(kù)”，“示蹤細(xì)胞庫(kù)”，“蛋白標(biāo)準(zhǔn)品庫(kù)”，“基因表達(dá)和突變數(shù)據(jù)庫(kù)”等產(chǎn)品和數(shù)據(jù)庫(kù)，同時(shí)開(kāi)發(fā)了分子生物學(xué)、蛋白工程、病毒包裝、抗體工程、細(xì)胞工程、藥物研發(fā)等一系列實(shí)驗(yàn)外包服務(wù)平臺(tái)。

公司十分重視研發(fā)創(chuàng)新，憑借我們細(xì)胞功能改造技術(shù)、高精度和靈活的基因編輯工具平臺(tái)，提供包括激酶，GPCR,腫瘤免疫等多類疾病靶點(diǎn)的藥物篩選細(xì)胞模型，以及數(shù)百種多種形式的用于基因診斷的標(biāo)準(zhǔn)參照品。我們?yōu)楦黝愃幬镅邪l(fā)和基因診斷機(jī)構(gòu)提供產(chǎn)品和服務(wù)，支持對(duì)所有物種的基因功能和人類疾病的基因驅(qū)動(dòng)因素的進(jìn)一步了解，以及個(gè)性化分子、細(xì)胞和基因治療的發(fā)展。

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細(xì)胞、標(biāo)準(zhǔn)品、生化試劑、分子試劑、試劑盒、

詳細(xì)信息 在線詢價(jià)

供貨周期	現(xiàn)貨	規(guī)格	T-25 Flask
貨號(hào)	CBP73197	應(yīng)用領(lǐng)域	生物產(chǎn)業(yè)
主要用途	僅限科研使用

CBP73197
I. Introduction
Cell Line Name：	KIF5B(E15)-RET(E12) [V804E]/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
Chromosomal rearrangements involving the gene that encodes the RET tyrosine kinase are known oncogenic drivers in 1% to 2% of patients with non–small cell lung cancer (NSCLC). These RET rearrangements occur with characteristic partners, most commonly KIF5B, but also CCDC6, NCOA, TRIM33, CUX1, KIAA1217, FRMD4A, and KIAA1468. They are typically identified in young patients with adenocarcinoma histology and minimal smoking history. Therapeutic targeting of RET-fusion–driven NSCLCs has taken the form of treatment with broad-spectrum tyrosine kinase inhibitors with anti-RET activity, such as cabozantinib (Cabometyx; Cometriq), vandetanib (Caprelsa), lenvatinib (Lenvima), RXDX-105, and sunitinib (Sutent). Cabozantinib and vandetanib have been the most heavily studied multi-kinase inhibitors (MKIs), with response rates of 20% to 50% in largely pretreated patients with RET-rearranged NSCLC. Sunitinib has been used in fewer patients to date with initial results demonstrating a 22% response rate. RXDX-105 has exhibited uniquely impressive response rates (75%) in patients with non–KIF5B-RET-fusion NSCLC, compared with 0% response in patients with KIF5B-RET-fusion–positive NSCLC. BLU-667 has demonstrated an objective response rate of 50% in patients with RET-fusion positive NSCLC, and LOXO-292 reported a 74% ORR in patients with RET-fusion positive NSCLC. Notably, RXDX-105, BLU- 667, and LOXO-292 have all demonstrated some central nervous system activity in these early phase trials. Future directions of RET inhibition in patients with RET-rearranged NSCLC include additional clinical validation of the next generation RET-selective inhibitors RXDX-105, BLU-667, and LOXO-292 and comparing multikinase inhibitors with RET-selective inhibitors to determine the optimal sequencing of RET-targeted therapies.

III. Representative Data
1. WB of KIF5B-RET [V804E]/BaF3
2. Sanger of KIF5B-RET [V804E]/BaF3
3. Anti-proliferation assay
Figure 4. CTG Proliferation Assay of BaF3 KIF5B-Ret (S) V804E Cells (C1).