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藥靶細(xì)胞株 > kinase激酶細(xì)胞株 > CBP73202LMNA-NTRK1/BaF3

LMNA-NTRK1/BaF3
名稱(chēng) LMNA-NTRK1/BaF3
型號(hào) CBP73202
報(bào)價(jià)
特點(diǎn) LMNA-NTRK1/BaF3,母細(xì)胞:BaF3,凍存條件:90% FBS+10% DMSO
  • 詳細(xì)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

CBP73202 WB.jpg



2. Sanger of LMNA-NTRK1/BaF3 expression


CBP73202 sanger.jpg

Figure 2. Sanger Sequencing of LMNA-NTRK1/BaF3


3. Anti-proliferation assay

CBP73202 fig.jpg

Figure 3. Anti-proliferation assay of two reference compounds on the LMNA-NTRK1/BaF3 Stable Cell Line



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