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						藥靶細(xì)胞株 > kinase激酶細(xì)胞株  >  CBP73287BCR-ABL1 Y253H/BaF3激酶細(xì)胞株
            
              
					
				
				
						- 詳細(xì)內(nèi)容
 
| CBP73287 | |
| I. Introduction | |
Cell Line Name:  | BCR-ABL1 [Y253H]/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 | |
Presence of a BCR-ABL1 fusion gene is necessary for the pathogenesis of CML. In up to 95% of cases, a t(9;22) (q34;q11) translocation results in the BCR-ABL1 fusion gene (Faderl et al. 1999). This translocation results in the Philadephia chromosome. In rare CML cases lacking the traditional t(9;22) translocation, other translocations result in the creation of the BCR-ABL1 fusion gene, which sometimes involve multiple chromosomes.  | |
| III. Representative Data | |
1. WB of BCR-ABL1 [Y253H]/BaF3 
  | |
2.Sanger of BCR-ABL1 [Y253H]/BaF3 
 Figure 2. BCR-ABL1 Y253H 
 Figure 3. BCR-ABL1 [Y253H]/BaF3 Fusion  | |
3. Anti-proliferation assay 
 Figure 4. CTG Proliferation Assay of BaF3 BCR-ABL1 Y253H Cells (C1).  | |








