| Background: | This gene encodes a member of the myeloid translocation gene family which interact with DNA-bound transcription factors and recruit a range of corepressors to facilitate transcriptional repression. The t(8;21)(q22;q22) translocation is one of the most frequent karyotypic abnormalities in acute myeloid leukemia. The translocation produces a chimeric gene made up of the 5'-region of the runt-related transcription factor 1 gene fused to the 3'-region of this gene. The chimeric protein is thought to associate with the nuclear corepressor/histone deacetylase complex to block hematopoietic differentiation. Alternative splicing results in multiple transcript variants. [provided by RefSeq]. | 
| Applications: | WB, IF | 
| Name of antibody: | RUNX1T1 | 
| Immunogen: | Fusion protein of human RUNX1T1 | 
| Full name: | runt-related transcription factor 1; translocated to, 1 (cyclin D-related) (RUNX1T1), transcript variant 3 | 
| Synonyms: | CDR; ETO; MTG8; AML1T1; ZMYND2; CBFA2T1; AML1-MTG8 | 
| SwissProt: | Q06455 | 
| WB Predicted band size: | 68 kDa | 
| WB Positive control: | Hela, SVT2, A549, COS7, Jurkat, PC12, MCF-7 cell lysates | 
| WB Recommended dilution: | 500-2000 | 
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