RUNX1T1 (NM_175636) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC200898L3V
- LentiORF®
Lenti ORF particles, RUNX1T1 (Myc-DDK tagged) - Human runt-related transcription factor 1; translocated to, 1 (cyclin D-related) (RUNX1T1), transcript variant 4, 200ul, >10^7 TU/mL
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Specifications
Product Data | |
Product Name | RUNX1T1 (NM_175636) Human Tagged ORF Clone Lentiviral Particle |
Synonyms | AML1-MTG8; AML1T1; CBFA2T1; CDR; ETO; MTG8; ZMYND2 |
Vector | pLenti-C-Myc-DDK-P2A-Puro |
ACCN | NM_175636 |
ORF Size | 1701 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC200898).
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OTI Disclaimer | The molecular sequence of this clone aligns with the gene accession number as a point of reference only. However, individual transcript sequences of the same gene can differ through naturally occurring variations (e.g. polymorphisms), each with its own valid existence. This clone is substantially in agreement with the reference, but a complete review of all prevailing variants is recommended prior to use. More info |
OTI Annotation | This clone was engineered to express the complete ORF with an expression tag. Expression varies depending on the nature of the gene. |
Reference Data | |
RefSeq | NM_175636.1 |
RefSeq Size | 7319 bp |
RefSeq ORF | 1704 bp |
Locus ID | 862 |
Protein Families | Transcription Factors |
Protein Pathways | Acute myeloid leukemia, Pathways in cancer |
MW | 63.2 kDa |
Gene Summary | 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, Nov 2010] |
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