CBFA2T3 (NM_005187) Human Tagged ORF Clone Lentiviral Particle
SKU
RC212257L1V
Lenti ORF particles, CBFA2T3 (Myc-DDK tagged) - Human core-binding factor, runt domain, alpha subunit 2; translocated to, 3 (CBFA2T3), transcript variant 1, 200ul, >10^7 TU/mL
Product Data | |
Type | Human Tagged ORF Clone Lentiviral Particle |
---|---|
Tag | Myc-DDK |
Target Symbol | CBFA2T3 |
Synonyms | ETO2; MTG16; MTGR2; RUNX1T3; ZMYND4 |
Vector | pLenti-C-Myc-DDK |
Mammalian Cell Selection | None |
Sequence Data |
ORF Nucleotide Sequence
The ORF insert of this clone is exactly the same as(RC212257).
|
ACCN | NM_005187 |
ORF Size | 1959 bp |
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. |
Shipping | Dry Ice |
Reference Data | |
RefSeq | NM_005187.4 |
RefSeq Size | 4372 bp |
RefSeq ORF | 1962 bp |
Locus ID | 863 |
UniProt ID | O75081 |
Cytogenetics | 16q24.3 |
Domains | TAFH, zf-MYND |
Protein Families | Transcription Factors |
MW | 71.2 kDa |
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(16;21)(q24;q22) translocation is one of the less common 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. This gene is also a putative breast tumor suppressor. Alternative splicing results in transcript variants. [provided by RefSeq, Nov 2010] |
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