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Rabbit Anti-RUNX1T1/FITC Conjugated antibody
background:
RUNX1T1 is a putative zinc finger transcription factor and oncoprotein. In acute myeloid leukemia, especially in the M2 subtype, the t(8;21)(q22;q22) translocation is one of the most frequent karyotypic abnormalities. The translocation produces a chimeric gene made up of the 5'-region of the RUNX1 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. Several transcript variants encoding multiple isoforms have been found for this gene.
Subunit:
Homotetramer. Heterotetramer with CSFA2T2 and CSFA2T3. Interacts with TCF12, SIN3A, HDAC1, HDAC2, HDAC3, NCOR1 and NCOR2. Interacts with ATN1 (via its N-terminus); the interaction enhances the transcriptional repression.
Subcellular Location:
Nucleus.
Tissue Specificity:
Most abundantly expressed in brain. Lower levels in lung, heart, testis and ovary.
Similarity:
Belongs to the CSFA2T family.
Contains 1 MYND-type zinc finger.
Contains 1 TAFH (NHR1) domain.
Database links:
Entrez Gene: 862 Human
Entrez Gene: 12395 Mouse
Entrez Gene: 362489 Rat
Omim: 133435 Human
SwissProt: Q06455 Human
SwissProt: Q61909 Mouse
Unigene: 368431 Human
Unigene: 470961 Mouse
Unigene: 4909 Mouse
Unigene: 218117 Rat
Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
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