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Rabbit Anti-TCF12 Antibody (CSB-PA023293ESR1HU)
Supplier: CUSABIO BIOTECH CO.
TCF-12 Antibody,Class B basic helix-loop-helix protein 20 Antibody,DNA-binding protein HTF4 Antibody,E-box-binding protein Antibody,Transcription factor HTF-4 Antibody,TCF12 Antibody,BHLHB20 Antibody, HEB Antibody, HTF4 AntibodyMore alternative names for the antibody
bHLHb20 antibody|Class B basic helix-loop-helix protein 20 antibody|DNA binding protein HTF4 antibody|DNA-binding protein HTF4 antibody|E box binding protein antibody|E-box-binding protein antibody|HEB antibody|Helix loop helix transcription factor 4 antibody|HsT17266 antibody|HTF4 antibody|HTF4_HUMAN antibody|TCF-12 antibody|Tcf12 antibody|Transcription factor 12 antibody|Transcription factor HTF-4 antibody|Transcription factor HTF4 antibody
Anti-TCF12 antibody (ab70746)
Anti-TCF12 antibody (ab70746)
Recommended applications: ELISA, IHC, IP
Recommended dilution: Recommended dilution:IHC:1:20-1:200,IP:1:200-1:2000
Recommended protocols: check protocols
|Catalogue No.|| |
Recombinant human Transcription factor 12 protein (443-682AA)
ELISA, IHC, IP
|Recommended dilution|| |
|Molecular weight|| |
Antigen Affinity Purified
Shipped at 4 Celcius Degree. Upon delivery aliquot and store at -20 Celcius Degree or -80 Celcius Degree. Avoid repeated freeze.
|Database links|| |
Entrez Gene:6938( Human), Entrez Gene:21406( Mouse), Entrez Gene:25720( Rat), Omim:600480( Human), SwissProt:Q99081( Human), SwissProt:Q61286( Mouse), SwissProt:P51514( Rat), Unigene:511504( Human), Unigene:171615( Mouse), Unigene:480117( Mouse), Unigene:9916( Rat)
|Protein function|| |
Transcriptional regulator. Involved in the initiation of neuronal differentiation. Activates transcription by binding to the E box (5′-CANNTG-3′).
|Protein tissue specificity|| |
Expressed in several tissues and cell types including skeletal muscle, thymus, and a B-cell line.
|Involvement in disease|| |
Craniosynostosis 3 (CRS3) [MIM:615314]: A primary abnormality of skull growth involving premature fusion of one or more cranial sutures. The growth velocity of the skull often cannot match that of the developing brain resulting in an abnormal head shape and, in some cases, increased intracranial pressure, which must be treated promptly to avoid permanent neurodevelopmental disability. . Note=The disease is caused by mutations affecting the gene represented in this entry.
|Protein sequence and domain|| |
the 9aaTAD motif is a transactivation domain present in a large number of yeast and animal transcription factors.
|Protein cellular localization|| |
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CUSABIO BIOTECH CO.
|Product type|| |
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