GTF2I Repeat Domain Containing Protein 2B (GTF2IRD2B)

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General Transcription Factor II-I Repeat Domain Containing Protein 2B; Transcription factor GTF2IRD2-beta

GTF2I Repeat Domain Containing Protein 2B (GTF2IRD2B)
The deduced human GTF2IRD2B protein contains 949 amino acids and has a calculated molecular mass of 107 kD. The N-terminal half of GTF2IRD2B contains a leucine zipper motif, followed by 2 helix-loop-helix motifs (I repeats) that share homology with the TFII-I family of transcription factors. The C-terminal half of GTF2IRD2B contains a CHARLIE8 transposable element-like sequence, including 3 transposase-related domains that may be functional, and a BED zinc finger DNA-binding motif. GTF2IRD2B also has 4 N-glycosylation sites and multiple putative phosphorylation sites. The 949-amino acid GTF2IRD2A protein has 6 C-terminal amino acid changes relative to GTF2IRD2B. Northern blot analysis detected a 3.5-kb GTF2IRD2B transcript in all tissues tested, and RT-PCR analysis confirmed ubiquitous expression.

Organism species: Homo sapiens (Human)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant GTF2I Repeat Domain Containing Protein 2B (GTF2IRD2B) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to GTF2I Repeat Domain Containing Protein 2B (GTF2IRD2B) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to GTF2I Repeat Domain Containing Protein 2B (GTF2IRD2B) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for GTF2I Repeat Domain Containing Protein 2B (GTF2IRD2B) CLIA Kit Customized Service Offer
n/a ELISA Kit for GTF2I Repeat Domain Containing Protein 2B (GTF2IRD2B) ELISA Kit Customized Service Offer
  1. "Isolation and characterisation of GTF2IRD2, a novel fusion gene and member of the TFII-I family of transcription factors, deleted in Williams-Beuren syndrome."Eur. J. Hum. Genet. 12:551-560(2004) [PubMed] [Europe PMC] [Abstract]
  2. "Comparison of TFII-I gene family members deleted in Williams-Beuren syndrome."Protein Sci. 13:2588-2599(2004) [PubMed] [Europe PMC] [Abstract]
  3. "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."Genome Res. 14:2121-2127(2004) [PubMed] [Europe PMC] [Abstract]
  4. "Complete sequencing and characterization of 21,243 full-length human cDNAs." Nat. Genet. 36:40-45(2004) [PubMed] [Europe PMC] [Abstract]
  5. "Hemizygosity at the NCF1 gene in patients with Williams-Beuren syndrome decreases their risk of hypertension."Am. J. Hum. Genet. 78:533-542(2006) [PubMed] [Europe PMC] [Abstract]
  6. "Solution structure of RSGI RUH-068, a GTF2I domain in human cDNA."Submitted (MAY-2007) to the PDB data bank