GTF2IRD1 (Human) Recombinant Protein (Q01)
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More Files
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Specification
Product Description
Human GTF2IRD1 partial ORF ( NP_005676, 431 a.a. - 530 a.a.) recombinant protein with GST-tag at N-terminal.
Sequence
IFTGNKFTKDTTKLEPASPPEDTSAEVSRATVLDLAGNARSDKGSMSEDCGPGTSGELGGLRPIKIEPEDLDIIQVTVPDPSPTSEEMTDSMPGHLPSED
Host
Wheat Germ (in vitro)
Theoretical MW (kDa)
36.74
Interspecies Antigen Sequence
Mouse (84); Rat (86)
Preparation Method
Purification
Glutathione Sepharose 4 Fast Flow
Quality Control Testing
12.5% SDS-PAGE Stained with Coomassie Blue.
Storage Buffer
50 mM Tris-HCI, 10 mM reduced Glutathione, pH=8.0 in the elution buffer.
Storage Instruction
Store at -80°C. Aliquot to avoid repeated freezing and thawing.
Note
Best use within three months from the date of receipt of this protein.
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Applications
Enzyme-linked Immunoabsorbent Assay
Western Blot (Recombinant protein)
Antibody Production
Protein Array
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Gene Info — GTF2IRD1
Entrez GeneID
9569GeneBank Accession#
NM_005685Protein Accession#
NP_005676Gene Name
GTF2IRD1
Gene Alias
BEN, CREAM1, GTF3, MUSTRD1, RBAP2, WBS, WBSCR11, WBSCR12, hMusTRD1alpha1
Gene Description
GTF2I repeat domain containing 1
Gene Ontology
HyperlinkGene Summary
The protein encoded by this gene contains five GTF2I-like repeats and each repeat possesses a potential helix-loop-helix (HLH) motif. It may have the ability to interact with other HLH-proteins and function as a transcription factor or as a positive transcriptional regulator under the control of Retinoblastoma protein. This gene is deleted in Williams-Beuren syndrome, a multisystem developmental disorder caused by deletion of multiple genes at 7q11.23. Alternative splicing of this gene generates at least 2 transcript variants. [provided by RefSeq
Other Designations
GTF2I repeat domain-containing 1|Williams-Beuren syndrome chromosome region 11|binding factor for early enhancer|general transcription factor 3|muscle TFII-I repeat domain-containing protein 1 alpha 1
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Interactome
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Pathway
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Disease
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