WBSCR1 (Human) Recombinant Protein (P01)
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More Files
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Specification
Product Description
Human WBSCR1 full-length ORF ( NP_071496.1, 1 a.a. - 248 a.a.) recombinant protein with GST-tag at N-terminal.
Sequence
MADFDTYDDRAYSSFGGGRGSRGSAGGHGSRSQKELPTEPPYTAYVGNLPFNTVQGDIDAIFKDLSIRSVRLVRDKDTDKFKGFCYVEFDEVDSLKEALTYDGALLGDRSLRVDIAEGRKQDKGGFGFRKGGPDDRGMGSSRESRGGWDSRDDFNSGFRDDFLGGRGGSRPGDRRTGPPMGSRFRDGPPLRGSNMDFREPTEEERAQRPRLQLKPRTVATPLNQVANPNSAIFGGARPREEVVQKEQE
Host
Wheat Germ (in vitro)
Theoretical MW (kDa)
53.8
Interspecies Antigen Sequence
Mouse (99); Rat (98)
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 — EIF4H
Entrez GeneID
7458GeneBank Accession#
NM_022170.1Protein Accession#
NP_071496.1Gene Name
EIF4H
Gene Alias
KIAA0038, WBSCR1, WSCR1
Gene Description
eukaryotic translation initiation factor 4H
Omim ID
603431Gene Ontology
HyperlinkGene Summary
This gene encodes one of the translation initiation factors, which functions to stimulate the initiation of protein synthesis at the level of mRNA utilization. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternative splicing of this gene generates 2 transcript variants. [provided by RefSeq
Other Designations
OTTHUMP00000024643|Williams-Beuren syndrome chromosome region 1
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Interactome
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Disease
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