EIF4H DNAxPab
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Specification
Product Description
Rabbit polyclonal antibody raised against a full-length human EIF4H DNA using DNAx™ Immune technology.
Technology
Immunogen
Full-length human DNA
Sequence
MADFDTYDDRAYSSFGGGRGSRGSAGGHGSRSQKELPTEPPYTAYVGNLPFNTVQGDIDAIFKDLSIRSVRLVRDKDTDKFKGFCYVEFDEVDSLKEALTYDGALLGDRSLRVDIAEGRKQDKGGFGFRKGGPDDRGMGSSRESRGGWDSRDDFNSGFRDDFLGGRGGSRPGDRRTGPPMGSRFRDGPPLRGSNMDFREPTEEERAQRPRLQLKPRTVATPLNQVANPNSAIFGGARPREEVVQKEQE
Host
Rabbit
Reactivity
Human
Purification
Protein A
Quality Control Testing
Antibody reactive against mammalian transfected lysate.
Storage Buffer
In 1x PBS, pH 7.4
Storage Instruction
Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
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Applications
Western Blot (Transfected lysate)
Immunofluorescence (Transfected cell)
Flow Cytometry (Transfected cell)
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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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