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Invitrogen
eIF4H Polyclonal Antibody
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Product Details
PA5-41898
Species Reactivity
Host/Isotype
Class
Type
Immunogen
Conjugate
Form
Concentration
Purification
Storage buffer
Contains
Storage conditions
Shipping conditions
RRID
Product Specific Information
Peptide sequence: DSRDDFNSGF RDDFLGGRGG SRPGDRRTGP PMGSRFRDGP PLRGSNMDFR
Sequence homology: Dog: 100%; Horse: 86%; Human: 100%; Mouse: 93%; Pig: 100%; Rat: 93%
Target Information
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.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
References (0)
Bioinformatics
Protein Aliases: eIF-4H; Eukaryotic translation initiation factor 4H; Williams-Beuren syndrome chromosomal region 1 protein; Williams-Beuren syndrome chromosome region 1
Gene Aliases: eIF-4H; EIF4H; KIAA0038; WBSCR1; WSCR1
UniProt ID: (Human) Q15056
Entrez Gene ID: (Human) 7458
Performance Guarantee
If an Invitrogen™ antibody doesn't perform as described on our website or datasheet,we'll replace the product at no cost to you, or provide you with a credit for a future purchase.*
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