EIF4H / Unconjugated /
Product Details
Description | Rabbit anti-eIF4H Antibody, Affinity Purified | |
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Conjugate | Unconjugated | |
Clone | ||
Target Species | Human | |
Applications | WB, IP, IHC | |
Supplier | Bethyl Laboratories | |
Catalog # | Sign in to view product details, citations, and spectra | |
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Antigen | ||
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About EIF4H
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, Jul 2008]
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, Jul 2008]
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146 EIF4H antibodies from over 16 suppliers available with over 36 conjugates.