EIF4H

gene product
KIAA0038, WBSCR1, WSCR1
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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38 antibodies from 15 providers.

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AntibodyRefsTypeWBELIFIPIHFC
antibodies-online
3 antibodies
ABIN1840561Polyclonal
ABIN314208Polyclonal
Bethyl Laboratories, Inc.
2 antibodies
A301-848APolyclonal
IHC-00609Polyclonal
Acris Antibodies GmbH
4 antibodies
AP51403PU-NPolyclonal
AP54923SU-NPolyclonal
Novus Biologicals
5 antibodies
H00007458-M07Monoclonal
NBP1-57248Polyclonal
Aviva Systems Biology
2 antibodies
ARP40978_T100Polyclonal
ARP40977_P050Polyclonal
Abnova Corporation
1 antibody
H00007458-M07Monoclonal
Atlas Antibodies
1 antibody
HPA030542Polyclonal
Proteintech Group
1 antibody
11012-1-AP1Polyclonal
Cell Signaling Technology, Inc
2 antibodies
3469Monoclonal
2444Polyclonal
GeneTex
3 antibodies
GTX47262Polyclonal
GTX121223Polyclonal
Thermo Fisher Scientific Pierce
2 antibodies
PA5-17211Polyclonal
PA5-31825Polyclonal
LifeSpan BioSciences, Inc.
3 antibodies
LS-C31538Polyclonal
LS-C65776Polyclonal (Antigen purified)
Creative Biomart
5 antibodies
CAB-3214MHMonoclonal
CABT-12305MHMonoclonal
Sigma-Aldrich
3 antibodies
HPA030542Polyclonal
AV40978Polyclonal
GenWay
1 antibody
18-003-43652Polyclonal