eIF4H Products

Antibodies
eIF4H Antibody
eIF4H Antibody
NBP1-83057
Species: Hu, Mu, Rt
Applications: WB, ICC/IF, IHC, IHC-P
Host: Rabbit Polyclonal
eIF4H Antibody
eIF4H Antibody
NBP1-57248
Species: Hu
Applications: WB, IHC, IHC-P
Host: Rabbit Polyclonal
eIF4H Antibody
eIF4H Antibody
NBP1-00105
Species: Hu
Applications: WB, IHC, IHC-P
Host: Rabbit Polyclonal
Lysates
eIF4H Overexpression Lysate ( ...
eIF4H Overexpression Lysate (Native)
NBL1-10212
Applications: WB
Proteins
eIF4H Recombinant Protein Ant ...
eIF4H Recombinant Protein Antigen
NBP1-83057PEP
Species: Hu
Applications: AC
Recombinant Human eIF4H Prote ...
Recombinant Human eIF4H Protein
NBP1-98965
Species: Hu
Applications: PAGE
RNAi
eIF4H RNAi
eIF4H RNAi
H00007458-R02
Species: Hu
Applications: RNAi, RNAi SP
eIF4H RNAi
eIF4H RNAi
H00007458-R01
Species: Hu
Applications: RNAi, RNAi SP

Description

eIF4H 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]

Bioinformatics

Entrez Human
Uniprot Human
Human
Human
Human
Human
Human
Product By Gene ID 7458
Alternate Names
  • WBSCR1
  • KIAA0038eIF-4H
  • WSCR1Williams-Beuren syndrome chromosomal region 1 protein
  • Williams-Beuren syndrome chromosome region 1
  • eukaryotic translation initiation factor 4H

Pathways for eIF4H

View related products by pathway and learn more about each of the pathways below.

Translation
Translational Initiation
Cell Proliferation
Cell Cycle
Associative Learning
Endocytosis
Stress Granule Assembly
Macropinocytosis
Rna Splicing

PTMs for eIF4H

Learn more about PTMs related to eIF4H.

Glycosylation

Bioinformatics Tool for eIF4H

Discover related pathways, diseases and genes to eIF4H. Need help? Read the Bioinformatics Tool Guide for instructions on using this tool.
 
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