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Anti-EIF4H Antibody

CAT: 0519-A05539-2Size: 100 µLDry Ice: NoHazardous: No
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CAT#:0519-A05539-2Size:100 µL
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Background
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.
Description
Boster Bio Anti-EIF4H Antibody catalog # A05539-2. Tested in WB, ELISA applications. This antibody reacts with Human.
Gene Name
EIF4H
UniProt
Q15056
Host
Rabbit
Reactivity
Human
Immunogen
E.coli-derived human EIF4H recombinant protein (Position: 3-185) .
Clonality
Polyclonal
Applications
WB, ELISA
Purification
Immunogen affinity purified.
Concentration
500 μg/mL
Form
Liquid
Storage Conditions
12 months from date of receipt, -20°C as supplied. 6 months 2 to 8°C after reconstitution. Avoid repeated freezing and thawing.
Contents
500 μg/mL antibody with PBS,0.02% NaN3, 1 mg BSA and 50% glycerol.

UniProtKB · Q15056

Eukaryotic translation initiation factor 4H

IF4H_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
Q15056
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
EIF4H
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
eIF-4H
EC number
—
Processing
—
Secondary accessions
A8K3R1, D3DXF6, D3DXF8
Protein keywords

PTM

AcetylationMethylationPhosphoprotein

Coding sequence diversity

Alternative splicing

Cellular component

Cytoplasm

Technical term

Direct protein sequencingProteomics identificationReference proteome

Biological process

Host-virus interactionProtein biosynthesis

Molecular function

Initiation factorRNA-binding

Disease

Williams-Beuren syndrome

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