EIF4H (NM_031992) Human Recombinant Protein
Product Specifications
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. [provided by RefSeq, Jul 2008]
Synonyms
EIF-4H; WBSCR1; WSCR1
Gene ID
7458
UniProt
Q15056
Accession Number mRNA
NM_031992
Chromosomal Location
7q11.23
Expression System
HEK293T
Tag
C-Myc/DDK
Concentration
>50 ug/mL as determined by microplate BCA method
Purity
> 80% as determined by SDS-PAGE and Coomassie blue staining
Form
Liquid
Buffer
25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10% glycerol
Molecular Weight
25 kDa
Storage Conditions
Stable for 1 year at -20°C or below from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. For long-term storage, aliquot and store at -20°C or below. Avoid repeated freeze-thaw cycles.
Symbol
EIF4H
Species
Human
Protein ID
NP_114381
Overview
Recombinant protein of human eukaryotic translation initiation factor 4H (EIF4H), transcript variant 2
Gene ID URL
https://www.ncbi.nlm.nih.gov/gene/7458
Uniprot URL
https://www.uniprot.org/uniprot/Q15056
Accession Number mRNA URL
https://www.ncbi.nlm.nih.gov/nuccore/NM_031992
Protein ID Link
https://www.ncbi.nlm.nih.gov/nuccore/NP_114381
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