WIPF1 (NM_003387) Human Recombinant Protein
Product Specifications
Background
This gene encodes a protein that plays an important role in the organization of the actin cytoskeleton. The encoded protein binds to a region of Wiskott-Aldrich syndrome protein that is frequently mutated in Wiskott-Aldrich syndrome, an X-linked recessive disorder. Impairment of the interaction between these two proteins may contribute to the disease. Two transcript variants encoding the same protein have been identified for this gene. [provided by RefSeq, Jul 2008]
Synonyms
PRPL-2; WAS2; WASPIP; WIP
Gene ID
7456
UniProt
O43516, A0A140VJZ9, Q2YDC4
Accession Number mRNA
NM_003387
Chromosomal Location
2q31.1
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
51.1 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
WIPF1
Species
Human
Protein ID
NP_003378
Overview
Recombinant protein of human WAS/WASL interacting protein family, member 1 (WIPF1), transcript variant 1
Gene ID URL
https://www.ncbi.nlm.nih.gov/gene/7456
Uniprot URL
https://www.uniprot.org/uniprot/O43516
Accession Number mRNA URL
https://www.ncbi.nlm.nih.gov/nuccore/NM_003387
Protein ID Link
https://www.ncbi.nlm.nih.gov/nuccore/NP_003378
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