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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]

Overview

Recombinant protein of human WAS/WASL interacting protein family, member 1 (WIPF1), transcript variant 1

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

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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