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SNTG1 (NM_018967) Human Recombinant Protein

Product Specifications

Background

The protein encoded by this gene is a member of the syntrophin family. Syntrophins are cytoplasmic peripheral membrane proteins that typically contain 2 pleckstrin homology (PH) domains, a PDZ domain that bisects the first PH domain, and a C-terminal domain that mediates dystrophin binding. This family member plays a role in mediating gamma-enolase trafficking to the plasma membrane and in enhancing its neurotrophic activity. Mutations in this gene are associated with idiopathic scoliosis. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Mar 2016]

Overview

Recombinant protein of human syntrophin, gamma 1 (SNTG1)

Synonyms

G1SYN; SYN4

Gene ID

54212

UniProt

Q9NSN8, A0A024R7Y0

Accession Number mRNA

NM_018967

Chromosomal Location

8q11.21

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

57.8 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

SNTG1

Species

Human

Protein ID

NP_061840

Gene ID URL

https://www.ncbi.nlm.nih.gov/gene/54212

Uniprot URL

https://www.uniprot.org/uniprot/Q9NSN8

Accession Number mRNA URL

https://www.ncbi.nlm.nih.gov/nuccore/NM_018967

Protein ID Link

https://www.ncbi.nlm.nih.gov/nuccore/NP_061840

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