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]
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
Overview
Recombinant protein of human syntrophin, gamma 1 (SNTG1)
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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