GPD1L (NM_015141) Human Recombinant Protein

Product Specifications

Background

The protein encoded by this gene catalyzes the conversion of sn-glycerol 3-phosphate to glycerone phosphate. The encoded protein is found in the cytoplasm, associated with the plasma membrane, where it binds the sodium channel, voltage-gated, type V, alpha subunit (SCN5A) . Defects in this gene are a cause of Brugada syndrome type 2 (BRS2) as well as sudden infant death syndrome (SIDS) . [provided by RefSeq, Jul 2010]

Overview

Recombinant protein of human glycerol-3-phosphate dehydrogenase 1-like (GPD1L)

Synonyms

GPD1-L

Gene ID

23171

UniProt

Q8N335

Accession Number mRNA

NM_015141

Chromosomal Location

3p22.3

Expression System

HEK293T

Tag

C-Myc/DDK

Related Pathways

Glycerophospholipid metabolism

Field of Research

Glycerophospholipid metabolism

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

38.2 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.