Recombinant human GPD1L protein
GPD1L, also known as glycerol-3-phosphate dehydrogenase 1-like protein, converts sn-glycerol 3-phosphate to glycerone phosphate. This protein is found in the cytoplasm, associated with the plasma membrane, where it binds the sodium channel, voltage-gated, type V, alpha subunit (SCN5A) . Mutations in GPD1L are the cause of sudden infant death syndrome (SIDS) and Brugada syndrome type 2, an autosomal dominant tachyarrhythmia. Recombinant human GPD1L protein, fused to His-tag at N-terminus, was expressed in E. coli and purified by using conventional chromatography.
Product Specifications
Product Name Alternative
Glycerol-3-phosphate dehydrogenase 1-like protein, GPD1-L
Expression System
E.coli
Antigen Species
Human
Tag
His-Tag
Applications
SDS-PAGE
Concentration
1 mg/mL (determined by Bradford assay)
Purity
> 95% by SDS-PAGE
Molecular Weight
40.6 kDa (371aa) confirmed by MALDI-TOF
Additionnal Information
References & Citations
Valdivia C.R., et al. (2009) Am. J. Physiol. 297:H1446-H1452; ; Van Norstrand D.W., et al. (2007) Circulation. 116:2253-2259
Storage Conditions
Can be stored at 2°C to 8°C for 1 week. For long term storage, aliquot and store at -20C to -80C. Avoid repeated freezing and thawing cycles.
Formulation
Liquid in. 20 mM Tris-HCl buffer (pH 8.0) containing 20% glycerol, 1mM DTT
Scientific Category
Metabolism
NCBI Accession Number
NP_055956
Uniprot Accession Number
Q8N335
Species
Human
AA Sequence
Explore Other Products
Discover premium biology products from our extensive collection of 20M+ items