GPD1L Polyclonal Antibody

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).

Research Area: Cancer, Cell Biology, Metabolism, Signal transduction

Synonyms:
2210409H23Rik, D9Ertd660e, Glycerol 3 phosphate dehydrogenase 1 like, Glycerol 3 phosphate dehydrogenase 1 like protein, Glycerol-3-phosphate dehydrogenase 1-like protein, GPD 1L, GPD1-L, gpd1l, GPD1L, KIAA0089, RGD1560123

Immunogen: Fusion protein of human GPD1L

Swissprot: Q8N335
Gene Accession: BC028726

Purification Method: Antigen affinity purification

Buffer: PBS with 0.05% NaN3 and 40% Glycerol, pH7.4

Concentration: 1.02 mg/mL
Dilution: IHC 1:50-1:300, ELISA 1:5000-1:10000

Storage:
Store at -20°C. Avoid freeze / thaw cycles.