• Product NameRecombinant Human GPD1L
• Brief DescriptionRecombinant Protein
• Immunogen DescriptionFusion protein corresponding to a region derived from 152-351 amino acids of human GPD1L
• Target Nameglycerol-3-phosphate dehydrogenase 1 like
• Alternative Names    GPD1-L
• Accession No. Swissprot:Q8N335
  Gene Accession:BC028726
• UniprotQ8N335
• Gene ID23171;
• Storage -20~-80˚C, pH 7.6 PBS

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).

Note: For in vitro research use only, not for diagnostic or therapeutic use. This product is not a medical device.

• Flow Cytometry (FCM) General Protocol
• Immunofluorescence(IC)
• Immunohistochemistry(Polymer)
• Western Blotting