- Description of Target:
- GPD1L belongs to the NAD-dependent glycerol-3-phosphate dehydrogenase family. Defects in GPD1L are the cause of Brugada syndrome type 2 (BRS2) and sudden infant death syndrome (SIDS).
- Gene Symbol:
- GABARAPL1
- Alias Symbols:
- APG8L; ATG8; ATG8L; GEC1; ATG8B; APG8-LIKE
- Protein Accession# :
- NP_113600
- Nucleotide Accession#:
- NM_031412
- Swissprot Id:
- Q9H0R8
- Protein Size (# AA):
- 117
- Molecular Weight:
- 14kDa
- Partner Proteins:
- KCNJ4, GNB1, GNB2, GNB4, KCNJ4
- Tag:
- GST
- Quality Control:
- This product was tested on western blot.
- Reconstitution and Storage:
- Add 100ul of distilled water. Final concentration is 1 mg/ml. For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
- Additional Information:
- Buffer Formulation: 0.1M Tris-HCl (pH 6.8) buffer containing 0.2M DTT, 4% SDS, 0.2% Bromophenol blue and 20% Sucrose.
- Key Reference:
- Tanida,I., (2006) FEBS J. 273 (11), 2553-2562
- Datasheets / Downloads:
- APL00006
- Protocol:
- Tips Information:
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