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The protein encoded by GPD1L catalyzes the conversion of sn-glycerol 3-phosphate to glycerone phosphate. Additionally we are shipping GPD1L Proteins (8) and GPD1L Kits (2) and many more products for this protein.
Showing 10 out of 41 products:
Cow (Bovine) Polyclonal GPD1L Primary Antibody for WB - ABIN2786083
London, Michalec, Mehdi, Zhu, Kerchner, Sanyal, Viswanathan, Pfahnl, Shang, Madhusudanan, Baty, Lagana, Aleong, Gutmann, Ackerman, McNamara, Weiss, Dudley: Mutation in glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) decreases cardiac Na+ current and causes inherited arrhythmias. in Circulation 2007
Human Polyclonal GPD1L Primary Antibody for EIA, IHC (p) - ABIN952587
Hanna, Kruskal, Ezekowitz, Bloom, Collier: Role of macrophage oxidative burst in the action of anthrax lethal toxin. in Molecular medicine (Cambridge, Mass.) 1996
In a nonreferred nationwide Danish cohort of SIDS (show IDS Antibodies) cases, up to 5/66 (7.5%) of SIDS (show IDS Antibodies) cases can be explained by genetic variants in the sodium channel complex genes.
The results of real-time PCR showed that, compared with the paired normal tissues, mRNA levels of GPD1L were decreased significantly in head and neck squamous cell carcinoma.
Common variations in or near CASQ2 (show CASQ2 Antibodies), GPD1L, and NOS1AP (show NOS1AP Antibodies) are associated with increased risk of sudden cardiac death in patients with coronary artery disease
hypoxia-induced miR (show MLXIP Antibodies)-210 represses GPD1L, contributing to suppression of prolyl hydroxylases activity, and increases of HIF-1alpha (show HIF1A Antibodies) protein levels.
mutations in GPD1-L as a pathogenic cause for a small subset of sudden infant death syndrome via a secondary loss-of-function mechanism
A GPD1-L mutation decreases SCN5A (show SCN5A Antibodies) surface membrane expression, reduces inward Na+ current, and causes Brugada syndrome
No non-synonymous mutations were found, indicating that GPD1L does not appear to be a major cause of Brugada syndrome in a Japanese population.
GPD1L links redox state to cardiac excitability by PKC (show PRRT2 Antibodies)-dependent phosphorylation of the sodium channel SCN5A (show SCN5A Antibodies).
Mutations of GPD1-L may downregulate Na(v)1.5 by altering the oxidized to reduced NAD(H) balance.
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).
glycerol-3-phosphate dehydrogenase 1-like protein
, glycerol-3-phosphate dehydrogenase 1-like
, glycerol-3-phosphate dehydrogenase 1-like protein-like