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Glycerol-3-Phosphate Dehydrogenase 1-Like (GPD1L) ELISA Kits

The protein encoded by GPD1L catalyzes the conversion of sn-glycerol 3-phosphate to glycerone phosphate. Additionally we are shipping GPD1L Antibodies (41) and GPD1L Proteins (8) and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
GPD1L 23171 Q8N335
GPD1L 333433 Q3ULJ0
Anti-Rat GPD1L GPD1L 363159  
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Top GPD1L ELISA Kits at antibodies-online.com

Showing 2 out of 2 products:

Catalog No. Reactivity Sensitivity Range Quantity Supplier Delivery Price Details
Mouse
96 Tests Log in to see 11 to 13 Days
$875.60
Details
Human
96 Tests Log in to see 11 to 13 Days
$875.60
Details

More ELISA Kits for GPD1L Interaction Partners

Human Glycerol-3-Phosphate Dehydrogenase 1-Like (GPD1L) interaction partners

  1. In a nonreferred nationwide Danish cohort of SIDS (show IDS ELISA Kits) cases, up to 5/66 (7.5%) of SIDS (show IDS ELISA Kits) cases can be explained by genetic variants in the sodium channel complex genes.

  2. 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.

  3. Common variations in or near CASQ2 (show CASQ2 ELISA Kits), GPD1L, and NOS1AP (show NOS1AP ELISA Kits) are associated with increased risk of sudden cardiac death in patients with coronary artery disease

  4. hypoxia-induced miR (show MLXIP ELISA Kits)-210 represses GPD1L, contributing to suppression of prolyl hydroxylases activity, and increases of HIF-1alpha (show HIF1A ELISA Kits) protein levels.

  5. mutations in GPD1-L as a pathogenic cause for a small subset of sudden infant death syndrome via a secondary loss-of-function mechanism

  6. A GPD1-L mutation decreases SCN5A (show SCN5A ELISA Kits) surface membrane expression, reduces inward Na+ current, and causes Brugada syndrome

  7. No non-synonymous mutations were found, indicating that GPD1L does not appear to be a major cause of Brugada syndrome in a Japanese population.

  8. GPD1L links redox state to cardiac excitability by PKC-dependent phosphorylation of the sodium channel SCN5A (show SCN5A ELISA Kits).

  9. Mutations of GPD1-L may downregulate Na(v)1.5 by altering the oxidized to reduced NAD(H) balance.

Mouse (Murine) Glycerol-3-Phosphate Dehydrogenase 1-Like (GPD1L) interaction partners

  1. Mutations of GPD1-L may downregulate Na(v)1.5 by altering the oxidized to reduced NAD(H) balance.

GPD1L Antigen Profile

Antigen Summary

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).

Gene names and symbols associated with GPD1L

  • glycerol-3-phosphate dehydrogenase 1-like (gpd1l) antibody
  • glycerol-3-phosphate dehydrogenase 1-like (GPD1L) antibody
  • glycerol-3-phosphate dehydrogenase 1-like (Gpd1l) antibody
  • 2210409H23Rik antibody
  • D9Ertd660e antibody
  • GPD1-L antibody
  • RGD1560123 antibody
  • wu:fi13g03 antibody
  • wu:fi45b08 antibody
  • zgc:92580 antibody

Protein level used designations for GPD1L

glycerol-3-phosphate dehydrogenase 1-like protein , glycerol-3-phosphate dehydrogenase 1-like , glycerol-3-phosphate dehydrogenase 1-like protein-like

GENE ID SPECIES
394623 Xenopus (Silurana) tropicalis
420664 Gallus gallus
485626 Canis lupus familiaris
750218 Pan troglodytes
100173675 Pongo abelii
100219677 Taeniopygia guttata
100547788 Meleagris gallopavo
449663 Danio rerio
379962 Xenopus laevis
23171 Homo sapiens
514456 Bos taurus
333433 Mus musculus
363159 Rattus norvegicus
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