anti-Glycerol-3-Phosphate Dehydrogenase 1 (Soluble) (GPD1) Antibodies

GPD1 encodes a member of the NAD-dependent glycerol-3-phosphate dehydrogenase family. Additionally we are shipping Glycerol-3-Phosphate Dehydrogenase 1 (Soluble) Proteins (21) and Glycerol-3-Phosphate Dehydrogenase 1 (Soluble) Kits (3) and many more products for this protein.

list all antibodies Gene Name GeneID UniProt
GPD1 60666 O35077
GPD1 2819 P21695
GPD1 14555 P13707
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Top anti-Glycerol-3-Phosphate Dehydrogenase 1 (Soluble) Antibodies at

Showing 10 out of 126 products:

Catalog No. Reactivity Host Conjugate Application Images Quantity Delivery Price Details
Cow Rabbit Un-conjugated WB WB Suggested Anti-GPD1 Antibody Titration:  0.2-1 ug/ml  ELISA Titer:  1:62500  Positive Control:  Transfected 293T 100 μL 2 to 3 Days
Cow Rabbit Un-conjugated IHC, WB WB Suggested Anti-GPD1 Antibody Titration:  0.2-1 ug/ml  ELISA Titer:  1:312500  Positive Control:  Human Lung Rabbit Anti-GPD1 Antibody   Formalin Fixed Paraffin Embedded Tissue: Human Liver Tissue Observed Staining: Cytoplasm in bile ductule Primary Antibody Concentration: 1:100 Other Working Concentrations: N/A Secondary Antibody: Donkey anti-Rabbit-Cy3 Secondary Antibody Concentration: 1:200 Magnification: 20X Exposure Time: 0.5 - 2.0 sec 100 μL 2 to 3 Days
Human Rabbit Un-conjugated ICC, IF, IHC (p), WB WB Image Sample(30 μg of whole cell lysate) A:Hep G2, 12% SDS PAGE antibody diluted at 1:1000 IHC-P Image Immunohistochemical analysis of paraffin-embedded human stomach , using GPD1, antibody at 1:100 dilution. 100 μL 3 to 4 Days
Human Rabbit Un-conjugated EIA, FACS, IHC (p), WB AP17436PU-N GPD1 Antibody (N-term) Flow Cytometry analysis of HepG2 cells (bottom histogram) compared to a negative control cell (top histogram). FITC-conjugated Goat-anti-Rabbit secondary antibodies were used for the analysis. AP17436PU-N GPD1 Antibody (N-term) staining of Formalin-Fixed, Paraffin-Embedded Human brain tissue using a peroxidase-conjugated to the secondary antibody, followed by DAB staining. 0.4 mL 6 to 8 Days
Human Rabbit Un-conjugated WB 100 μL 11 to 14 Days
Dog Rabbit Un-conjugated WB 100 μL 11 to 14 Days
Rabbit Goat HRP ELISA, WB Western Blot results of Goat Anti-Glycerol 3 Phosphate-Dehydrogenase Peroxidase Conjugated. Lane 1: Opal Prestained Molecular weight Ladder . Lane 2: Glycerol 3 Phosphate-Dehydrogenase. Load: 1µg. Primary Antibody: Goat anti-Glycerol 3 Phosphate-Dehydrogenase Peroxidase Conjugated Antibody at 1µg/mL overnight at 4°C. Secondary Antibody: Donkey Anti-Goat HRP  at 1:40,000 for 30min at RT. Blocking: BlockOut  for 30 min at RT. Expect: ~37kDa. 100 μg 5 to 7 Days
Human Rabbit Un-conjugated IHC, WB Western blot analysis of extracts of various cell lines, using GPD1 antibody (ABIN5973343) at 1/1000 dilution. Immunohistochemistry of paraffin-embedded rat heart using GPD1 Antibody (ABIN5973343) at dilution of 1/100 (40x lens). 100 μL 11 to 16 Days
Human Rabbit Un-conjugated FACS, IHC (p), WB Western blot analysis of GPD1 Antibody (N-term) (ABIN652446) in mouse brain tissue lysates (35 µg/lane). GPD1 (arrow) was detected using the purified polyclonal antibody. Formalin-fixed and paraffin-embedded human brain tissue reacted with GPD1 Antibody (N-term), which was peroxidase-conjugated to the secondary antibody, followed by DAB staining. 400 μL 10 to 11 Days
Human Rabbit Un-conjugated ELISA, WB Western blot analysis GPD1 using COLO205 whole cell lysates 100 μL 11 to 12 Days

Top referenced anti-Glycerol-3-Phosphate Dehydrogenase 1 (Soluble) Antibodies

  1. Human Polyclonal GPD1 Primary Antibody for ICC, IF - ABIN4314742 : Joshi, Eagan, Desai, Newton, Towne, Marinakis, Esteves, De Ferranti, Bennett, McIntyre, Beggs, Berry, Agrawal: A compound heterozygous mutation in GPD1 causes hepatomegaly, steatohepatitis, and hypertriglyceridemia. in European journal of human genetics : EJHG 2014 (PubMed)

More Antibodies against Glycerol-3-Phosphate Dehydrogenase 1 (Soluble) Interaction Partners

Human Glycerol-3-Phosphate Dehydrogenase 1 (Soluble) (GPD1) interaction partners

  1. These results support the conclusion that the rate acceleration for Glycerol-3-Phosphate Dehydrogenase-catalyzed reactions is due to the stabilization of the transition state for hydride transfer by interactions with the protein catalyst.

  2. To recognize this entity by considering GPD1 mutations in appropriate clinical settings.

  3. Although these data indicate that a lack of GPD1 inhibits gluconeogenesis from glycerol, chronic GPD1 deficiency may induce an adaptation that enhances gluconeogenesis from glycogenic amino acids

  4. The R269A mutation of GPDH1 results in a 110-fold increase in K(m) (2.8 kcal/mol effect) and a 41,000-fold decrease in k(cat) (6.3 kcal/mol effect), which corresponds to a 9.1 kcal/mol destabilization of the transition state.

  5. massive hepatomegaly, fatty liver and severe hypertriglyceridemia carrying a compound heterozygous mutation in GPD1

  6. Mutation analysis revealed a homozygous splicing mutation, c.361-1G>C, which resulted in an aberrantly spliced mRNA in the ten affected individuals.

  7. The expression levels of the GPD1 gene did not differ between patients with OSA and their matched controls. The results were not affected by the clinical and biochemical measurements, the sleep parameters or the severity of nocturnal hypoxemia.

  8. Identification and function of mutations in FAD-binding domain of mitochonrial glycerophosphate dehydrogenase in caucasians with type 2 diabetes mellitus.

  9. GPD1 has a role in increased triacylglycerol production in adipose tissue of obese humans

  10. The apoenzyme structure of GPD1 has been determined; an electrophilic catalytic mechanism by the epsilon-NH3+ group of Lys204 is proposed on the basis of structural analyses.

  11. GpD1 is a weight-loss-responsive gene in skeletal muscle. Its observed transcriptional modulation may decrease triglyceride synthesis, with weight loss.

  12. The activities of glycerol phosphate dehydrogenase were decreased by 73% in pancreatic islets of patients with type 2 diabetes.

  13. the discovery overexpression of GPD1 and RRBP1 proteins and lack of expression for HNRNPH1 and SERPINB6 proteins which are new candidate biomarkers of colon cancer.

Fruit Fly (Drosophila melanogaster) Glycerol-3-Phosphate Dehydrogenase 1 (Soluble) (GPD1) interaction partners

  1. Gene trees for the GPDH and GPO paralogs indicate that the genes expressed in the flight muscles are evolving very slowly presumably under strong purifying selection whereas the paralogs expressed in the testes are evolving more rapidly.

  2. Molecular analysis of alpha glycerophosphate dehydrogenase and alpha glycerophosphate oxidase mutants.

  3. molecular polymorphism associated with GPDH activity could be maintained in natural populations by selection related to adaptation to alcohol

Mouse (Murine) Glycerol-3-Phosphate Dehydrogenase 1 (Soluble) (GPD1) interaction partners

  1. GPD1 null mice showed increased exercise capacity. Exercise-induced lipid oxidation was enhanced in GPD1 null mice.

  2. GPD1 and glycolytic gene expression is up-regulated by ethanol, and GPD1-mediated incorporation of glucose into triglycerides glycerol moieties together with increased lipogenesis plays a role in ethanol-induced hepatic triglycerides accumulation.

  3. Knockout mice deficient in both cytosolic and mitochondrial GPD have lethal hypoglycemic ketosis and glyceroluria.

Pig (Porcine) Glycerol-3-Phosphate Dehydrogenase 1 (Soluble) (GPD1) interaction partners

  1. the pig GPD1 gene is regulated negatively by C/EBP beta in cultured kidney cells

  2. The full-length genomic sequence of porcine GPD1 gene including promoter region, is reported.

Glycerol-3-Phosphate Dehydrogenase 1 (Soluble) (GPD1) Antigen Profile

Protein Summary

This gene encodes a member of the NAD-dependent glycerol-3-phosphate dehydrogenase family. The encoded protein plays a critical role in carbohydrate and lipid metabolism by catalyzing the reversible conversion of dihydroxyacetone phosphate (DHAP) and reduced nicotine adenine dinucleotide (NADH) to glycerol-3-phosphate (G3P) and NAD+. The encoded cytosolic protein and mitochondrial glycerol-3-phosphate dehydrogenase also form a glycerol phosphate shuttle that facilitates the transfer of reducing equivalents from the cytosol to mitochondria. Mutations in this gene are a cause of transient infantile hypertriglyceridemia. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene.

Gene names and symbols associated with GPD1

  • glycerol-3-phosphate dehydrogenase 1 (Gpd1) antibody
  • Glycerol-3-phosphate dehydrogenase [NAD(+)] (gpdh-1) antibody
  • glycerol-3-phosphate dehydrogenase 1 (GPD1) antibody
  • glycerol-3-phosphate dehydrogenase (Tb11.02.5280) antibody
  • Glycerol 3 phosphate dehydrogenase (Gpdh) antibody
  • glycerol-3-phosphate dehydrogenase 1 (soluble) (Gpd1) antibody
  • glycerol-3-phosphate dehydrogenase 1 L homeolog (gpd1.L) antibody
  • glycerol-3-phosphate dehydrogenase 1c (gpd1c) antibody
  • glycerol-3-phosphate dehydrogenase 1 (gpd1) antibody
  • glycerol-3-phosphate dehydrogenase 1 (soluble) (GPD1) antibody
  • glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic (LOC101071719) antibody
  • glycerol-3-phosphate dehydrogenase 1b (gpd1b) antibody
  • AI747587 antibody
  • alpha-GPD antibody
  • alpha-Gpdh antibody
  • alpha-GPDH-1 antibody
  • alphaGpd antibody
  • alphaGpdh antibody
  • alphaGpdh-1 antibody
  • CG9042 antibody
  • Dmel\\CG9042 antibody
  • DmG3PDH antibody
  • DROGPDHA antibody
  • G3pdh antibody
  • GAPDH antibody
  • Gdc-1 antibody
  • Gdc1 antibody
  • Gdh antibody
  • Gpd antibody
  • GPD-C antibody
  • Gpd1 antibody
  • gpd1h antibody
  • gpd1l antibody
  • Gpd3 antibody
  • GPDA antibody
  • gpdh antibody
  • gpdh-1 antibody
  • GPDH-C antibody
  • HTGTI antibody
  • LG3P antibody
  • MGC79676 antibody
  • mKIAA4010 antibody
  • sn-Gpdh antibody
  • wu:fc30a07 antibody
  • wu:fc58b05 antibody
  • zgc:63859 antibody
  • zgc:66051 antibody
  • zgc:85742 antibody

Protein level used designations for GPD1

GPD-C , GPDH-C , glycerol 3-phosphate dehydrogenase , glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic , glycerol-3-phosphate dehydrogenase [NAD+], cytoplasmic , Glycerol-3-Phosphate DeHydrogenase family member (gpdh-1) , glycerophosphate dehydrogenase , glycerol-3-phosphate dehydrogenase , 5' gene , Alpha-Glycerophosphate dehydrogenase , CG9042-PA , CG9042-PB , CG9042-PC , CG9042-PD , CG9042-PE , CG9042-PF , CG9042-PG , Gpdh-PA , Gpdh-PB , Gpdh-PC , Gpdh-PD , Gpdh-PE , Gpdh-PF , Gpdh-PG , alpha glycerophosphate dehydrogenase , alpha-glycerol phosphate dehydrogenase , alpha-glycerol-3-phosphate dehydrogenase , dehydrogenase , glycerol 3 phosphate dehydrogenase , sn-glycerol 3-phosphate dehydrogenase , sn-glycerol-3-phosphate , sn-glycerol-3-phosphate dehydrogenase , glycerol phosphate dehydrogenase 1, cytoplasmic adult , glycerolphosphate dehydrogenase 1, cytoplasmic adult , fc30a07 , glycerol-3-phosphate dehydrogenase 1 (soluble) , Glycerol-3-phosphate dehydrogenase [NAD+], cytoplasmic , Glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic , glycerol-3-phosphate dehydrogenase 1 (soluble), like , glycerol-3-phosphate dehydrogenase 1b , glycerol-3-phosphate dehydrogenase 1h

60666 Rattus norvegicus
173272 Caenorhabditis elegans
2819 Homo sapiens
3665563 Trypanosoma brucei brucei strain 927/4 GUTat10.1
33824 Drosophila melanogaster
14555 Mus musculus
399227 Xenopus laevis
406615 Danio rerio
448519 Xenopus (Silurana) tropicalis
525042 Bos taurus
607942 Canis lupus familiaris
713384 Macaca mulatta
741054 Pan troglodytes
100052204 Equus caballus
100153250 Sus scrofa
100172201 Pongo abelii
100594138 Nomascus leucogenys
101071719 Takifugu rubripes
100720368 Cavia porcellus
325181 Danio rerio
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