GPD1 Polyclonal Antibody
€0.00
In stock
SKU
E-AB-61081
Catalog Number: E-AB-61081
Isotype: Rabbit IgG
Reactivity: human, mouse, rat
Applications: WB,IHC
Datasheet, Questions? Contact us!
Isotype: Rabbit IgG
Reactivity: human, mouse, rat
Applications: WB,IHC
Datasheet, Questions? Contact us!
Background:
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.
Research Area: Cancer, Cardiovascular, Metabolism, Signal Transduction
Synonyms:
GPD1, GPD-C, GPDH-C, HTGTI
Immunogen: Recombinant fusion protein of human GPD1 (NP_005267.2).
Swissprot: P21695
Gene ID: 2819
Calculated MW: 35 kDa/37 kDa
Observed MW: 38 kDa
Purification Method: Affinity purification
Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3
Concentration: 1 mg/mL
Dilution: "WB 1:500-1:2000 IHC 1:50-1:200"
Storage:
Store at -20°C. Avoid freeze / thaw cycles.
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.
Research Area: Cancer, Cardiovascular, Metabolism, Signal Transduction
Synonyms:
GPD1, GPD-C, GPDH-C, HTGTI
Immunogen: Recombinant fusion protein of human GPD1 (NP_005267.2).
Swissprot: P21695
Gene ID: 2819
Calculated MW: 35 kDa/37 kDa
Observed MW: 38 kDa
Purification Method: Affinity purification
Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3
Concentration: 1 mg/mL
Dilution: "WB 1:500-1:2000 IHC 1:50-1:200"
Storage:
Store at -20°C. Avoid freeze / thaw cycles.
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