GTX32630
GPD1 antibody
Cannot supply to this region.
- SKU:
- GTX32630
- Additional Names:
- glycerol-3-phosphate dehydrogenase 1 , GPD-C , GPDH-C , HTGTI
- Application:
- WB, IHC-P
- Physical State:
- Liquid
- Species Reactivity:
- Human
- Purification:
- Affinity Purified
- Storage Conditions:
- -20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
- Supplier:
- Genetex
- Host:
- Rabbit
- Reactivities:
- Human, Mouse, Rat
- Buffer:
- PBS, 50% Glycerol, 0.02% Sodium azide.
- Immunogen:
- Recombinant fusion protein containing a sequence corresponding to amino acids 1-349 of human GPD1 (NP_005267.2).
- Uniprot:
- P21695
- Synonyms:
- epididymis secretory sperm binding protein;glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic;glycerol-3-phosphate dehydrogenase [NAD+], cytoplasmic;glycerol-3-phosphate dehydrogenase 1 (soluble);glycerophosphate dehydrogenase;GPD-C;GPDH-C;HTGTI
- Extra Details:
- 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. [provided by RefSeq, Mar 2012]
- Shipping Conditions:
- Blue Ice