GPD1 antibody [HL1959]

Cannot supply to this region.

SKU:: GTX637796
Additional Names:: glycerol-3-phosphate dehydrogenase 1 , GPD-C , GPDH-C , HTGTI
Application:: WB, IHC-P, IF, ICC
Concentration:: 1 mg/ml
Physical State:: Liquid
Species Reactivity:: Human
Purification:: Protein A 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, no preservatives.
Immunogen:: Recombinant protein encompassing a sequence within the C-term region of human GPD1. The exact sequence is proprietary.
Clone:: HL1959
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