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Pyruvate Dehydrogenase E1-alpha subunit Rabbit pAb

Cat No.: APA1235
Size:
Product Name: Pyruvate Dehydrogenase E1-alpha subunit Rabbit pAb
Cat No.: APA1235
source: Rabbit
reactivity: Human, Mouse, Rat
applications: WB,IHC,ICC/IF,FC,IP
clonality: Polyclonal
recommended dilution: WB: 1:1000-1:2000
IHC: 1:20-1:100
ICC/IF: 1:20-1:100
FC: 1:20
IP: 1:20-1:50
format: Liquid
isotype: IgG
immunogen: A synthetic peptide of human Pyruvate Dehydrogenase E1-alpha subunit
calculated molecular weight: 43 kDa
observed molecular weight: 43 kDa
genbank accession number: P08559
gene id (ncbi): 5160
purification method: Affinity Purification
conjugate: Un-conjugated
storage: Store at -20°C. Supplied in 50nM Tris-Glycine(pH 7.4), 0.15M NaCl, 40%Glycerol, 0.01% sodium azide and 0.05% BSA. Stable for 12 months from date of receipt.
synonyms: PDHA; PDHAD; PHE1A; PDHCE1A
category: Primary Ab
concentration: 0.5mg/ml
background: The pyruvate dehydrogenase (PDH) complex is a nuclear-encoded mitochondrial multienzyme complex that catalyzes the overall conversion of pyruvate to acetyl-CoA and CO(2), and provides the primary link between glycolysis and the tricarboxylic acid (TCA) cycle. The PDH complex is composed of multiple copies of three enzymatic components: pyruvate dehydrogenase (E1), dihydrolipoamide acetyltransferase (E2) and lipoamide dehydrogenase (E3). The E1 enzyme is a heterotetramer of two alpha and two beta subunits. This gene encodes the E1 alpha 1 subunit containing the E1 active site, and plays a key role in the function of the PDH complex. Mutations in this gene are associated with pyruvate dehydrogenase E1-alpha deficiency and X-linked Leigh syndrome. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Mar 2010]