Phospho-Pyruvate Dehydrogenase E1-alpha subunit Rabbit Monoclonal Antibody

Phospho-Pyruvate Dehydrogenase E1-alpha subunit Rabbit Monoclonal Antibody

Cat: AMRe87115
Size:50μL Price:$168
Size:100μL Price:$300
Application:WB,IHC,IP

Reactivity:Human,Mouse,Rat
Conjugate:Unconjugated
Optional conjugates: Biotin, FITC (free of charge).
See other 26 conjugates.

Gene Name:Phospho-Pyruvate Dehydrogenase E1-alpha subunit
Category: Recombinant Monoclonal Antibody Tags: , , , , , , ,

Summary

Production Name

Phospho-Pyruvate Dehydrogenase E1-alpha subunit Rabbit Monoclonal Antibody

Description

Recombinant rabbit monoclonal antibody

Host

Rabbit

Application

WB,IHC,IP

Reactivity

Human,Mouse,Rat

 

Performance

Conjugation

Unconjugated

Modification

Phosphorylated

Isotype

IgG

Clonality

Monoclonal

Form

Liquid

Storage

Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.

Buffer

Supplied in 50mM Tris-Glycine(pH 7.4), 0.15M NaCl, 40% Glycerol, 0.01% sodium azide and 0.05% protective protein. Stable for 12 months from date of receipt.

Purification

Affinity Purification

 

Immunogen

Gene Name

Phospho-Pyruvate Dehydrogenase E1-alpha subunit

Alternative Names

PDHA; PDHAD; PHE1A; PDHCE1A

Gene ID

5160

SwissProt ID

P08559

 

Application

Dilution Ratio

WB 1:1000-1:5000,IHC 1:100-1:200,IP 1:10-1:100

Molecular Weight

Calculated MW:43 kDa; Observed MW:43 kDa

 

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]

 

Research Area

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