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Rabbit anti-Human PDHA1 Monoclonal Antibody

The antibody against PDHA1 was raised in Rabbit using a synthetic peptide corresponding to a sequence within amino acids 248-348 of human PDHA1 (NP_000275.1) as the immunogen. The monoclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, ELISA.

ADA-14767A

The antibody against PDHA1 was raised in Rabbit using a synthetic peptide corresponding to a sequence within amino acids 248-348 of human PDHA1 (NP_000275.1) as the immunogen. The monoclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, ELISA.

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Specifications


Cat.No ADA-14767A ClonalityMonoclonal
Host SpeciesRabbitTarget NamePDHA1
Target SynonymsPDHA; PDHAD; PHE1A; E1alpha; PDHCE1A; PDHA1FormLiquid
Species ReactivityHuman, MouseIsotypeIgG
Storage Buffer50% Glycerol, 0.05% BSA, PBS with 0.05% proclin300, pH7.3.Purification MethodAffinity purification
Positive SamplesNIH/3T3, HepG2ApplicationELISA, WB

Immunogen Information


Immunogen DescriptionA synthetic peptide corresponding to a sequence within amino acids 248-348 of human PDHA1 (NP_000275.1).Target SpeciesHuman
Immunogen SequenceIPGLRVDGMDILCVREATRFAAAYCRSGKGPILMELQTYRYHGHSMSDPGVSYRTREEIQEVRSKSDPIMLLKDRMVNSNLASVEELKEIDVEVRKEIEDUniprot IDP08559
Background Information
  • Uniprot Id

    P08559

  • Target Species

    Human

  • Target Name

    PDHA1

  • Target Full Name

    Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial

  • Target Function

    The pyruvate dehydrogenase complex catalyzes the overall conversion of pyruvate to acetyl-CoA and CO(2), and thereby links the glycolytic pathway to the tricarboxylic cycle.

  • Target Involvement

    Pyruvate dehydrogenase E1-alpha deficiency (PDHAD)

  • Target Subcellular Location

    Mitochondrion matrix.

  • Target Tissue Specificity

    Ubiquitous.

  • Target Research Area

    Metabolism

  • Target Synonyms

    ODPA_HUMAN; PDH; PDHA; PDHA1; PDHCE1A; PDHE1 A type I ; PDHE1-A type I; PHE1A; Pyruvate Dehydrogenase (lipoamide) alpha 1; Pyruvate dehydrogenase complex, E1 alpha polypeptide 1; Pyruvate Dehydrogenase E1 alpha; Pyruvate dehydrogenase E1 component subunit alpha; Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial

  • Target 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.

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