ALDH4A1 (Human) Matched Antibody Pair

Catalog # H00008659-AP51

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Size:1 Set
Price: USD $ 607.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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QC Test

Sandwich ELISA detection sensitivity ranging from approximately 729x to 3x dilution of the ALDH4A1 293T overexpression lysate (non-denatured).

  • Specification

    Product Description

    This antibody pair set comes with a matched antibody pair to detect and quantify the protein level of human ALDH4A1.

    Reactivity

    Human

    Interspecies Antigen Sequence

    Mouse (91); Rat (91)

    Quality Control Testing

    Standard curve using ALDH4A1 293T overexpression lysate (non-denatured) as an analyte.

    Sandwich ELISA detection sensitivity ranging from approximately 729x to 3x dilution of the ALDH4A1 293T overexpression lysate (non-denatured).

    Supplied Product

    Antibody pair set content:
    1. Capture antibody: mouse monoclonal anti-ALDH4A1 (100 ug)
    2. Detection antibody: rabbit purified polyclonal anti-ALDH4A1 (50 ug)
    *Reagents are sufficient for at least 3-5 x 96 well plates using recommended protocols.

    Storage Instruction

    Store reagents of the antibody pair set at -20°C or lower. Please aliquot to avoid repeated freeze thaw cycle. Reagents should be returned to -20°C storage immediately after use.

  • Applications

    ELISA Pair (Transfected lysate)

  • Gene Info — ALDH4A1

    Entrez GeneID

    8659

    Gene Name

    ALDH4A1

    Gene Alias

    ALDH4, P5CD, P5CDh, P5CDhL, P5CDhS

    Gene Description

    aldehyde dehydrogenase 4 family, member A1

    Omim ID

    239510 606811

    Gene Ontology

    Hyperlink

    Gene Summary

    This protein belongs to the aldehyde dehydrogenase family of proteins. This enzyme is a mitochondrial matrix NAD-dependent dehydrogenase which catalyzes the second step of the proline degradation pathway, converting pyrroline-5-carboxylate to glutamate. Deficiency of this enzyme is associated with type II hyperprolinemia, an autosomal recessive disorder characterized by accumulation of delta-1-pyrroline-5-carboxylate (P5C) and proline. Alternatively spliced transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq

    Other Designations

    OTTHUMP00000002544|OTTHUMP00000002545|P5C dehydrogenase|aldehyde dehydrogenase 4A1|mitochondrial delta-1-pyrroline 5-carboxylate dehydrogenase

  • Interactome
  • Pathway
  • Disease
Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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