OAT monoclonal antibody, clone AT23A2

Catalog # MAB16138

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Size:50 uL
Price: USD $ 531.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
Images
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
Application

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)

Immunohistochemical staining (Formalin-fixed paraffin-embedded sections) of human kidney with OAT monoclonal antibody, clone AT23A2 (Cat # MAB16138).

  • Specification

    Product Description

    Mouse monoclonal antibody raised against recombinant human OAT.

    Immunogen

    Recombinant protein corresponding to human OAT.

    Host

    Mouse

    Reactivity

    Human

    Form

    Liquid

    Purification

    Protein G purification

    Isotype

    IgG1, kappa

    Recommend Usage

    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) (5 ug/mL)
    The optimal working dilution should be determined by the end user.

    Storage Buffer

    In PBS, pH 7.4 (0.09% sodium azide).

    Storage Instruction

    Store at 4°C. For long term storage store at -20°C.
    Aliquot to avoid repeated freezing and thawing.

    Note

    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

  • Applications

    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)

    Immunohistochemical staining (Formalin-fixed paraffin-embedded sections) of human kidney with OAT monoclonal antibody, clone AT23A2 (Cat # MAB16138).
  • Gene Info — OAT

    Entrez GeneID

    4942

    Protein Accession#

    P04181

    Gene Name

    OAT

    Gene Alias

    DKFZp781A11155, HOGA

    Gene Description

    ornithine aminotransferase (gyrate atrophy)

    Omim ID

    258870

    Gene Ontology

    Hyperlink

    Gene Summary

    This gene encodes the mitochondrial enzyme ornithine aminotransferase, which is a key enzyme is the pathway that converts arginine and ornithine into the major excitatory and inhibitory neurotransmitters glutamate and GABA. Mutations that result in a deficiency of this enzyme cause the autosomal recessive eye disease Gyrate Atrophy. [provided by RefSeq

    Other Designations

    OTTHUMP00000020690|ornithine aminotransferase

  • 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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