HPGD monoclonal antibody, clone AEFF-8

Catalog # MAB22227

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Size:100 uL
Price: USD $ 428.00
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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
Western Blot (Cell lysate)
Application

Western Blot (Cell lysate)

Western blot analysis of SW480 cell lysate.

  • Specification

    Product Description

    Rabbit monoclonal antibody raised against synthetic peptide of human HPGD.

    Immunogen

    A synthetic peptide corresponding to human HPGD.

    Host

    Rabbit

    Reactivity

    Human

    Specificity

    The antibody reacts with human HPGD, in native form and recombinant. Superfamily members of HPGD are not reactive to this antibody.

    Form

    Liquid

    Purification

    Affinity purification

    Isotype

    IgG

    Recommend Usage

    Flow Cytometry (1:60)
    Immunocytochemistry (1:50-1:200)
    Immunofluorescence (1:50-1:200)
    Immunohistochemistry (1:50-1:200)
    Western Blot (1:500-1:2000)
    The optimal working dilution should be determined by the end user.

    Storage Buffer

    In PBS, 150 mM NaCl, pH 7.4 (50% glycerol, 0.02% sodium azide).

    Storage Instruction

    Store at 4°C for short term storage. 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

    Western Blot (Cell lysate)

    Western blot analysis of SW480 cell lysate.

    Immunohistochemistry

    Immunocytochemistry

    Immunofluorescence

    Flow Cytometry

  • Gene Info — HPGD

    Entrez GeneID

    3248

    Protein Accession#

    P15428

    Gene Name

    HPGD

    Gene Alias

    15-PGDH, PGDH, PGDH1, SDR36C1

    Gene Description

    hydroxyprostaglandin dehydrogenase 15-(NAD)

    Omim ID

    601688

    Gene Ontology

    Hyperlink

    Gene Summary

    This gene encodes a member of the short-chain nonmetalloenzyme alcohol dehydrogenase protein family. The encoded enzyme is responsible for the metabolism of prostaglandins, which function in a variety of physiologic and cellular processes such as inflammation. Mutations in this gene result in primary autosomal recessive hypertrophic osteoarthropathy and cranioosteoarthropathy. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq

    Other Designations

    15-hydroxy prostaglandin dehydrogenase|15-hydroxyprostaglandin dehydrogenase|NAD+-dependent 15-hydroxyprostaglandin dehydrogenase|short chain dehydrogenase/reductase family 36C, member 1

  • Interactome
  • 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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