HSD17B10 monoclonal antibody, clone ACOD-8

Catalog # MAB22297

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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 (cell lysate) analysis of HeLa cell lysate.

  • Specification

    Product Description

    Rabbit monoclonal antibody raised against synthetic protein of human HSD17B10.

    Immunogen

    A synthetic peptide corresponding to human HSD17B10.

    Host

    Rabbit

    Reactivity

    Human

    Specificity

    This antibody reacts with human, mouse, rat HSD17B10, in native form and recombinant. Superfamily members of HSD17B10 are not reactive to antibody.

    Form

    Liquid

    Purification

    Affinity purification

    Isotype

    IgG

    Recommend Usage

    Immunofluorescence (1:50-200)
    Western Blot (1:1000-5000)
    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 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 (cell lysate) analysis of HeLa cell lysate.

    Immunofluorescence

  • Gene Info — HSD17B10

    Entrez GeneID

    3028

    Protein Accession#

    Q99714

    Gene Name

    HSD17B10

    Gene Alias

    17b-HSD10, ABAD, CAMR, DUPXp11.22, ERAB, HADH2, HCD2, MHBD, MRPP2, MRX17, MRX31, MRXS10, SCHAD, SDR5C1

    Gene Description

    hydroxysteroid (17-beta) dehydrogenase 10

    Omim ID

    300256 300438

    Gene Ontology

    Hyperlink

    Gene Summary

    This gene encodes 3-hydroxyacyl-CoA dehydrogenase type II, a member of the short-chain dehydrogenase/reductase superfamily. The gene product is a mitochondrial protein that catalyzes the oxidation of a wide variety of fatty acids, alcohols, and steroids. The protein has been implicated in the development of Alzheimer's disease, and mutations in the gene are the cause of 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency (MHBD). Several alternatively spliced transcript variants have been identified, but the full-length nature of only two transcript variants has been determined. [provided by RefSeq

    Other Designations

    17-beta-hydroxysteroid dehydrogenase type 10|3-hydroxy-2-methylbutyryl-CoA dehydrogenase|AB-binding alcohol dehydrogenase|OTTHUMP00000023348|OTTHUMP00000023349|amyloid-beta binding polypeptide|amyloid-beta peptide binding alcohol dehydrogenase|mental reta

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