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HSD17B10 Antikörper

Dieses Kaninchen Monoklonal-Antikörper erkennt spezifisch HSD17B10 in WB. Er zeigt eine Reaktivität gegenüber Human.
Produktnummer ABIN1513420

Kurzübersicht für HSD17B10 Antikörper (ABIN1513420)

Target

Alle HSD17B10 Antikörper anzeigen
HSD17B10 (Hydroxysteroid (17-Beta) Dehydrogenase 10 (HSD17B10))

Reaktivität

  • 56
  • 26
  • 18
  • 3
  • 2
  • 2
  • 2
Human

Wirt

  • 50
  • 9
  • 1
Kaninchen

Klonalität

  • 53
  • 7
Monoklonal

Konjugat

  • 39
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Dieser HSD17B10 Antikörper ist unkonjugiert

Applikation

  • 36
  • 23
  • 19
  • 15
  • 13
  • 12
  • 10
  • 6
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Kreuzreaktivität

    Human, Maus, Ratte

    Produktmerkmale

    Monoclonal Antibodies

    Aufreinigung

    Affinity purification

    Immunogen

    A synthesized peptide derived from human ERAB/HSD17B10

    Isotyp

    IgG
  • Applikationshinweise

    WB,1:500 - 1:2000

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,0.05 % BSA,50 % glycerol, pH 7.3.

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

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

    Handhabung

    Avoid freeze / thaw cycles

    Lagerung

    -20 °C

    Informationen zur Lagerung

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    HSD17B10 (Hydroxysteroid (17-Beta) Dehydrogenase 10 (HSD17B10))

    Andere Bezeichnung

    HSD17B10

    Hintergrund

    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 and steroids, and is a subunit of mitochondrial ribonuclease P, which is involved in tRNA maturation. The protein has been implicated in the development of Alzheimer disease, and mutations in the gene are the cause of 17beta-hydroxysteroid dehydrogenase type 10 (HSD10) deficiency. Several alternatively spliced transcript variants have been identified, but the full-length nature of only two transcript variants has been determined. [provided by RefSeq, Aug 2014],17b-HSD10, ABAD, CAMR, DUPXp11.22, ERAB, HADH2, HCD2, MHBD, MRPP2, MRX17, MRX31, MRXS10, SCHAD, SDR5C1,Endocrine & Metabolism,Mitochondrial metabolism,Mitochondrial metabolism_Mitochondrial markers,Neurodegenerative Diseases,Neurodegenerative Diseases_Amyloid Plaque and Neurofibrillary Tangle Formation in Alzheimers Disease,Neuroscience,HSD17B10

    Molekulargewicht

    27 kDa

    Gen-ID

    3028

    UniProt

    Q99714
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