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SCCPDH Antikörper

Der Kaninchen Polyklonal Anti-SCCPDH-Antikörper wurde für WB, IHC und ELISA validiert. Er ist geeignet, SCCPDH in Proben von Human, Maus und Ratte zu detektieren.
Produktnummer ABIN7247165

Kurzübersicht für SCCPDH Antikörper (ABIN7247165)

Target

Alle SCCPDH Antikörper anzeigen
SCCPDH (Saccharopine Dehydrogenase (SCCPDH))

Reaktivität

  • 17
  • 11
  • 10
  • 3
  • 3
  • 2
  • 2
  • 1
Human, Maus, Ratte

Wirt

  • 15
  • 2
Kaninchen

Klonalität

  • 17
Polyklonal

Konjugat

  • 10
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser SCCPDH Antikörper ist unkonjugiert

Applikation

  • 10
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), ELISA
  • Produktmerkmale

    Polyclonal Antibody

    Aufreinigung

    Antigen affinity purification

    Immunogen

    Fusion protein of human SCCPDH

    Isotyp

    IgG
  • Applikationshinweise

    WB 1:1000-1:5000, IHC 1:50-1:300, ELISA 1:5000-1:10000

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Konzentration

    1.5 mg/mL

    Buffer

    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

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

    Lagerung

    -20 °C

    Informationen zur Lagerung

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

    SCCPDH (Saccharopine Dehydrogenase (SCCPDH))

    Andere Bezeichnung

    SCCPDH

    Hintergrund

    SCCPDH (Probable saccharopine dehydrogenase) is a 429 amino acid protein that belongs to the saccharopine dehydrogenase family. The SCCPDH gene is conserved in chimpanzee, dog, cow, mouse, rat, chicken, fruit fly, mosquito and C.elegans, and maps to human chromosome 1q44. Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8 % of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma.

    Molekulargewicht

    Observed_MW: Refer to figures

    Calculated_MW: 47 kDa

    UniProt

    Q8NBX0

    Pathways

    SARS-CoV-2 Protein Interaktom
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