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SCCPDH Antikörper

SCCPDH Reaktivität: Human, Maus WB Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN7260229
  • Target Alle SCCPDH Antikörper anzeigen
    SCCPDH (Saccharopine Dehydrogenase (SCCPDH))
    Reaktivität
    • 16
    • 11
    • 11
    • 3
    • 3
    • 2
    • 2
    • 1
    Human, Maus
    Wirt
    • 14
    • 2
    Kaninchen
    Klonalität
    • 16
    Polyklonal
    Konjugat
    • 9
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser SCCPDH Antikörper ist unkonjugiert
    Applikation
    • 9
    • 2
    • 1
    • 1
    Western Blotting (WB)
    Produktmerkmale
    Polyclonal Antibody
    Aufreinigung
    Affinity purification
    Immunogen
    Recombinant fusion protein of human SCCPDH (NP_057086.2).
    Isotyp
    IgG
    Top Product
    Discover our top product SCCPDH Primärantikörper
  • Applikationshinweise
    WB 1:500-1:2000
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    1 mg/mL
    Buffer
    PBS with 0.02 % sodium azide, 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.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    SCCPDH (Saccharopine Dehydrogenase (SCCPDH))
    Andere Bezeichnung
    SCCPDH (SCCPDH Produkte)
    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: 45 kDa

    Calculated_MW: 47 kDa

    Gen-ID
    51097
    UniProt
    Q8NBX0
    Pathways
    SARS-CoV-2 Protein Interaktom
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