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SMCR7 Antikörper

SMCR7 Reaktivität: Human WB Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN7468985
  • Target Alle SMCR7 Antikörper anzeigen
    SMCR7 (Smith-Magenis Syndrome Chromosome Region, Candidate 7 (SMCR7))
    Reaktivität
    • 5
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    Human
    Wirt
    • 4
    • 1
    Kaninchen
    Klonalität
    • 4
    • 1
    Polyklonal
    Konjugat
    • 5
    Dieser SMCR7 Antikörper ist unkonjugiert
    Applikation
    • 5
    • 3
    • 2
    Western Blotting (WB)
    Kreuzreaktivität
    Human, Maus
    Aufreinigung
    Purified by antigen-affinity chromatography.
    Immunogen
    Recombinant protein encompassing a sequence within the center region of human SMCR7. The exact sequence is proprietary.
    Isotyp
    IgG
    Top Product
    Discover our top product SMCR7 Primärantikörper
  • Applikationshinweise
    WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.
    Kommentare

    Positive Control: Raji , Mouse brain , RD

    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    1.01 mg/mL
    Buffer
    0.1M Tris-Glycine ( pH 7), 20 % Glycerol, 0.01 % Thimerosal
    Konservierungsmittel
    Thimerosal (Merthiolate)
    Vorsichtsmaßnahmen
    This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Lagerung
    4 °C,-20 °C
    Informationen zur Lagerung
    Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
  • Target
    SMCR7 (Smith-Magenis Syndrome Chromosome Region, Candidate 7 (SMCR7))
    Andere Bezeichnung
    mitochondrial elongation factor 2 (SMCR7 Produkte)
    Hintergrund

    Synonyms: mitochondrial elongation factor 2 , MID49 , SMCR7

    Background: This gene encodes a protein of unknown function. The gene is located within the Smith-Magenis syndrome region on chromosome 17. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms. [provided by RefSeq]

    Molekulargewicht
    49 kDa
    Gen-ID
    125170
    UniProt
    Q96C03
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