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MMAA Antikörper (Alexa Fluor 488)

MMAA Reaktivität: Human, Maus, Ratte WB, IF (p) Wirt: Kaninchen Polyclonal Alexa Fluor 488
Produktnummer ABIN1405690
  • Target Alle MMAA Antikörper anzeigen
    MMAA (Methylmalonic Aciduria (Cobalamin Deficiency) Type A (MMAA))
    Reaktivität
    • 33
    • 22
    • 15
    • 1
    • 1
    • 1
    • 1
    • 1
    Human, Maus, Ratte
    Wirt
    • 30
    • 3
    Kaninchen
    Klonalität
    • 32
    • 1
    Polyklonal
    Konjugat
    • 10
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser MMAA Antikörper ist konjugiert mit Alexa Fluor 488
    Applikation
    • 33
    • 14
    • 12
    • 12
    • 6
    • 1
    Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
    Kreuzreaktivität
    Human, Maus, Ratte
    Aufreinigung
    Purified by Protein A.
    Immunogen
    KLH conjugated synthetic peptide derived from human MMAA/cblA
    Isotyp
    IgG
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  • Applikationshinweise
    IF(IHC-P) 1:50-200
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    1 μg/μL
    Buffer
    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
    Konservierungsmittel
    ProClin
    Vorsichtsmaßnahmen
    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
    Haltbarkeit
    12 months
  • Target
    MMAA (Methylmalonic Aciduria (Cobalamin Deficiency) Type A (MMAA))
    Andere Bezeichnung
    cblA (MMAA Produkte)
    Synonyme
    2810018E08Rik antikoerper, AI840684 antikoerper, cblA antikoerper, methylmalonic aciduria (cobalamin deficiency) type A antikoerper, methylmalonic aciduria (cobalamin deficiency) cblA type antikoerper, Mmaa antikoerper, MMAA antikoerper
    Hintergrund

    Synonyms: mitochondrial, cblA, MMAA protein, Methylmalonic aciduria cobalamin deficiency cblA type, Methylmalonic aciduria cobalamin deficiency type A, Methylmalonic aciduria type A protein, Methylmalonic aciduria type A protein mitochondrial, MMAA, MMAA_HUMAN.

    Background: The protein encoded by this gene is involved in the translocation of cobalamin into the mitochondrion, where it is used in the final steps of adenosylcobalamin synthesis. Adenosylcobalamin is a coenzyme required for the activity of methylmalonyl-CoA mutase. Defects in this gene are a cause of methylmalonic aciduria. [provided by RefSeq, Jul 2008].

    Gen-ID
    166785
    Pathways
    Monocarboxylic Acid Catabolic Process
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