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MMAB anticorps

MMAB Reactivité: Humain WB, IHC, FACS Hôte: Souris Monoclonal 2G5 unconjugated
N° du produit ABIN2726118
  • Antigène Voir toutes MMAB Anticorps
    MMAB (Methylmalonic Aciduria (Cobalamin Deficiency) CblB Type (MMAB))
    Reactivité
    • 8
    • 3
    Humain
    Hôte
    • 5
    • 3
    Souris
    Clonalité
    • 6
    • 2
    Monoclonal
    Conjugué
    • 8
    Cet anticorp MMAB est non-conjugé
    Application
    • 8
    • 4
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC), Flow Cytometry (FACS)
    Attributs du produit
    Homo sapiens methylmalonic aciduria (cobalamin deficiency) cblB type (MMAB), nuclear gene encoding mitochondrial protein, transcript variant 1
    Purification
    Purified from mouse ascites fluids by affinity chromatography
    Immunogène
    Full length human recombinant protein of human MMAB (NP_443077) produced in HEK293T cell.
    Clone
    2G5
    Isotype
    IgG1
    Top Product
    Discover our top product MMAB Anticorps primaire
  • Indications d'application
    WB 1:2000, IHC 1:150, FLOW 1:100
    Commentaires

    The concentration of the product may vary between diferrent lots.

    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.5-1.0 mg/mL
    Buffer
    PBS (PH 7.3) containing 1 % BSA, 50 % glycerol and 0.02 % sodium azide.
    Agent conservateur
    Sodium azide
    Précaution d'utilisation
    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Stock
    -20 °C
  • Antigène
    MMAB (Methylmalonic Aciduria (Cobalamin Deficiency) CblB Type (MMAB))
    Autre désignation
    MMAB (MMAB Produits)
    Synonymes
    anticorps ATR, anticorps cblB, anticorps cob, anticorps 9130222L19Rik, anticorps methylmalonic aciduria (cobalamin deficiency) cblB type, anticorps methylmalonic aciduria (cobalamin deficiency) cblB type homolog (human), anticorps MMAB, anticorps Mmab
    Sujet
    This gene encodes a protein that catalyzes the final step in the conversion of vitamin B(12) into adenosylcobalamin (AdoCbl), a vitamin B12-containing coenzyme for methylmalonyl-CoA mutase. Mutations in the gene are the cause of vitamin B12-dependent methylmalonic aciduria linked to the cblB complementation group.
    Poids moléculaire
    24.0 kDa
    ID gène
    326625
    NCBI Accession
    NM_052845
    HGNC
    326625
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