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MMAB anticorps (Middle Region)

MMAB Reactivité: Humain WB Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN5517725
  • Antigène Voir toutes MMAB Anticorps
    MMAB (Methylmalonic Aciduria (Cobalamin Deficiency) CblB Type (MMAB))
    Épitope
    • 1
    • 1
    • 1
    • 1
    Middle Region
    Reactivité
    • 8
    • 3
    Humain
    Hôte
    • 5
    • 3
    Lapin
    Clonalité
    • 6
    • 2
    Polyclonal
    Conjugué
    • 8
    Cet anticorp MMAB est non-conjugé
    Application
    • 8
    • 4
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    Western Blotting (WB)
    Séquence
    PRIPKIYTKT GDKGFSSTFT GERRPKDDQV FEAVGTTDEL SSAIGFALEL
    Purification
    Affinity purified
    Immunogène
    The immunogen is a synthetic peptide directed towards the middle region of human MMAB
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    Discover our top product MMAB Anticorps primaire
  • Indications d'application
    Optimal working dilution should be determined by the investigator.
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
    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
    Stockage commentaire
    For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
  • 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. Alternatively spliced transcript variants have been found.

    Alias Symbols: ATR, cob, cblB, CFAP23

    Protein Size: 173
    ID gène
    326625
    NCBI Accession
    NP_443077
    UniProt
    F5H4Z7
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