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SAMD9 anticorps

SAMD9 Reactivité: Humain, Souris, Rat IF (p), IHC (p) Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN1385330
  • Antigène Voir toutes SAMD9 Anticorps
    SAMD9 (Sterile alpha Motif Domain Containing 9 (SAMD9))
    Reactivité
    Humain, Souris, Rat
    Hôte
    • 34
    Lapin
    Clonalité
    • 34
    Polyclonal
    Conjugué
    • 7
    • 4
    • 4
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp SAMD9 est non-conjugé
    Application
    • 16
    • 16
    • 14
    • 12
    • 5
    • 1
    Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
     Réactivité croisée
    Humain, Souris, Rat
    Purification
    Purified by Protein A.
    Immunogène
    KLH conjugated synthetic peptide derived from human SAMD9
    Isotype
    IgG
    Top Product
    Discover our top product SAMD9 Anticorps primaire
  • Indications d'application
    IHC-P 1:200-400
    IF(IHC-P) 1:50-200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 μg/μL
    Buffer
    0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
    Agent conservateur
    ProClin
    Précaution d'utilisation
    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
    Stock
    4 °C,-20 °C
    Stockage commentaire
    Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
    Date de péremption
    12 months
  • Antigène
    SAMD9 (Sterile alpha Motif Domain Containing 9 (SAMD9))
    Autre désignation
    SAMD9 (SAMD9 Produits)
    Synonymes
    anticorps C7orf5, anticorps DRIF1, anticorps NFTC, anticorps OEF1, anticorps OEF2, anticorps sterile alpha motif domain containing 9, anticorps SAMD9
    Sujet

    Synonyms: SAM domain-containing protein 9, SAMD9, SAMD9_HUMAN, sterile alpha mot domain containing 9, Sterile alpha mot domain-containing protein 9, C7orf5.

    Background: Defects in SAMD9 are the cause of normophosphatemic familial tumoral calcinosis (NFTC). NFTC is an uncommon life-threatening disorder characterized by massive periarticular, and seldom visceral, deposition of calcified tumors.

    ID gène
    54809
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