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SAMD9 antibody (FITC)

SAMD9 Reactivity: Human, Mouse, Rat IF (p) Host: Rabbit Polyclonal FITC
Catalog No. ABIN1400270
  • Target See all SAMD9 Antibodies
    SAMD9 (Sterile alpha Motif Domain Containing 9 (SAMD9))
    Reactivity
    Human, Mouse, Rat
    Host
    • 34
    Rabbit
    Clonality
    • 34
    Polyclonal
    Conjugate
    • 8
    • 4
    • 4
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This SAMD9 antibody is conjugated to FITC
    Application
    • 16
    • 16
    • 14
    • 12
    • 6
    • 1
    Immunofluorescence (Paraffin-embedded Sections) (IF (p))
    Cross-Reactivity
    Human, Mouse, Rat
    Purification
    Purified by Protein A.
    Immunogen
    KLH conjugated synthetic peptide derived from human SAMD9
    Isotype
    IgG
    Top Product
    Discover our top product SAMD9 Primary Antibody
  • Application Notes
    IF(IHC-P) 1:50-200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 μg/μL
    Buffer
    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
    Preservative
    ProClin
    Precaution of Use
    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
    Expiry Date
    12 months
  • Target
    SAMD9 (Sterile alpha Motif Domain Containing 9 (SAMD9))
    Alternative Name
    SAMD9 (SAMD9 Products)
    Synonyms
    C7orf5 antibody, DRIF1 antibody, NFTC antibody, OEF1 antibody, OEF2 antibody, sterile alpha motif domain containing 9 antibody, SAMD9 antibody
    Background

    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.

    Gene ID
    54809
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