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C12ORF50 Antikörper (Chromosome 12 Open Reading Frame 50) Primary Antibody

C12ORF50 Reaktivität: Human, Maus, Ratte IF (p), IHC (p), WB Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN1385100
$374.00
Zzgl. Versandkosten $45.00
100 μL
local_shipping Lieferung nach: Vereinigte Staaten von Amerika
Lieferung in 4 bis 6 Werktagen
  • Target See all C12ORF50 products
    C12ORF50
    Reaktivität
    • 22
    • 15
    • 14
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    Human, Maus, Ratte
    Wirt
    • 22
    Kaninchen
    Klonalität
    • 22
    Polyklonal
    Konjugat
    • 5
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser C12ORF50 Antikörper ist unkonjugiert
    Applikation
    • 12
    • 6
    • 5
    • 2
    Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Western Blotting (WB)
    Aufreinigung
    Purified by Protein A.
    Immunogen
    KLH conjugated synthetic peptide derived from human C12ORF50
    Isotyp
    IgG
  • Applikationshinweise
    WB 1:300-5000
    IHC-P 1:200-400
    IF(IHC-P) 1:50-200
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    1 μg/μL
    Buffer
    0.01M TBS( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
    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 for one year. Avoid repeated freeze/thaw cycles.
    Haltbarkeit
    12 months
  • Target
    C12ORF50
    Andere Bezeichnung
    C12ORF50 (C12ORF50 Produkte)
    Synonyme
    C12orf50, MGC134438, chromosome 1 C12orf50 homolog, chromosome 12 open reading frame 50, chromosome 5 open reading frame, human C12orf50, C1H12orf50, C12orf50, C5H12orf50
    Hintergrund

    Encoding over 1,100 genes within 132 million bases, chromosome 12 makes up about 4.5 % of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The C12orf50 gene product has been provisionally designated C12orf50 pending further characterization.

    Synonyms: C5H12orf50, Chromosome 12 open reading frame 50, chromosome 12 open reading frame 50 ortholog, Hypothetical protein LOC160419, CL050_HUMAN.

    Gen-ID
    160419
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