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C12ORF50 Antikörper

Dieses Anti-C12ORF50-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von C12ORF50 in WB, IF (p) und IHC (p). Geeignet für Human, Ratte und Maus.
Produktnummer ABIN1385100

Kurzübersicht für C12ORF50 Antikörper (ABIN1385100)

Target

C12ORF50 (Chromosome 12 Open Reading Frame 50 (C12ORF50))

Reaktivität

  • 22
  • 15
  • 14
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Human, Ratte, Maus

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

  • 18
  • 12
  • 5
  • 2
Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • Kreuzreaktivität

    Human, Maus, Ratte

    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, 0.02 % Proclin300 and 50 % Glycerol.

    Konservierungsmittel

    ProClin

    Vorsichtsmaßnahmen

    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

    Lagerung

    4 °C,-20 °C

    Informationen zur Lagerung

    Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

    Haltbarkeit

    12 months
  • Target

    C12ORF50 (Chromosome 12 Open Reading Frame 50 (C12ORF50))

    Andere Bezeichnung

    C12ORF50

    Hintergrund

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

    Background: 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.

    Gen-ID

    160419
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