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C9ORF135 Antikörper (AA 151-229) (Cy3)

Der Kaninchen Polyklonal Anti-C9ORF135-Antikörper wurde für WB, IF (cc) und IF (p) validiert. Er ist geeignet, C9ORF135 in Proben von Human zu detektieren.
Produktnummer ABIN1702043

Kurzübersicht für C9ORF135 Antikörper (AA 151-229) (Cy3) (ABIN1702043)

Target

C9ORF135 (Chromosome 9 Open Reading Frame 135 (C9ORF135))

Reaktivität

Human

Wirt

  • 15
Kaninchen

Klonalität

  • 15
Polyklonal

Konjugat

  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser C9ORF135 Antikörper ist konjugiert mit Cy3

Applikation

  • 15
  • 12
  • 12
  • 3
  • 3
  • 3
  • 1
Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • Bindungsspezifität

    • 14
    • 1
    AA 151-229

    Homologie

    Human,Mouse,Rat,Horse,Rabbit

    Aufreinigung

    Purified by Protein A.

    Immunogen

    KLH conjugated synthetic peptide derived from human C9orf135

    Isotyp

    IgG
  • Applikationshinweise

    IF(IHC-P) 1:50-200
    IF(IHC-F) 1:50-200
    IF(ICC) 1:50-200

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Konzentration

    1 μg/μL

    Buffer

    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % 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

    -20 °C

    Informationen zur Lagerung

    Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

    Haltbarkeit

    12 months
  • Target

    C9ORF135 (Chromosome 9 Open Reading Frame 135 (C9ORF135))

    Andere Bezeichnung

    C9orf135

    Hintergrund

    Synonyms: C9orf135, CI135_HUMAN, Uncharacterized protein C9orf135.

    Background: C9orf135 (chromosome 9 open reading frame 135) is a 229 amino acid single-pass membrane protein encoded by a gene that maps to human chromosome 9q21.11. Chromosome 9 consists of about 145 million bases, represents 4 % of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.

    Gen-ID

    138724
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