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CCDC19 Antikörper (Cy7)

Der Kaninchen Polyklonal Anti-CCDC19-Antikörper wurde für WB validiert. Er ist geeignet, CCDC19 in Proben von Human, Ratte und Maus zu detektieren.
Produktnummer ABIN719147

Kurzübersicht für CCDC19 Antikörper (Cy7) (ABIN719147)

Target

Alle CCDC19 Antikörper anzeigen
CCDC19 (Coiled-Coil Domain Containing 19 (CCDC19))

Reaktivität

  • 35
  • 13
  • 11
  • 4
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
Human, Ratte, Maus

Wirt

  • 35
Kaninchen

Klonalität

  • 35
Polyklonal

Konjugat

  • 11
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser CCDC19 Antikörper ist konjugiert mit Cy7

Applikation

  • 28
  • 11
  • 9
  • 3
  • 1
Western Blotting (WB)
  • Homologie

    Human,Mouse,Rat,Cow,Sheep,Horse,Rabbit

    Aufreinigung

    Purified by Protein A.

    Immunogen

    KLH conjugated synthetic peptide derived from human CCDC19

    Isotyp

    IgG
  • Applikationshinweise

    IF(IHC-P) 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

    Sodium azide

    Vorsichtsmaßnahmen

    This product contains Sodium azide: 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

    CCDC19 (Coiled-Coil Domain Containing 19 (CCDC19))

    Andere Bezeichnung

    Ccdc19

    Hintergrund

    Synonyms: Coiled coil domain containing 19, Nasopharyngeal epithelium specic protein 1, NESG1, RP11 190A12.6, CCD19_HUMAN.

    Background: CCDC19 is a 466 amino acid protein encoded by a gene mapping to human chromosome 1. Chromosome 1 is the largest human chromosome, spanning about 260 million base pairs and making up 8 % of the human genome. There are about 3,000 genes on chromosome 1 and, considering the great number of genes, there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes Lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinson?s, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma.

    Gen-ID

    25790
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