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CCDC19 Antikörper

Der Kaninchen Polyklonal Anti-CCDC19-Antikörper wurde für ELISA und IHC validiert. Er ist geeignet, CCDC19 in Proben von Human zu detektieren.
Produktnummer ABIN7190228

Kurzübersicht für CCDC19 Antikörper (ABIN7190228)

Target

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

Reaktivität

  • 35
  • 14
  • 12
  • 4
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
Human

Wirt

  • 35
Kaninchen

Klonalität

  • 35
Polyklonal

Konjugat

  • 10
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser CCDC19 Antikörper ist unkonjugiert

Applikation

  • 29
  • 10
  • 8
  • 3
  • 1
ELISA, Immunohistochemistry (IHC)
  • Kreuzreaktivität

    Human

    Aufreinigung

    Antigen affinity purification

    Immunogen

    Synthetic peptide of Human CFAP45

    Isotyp

    IgG
  • Applikationshinweise

    ELISA:1:2000-1:5000, IHC:1:25-1:100,

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Buffer

    -20 °C, pH 7.4 PBS, 0.05 % Sodium azide, 40 % 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,-80 °C

    Informationen zur Lagerung

    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • Target

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

    Andere Bezeichnung

    CFAP45

    Hintergrund

    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.

    Aliases: CCD19_HUMAN antibody, CCDC19 antibody, Coiled coil domain containing 19 antibody, Coiled-coil domain-containing protein 19 antibody, mitochondrial antibody, Nasopharyngeal epithelium specific protein 1 antibody, Nasopharyngeal epithelium-specific protein 1 antibody, NESG1 antibody, OTTHUMP00000033461 antibody, RP11 190A12.6 antibody

    UniProt

    Q9UL16
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