CCDC19 Antikörper

Produktnummer ABIN7190228

Produktdetails anti-CCDC19 Antikörper

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

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser CCDC19 Antikörper ist unkonjugiert

Applikation: ELISA, Immunohistochemistry (IHC)

Kreuzreaktivität: Human

Aufreinigung: Antigen affinity purification

Immunogen: Synthetic peptide of Human CFAP45

Isotyp: IgG

Anwendungsinformationen

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

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

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.

Details zu CCDC19

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

Andere Bezeichnung: CFAP45 (CCDC19 Produkte)

Synonyme: nesg1 antikoerper, MGC76242 antikoerper, CCDC19 antikoerper, NESG1 antikoerper, 1700028D05Rik antikoerper, Nesg1 antikoerper, cilia and flagella associated protein 45 antikoerper, cilia and flagella associated protein 45 S homeolog antikoerper, coiled-coil domain-containing protein 19, mitochondrial antikoerper, cfap45 antikoerper, CFAP45 antikoerper, cfap45.S antikoerper, LOC748703 antikoerper, Cfap45 antikoerper

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