CCDC19 Antikörper (Alexa Fluor 750)

Produktnummer ABIN4999235

Produktdetails anti-CCDC19 Antikörper (Alexa Fluor 750)

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

Reaktivität: Human, Ratte, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser CCDC19 Antikörper ist konjugiert mit Alexa Fluor 750

Applikation: 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

Anwendungsinformationen

Applikationshinweise: IF(IHC-P) 1:50-200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

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.

Lagerung: -20 °C

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

Haltbarkeit: 12 months

Details zu CCDC19

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

Andere Bezeichnung: CCDC19 (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:

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