CCDC19 anticorps

N° du produit ABIN7190228

L’anticorps Lapin Polyclonal anti-CCDC19 a été validé pour ELISA et IHC. Il convient pour détecter CCDC19 dans des échantillons de Humain.

Aperçu rapide pour CCDC19 anticorps (ABIN7190228)

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

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp CCDC19 est non-conjugé

Application: ELISA, Immunohistochemistry (IHC)

Détail du produit anti-CCDC19 anticorps

Fonction: CFAP45 Antibody

Purification: Antigen affinity purification

Immunogène: Synthetic peptide of Human CFAP45

Isotype: IgG

Information d'application

Indications d'application: Optimal working dilution should be determined by the investigator.

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer:  pH 7.4 PBS, 0.05 % Sodium azide, 40 % Glycerol

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C,-80 °C

Stockage commentaire: Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.

Détails sur CCDC19

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

Autre désignation: CFAP45

Sujet:

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