CCDC19 antibody

Catalog No. ABIN7190228

The Rabbit Polyclonal anti-CCDC19 antibody has been validated for ELISA and IHC. It is suitable to detect CCDC19 in samples from Human.

Quick Overview for CCDC19 antibody (ABIN7190228)

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

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This CCDC19 antibody is un-conjugated

Application: ELISA, Immunohistochemistry (IHC)

Product Details anti-CCDC19 Antibody

Cross-Reactivity: Human

Purification: Antigen affinity purification

Immunogen: Synthetic peptide of Human CFAP45

Isotype: IgG

Application Details

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

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: -20 °C, pH 7.4 PBS, 0.05 % Sodium azide, 40 % Glycerol

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C,-80 °C

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

Target Details for CCDC19

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

Alternative Name: CFAP45

Background:

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