| Product Name | CFAP45 Antibody |
|---|---|
| Description | Rabbit polyclonal antibody to CFAP45 |
| Synonyms | 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 |
| Host | Rabbit |
| Clonality | Polyclonal |
| Conjugate | Unconjugated |
| Immunogen | Synthetic peptide of human CFAP45 |
| Isotype | IgG |
| Target | CFAP45 |
| Reactivity | Human |
| Applications | ELISA, IHC |
| Form | Liquid |
| Diluent Buffer | -20°C, pH7.4 PBS, 0.05% NaN3, 40% Glycerol |
| Uniprot | Q9UL16 |
| Storage | Upon receipt, store at -20°C or -80°C. Avoid repeated freeze. |
| 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, ParkinsonÕs, Gaucher disease and Usher syndrome are also associated with chromosome 1. |
| Supplier | Cusabio |
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