| Product Name | R3HCC1L Antibody |
|---|---|
| Description | Rabbit polyclonal antibody to R3HCC1L |
| Synonyms | R3HCC1L antibody; C10orf28 antibody; GIDRP88 antibody; Coiled-coil domain-containing protein R3HCC1L antibody; Growth inhibition and differentiation-related protein 88 antibody; Putative mitochondrial space protein 32.1 antibody; R3H and coiled-coil domain-containing protein 1-like antibody |
| Host | Rabbit |
| Clonality | Polyclonal |
| Conjugate | Unconjugated |
| Immunogen | Synthetic peptide of human R3HCC1L |
| Isotype | IgG |
| Target | R3HCC1L |
| Reactivity | Human, Mouse |
| Applications | ELISA, IHC |
| Form | Liquid |
| Diluent Buffer | -20°C, pH7.4 PBS, 0.05% NaN3, 40% Glycerol |
| Uniprot | Q7Z5L2 |
| Storage | Upon receipt, store at -20°C or -80°C. Avoid repeated freeze. |
| Background | C10orf28 (chromosome 10 open reading frame 28), also known as GIDRP88 (growth inhibition and differentiation-related protein 88) or putative mitochondrial space protein 32.1, is a 792 amino acid protein that exists as three alternatively spliced isoforms. The gene encoding C10orf28 maps to human chromosome 10, which spans nearly 135 million base pairs, makes up approximately 4.5% of total DNA in cells and encodes nearly 1,200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, WolmanÕs syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria. |
| Supplier | Cusabio |
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