| Overview |
| bs-9772R |
| C10orf93 Polyclonal Antibody |
| WB, ELISA, IHC-P, IHC-F, IF |
| Human, Mouse, Rat |
| Specifications |
| Unconjugated |
| Rabbit |
| KLH conjugated synthetic peptide derived from human C10orf93 |
| Polyclonal |
| #REF! |
| IgG |
| 1ug/ul |
| Purified by Protein A. |
| 0.01M TBS(pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol. |
| Shipped at 4C. Store at -20C for one year. Avoid repeated freeze/thaw cycles. |
| Target |
| 54777 |
| Q8IYW2 |
| TTC40; C10orf92; C10orf93; C10orf123; C10orf124; bA288G11.4; bA288G11.5; bB137A17.2; bB137A17.3; Protein CFAP46; Cilia- and flagella-associated protein 46; Tetratricopeptide repeat protein 40; CFAP46 |
| C10orf93 , also known as C10orf124 or TPR repeat-containing protein C10orf93, is a 1,530 amino acid protein that contains two TPR repeats and exists as three alternatively spliced isoforms. The gene encoding C10orf93 maps to human chromosome 10q26.3. Spanning nearly 135 million base pairs, chromosome 10 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, Wolman?s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria. |
| Application Dilution |
| WB |
IHC-P1:200-400 |
| ELISA |
IFIHC-P1:50-200 |
| IHC-P |
|
| IHC-F |
|
| IF |
|