CFAP418 (NM_177965) Human Recombinant Protein
CAT#: TP761071
Purified recombinant protein of Human chromosome 8 open reading frame 37 (C8orf37), full length, with N-terminal HIS tag, expressed in E. coli, 50ug
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CNY 2040.00
货期*
现货
规格
Specifications
| Product Data | |
| Species | Human |
| Expression Host | E. coli |
| Expression cDNA Clone or AA Sequence |
A DNA sequence encoding human full-length C8orf37
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| Tag | N-His |
| Predicted MW | 23.2 kDa |
| Concentration | >0.05 µg/µL as determined by microplate BCA method |
| Purity | > 80% as determined by SDS-PAGE and Coomassie blue staining |
| Buffer | 25 mM Tris-HCl, pH 8.0, 150 mM NaCl, 1% sarkosyl, 10% glycerol |
| Note | For testing in cell culture applications, please filter before use. Note that you may experience some loss of protein during the filtration process. |
| Storage | Store at -80°C. |
| Stability | Stable for 12 months from the date of receipt of the product under proper storage and handling conditions. Avoid repeated freeze-thaw cycles. |
| Reference Data | |
| RefSeq | NP_808880 |
| Locus ID | 157657 |
| UniProt ID | Q96NL8 |
| Refseq Size | 2254 |
| Cytogenetics | 8q22.1 |
| Refseq ORF | 621 |
| Synonyms | BBS21; C8orf37; CORD16; FAP418; MOT25; RP64; smalltalk |
| Summary | This gene encodes a ubiquitously expressed protein of unknown function. It has high levels of mRNA expression in the brain, heart, and retina and the protein co-localizes with polyglutamylated tubulin at the base of the primary cilium in human retinal pigment epithelial cells. Mutations in this gene have been associated with autosomal recessive cone-rod dystrophy (arCRD) and retinitis pigmentosa (arRP). [provided by RefSeq, Mar 2012] |
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