Senataxin (SETX) Mutant (NM_015046) Human Recombinant Protein
CAT#: TP701002
Purified recombinant protein of Human senataxin (SETX), (L389S) mutant protein, esidues Met1-Phe500, expressed in HEK293 cells, 20ug
Other products for "SETX"
Specifications
| Product Data | |
| Species | Human |
| Expression Host | HEK293 |
| Expression cDNA Clone or AA Sequence | A DNA sequence from TrueORF clone, RC222616, encoding the region (Met1-Phe500) of SETX(L389S) |
| Tag | C-Myc/DDK |
| Predicted MW | 57.8 kDa |
| Concentration | >50 ug/mL as determined by microplate BCA method |
| Purity | > 80% as determined by SDS-PAGE and Coomassie blue staining |
| Buffer | 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10% glycerol |
| 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_055861 |
| Locus ID | 23064 |
| Cytogenetics | 9q34.13 |
| Refseq Size | 8583 |
| Refseq ORF | 8031 |
| Synonyms | ALS4; AOA2; bA479K20.2; SCAN2; SCAR1; Sen1 |
| Summary | This gene encodes a protein named for its homology to the Sen1p protein of fungi which has RNA helicase activity encoded by a domain at the C-terminal end of the protein. The protein encoded by this gene contains a DNA/RNA helicase domain at its C-terminal end which suggests that it may be involved in both DNA and RNA processing. Mutations in this gene have been associated with ataxia-ocular apraxia-2 (AOA2) and an autosomal dominant form of juvenile amyotrophic lateral sclerosis (ALS4). [provided by RefSeq, Jul 2008] |
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