CLPB (NM_030813) Human Recombinant Protein
CAT#: TP761474
Purified recombinant protein of Human ClpB caseinolytic peptidase B homolog (E.coli) (CLPB), full length, with N-terminal HIS tag, expressed in E.coli, 50ug
View other "CLPB" proteins (2)
Need it in bulk or customized? Get a free quote |
CN¥ 2,040.00
货期*
现货
规格
经常一起买 (1)
Specifications
Product Data | |
Species | Human |
Expression Host | E. coli |
Expression cDNA Clone or AA Sequence |
A DNA sequence encoding human full-length CLPB
|
Tag | N-His |
Predicted MW | 78.5 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_110440 |
Locus ID | 81570 |
UniProt ID | Q9H078 |
Refseq Size | 3272 |
Cytogenetics | 11q13.4 |
Refseq ORF | 2121 |
Synonyms | ANKCLB; HSP78; MEGCANN; MGCA7; SKD3 |
Summary | This gene belongs to the ATP-ases associated with diverse cellular activities (AAA+) superfamily. Members of this superfamily form ring-shaped homo-hexamers and have highly conserved ATPase domains that are involved in various processes including DNA replication, protein degradation and reactivation of misfolded proteins. All members of this family hydrolyze ATP through their AAA+ domains and use the energy generated through ATP hydrolysis to exert mechanical force on their substrates. In addition to an AAA+ domain, the protein encoded by this gene contains a C-terminal D2 domain, which is characteristic of the AAA+ subfamily of Caseinolytic peptidases to which this protein belongs. It cooperates with Hsp70 in the disaggregation of protein aggregates. Allelic variants of this gene are associated with 3-methylglutaconic aciduria, which causes cataracts and neutropenia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2015] |
Documents
FAQs |
SDS |
Resources
蛋白相关资源 |
Customer
Reviews
Loading...