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Description:Purified recombinant protein of Human non-SMC element 2, MMS21 homolog (S. cerevisiae) (NSMCE2), full length, with N-terminal HIS tag, expressed in E. coli, 50ug
Accn:NM_173685
Unipro ID:Q96MF7
Synonyms:C8orf36; MMS21; NSE2; ZMIZ7
Species:Human
Amount:50 ug
Delivery time:现货
Expression sequence:A DNA sequence encoding human full-length NSMCE2
Tags:N-His
PredictedMW:27.8 kDa
Buffer:25 mM Tris-HCl, pH 8.0, 150 mM NaCl, 1% sarkosyl, 10% glycerol
Stability:Stable for 12 months from the date of receipt of the product under proper storage and handling conditions. Avoid repeated freeze-thaw cycles.
Bioactivity
Purity:> 80% as determined by SDS-PAGE and Coomassie blue staining
Concentration:>0.05 µg/µL as determined by microplate BCA method
Preparation
Endotoxin
Shipping
Background:This gene encodes a member of a family of E3 small ubiquitin-related modifier (SUMO) ligases that mediates the attachment of a SUMO protein to proteins involved in nuclear transport, transcription, chromosome segregation and DNA repair. The encoded protein is part of the structural maintenance of chromosomes (SMC) 5/6 complex which plays a key role genome maintenance, facilitating chromosome segregation and suppressing mitotic recombination. A knockout of the orthologous mouse gene is lethal prior to embryonic day 10.5. Naturally occurring mutations in this gene, that abolish the SUMO ligase activity, are associated with primordial dwarfism and extreme insulin resistance. [provided by RefSeq, Mar 2017]
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文献和实验Preparation of Recombinant Protein Spotted Arrays for Proteome‐Wide Identification of Kinase Targets
Pin/pin head cleaning solution (Arrayit), optional 384‐well plate containing purified protein samples ( protocol
Introduction of human 14-3-3 proteins
The human and bovine 14-3-3 eta protein mRNAs are highly conservedEvolutionary conservation of the 14-3-3 proteinExpression and structural analysis of 14-3-3 proteinsCrystal structure of the zeta isoform of the 14-3-3 proteinStructure of a 14
of the unknown protein SMC protein from B. subtilis was determined by gel filtration. Fig. 3 Determination of R s of BsSMC by gel filtration. The column was calibrated by running standard proteins BSA, catalase, and thyroglobulin
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