


产品介绍 评论(0)
物种
Yeast表达宿主
E.coli分子量
27 kDa (Reducing)
纯度
>95% by SDS-PAGE and RP-HPLC
内毒素含量
<1EU/μg活性
10U/μl标记
Unconjugated标签
His Tag性状
Liquid缓冲体系
20mM PB, pH7.4, 200mM NaCl, 0.1% NP-40, 0.5mM DTT, 50%(v/v) Glycerol
储存条件
· 12 months from date of receipt, -20 to -70 °C as supplied.
· 6 months, -20 to -70 °C under sterile conditions after reconstitution.
· 1 week, 2 to 8 °C under sterile conditions after reconstitution.
· Please avoid repeated freeze-thaw cycles.
Saccharomyces cerevisiae-derived Small ubiquitin-like modifier (SUMO, Smt3) is commonly used as a protein fusion domain to facilitate expression and purification of recombinant proteins, and a Saccharomyces cerevisiae-derived SUMO-specific protease(Ulp1) is then used to remove SUMO tag from these proteins in a ‘scarless’ manner. SUMO Protease cleaves in a highly specific manner, recognizing the tertiary structure of the SUMO tag, rather than an amino acid sequence, and hydrolyzes the peptide bond in the x-Gly-Gly-x sequence after the Gly-Gly bond at the C-terminus of the SUMO tag. The SUMO Protease cleavage proteins over wide ranges of temperature (4℃-30℃), ionic strengths(0-400 mM NaCl) and pH(7.0-9.0), and easily removed from the cleavage reaction by Immobilized Metal Affinity chromatography (IMAC).
1. SUMO Protease;
2. 10X SUMO Protease Buffer + Salt: 500 mM PB, pH 7.4, 2% Igepal (NP-40), 1.5 M NaCl, 10 mM DTT;
3. 10X SUMO Protease Buffer – Salt: 500 mM PB, pH 7.4, 2% Igepal (NP-40), 10 mM DTT;
- One unit of SUMO Protease cleaves ≥85% of 2 μg control substrate in 1 h at 30°C.
生物活性
The substrate of 2 μg fusion protein was digested by SUMO Protease at 30 ℃ for 1 hour. The addition amount of SUMO Protease were 0U, 0.25U, 0.5U, 0.75U and 1U, respectively. The substrate is a fusion protein with a molecular weight of 20 KD and digested completely into two bands.
电泳
- 1μg (N: non-reducing condition, R: reducing condition).
反相高效液相色谱(RP-HPLC)







评论(0)