推荐产品
应用
蛋白酶是一种通过水解肽键来分解蛋白质的酶。蛋白酶用于降解蛋白质、研究蛋白酶抑制剂和研究热灭活动力学。蛋白酶用于孵育过程中的核酸分离程序。它被用于研究蛋白酶激活受体,如炎症和免疫反应中蛋白酶介导的信号转导 。产品 P4032 来自 黑曲霉 ,已用于霍氏链霉菌木聚糖酶的非特异性降解。
生化/生理作用
蛋白酶通过水解肽键使蛋白质分解代谢。丝氨酸活性部位抑制剂可灭活蛋白酶,如苯甲基磺酰氟 (PMSF) 和二异丙基氟磷酸盐。
单位定义
除非另有说明,否则一个单位将水解酪蛋白以在 pH7.5,37°C 下每分钟产生相当于1.0μmole (181μg) 酪氨酸的颜色(Folin-Ciocalteu 试剂的颜色)。
警示用语:
Danger
危险分类
Eye Irrit. 2 - Resp. Sens. 1 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
11 - Combustible Solids
WGK
WGK 1
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
法规信息
常规特殊物品
从最新的版本中选择一种:
分析证书(COA)
Endocrine reviews, 26(1), 1-43 (2005-02-04)
Serine proteinases such as thrombin, mast cell tryptase, trypsin, or cathepsin G, for example, are highly active mediators with diverse biological activities. So far, proteinases have been considered to act primarily as degradative enzymes in the extracellular space. However, their
Scientific reports, 10(1), 15078-15078 (2020-09-17)
Understanding the mechanisms by which neurons create or suppress connections to enable communication in brain-derived neuronal cultures can inform how learning, cognition and creative behavior emerge. While prior studies have shown that neuronal cultures possess self-organizing criticality properties, we further
Microbiology (Reading, England), 149(Pt 7), 1623-1632 (2003-07-12)
The xylanase Xys1L from Streptomyces halstedii JM8 is known to be processed extracellularly, to produce a protein of 33.7 kDa, Xys1S, that retains catalytic activity but not its cellulose-binding capacity. This paper demonstrates that at least five serine proteases isolated
The British journal of nutrition, 79(6), 519-525 (1998-10-15)
Differences between the fermentation characteristics of cell contents (CC) and protease-treated cell walls (CW) of young leaves of Italian ryegrass (Lolium multiflorum Lam.) cultivar Multimo (tetraploid), were studied in vitro. Gas and volatile fatty acid (VFA) production rates were measured
Nature communications, 10(1), 4691-4691 (2019-10-18)
Multiple scattering and absorption limit the depth at which biological tissues can be imaged with light. In thick unlabeled specimens, multiple scattering randomizes the phase of the field and absorption attenuates light that travels long optical paths. These obstacles limit
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