跳转至内容
Merck
CN

539137

Protease Inhibitor Cocktail V

EDTA-Free, lyophilized, A cocktail of four protease inhibitors for the inhibition of serine, cysteine, but not metalloproteases.

别名:

EDTA free Protease inhibitor

登录 查看组织和合同定价。

选择尺寸


关于此项目

UNSPSC Code:
12352200
NACRES:
NA.54
Form:
lyophilized
Solubility:
water: soluble
Storage temp.:
−20°C
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助

产品名称

蛋白酶抑制剂混合物套装V,无EDTA, A cocktail of four protease inhibitors for the inhibition of serine, cysteine, but not metalloproteases.

form

lyophilized

manufacturer/tradename

Calbiochem®

storage condition

OK to freeze, desiccated (hygroscopic)

solubility

water: soluble

shipped in

wet ice

storage temp.

−20°C

Quality Level

正在寻找类似产品? 访问 产品对比指南

General description

四种蛋白酶抑制剂的混合物,用于抑制丝氨酸、半胱氨酸,但不用于抑制金属蛋白酶。用1 ml H2O复溶每个小瓶,以获得100X溶液。1X贮备溶液,含有500 µM AEBSF、HCl(目录号101500)、150 nM抑肽酶(目录号616370)、1 µM E-64(目录号324890)和1 µM亮抑蛋白酶肽(目录号108975)。随附数据表。

Biochem/physiol Actions

主靶
丝氨酸和半胱氨酸蛋白酶,但不用于抑制金属蛋白酶。
产物不与ATP竞争。
可逆:否
抑制丝氨酸蛋白酶、半胱氨酸蛋白酶。切勿抑制金属蛋白酶。
细胞可渗透性:否

Preparation Note

复溶后,等分并冷冻保存(-20°C)。贮备溶液在-20°C下可稳定保存至多6个月。
用1 ml H₂O复溶每个小瓶,以获得100X溶液。

Legal Information

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

Disclaimer

毒性:标准处理(A)

pictograms

Corrosion

signalword

Danger

hcodes

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1A

存储类别

8A - Combustible corrosive hazardous materials

wgk

WGK 3


分析证书(COA)

输入产品批号来搜索 分析证书(COA) 。批号可以在产品标签上"批“ (Lot或Batch)字后找到。

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库

Mario Lebendiker et al.
Methods in molecular biology (Clifton, N.J.), 1485, 257-273 (2016-10-13)
Maltose-Binding Protein (MBP) is one of the most popular fusion partners being used for producing recombinant proteins in bacterial cells. MBP allows the use of a simple capture affinity step on Amylose-Agarose or Dextrin-Sepharose columns, resulting in a protein that
Emery T Usher et al.
The Journal of biological chemistry, 296, 100693-100693 (2021-04-25)
Speckle-type POZ protein (SPOP) is a ubiquitin ligase adaptor that binds substrate proteins and facilitates their proteasomal degradation. Most SPOP substrates present multiple SPOP-binding (SB) motifs and undergo liquid-liquid phase separation with SPOP. Pancreatic and duodenal homeobox 1 (Pdx1), an
Jin Wen et al.
Bioorganic & medicinal chemistry, 28(20), 115711-115711 (2020-10-18)
Cyclic peptides are capable of binding to challenging targets (e.g., proteins involved in protein-protein interactions) with high affinity and specificity, but generally cannot gain access to intracellular targets because of poor membrane permeability. In this work, we discovered a conformationally
Kirby Martinez-Fonts et al.
Nature communications, 11(1), 477-477 (2020-01-26)
Proteins are targeted to the proteasome by the attachment of ubiquitin chains, which are markedly varied in structure. Three proteasome subunits-Rpn10, Rpn13, and Rpn1-can recognize ubiquitin chains. Here we report that proteins with single chains of K48-linked ubiquitin are targeted
Chinyere Agbaegbu Iweka et al.
Journal of neurochemistry, 157(3), 494-507 (2020-12-16)
Phospholipid Phosphatase-Related Protein Type 1 (PLPPR1) is a member of a family of lipid phosphatase related proteins, integral membrane proteins characterized by six transmembrane domains. This family of proteins is enriched in the brain and recent data indicate potential pleiotropic

我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系客户支持