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Merck
CN

T4665

胰蛋白酶 来源于牛胰腺

lyophilized powder, ≥7,500 BAEE units/mg solid

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化学文摘社编号:
UNSPSC Code:
12352204
EC Number:
232-650-8
MDL number:
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form

lyophilized powder

specific activity

≥7,500 BAEE units/mg solid, ≥7,500 units/mg solid

mol wt

23.8 kDa

foreign activity

Chymotrypsin <3 BTEE units/mg solid

storage temp.

−20°C

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Application

对于胰蛋白酶消化肽,胰蛋白酶:肽 使用约为 1:100 至 1:20 的比例。从培养表面除去粘附细胞是本产品的一个典型应用。 从其底物中去除细胞所需的胰蛋白酶浓度主要取决于细胞类型和培养物的年龄。 胰蛋白酶也被用于细胞培养期间细胞的再悬浮、蛋白质组学研究中的蛋白质消化和各种凝胶内消化。 其他应用包括:通过基于膜的技术评估结晶,用在确定动力学陷阱的存在会限制蛋白质的折叠速率和产量的一项研究中。

Biochem/physiol Actions

胰蛋白酶切割赖氨酸和精氨酸残基的 C 端肽。 如果酸性残基位于切割位点的任一侧,则该反应的水解速度减慢,并且如果脯氨酸残基位于切割位点的羧基侧,则停止水解。 胰蛋白酶活性的最适 pH 为 7-9。 胰蛋白酶还可以起到裂解氨基酸合成衍生物的酯和酰胺键的作用。 将 EDTA 作为螯合剂添加到胰蛋白酶溶液中,用于中和钙离子和镁离子,这些离子遮蔽胰蛋白酶作用的肽键。 去除这些离子会增加酶活性。

丝氨酸蛋白酶抑制剂,包括 DFP、TLCK、APMSF、AEBSEF 和抑肽酶等,将抑制胰蛋白酶。

Physical form

Lyophilized powder containing lactose

Other Notes

使用 BAEE 作为底物,一个 BAEE 单元,将在 pH 7.6,25℃ 下,每分钟产生 0.001 的 A253
One BAEE unit will produce a ΔA253 of 0.001 per min at pH 7.6 at 25 °C using BAEE as substrate. Reaction volume = 3.2 ml (1 cm light path).

pictograms

Health hazardExclamation mark

signalword

Danger

Hazard Classifications

Eye Irrit. 2 - Resp. Sens. 1 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

11 - Combustible Solids

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

法规信息

新产品

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Monika Gulia-Nuss et al.
PloS one, 6(5), e20401-e20401 (2011-06-08)
Mosquitoes are insects that vector many serious pathogens to humans and other vertebrates. Most mosquitoes must feed on the blood of a vertebrate host to produce eggs. In turn, multiple cycles of blood feeding promote frequent contacts with hosts and
R J Read et al.
Biochemistry, 23(26), 6570-6575 (1984-12-18)
The X-ray crystal structure of Streptomyces griseus trypsin has been solved and refined at 1.7-A resolution. The structure of this protein had been predicted in two models on the basis of its expected homology to structures of bovine trypsin and
Fikadu G Tafesse et al.
Proceedings of the National Academy of Sciences of the United States of America, 110(16), 6406-6411 (2013-04-12)
Cells genetically deficient in sphingomyelin synthase-1 (SGMS1) or blocked in their synthesis pharmacologically through exposure to a serine palmitoyltransferase inhibitor (myriocin) show strongly reduced surface display of influenza virus glycoproteins hemagglutinin (HA) and neuraminidase (NA). The transport of HA to
Bernard A Fang et al.
Biochimica et biophysica acta, 1845(1), 1-19 (2013-11-26)
N-myc down-regulated gene 1 (NDRG1) is a known metastasis suppressor in multiple cancers, being also involved in embryogenesis and development, cell growth and differentiation, lipid biosynthesis and myelination, stress responses and immunity. In addition to its primary role as a
Norelle L Daly et al.
The Journal of biological chemistry, 288(50), 36141-36148 (2013-10-31)
MCoTI-II is a head-to-tail cyclic peptide with potent trypsin inhibitory activity and, on the basis of its exceptional proteolytic stability, is a valuable template for the design of novel drug leads. Insights into inhibitor dynamics and interactions with biological targets

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