跳转至内容
Merck

K2638

Sigma-Aldrich

激肽释放酶 来源于人类血浆

buffered aqueous solution, ≥5 units/mg protein

别名:

激肽原, 激肽原酶

登录查看公司和协议定价


About This Item

CAS号:
MDL號碼:
分類程式碼代碼:
12352204
NACRES:
NA.54

形狀

buffered aqueous solution

品質等級

比活性

≥5 units/mg protein

UniProt登錄號

運輸包裝

dry ice

儲存溫度

−20°C

基因資訊

human ... KLK1(3816)

正在寻找类似产品? 访问 产品对比指南

一般說明

Kallikrein肽酶属于15个高度保守的胰蛋白酶或胰凝乳蛋白酶家庭的成员。血浆激肽释放酶(PK)是一种来源于血浆前激肽释放酶的丝氨酸蛋白酶,也是一种在血液循环中含量较高的酶原。KLKB1基因位于人染色体4q35.2上。

應用

从人血浆中提取的激肽释放酶已用于:

  • 培养人肝癌细胞系
  • 研究其对来自脑膜炎奈瑟氏菌的奈瑟球菌肝素结合抗原(NHBA)的裂解作用
  • 肽酶抑制分析

生化/生理作用

血浆激肽释放酶(PK)参与缓激肽的合成,可维持血液代谢物水平和高血压。它还参与凝血因子XII的激活,促进炎症和内源性凝血途径。PK控制心血管系统中的蛋白水解级联反应,如激肽酶激肽系统、肾素血管紧张素系统、纤维蛋白溶解系统和补体旁路等。它参与胰高血糖素样肽-1(GLP-1)和神经肽Y(NPY) 的裂解,这表明血浆激肽释放酶可能会影响代谢和糖尿病。

單位定義

一个酶活性单位是指在pH 8.7、25°C条件下,每分钟将1.0 μMNα-苯甲酰基-L-精氨酸乙酯(BAEE)水解为Nα-苯甲酰基-L-精氨酸和乙醇所需的酶量。

外觀

溶于20 mM Tris-HCl (pH 7.8)和100 mM NaCl的溶液中。

儲存類別代碼

12 - Non Combustible Liquids

水污染物質分類(WGK)

WGK 1

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)


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

Xueqing Xu et al.
Nucleic acids research, 37(22), 7381-7393 (2009-10-13)
A subtelomeric region, 4q35.2, is implicated in facioscapulohumeral muscular dystrophy (FSHD), a dominant disease thought to involve local pathogenic changes in chromatin. FSHD patients have too few copies of a tandem 3.3-kb repeat (D4Z4) at 4q35.2. No phenotype is associated
Elisa Pantano et al.
PloS one, 14(8), e0203234-e0203234 (2019-08-02)
Neisserial Heparin Binding Antigen (NHBA) is a surface-exposed lipoprotein of Neisseria meningitidis and a component of the Bexsero vaccine. NHBA is characterized by the presence of a highly conserved Arg-rich region involved in binding to heparin and heparan sulphate proteoglycans
H Austin et al.
Journal of thrombosis and haemostasis : JTH, 9(3), 489-495 (2011-01-15)
We evaluated 10 single-nucleotide polymorphisms (SNPs) identified in three European case-control studies as risk factors for venous thrombosis. We sought to replicate the positive findings from this report among Whites and to evaluate the association of these SNPs with venous
L E Stolz et al.
Drugs of today (Barcelona, Spain : 1998), 46(8), 547-555 (2010-09-11)
Hereditary angioedema (HAE) is a debilitating, potentially fatal disease characterized by variable and unpredictable acute attacks of swelling affecting the subcutaneous tissue and mucosa. It is an autosomal dominant disorder resulting from a genetic deficiency of functional C1-esterase inhibitor. Available
A new case of homozygous C1-inhibitor deficiency suggests a role for Arg378 in the control of kinin pathway activation.
Alberto López-Lera et al.
The Journal of allergy and clinical immunology, 126(6), 1307-1310 (2010-09-25)

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.

联系技术服务部门