推荐产品
产品名称
胰蛋白酶抑制剂 来源于大豆, lyophilized powder
生物来源
Glycine max (soybean)
类型
Type II-S
表单
lyophilized powder
分子量
20,100 Da
技术
inhibition assay: suitable
溶解性
balanced salt solution: 1 mg/mL
concentrate: >10 mg/mL, hazy, amber-yellow
phosphate buffer: 10 mg/mL
water: 10 mg/mL
serum-free medium: soluble
运输
ambient
储存温度
2-8°C
正在寻找类似产品? 访问 产品对比指南
生化/生理作用
该抑制剂能够在较小程度上抑制胰蛋白酶、胰凝乳蛋白酶和纤溶酶。它还能抑制蛋白酶血浆激肽释放酶和凝血因子X,机制与抑制胰蛋白酶类似。胰蛋白酶抑制剂不会抑制金属蛋白酶、基于组织的激肽释放酶、酸性蛋白酶或硫代蛋白酶。该抑制剂通过与蛋白酶活性位点按1:1化学计量形成复合物,然后在抑制剂上切割单个精氨酸-异亮氨酸键。抑制作用是可逆的且具有pH依赖性。
组分
大豆胰蛋白酶抑制剂是在由两个二硫键交联的单个多肽链中含有 181 个氨基酸残基的单体蛋白质。
单位定义
一个胰蛋白酶单位是指在25°C、pH 7.6条件下,以N-α-苯甲酰基-L-精氨酸乙酯(BAEE)为底物,每分钟产生0.001的 A253所需的酶量。
一个胰蛋白酶单位每分钟将产生 0.001 的 ΔA253,BAEE 作为底物,pH 值为 7.6,温度为 25℃;反应体积 3.2 ml,光程为 1 cm。
制备说明
胰蛋白酶抑制剂能够以10 mg/mL溶于水和磷酸盐缓冲液。它能够以1 mg/mL溶于平衡盐溶液和无血清培养基中。浓度大于10 mg/mL的浓缩液可能浑浊,呈黄色至琥珀色。使用胰蛋白酶消化细胞后,重悬于胰蛋白酶抑制剂溶液中,使得用于解离的胰蛋白酶溶液浓度达到1 mg/mL。然后将细胞悬浮液以1000rpm离心,得到细胞沉淀。
在2-8℃下短期储存时,溶液可保持活性。溶液分装后可在-20℃冷冻并保持稳定。
在2-8℃下短期储存时,溶液可保持活性。溶液分装后可在-20℃冷冻并保持稳定。
分析说明
1 mg 胰蛋白酶抑制剂,将抑制最低 1.0 mg 胰蛋白酶活性,约 10,000 BAEE 单位/mg 胰蛋白酶。
警示用语:
Danger
危险声明
危险分类
Resp. Sens. 1 - Skin Sens. 1
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
历史批次信息供参考:
分析证书(COA)
Lot/Batch Number
其他客户在看
Dolores D Mruk et al.
Methods in molecular biology (Clifton, N.J.), 763, 237-252 (2011-08-30)
The use of an in vitro system based on primary cultures of Sertoli cells isolated from rat testes has greatly facilitated the study of the blood-testis barrier in recent years. Herein, we summarize the detailed procedures on the isolation of
Ho Am Jang et al.
Developmental and comparative immunology, 67, 97-106 (2016-11-09)
Riptortus pedestris, a common pest in soybean fields, harbors a symbiont Burkholderia in a specialized posterior midgut region of insects. Every generation of second nymphs acquires new Burkholderia cells from the environment. We compared in vitro cultured Burkholderia with newly in vivo
Patrik Hollos et al.
eNeuro, 7(1) (2020-01-16)
In this study, we use an optogenetic inhibitor of c-Jun NH2-terminal kinase (JNK) in dendritic spine sub-compartments of rat hippocampal neurons. We show that JNK inhibition exerts rapid (within seconds) reorganization of actin in the spine-head. Using real-time Förster resonance
I T Padol et al.
Infection and immunity, 69(6), 3891-3896 (2001-05-12)
As a bacterial product, Helicobacter pylori lipopolysaccharide (LPS) can originate in close proximity to parietal cells, but the role of this uniquely structured endotoxin on acid secretion has not been fully investigated and remains unclear. The purpose of this study
Graeme S Cottrell et al.
Gastroenterology, 132(7), 2422-2437 (2007-06-16)
We studied the role of protease-activated receptor 2 (PAR(2)) and its activating enzymes, trypsins and tryptase, in Clostridium difficile toxin A (TxA)-induced enteritis. We injected TxA into ileal loops in PAR(2) or dipeptidyl peptidase I (DPPI) knockout mice or in
实验方案
This technical article described the Enzymatic Assay of Trypsin Inhibitor.
Chromatograms
application for HPLC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