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Merck
CN
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主要文件

安全信息

D4693

Sigma-Aldrich

分散酶®II

protease

别名:

蛋白酶 来源于多粘芽孢杆菌

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About This Item

CAS号:
42613-33-2
EC 号:
255-914-4
MDL编号:
MFCD02253017
UNSPSC代码:
12352204
NACRES:
NA.54

质量水平

100

表单

lyophilized solid

比活

≥0.5 units/mg solid

技术

cell culture | mammalian: suitable
single cell analysis: suitable

溶解性

10 mM NaAc (pH 7.5) and 5 mM CaAc: soluble

储存温度

2-8°C

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应用

来自Sigma的该酶已被用于开发用于离体培养小鼠胚胎乳腺芽的实验方法。它已被用于在从大鼠心脏分离线粒体的过程中对大鼠心脏碎片进行处理。它还被用于通过酶水解来分离牙髓干细胞（DPSC）。这些细胞已与通过外植体方法而分离的DPSC进行了比较，以分析它们的干细胞和分化特性。
中性蛋白酶® II已用于荧光激活细胞分选（FACS）。它还被用于分离内脏卵黄囊层。
适用于制备测序用单细胞悬浮液。

生化/生理作用

中性蛋白酶®II是一种中性的蛋白酶，可水解非极性氨基酸残基的N-末端肽键。它可用于分离生长在体外的多种组织和细胞。该酶非常温和，不会对细胞膜造成损伤。它还可用于防止悬浮培养物中的细胞结块。该蛋白酶可水解纤连蛋白和IV型胶原蛋白，但不能水解层粘连蛋白、V型胶原蛋白、血清白蛋白或转铁蛋白。中性蛋白酶®II具有切割亮氨酸-苯丙氨酸键的特异性。Ca2+、Mg2+、Mn2+、Fe2+、Fe3+和Al3+ 可灭活分散酶I。EDTA、EGTA、Hg2+ 和其他重金属可抑制该酶活性。每g-mol纯化分散酶I含有1g锌原子。如果通过EDTA或EGTA等螯合剂除去锌成分，则产生无活性的酶蛋白。该酶不受血清抑制。

单位定义

除特殊说明，在pH 7.5，37 °C 条件下，一单位的酶每分钟将会水解酪蛋白以产生与1.0 μ摩尔 (181 μg) 酪氨酸等同的颜色（Folin-Ciocalteu试剂提供的颜色）。

外形

含有乙酸钙和乳糖的冻干粉

制备说明

可通过将粉末溶解在含有10 mM NaAc (pH 7.5)和5 mM CaAc的缓冲液中制备50 U/mL的储备溶液。它应当被储存在4 °C。

分析说明

该酶初始可以10 mg/ml溶解于50 mM Hepes/KOH pH 7.4, 150 mM NaCl中。 进一步的稀释应当在最适于待解离细胞的培养基中进行。 中性蛋白酶是一种金属蛋白酶，可通过包括Ca2+ , Mg2+, Mn2+以及Fe2+在内的二价阳离子激活。

法律信息

Dispase is a registered trademark of Godo Shusei Co., Ltd.

象形图

Health hazardExclamation mark
GHS08,GHS07

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 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

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)

Lot/Batch Number
BCCL2638
BCCM1253
BCCL7124
BCCJ7416
BCCK9179

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  1. Which document(s) contains shelf-life or expiration date information for a given product?

    If available for a given product, the recommended re-test date or the expiration date can be found on the Certificate of Analysis.

  2. How do I get lot-specific information or a Certificate of Analysis?

    The lot specific COA document can be found by entering the lot number above under the "Documents" section.

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Maria Voutilainen et al.
Journal of mammary gland biology and neoplasia, 18(2), 239-245 (2013-05-16)
The explant culture techniques of embryonic tissues allow continuous monitoring of organ growth and morphogenesis ex vivo. The effect of growth factors and other soluble molecules can be examined by applying them to the culture medium. Relatively few studies have
P Hilkens et al.
Cell and tissue research, 353(1), 65-78 (2013-05-30)
Dental pulp stem cells (DPSCs) are an attractive alternative mesenchymal stem cell (MSC) source because of their isolation simplicity compared with the more invasive methods associated with harvesting other MSC sources. However, the isolation method to be favored for obtaining
Magdalena Labieniec-Watala et al.
International journal of molecular sciences, 12(11), 8013-8026 (2011-12-17)
Diabetes is associated with a mitochondrial dysfunction. Hyperglycaemia is also clearly recognized as the primary culprit in the pathogenesis of cardiac complications. In response to glycation and oxidative stress, cardiac mitochondria undergo cumulative alterations, often leading to heart deterioration. There
Some properties of a protease from Bacillus polymyxa.
P J Griffin et al.
The Biochemical journal, 125(4), 109P-109P (1971-12-01)
Feng-Ming Ding et al.
Molecular medicine reports, 16(1), 778-786 (2017-06-01)
Neutrophilic airway inflammation in chronic lung infections caused by Pseudomonas aeruginosa (PA) is associated with T helper (Th)17 responses. Suppressor of cytokine signaling 3 (SOCS3) is the major negative modulator of Th17 function through the suppression of signal transducer and activator
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