苏科商城

产品介绍

蛋白酶K(Proteinase K)，属丝氨酸蛋白酶类，1974年，Wolfgang Ebeling等利用沉淀、离子交换层析和凝聚层析等方法在林伯氏白色念球菌的培养基中分离纯化出蛋白酶K。因能合成该种蛋白酶的微生物能在以角蛋白(Keratin)为唯一碳氮源的环境中生长，即能够消化角蛋白，因此被命名为蛋白酶K(Proteinase K)。蛋白酶K由一条肽链组成，包含277个氨基酸残基，相对分子质量为28.9kDa。与其它的蛋白酶相比较，蛋白酶K具有高活力和高稳定性，其酶活不会被尿素、SDS和EDTA等变性剂抑制，且在高温、高盐或较高的pH等条件下，蛋白酶K仍能保持较高活性。因该酶在较广的pH范围(4～12.5)内及高温(50～70℃)均有活性，在提取DNA和RNA的缓冲液中具有很高的活性，可用于质粒或基因组DNA、RNA的分离，是DNA提取的关键试剂。

近年来，随着研究的深入，蛋白酶K(Proteinase K)的应用不仅仅局限在医疗诊断及科研领域。在实现规模化工业生产的前提下，蛋白酶K还可以替代作用范围较窄的其它蛋白酶，应用于工业制革、食品加工、饲料生产、造纸等行业中。另外，蛋白酶K也可以替代传统的可能存在污染的化学方法处理原材料，去除不必要的蛋白质杂质。

阿拉丁推出的蛋白酶K(Proteinase K)，纯度高，比酶活高。该产品应用于新冠核酸提取试剂盒，能完全消化各种核酸酶和其他蛋白质，防止病毒核酸降解，优化提取效率，可满足COVID-19/HCV/HBV等检测需求。

特点

1、According to the SDS-PAGE image,the purity of Proteinase K is more than 95% and the molecular weight is 28.9 kDa.

2、Detect DNase residue by agarose gel electrophores.

3、Detect Nucleic acid residue by agarose gel electrophores.

4、Detect RNase residue by agarose gel electrophores.

5、Using the absorbance A275 as the vertical axis and different concentrations of tyrosine as the horizontal axis, a standard curve was drawn, and the enzyme activity was calculated>30U/mg.

Product Introduce

Proteinase K, originally isolated from the mold Tritirachium album, is a serine protease with broad substrate specificity and relatively high proteolytic activity. It preferentially cleaves ester and peptide bonds adjacent to the C-termini of hydrophobic, aliphatic, or aromatic amino acids. aladdin's proteinase K is characterized by high purity, sterility, no bio-burden, and no presence of DNAse, RNAse, DNA, and RNA contaminants. It is a good partner in DNA and RNA extraction for you.

Features

1、According to the SDS-PAGE image,the purity of Proteinase K is more than 95% and the molecular weight is 28.9 kDa.

2、Detect DNase residue by agarose gel electrophores.

3、Detect Nucleic acid residue by agarose gel electrophores.

4、Detect RNase residue by agarose gel electrophores.

5、Using the absorbance A275 as the vertical axis and different concentrations of tyrosine as the horizontal axis, a standard curve was drawn, and the enzyme activity was calculated>30U/mg.