RNA 级蛋白酶 K 溶液 (20 mg/mL)
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RNA 级蛋白酶 K 溶液 (20 mg/mL)
Invitrogen™

RNA 级蛋白酶 K 溶液 (20 mg/mL)

真菌中的蛋白酶 K 白色侧齿霉菌是一种对蛋白常规消化有用的非特异性丝氨酸蛋白酶。蛋白酶 K 保持活性:•在较宽 pH 范围内(在 6.5—9.5了解更多信息
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货号数量
255300495 mL
货号 25530049
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数量:
5 mL
价格(CNY)
1,730.00
Online Exclusive
Ends: 31-Dec-2025
2,591.00
共减 861.00 (33%)
Each
添加至购物车
真菌中的蛋白酶 K 白色侧齿霉菌是一种对蛋白常规消化有用的非特异性丝氨酸蛋白酶。蛋白酶 K 保持活性:

•在较宽 pH 范围内(在 6.5—9.5 之间活性较佳)
• 在变性条件下—例如存在 SDS 或尿素
• 在存在金属螯合剂的情况下—例如 EDTA
• 在相对较高的温度下—最佳酶切温度为 65°C

应用
在制备 DNA 和 RNA 过程中去除内源性核酸酶;制备用于原位杂交的组织切片。

性能和质量测试
脱氧核糖核酸内切酶和脱氧核糖核酸外切酶测定;检测液体剂型是否缺乏 RNase 活性。

单位定义
一个 mAnson 单位描述为在 37°C 下以血红蛋白为底物在 1 min 内释放 1 µ 摩尔福林阳性氨基酸的酶量。
仅供科研使用。不可用于诊断程序。
规格
适用于(应用)染色质生物学/RNA 提取/DNA 提取
产品类型蛋白酶 K
纯度无 DNase、无 RNase
数量5 mL
运输条件经批准可置于湿冰或干冰上运输
最大浓度20 mg/mL
形式液体
Unit SizeEach
内容与储存
在冰箱(-5 至 -30°C)中储存。

常见问题解答 (FAQ)

蛋白酶K应该如何储存?

建议将其储存在4°C。

How do you recommend storing proteinase K?

We recommend storing it at 4°C.

How do I isolate DNA from single bacterial colonies before PCR?

Scrape a single colony from the surface of an agar plate and transfer to 12 µL of SCL solution [10 mM Tris-HCl (pH 7.5), 1 mM EDTA, 50 µg/mL proteinase K] and incubate for 15 min at 55 degrees C. Inactivate proteinase K for 15 min at 80 degrees C and add 20 µL of deionized water. Centrifuge at 12,000 x g for 3 min. Transfer the supernatant to a new tube.

What are the recommended conditions for proteinase K treatment when isolating RNA or DNA samples?

Concentration: Generally proteinase K is used in the concentration range of 50 to 500 µg/mL at 65 degrees C in the presence of SDS (0.5-1%).

Temperature optimum: 65 degrees C; 12X more active at 65 degrees C than at 25 degrees C.

pH: Proteinase K is stable over a wide pH range (4.0 to 12.5), with optimal activity at pH 6.5 to 9.5. It is most stable at pH 8.
Inactivation: Heat inactivate Proteinase K at 80 degrees C for 15 min. Phenol extraction is the recommended method to ensure complete inactivation.

Inhibited by: PMSF (0.1 to 1.0 mM of PMSF is usually sufficient for inhibition of Proteinase K)

Not inhibited by: Proteinase K is not inactivated by metal ions, chelating agents (e.g., EDTA), sulfhydryl reagents or by trypsin or chymotrypsin inhibitors. Activity can be stimulated by addition of denaturing agents (SDS and urea).