上海金畔生物科技有限公司代理New England Biolabs(NEB)酶试剂全线产品,欢迎访问官网了解更多产品信息和订购。
产品信息
and 2´,3´ cyclic monophosphate (1). It has a preference for single-stranded RNA over double-stranded RNA in the absence of calcium (2). RNase If is a recombinant protein fusion of RNase I (from E. coli) and maltose-binding protein. It has identical activity to RNase I.
产品来源
An E. coli strain containing a genetic fusion of the E. coli RNase I gene (2nd) and the gene coding for maltose binding protein (MBP).
- 产品类别:
- RNases
-
产品组分信息
本产品提供以下试剂或组分:
NEB # 名称 组分货号 储存温度 数量 浓度 -
M0243S -20 RNase If M0243SVIAL -20 1 x 0.1 ml 50,000 units/ml NEBuffer™ 3 B7003SVIAL -20 1 x 1.25 ml 10 X
-
M0243L -20 RNase If M0243LVIAL -20 1 x 0.5 ml 50,000 units/ml NEBuffer™ 3 B7003SVIAL -20 1 x 1.25 ml 10 X
-
-
特性和用法
单位定义
One unit is defined as the amount of enzyme required to fully digest 1 picomole of synthetic ssRNA 33-mer in a total reaction volume of 10 µl in 15 minutes in 1X NEBuffer 3 as visualized on a 20% acrylamide gel.
反应条件
1X NEBuffer™ 3
Incubate at 37°C1X NEBuffer™ 3
100 mM NaCl
50 mM Tris-HCl
10 mM MgCl2
1 mM DTT
(pH 7.9 @ 25°C)贮存溶液
10 mM Tris-HCl
100 mM NaCl
1 mM DTT
0.5 mM EDTA
50% Glycerol
pH 8 @ 25°C热失活
70°C for 20 minutes
-
优势和特性
应用特性
- Degradation of single-stranded RNA to mono-, di- and trinucleotide (3)
- Used in ribonuclease protection assays
-
相关产品
单独销售的组分
- NEBuffer 3
-
注意事项
- RNase If will not degrade DNA. It has a preference for single-stranded RNA over double-stranded RNA.
-
参考文献
- Spahr, P.F. and Hollingworth, B.R. (1961). J. Biol. Chem.. 236, 823-831.
- Grünberg S, Coxam B, Chen TH, Dai N, Saleh L, Corrêa IR, Nichols NM, Yigit E. (2021). Nucleic Acids Res.. May 21;49(9), 5265-5277.
- Meador, J. III and Kennell, D. (1990). Gene. 95, 1-7.
- Meador, J. III, Cannon, B., Cannistraro, V.J. and Kennell, D. (1990). Eur. J. Biochem.. 187, 549-553.
操作说明、说明书 & 用法
-
操作说明
- Cleavage of ssRNA with RNase If (NEB #M0243)