RNase I (10 U/μL)
RNase I (10 U/μL)
Thermo Scientific™

RNase I (10 U/μL)

Thermo Scientific Ribonuclease I (RNase I) is an endoribonuclease that preferentially hydrolyzes single-stranded RNA to nucleoside 3'-monophosphates via nucleoside 2',자세히 알아보기
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카탈로그 번호수량
EN06011,000 units
EN06025,000 units
카탈로그 번호 EN0601
제품 가격(KRW)
140,000
온라인 행사
Ends: 31-Mar-2026
159,000
할인액 19,000 (12%)
Each
카트에 추가하기
수량:
1,000 units
대량 주문 또는 맞춤형 요청
제품 가격(KRW)
140,000
온라인 행사
Ends: 31-Mar-2026
159,000
할인액 19,000 (12%)
Each
카트에 추가하기
Thermo Scientific Ribonuclease I (RNase I) is an endoribonuclease that preferentially hydrolyzes single-stranded RNA to nucleoside 3'-monophosphates via nucleoside 2', 3'-cyclic monophosphate intermediates.

The enzyme does not require any metal ions for activity.

Highlights

• Stable and active under a wide variety of reaction conditions
• Can be heat inactivated in 30 minutes at 100°C

Applications

• Removal of RNA from DNA solutions
• Removal of RNA from recombinant protein preparations
• Ribonuclease protection assays

Notes

Mammalian ribonuclease inhibitors have no effect on RNase I. RNase I binds to DNA, but does not degrade it. RNase I amino acid sequence is typical for the RNase T2 family. Non-ionic detergents (e.g., Triton X-100) do not inhibit RNase I, and may even slightly stimulate its activity and stabilize it against heat inactivation. Triton X-100 or BSA (at 0.1 mg/mL) may prevent RNase I from sticking to glass vessels when working with dilute solutions. Polyamines stimulate the activity of RNase I.
For Research Use Only. Not for use in diagnostic procedures.
사양
제품 유형RNase I
수량1,000 units
농도10 U/μL
효소RNase
Unit SizeEach

자주 묻는 질문(FAQ)

What are your recommendations for removal of RNA from DNA solutions using Thermo Scientific RNase I?

1. Add 15-20 u of RNase I per 1 µg of RNA. RNase I is ≥ 90% active within pH range 7.0-8.8 at salt concentration 100-200 mM. Incubation with RNase I can be performed simultaneously with the digestion of DNA by restriction endonucleases.

2. Incubate at 37 degrees C for 30 minutes.

3. Purify DNA by spin column or phenol/chloroform extraction.