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Merck
모든 사진(1)

주요 문서

10786357001

Roche

Ribonuclease H (RNase H)

from Escherichia coli H 560 pol A1

동의어(들):

rnase h

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About This Item

UNSPSC 코드:
12352204

생물학적 소스

Escherichia coli ( H 560 pol A1)

Quality Level

분석

100%

형태

solution

특이 활성도

~40000 units/mg protein

포장

pkg of 100 U

제조업체/상표

Roche

기술

cDNA synthesis: suitable

색상

colorless

최적 pH

7.5-9.1

solubility

water: miscible

적합성

suitable for molecular biology

NCBI 수납 번호

응용 분야

life science and biopharma

외래 활성

RNase, none detected (up to 10 U with MS- II- RNA)
endonuclease ~10 units, none detected (using lambda-DNA)
nicking activity 10 units, none detected

배송 상태

dry ice

저장 온도

−20°C (−15°C to −25°C)

유전자 정보

Escherichia coli ... rnhA(946955)

일반 설명

Nonspecific endoribonuclease that specifically cleaves RNA in RNA:DNA hybrids. A minimum of four continuous base pairs (RNA:DNA) is required for activity. RNase H cleaves RNA to release 5′-oligoribonucleotides.

Source: E. coli H560 pol A1
Storage Buffer: 25 mM Tris-HCl, 50 mM KCl, 1 mM dithiothreitol, 0.1 mM EDTA, 50% glycerol (v/v), pH 8.0 (+4°C)
Volume Activity: 1 x 103 U/ml assayed according to Hillenbrand & Staudenbauer.
Ribonuclease H (RNase H) is a nonspecific endoribonuclease, localized to the nucleus and cytoplasm. It is ubiquitously found and widely present among many organisms including viruses and human.

애플리케이션

Ribonuclease H (RNase H) has been used for:
  • In vivo RNA-primed initiation of DNA synthesis
  • Elimination of mRNA during second-strand cDNA synthesis
  • Site-specific cleavage of RNA
  • Detection of RNA:DNA regions in double-stranded DNA of natural origin
  • Removal of poly (A) sequences of mRNA if oligo (dT) is present
  • RNA extraction and quantitative reverse transcriptase polymerase chain reaction (RT-PCR)

생화학적/생리학적 작용

Ribonuclease H (RNase H) specifically cleaves RNA in RNA:DNA hybrids. A minimum of four continuous base pairs (RNA:DNA) is required for activity. RNase H cleaves RNA to release 5′-oligoribonucleotides. RNase H is associated with nucleic acid immunity. Using RNase H for degrading mRNA results in 80% depletion of mRNA and protein expression. RNase H recognizes the start codon and the 3′ and 5′ untranslated regions. This enzyme participates in DNA replication.

특징 및 장점

  • Eliminate potential sources of PCR errors.
  • Increase accessibility of primers during subsequent PCR.

품질

Absence of endonucleases, nicking activities, and ribonucleases.

단위 정의

RNase H is assayed according to Hillenbrand and Staudenbauer. One unit of RNase H is the amount of enzyme which produces 1 nmol acid-soluble ribonucleotides from[3H] poly(A) x poly(dT) in 20 minutes at +37 °C under the stated assay conditions.

Volume Activity: Approximately 1 U/μl

제조 메모

Activator: The enzyme has its maximal activity in presence of SH-reagents

저장 및 안정성

Store at -15–-25 °C. (unopened)

기타 정보

For life science research only. Not for use in diagnostic procedures. Using RNase H after the cDNA synthesis step can increase the sensitivity of a two-step RT-PCR assay.

Storage Class Code

12 - Non Combustible Liquids

WGK

WGK 1

Flash Point (°F)

does not flash

Flash Point (°C)

does not flash


시험 성적서(COA)

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문서 라이브러리 방문

Amandine Bonnet et al.
Molecular cell, 67(4), 608-621 (2017-08-02)
Transcription is a source of genetic instability that can notably result from the formation of genotoxic DNA:RNA hybrids, or R-loops, between the nascent mRNA and its template. Here we report an unexpected function for introns in counteracting R-loop accumulation in
Antisense oligonucleotides and rna interference
Kher G, et al.
Chalcogenide Lett null
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Houben A, et al.
Development, dev-137489 (2016)
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PLoS genetics, 17(8), e1009784-e1009784 (2021-09-01)
Aberrant repair of DNA double-strand breaks can recombine distant chromosomal breakpoints. Chromosomal rearrangements compromise genome function and are a hallmark of ageing. Rearrangements are challenging to detect in non-dividing cell populations, because they reflect individually rare, heterogeneous events. The genomic
Anirudh Chakravarthy et al.
Life science alliance, 4(12) (2021-10-02)
The continued resurgence of the COVID-19 pandemic with multiple variants underlines the need for diagnostics that are adaptable to the virus. We have developed toehold RNA-based sensors across the SARS-CoV-2 genome for direct and ultrasensitive detection of the virus and

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