dsDNase
dsDNase
Thermo Scientific™

dsDNase

dsDNase is a heat inactivatable recombinant shrimp DNase used to remove genomic DNA contamination of RNA samples before reverse transcription.
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카탈로그 번호수량
EN077150 reactions
카탈로그 번호 EN0771
제품 가격(KRW)
220,000
온라인 행사
Ends: 31-Mar-2026
251,000
할인액 31,000 (12%)
Each
카트에 추가하기
수량:
50 reactions
대량 주문 또는 맞춤형 요청
제품 가격(KRW)
220,000
온라인 행사
Ends: 31-Mar-2026
251,000
할인액 31,000 (12%)
Each
카트에 추가하기

Thermo Scientific dsDNase is an engineered shrimp DNase designed for rapid and safe removal of contaminating genomic DNA from RNA samples. It is an endonuclease that cleaves phosphodiester bonds in DNA to yield oligonucleotides with 5'-phosphate and 3'-hydroxyl termini. Highly specific activity towards double-stranded DNA ensures that RNA and single-stranded DNA such as cDNA and primers are not cleaved. dsDNase is easily inactivated by modetate heat treatment (55°C). These features make dsDNase an excellent choice for gDNA elimation prior reverse transcription. It allows for dramatically simplified workflow which combines genomic DNA elimination and cDNA synthesis into one-tube procedure.

Highlights

  • Highly specific degradation of double-stranded DNA
  • Fast 2 min protocol for gDNA removal prior reverse transcription
  • Heat-labile—irreversibly inactivated by moderate heat treatment (55°C)

Applications

  • Genomic DNA removal from RNA samples prior first strand cDNA synthesis, RT-PCR and RT-qPCR

Specificities of dsDNase—dsDNase activity towards double- and single-stranded DNA and RNA oligonucleotides was measured. Relative activity values indicate that dsDNase is highly specific to double-stranded DNA.

  • dsDNA - 100% relative activity
  • ssDNA - <0.03% relative activity
  • dsRNA - <0.01% relative activity
  • ssRNA - <0.01% relative activity
For Research Use Only. Not for use in diagnostic procedures.
사양
설명DNase
수량50 reactions
Unit SizeEach

자주 묻는 질문(FAQ)

Does dsDNase cleave ssDNA?

No, dsDNase cleaves only double-stranded DNA. However, if ssDNA forms double-stranded structures, it will act as a target for dsDNase. Because of this, long and complex ssDNA may be partially degraded. Therefore we recommend additional dsDNase inactivation step for RT-PCR amplification of targets 3 kb or longer. The inactivation step should be performed by 5 min incubation at 55 degrees C in the presence of 10 mM DTT.

Can dsDNase be added directly to a reverse transcription reaction to remove genomic DNA?

No. RT reaction composition inhibits dsDNase activity, and genomic DNA removal may be incomplete.

When using the Maxima or Maxima H Minus First Strand cDNA Synthesis kits with dsDNase, can the genomic DNA elimination step be omitted?

Yes. dsDNase buffer is not needed for subsequent reverse transcription reaction. If RNA sample is not contaminated with gDNA, dsDNase treatment may be omitted.