DreamTaq™ Hot Start DNA Polymerase
DreamTaq™ Hot Start DNA Polymerase
Thermo Scientific™

DreamTaq™ Hot Start DNA Polymerase

Thermo Scientific DreamTaq Hot Start DNA Polymerase is an enhanced hot start Taq DNA polymerase that enables higher PCR specificity, sensitivity, and yields compared to conventional hot start Taq DNA polymerases.
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카탈로그 번호색상수량
EP1711Green200 U
EP1701Colorless200 U
EP1702Colorless500 U
EP1703Colorless2500 U
EP1712Green500 U
EP1713Green2500 U
카탈로그 번호 EP1711
제품 가격(KRW)
139,000
온라인 행사
Ends: 31-Dec-2025
163,000
할인액 24,000 (15%)
Each
카트에 추가하기
색상:
Green
수량:
200 U
대량 주문 또는 맞춤형 요청
제품 가격(KRW)
139,000
온라인 행사
Ends: 31-Dec-2025
163,000
할인액 24,000 (15%)
Each
카트에 추가하기
Thermo Scientific DreamTaq Hot Start DNA Polymerase, available in colorless and green formats, is an enhanced hot start Taq DNA polymerase that enables higher PCR specificity, sensitivity, and yields compared to conventional hot start Taq DNA polymerases.

DreamTaq Hot Start DNA Polymerase employs antibody-based inhibition of DNA polymerase activity at ambient temperatures to prevent the amplification of non-specific products prior to the amplification step. With DreamTaq Hot Start DNA Polymerase, reactions can be set up at room temperature using the same protocol and cycling conditions as conventional Taq DNA polymerases. The enzyme is supplied with an optimized 10X DreamTaq Buffer containing magnesium chloride, which eliminates the need for extensive optimization of reaction conditions. DreamTaq Hot Start DNA Polymerase is also available with pre-added density reagent and electrophoresis tracking dyes, as well as in master mix format.

The 10X DreamTaq Green Buffer also includes a density reagent and two tracking dyes for convenient direct loading of PCR products on a gel.

DreamTaq Hot Start DNA Polymerase is formulated to enhance productivity through:

  • Better reaction outcomes
    • Higher yield of target amplicons from low template amounts
    • Increased reaction specificity due to reliable hot-start technology
    • Wider range of amplicon lengths with routine amplification of genomic DNA fragments up to 6 kb
  • Enhanced convenience
    • Room temperature reaction setup
    • Minimized optimization of Mg2+ concentration and of primer annealing temperatures due to optimized reaction buffer
    • Direct loading of PCR products on a gel with DreamTaq Green Buffer

Applications

  • Generation of PCR products for TA cloning
  • Routine PCR
  • Colony PCR
  • Genotyping
  • RT-PCR
사양
색상Green
핫 스타트Built-In Hot Start
오버행3'-A
중합효소DreamTaq DNA Polymerase
수량200 U
반응 형식Separate Components
배송 조건Dry Ice
농도5 U/μL
용도(애플리케이션)Hot-start PCR
GC-Rich PCR PerformanceLow
반응 속도Standard
Unit SizeEach
구성 및 보관
• DreamTaq Hot Start DNA Polymerase (5 U/μL), 40 μL
• 10X DreamTaq Green Buffer (with 20 mM MgCl2), 1.25 mL

Store at -20°C.

자주 묻는 질문(FAQ)

Which nucleotide analogues can be used with DreamTaq Hot Start DNA Polymerase?

DreamTaq Hot Start DNA Polymerase can incorporate dUTP and a variety of modified nucleotides, such as: dITP, 7-deaza-dGTP, fluorescein-12-dUTP, Biotin-11-dUTP, dm5CTP, alpha-thio-dCTP, and aminoallyl-dUTP.

Are DreamTaq buffers the same for DreamTaq DNA Polymerase and DreamTaq Hot Start DNA Polymerase?

Yes. 10X DreamTaq Buffer and 10X DreamTaq Green Buffer are the same for both polymerases.

My experiments require extra DreamTaq Buffer. Do you offer the buffer as a separate product?

Yes, DreamTaq Buffer (Cat. No. B65, 4 x 1.25 mL) and DreamTaq Green Buffer (Cat. No. B71, 4 x 1.25 mL) are available as stand-alone products.

Can DreamTaq Hot Start DNA Polymerase be used for amplification of bisulfite converted DNA?

Yes. DreamTaq Hot Start DNA Polymerase can read uracil in the template strand and therefore can be used for amplification of bisulfite converted DNA.

What is the limit of amplicon size using DreamTaq Hot Start DNA Polymerase?

DreamTaq Hot Start DNA Polymerase amplifies up to 6 kb from human genomic DNA and up to 20 kb from lambda DNA with high yields and specificity. Amplification of even longer fragments up to 9 kb from human genomic DNA has been demonstrated, but may require additional optimization of reaction conditions and primer design.