상품 옵션 정보 | ||||||
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카탈로그 번호 | 설명 | 상태 | 단위 | 가격 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
R300B | Takara R300B TaKaRa Taq™ HS Perfect Mix, 400 Rxns pk | 재고문의 | pk | 608,000원 | 668,800원 | |
R007B | Takara R007B TaKaRa Taq™ DNA Polymerase Hot Start Version, 1,000 Units pk | 재고문의 | pk | 500,000원 | 550,000원 | |
R300A | Takara R300A TaKaRa Taq™ HS Perfect Mix, 100 Rxns pk | 재고문의 | pk | 168,000원 | 184,800원 | |
R007A | Takara R007A TaKaRa Taq™ DNA Polymerase Hot Start Version, 250 Units pk | 재고문의 | pk | 139,000원 | 152,900원 | |
R028A | Takara R028A Premix Taq™ DNA Polymerase Hot-Start Version, 100 Rxns pk | 재고문의 | pk | 120,000원 | 132,000원 |
The hot-start versions of TaKaRa Taq DNA Polymerase contain a mixture of Taq polymerase and a monoclonal antibody that binds to Taq polymerase, thereby preventing DNA synthesis at room temperature. During the initial DNA denaturation step (reaction temperature ~94°C), the antibody is denatured, releasing the polymerase and allowing DNA synthesis to proceed. The use of a hot-start PCR enzyme prevents nonspecific amplification due to mispriming and/or the formation of primer dimers during PCR assembly.
Several hot-start versions of Takara Taq are available:
The hot-start versions of TaKaRa Taq DNA Polymerase contain a mixture of Taq polymerase and a monoclonal antibody that binds to Taq polymerase, thereby preventing DNA synthesis at room temperature. During the initial DNA denaturation step (reaction temperature ~94°C), the antibody is denatured, releasing the polymerase and allowing DNA synthesis to proceed. The use of a hot-start PCR enzyme prevents nonspecific amplification due to mispriming and/or the formation of primer dimers during PCR assembly.
Several hot-start versions of Takara Taq are available:
- TaKaRa Taq DNA Polymerase Hot Start Version—enzyme, buffer, and dNTPs are supplied as separate components
- Premix Taq DNA Polymerase Hot Start Version—2X premix containing Takara Taq HS enzyme, dNTPs, and an optimized reaction buffer
- TaKaRa Taq HS Perfect Mix—2X hot-start premix optimized for fast reactions. It contains a modified Taq DNA polymerase, which lacks exonuclease activities, and is compatible with a 20 sec/kb extension step
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