- 商品介绍
- 规格参数
- 包装参数
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规格 |
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| For Use With (Application): | Real-Time Quantitative PCR (qPCR), Reverse Transcriptase PCR (RT-PCR) |
| Primer: | Random Primers, Oligo dT Primers |
| Optimal Reaction Temperature: | 50° C |
| Reaction Format: | SuperMix or Master Mix |
| Reverse Transcriptase: | SuperScript™ III |
| Shipping Condition: | Dry Ice |
| Product Line: | SuperScript™ |
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储存 |
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Contains: • 2X Reaction Mix (500 µl) • SuperScript® III Enzyme Mix (100 µl) • Oligo(dT)20 (50 µl total provided at 50 µM) • Random hexamers (50 µl total provided at 50 ng/µl) • Annealing buffer (50 µl) Enough material provided for 50 reactions (20 µl each). Store at -20°C. |
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描述 |
The SuperScript® III First-Strand Synthesis SuperMix is an optimized SuperMix formulation for first-strand cDNA synthesis from purified poly(A)+ or total RNA. RNA targets from 100 bp to >12 kb can be detected with this system. The amount of starting material can vary from 0.1 pg to 5 µg of total RNA.
Using the SuperScript® III First-Strand Synthesis SuperMix
The kit includes SuperScript® III/RNaseOUT™ Enzyme Mix, 2X First-Strand Reaction Mix, and Annealing Buffer. SuperScript® III Reverse Transcriptase, included in the Enzyme Mix, is a version of M-MLV RT that has been engineered to reduce RNase H activity and provide increased thermal stability. The enzyme can be used to synthesize cDNA at a temperature range of 45–55°C, providing increased specificity, higher yields of cDNA, and more full-length product than other reverse transcriptases. Because SuperScript® III RT is not significantly inhibited by ribosomal and transfer RNA, it can be used to synthesize cDNA from total RNA. RNaseOUT™ Recombinant RNase Inhibitor is included in the Enzyme Mix to safeguard against degradation of target RNA due to ribonuclease contamination. The 2X First-Strand Reaction Mix includes 10 mM MgCl2 and 1 mM of each dNTP in a buffer formulation that has been optimized for first-strand synthesis of cDNA. The Annealing Buffer is used in the initial template-primer annealing step. Separate tubes of oligo(dT)20 and random hexamers are also provided. cDNA synthesis can be performed using either total RNA or poly(A)+-selected RNA primed with oligo(dT), random primers, or a gene-specific primer.
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