Promega TNT® T7 Quick for PCR DNA Kit User Manual

The Promega TNT® T7 Quick for PCR DNA kit manual provides step‑by‑step instructions, component details, storage conditions, and troubleshooting for in‑vitro…


Promega TNT® T7 Quick for PCR DNA Kit User Manual - cover page
Brand
Promega
Category
Other
Document type
User Manual
Language
Chinese
Pages
11
File format
PDF
File size
323 KB
Published
08 October, 2026
Updated
08 October, 2026
MD5 checksum
8D25EE100915649D0D5581FAFE35D400

About this manual

The TNT® T7 Quick for PCR DNA kit enables rapid, coupled transcription‑translation of PCR‑generated DNA templates. The kit contains a master mix and reagents that allow direct use of PCR products without purification, producing high protein yields.

The manual covers template considerations, component list and storage, general lab practices, detailed transcription/translation procedures (including radioactive, non‑radioactive, and fluorescent detection options), post‑translation analysis, and a FAQ section for common problems. This manual is written in Chinese.

What's inside

  • Overview
  • Considerations for PCR DNA Templates
  • Components and Storage Conditions
  • General Considerations
  • Transcription/Translation Procedure
  • Post‑translation Protein Analysis
  • Frequently Asked Questions
  • References
  • Appendix

Specifications

Master Mix storage temperature-70 °C
Typical reaction volume≈40 × 50 µl
Master Mix composition1.6 ml TNT® T7 PCR Quick Master Mix (8 × 200 µl)
Methionine supplement50 µl, 1 mM
Incubation temperature for transcription/translation30 °C

Frequently asked questions

What temperature should the transcription/translation reaction be incubated at?

Incubate the reaction at 30 °C for 60–90 minutes.

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