InviTrans T7 In Vitro Transcription Kit

Product Code: AG51201

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¥1,200

Product Description

This is a kit that utilizes T7 RNA Polymerase for in vitro transcription to obtain large amounts of RNA in a short period of time. T7 RNA Polymerase synthesizes RNA downstream of the T7 promoter sequence using a template such as linearized plasmid DNA with the T7 promoter, PCR products or chemically synthesized DNA fragments (T7 promoter sequence “TAATACGACTCACTATA”), and NTP as the substrate. The T7 RNA Polymerase synthesizes RNA downstream of the T7 promoter, using NTP as the substrate, and synthesizes 100 to 200 μg of RNA per system, while transcribing fragments up to 10 kb in length. The transcribed RNA product can be used for RNA structure and function, RNAase protection, probe hybridization, RNAi, microinjection, in vitro translation and mRNA vaccines.

 

Product Advantages

1. The substrate and enzyme in this product are presented in the form of premix, which reduces the experimental steps and is simple and convenient.
2. This product has a high RNA yield for transcription, each reaction system can obtain 100 ~ 200 μg of high quality RNA.

Product Composition
ingredient norm
10X In Vitro Transcription Buffer 100 μl
NTP Mix (25 mM each) 400 μl
T7 RNA Polymerase Mix 100 μl
RNase free water 1 ml
Preservation and transportation

Storage temperature: -20℃ storage
Transportation temperature: dry ice transportation or -20℃ ice bag transportation

Experiment example 1

Using 1 μg of T7 promoter-containing DNA fragments as template, this product can be used for in vitro transcription of fragments ranging from 1 to 8 kb in length.

The electrophoresis results are shown in the figure below, where M is the ssRNA Ladder (Code No. N0362S) from NEB:

 

Example 2

The DNA fragments containing T7 promoter with lengths of 0.1 kb, 1.0 kb, 2.0 kb and 4.0 kb and a template amount of 1 μg were used as templates, and different reaction times (0.5 ~ 8 h) were set to carry out the in vitro transcription using this product, and the results are shown below: