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GNX T7 RNA Polymerase (250U/µL)

Product information "GNX T7 RNA Polymerase (250U/µL)"

High-Purity Enzyme for In Vitro Transcription


GNX T7 RNA Polymerase is a recombinant enzyme derived from bacteriophage T7 and expressed in Escherichia coli. It catalyzes the 5'→3' synthesis of RNA using double-stranded DNA containing a T7 promoter sequence (5'-TAATACGACTCACTATAGG-3') as a template and NTPs (ATP, CTP, GTP, UTP) as substrates for in vitro transcription.

The polymerase is compatible with linear double-stranded DNA templates with either blunt ends or 5'-protruding ends. This makes it suitable for use with both linearized plasmid DNA and PCR products containing a T7 promoter.

Supplied in a convenient liquid format, this enzyme is ideal for a variety of molecular biology applications such as RNA synthesis, RNA interference (RNAi), hybridization, in vitro translation, and the preparation of RNA probes.

Key Features:
  • High activity and specificity for T7 promoter sequences
  • Suitable for short and long RNA transcripts
  • Compatible with PCR products and linearized plasmids (blunt end or 5'-overhang)
  • Liquid formulation for immediate use

Synthesis principle:
null

Specifications:
Source: Recombinantly produced in Escherichia coli
Concentration: mind. 250U/µL
Storage: The enzyme is stable upon storage at - 20°C for up to 1 year

Applikation / Application:

In vitro RNA Transcription

Einheiten / Units:

The amount of enzyme required to incorporate 1 nmol of [3H] GMP into the acid-insoluble precipitate within 1 hour at 37°C and pH 8.0 is defined as 1 unit.

Quelle / Source:

recombinant

Klassifizierungen / Classification

eclass No.: 32-16-05-90
Documents - Protocols - Downloads :
Here you will find information and further literature. For further documents (certificates with additional lot numbers, safety data sheets in other languages, further product information) please contact Genaxxon biosience at: info@genaxxon.com or phone: +49 731 3608 123.


Documents:

Manuals