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GMP-grade T7 RNA Polymerase 3.0 for in vitro transcription with reduced dsRNA by-product formation, high catalytic activity, and reliable performance for mRNA synthesis workflows.

T7 RNA Polymerase 3.0 GMP-grade (low dsRNA), GMP-BP-E11

USD
$0.00
GMP-BP-E11
Features
  • Reduced dsRNA by-product generation compared with conventional T7 RNA polymerase
  • High transcriptional catalytic activity across different DNA templates and nucleic acid types
  • Precise recognition of the T7 promoter sequence (5′-TAATACGACTCACTATAG-3′)
  • Supports RNA synthesis with natural or modified nucleotide substrates
  • GMP-grade manufacturing with multi-step purification and stringent quality control
  • Free of exogenous DNase, RNase, exonuclease, and endonuclease activity
  • Low residual host-cell DNA, low endotoxin, and high protein purity for demanding IVT workflows
  • In vitro transcription (IVT) for mRNA synthesis and process development
  • Preparation of RNA from DNA templates containing the T7 promoter
  • Workflows requiring reduced dsRNA by-product formation to support downstream translational performance and lower innate immune activation risk
  • Research, preclinical, and manufacturing-oriented therapeutic RNA development
  • Use with natural or modified nucleotides in advanced RNA production workflows
No. Component Catalog No. Quantity Volume
1 T7 RNA Polymerase 3.0 GMP-grade (low dsRNA) GMP-BP-E11-5K 5 KU 100 μL
2 T7 RNA Polymerase 3.0 GMP-grade (low dsRNA) GMP-BP-E11-50K 50 KU 1 mL
3 T7 RNA Polymerase 3.0 GMP-grade (low dsRNA) GMP-BP-E11-500K 500 KU 10 mL
Condition Recommendation
Storage Store at -20 ± 5 °C.
Handling Mix thoroughly before use and avoid repeated freeze-thaw cycles.
RNase precautions Use RNase-free consumables and wear gloves throughout the workflow.
Storage Buffer 50 mM Tris-HCl, 1 mM EDTA, 10 mM DTT, 100 mM NaCl, 0.1% (v/v) Triton X-100, 50% (v/v) glycerol, pH 7.9 at 25 °C.

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