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ParTasR mRNA (Cap1, m1Ψ)

ParTasR mRNA encodes human-codon-optimized Tas nuclease from the TIGR-Tas system. Features Cap1, m1Ψ modification, X5 codon optimization, and 100A tail. Ideal for programmable DNA targeting and precision genome editing.
¥1500
RP-A00075-0.2

Description

The GenScript ParTasR mRNA encodes human-codon-optimized Tas nuclease, an ortholog of the recently discovered TIGR-Tas RNA-guided DNA-targeting system (Tandem Interspaced Guide RNA array–TIGR-associated (Tas) protein) as described by Faure et al., Science, 2025. ParTasR enables programmable DNA targeting, providing a novel tool for genome engineering and functional genomics studies.  
 
This mRNA features: 
- A Cap 1 structure with high capping efficiency for enhanced translation 
- Codon optimization via GenScript X5 algorithm for improved protein expression 
- 100% substitution with N1-methyl-pseudouridine (m1Ψ) to enhance expression and reduce innate immune activation 
- A 100A poly(A) tail to mimic mature mRNA 
 
This construct provides a reliable RNA-guided DNA-targeting tool, ideal for precision genome editing and advanced DNA manipulation research.

Form Liquid
Concentration 1mg/mL
Full mRNA length 1374 nt
Full mRNA Molecular Weight 4.46×10^5 Da
Storage buffer 1mM Sodium citrate, pH 6.5
Storage condition Store at -20°C for short term (<3 months), store at -80°C for long term.
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Appearance Clear and free of foreign particles
RNA Length Expected size band detected
RNA Content Target ± 5%
Integrity ≥ 75%
OD260/OD280 1.70 ~ 2.30
Capping Efficiency ≥ 90%
Endotoxin < 10 EU/mg
pH Target ± 0.5
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1.2 µg of ParTasR mRNA and 0.7 µg of gRNA were electroporated into 200,000 HEK293T cells. After 72 hours of incubation, total genomic DNA was extracted, and an amplicon-based NGS library was prepared. Indel percentages at the target site were analyzed.
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ParTasR MRNA (Cap1, M1Ψ)

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ParTasR MRNA (Cap1, M1Ψ)

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For laboratory research use only. Direct human use, including taking orally and injection and clinical use are forbidden.