HyperScribe™ Two-Step sgRNA Synthesis Kit
The CRISPR/Cas9 system is a widely used genome editing technology, which uses Cas9 nuclease to cut specific sites of targeted sequences of genomic DNA under the guidance of sgRNA, also known as gRNA (guide RNA). gRNA is a fusion product consisting of 18-20 bp CRISPR RNA (crRNA) sequences that complement the target gene sequences, and Trans-activating crRNA (tracrRNA) sequences that bind to Cas9 nucleases.In the cell, gRNA bound to Cas9 nuclease and guided Cas9 nuclease to cut the target gene at the upstream position of the proto-spacer adjacent motif (PAM) sequence, causing frameshift mutations in the target gene locus and eventually resulting in deletion mutations of the target gene.
This kit is a two-step method for the synthesis of sgRNA based on PCR amplification and in vitro transcription dependent on T7 RNA polymerase. The kit provides a Template Mix, including a Scaffold Template sequence and a downstream primer for amplification of the sequence. Users only need to design and synthesize the Target-specific DNA oligo (i.e. the upstream primer) to obtain the corresponding sgRNA through this kit. After purification, the synthesized sgRNA can be co-transfected with Cas9 mRNA (No.R1015), or gene edited in cells expressing Cas9 protein, or mixed with Cas9 nuclease for enzyme digestion identification experiment.
Components |
20 rxns |
100 rxns |
2× Template Mix |
200 μL |
1 mL |
Phusion high-fidelity DNA polymerase |
10 μL |
50 μL |
ATP (100 mM) |
40 μL |
200 μL |
GTP (100 mM) |
40 μL |
200 μL |
UTP (100 mM) |
40 μL |
200 μL |
CTP (100 mM) |
40 μL |
200 μL |
T7 RNA polymerase Mix |
40 μL |
200 μL |
10× Reaction Buffer |
40 μL |
200 μL |
DNase I |
20 μL |
100 μL |
RNase-free H2O |
400 μL |
2 mL |
Store the components at -20 °C for at least one year. |