PfAGO (Pfu Argonaute)
¥1,984.00
Prokaryotic Argonautes (pAgo) is the key protein in the host defense system by mediating nucleic acid molecules.
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| SKU | OPTIONS | 价格 | |
|---|---|---|---|
| PfAGO-50 | 250 pmol, 50 µl (5 µM) | ¥1,984.00 |
- Description
- Additional information
- Documents
Description
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Description
Prokaryotic Argonaute (pAGO) is the key protein in the host defense system by mediating nucleic acid molecules. As the DNA-guided endonuclease from hyperthermophilic archaeon Pyrococcus furiosus, pfAGO protein targets cognate DNA without the requirements of a PAM (protospacer adjacent motif) or PFS (protospacer flanking site) on the target sequence, which largely extends the application in selection of available target DNA sequence. Besides, compared to CRISPR/Cas systems, PfAGO endonuclease exploits guide DNA rather than guide RNA in stimulating target DNA cleavage, which is more convenient for in vitro use as guide DNA is more stable and easier, cost-saver to synthesis than guide RNA.
These properties enable pfAGO as a programmable DNA endonuclease guided by short guide DNAs in efficient, rapid and cost-effective Nucleic Acid Detection systems as well as in versatile Synthetic Biology platforms.
Features
High Biological Activity
Highly Specific
Low Endotoxin Level
Application
Nucleic Acid Detection, Cancer Diagnostics, Synthetic Biology, Genetic Screening
Source
PfAgo gene from Pyrococcus furiosus (NCBI-Protein ID: AAL80661) expressed in E. coli
Purity
Greater than 95% as determined by SDS-PAGE and FPLC
Activity
Linear pUC19 plasmid digested after 10 min reaction at 95°C.
The reaction is performed as follow:
System 20 µl, including 0.16 µM PfAGO Enzyme, 4 µM each of guide DNA, 600 ng linear pUC19 plasmid as target DNA and 2ul 10x reaction buffer.
Pre-incubate PfAGO-guide DNAs complex in reaction buffer at 75°C for 10 min. Then add target DNA, incubating at 95°C for 10 min, and slowly cooling down to 10°C.
Storage Condition
-20 °C
10 X Reaction Buffer
200 mM HEPES, pH 7.5,
2.5 M NaCl,
5 mM MnCl2
Storage Buffer
20 mM Tris-HCl, pH 8.0,
300 mM NaCl,
0.5 mM MnCl2,
50% (v/v) glycerol
Experimental Data
References
1. Ji-Joon Song et. al. (2004). Science. 305 (5689).
2. Daan C. Swarts et. al. (2015). Nucleic Acids Res. 43(10):5420-5129.
3. Yuqing Qin et. al. (2022). Trends Biotechnol. 40(8):910-914.
Additional information
| OPTIONS | 250 pmol, 50 µl (5 µM), 250 pmol, 50 µl (5 µM) |
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