Fully Automated Protein Synthesis/purification
Negotiable Min Order Quantity Unit
- Required Quantity
-
- Place of Origin
- South Korea
- Brand name
- ExiProgen™
- Payment Terms
- Negotiable
- Production method
- Negotiable
- Shipping / Lead Time
- Negotiable / Negotiable
Product name | Fully Automated Protein Synthesis/purification | Certification | - |
---|---|---|---|
Category |
Other Extracts
Chemical Reagents & Products Amino Acids and Coenzymes |
Ingredients | - |
Keyword | protein purification , protein synthesis system , nucleic acid extraction system , protein synthesis/purification | Unit Size | 320.0 * 500.0 * 535.0 mm |
Brand name | ExiProgen™ | Unit Weigh | 27 kg |
origin | South Korea | Stock | - |
Supply type | - | HS code | 902580 |
Product Information
ExiProgen™ is an instrument that automatically synthesizes protein from DNA. This product performs In-vitro transcription and translation automatically when loaded with DNA coding a protein and a protein synthesis kit. By purifying this protein through affinity chromatography method, more than 90% pure protein can be obtained within 6 hours and up to 16 species can be produced at one time. In addition, highly expressed affinity tagged proteins can be purified in cell lines with high purity.
- Built-in optimized nucleic acid and protein synthesis protocol
Simplified usage and reproducible results with built-in nucleic acid extraction and protein purification protocols optimized for various samples (whole blood, tissue, cell, bacteria, plant, etc.)
- High stability
Minimized protein denaturation by installing cooling reaction block inside the instrument keeping the temperature of elution tube rack below 10°C
- High-pure nucleic acid extraction & protein purification
Quick performance of nucleic acid extraction and protein purification with great purity and efficiency by attaching magnetic particles to the bottom of each well equally and rapidly by magnetic blocks attached to the instrument
Increased elution efficiency allowing complete evaporation of alcohols by its heating block (Korean Patent No. 10-1025135) - Contamination prevention device
Substantial blocking of cross-contamination, which may occur in other wells by the aerosols generated from the tip, through the sophisticated designs drop-contamination prevention device located at the bottom of the filter tip
- Automatic UV sterilization Function
Sterilization to prevent infection for the users by the samples through the UV lamp installed inside the instrument
- Easy-to-use
User-friendly UI capable of checking the experimental progress rate real-time without the need of seperate PC by equipping with a 13.3-inch touch screen on the front of the device
- Excellent precision
Minimized error range, that may occur during the automatic dispensing of the solution, through installment of an adjustable syringe motor up to 0.1 mm capable of stably distributing in a volume of 25 ㎕ ~ 1000 ㎕ for application to various protocols and obtaining of experimental results
▶ Specifications
Dimensions (cm) | 32 (W) x 53.5 (D) x 50 (H) |
Weight (kg) | 27 |
Temperature range | 15-35℃ |
Humidity range | 20-80%, no condensation |
Operating system | Standalone |
User interface | 320 x 240 touch screen graphic LCD |
Input voltage | 100 – 240 VAC |
Frequency | 50 / 60 Hz |
UV sterilization | 15 minute cycle |
Communications | TCP/IP |
Heat block | 40-90℃ |
▶ Function
DNA/RNA Extraction | O |
Protein Expression | O |
Protein Purification | O |
TFT Touch Screen | O |
Sample Number | 16 samples |
UV sterilization | O |
Heating & magnetic block | O |
Cartridge Contamination shield | O |
TCP/IP network connection | Numerous equipment can be connected |
Cooling system for sample store | O |
Automatic dispensing | O |
Power supply | 24 VDC, 7.5 A(180 W) |
* Specifications of this product are subject to change without notice to improve product performance.
▶ Experimental data
1Protein expression and purification
- DNA concentration used: 6 - 10 μg (purity > 1.8)
- Protocol number : 902
- Total run time : < 6 h
- yield : <100 μg
Experimental Process
SDS-PAGE analysis | |
<Simultaneous expression/purification of the same protein (GFP) 16 wells> Figure 1. GFP protein (His-tagged protein)'s expression/purification with ExiProgen™ M; AccuLadder™ Protein Size Maker (Low), E; expression sample P; purification sample | |
<Simultaneous expression/purification of different kinds of proteins> Figure 2. His-tagged proteins expression/purification with ExiProgen™ M; AccuLadder™ Protein Size Maker (Low) E; expression sample, P; purification sample |
2Total RNA Extraction From Tissue or cultured mammalian cell
- Sample: 15 ㎎ (rat liver tissue) or 1 X 106 cells (HeLa)
- Protocol number: 202
- Average yield: 25 ㎍ (rat liver tissue), 10 ㎍ (HeLa)
- Average RQS: 9.5 over
※ RQS(RNA quality score): The quality of the extracted RNA is expressed as a numerical value, the height and width of each rRNA peak, and the peak of degraded RNA fragments are comprehensively calculated and displayed. It is the same concept as the RNA integrity number (RIN) developed by Agilent. It is usually expressed as a value from 0 to 10. The closer to 10, the better the quailty of RNA.
Experimental Process
• Analysis results of Total RNA extracted from tissues of Rat
Figure 3. Since each subunit of rRNA is well observed, it can be confirmed that RNA was intactly extracted without decomposition of RNA during total RNA extraction process.
• Results of Real-Time PCR using Total RNA extracted from tissues of Rat
Figure 4.Results of real time RT-PCR using AccuPower® RocketScrpt ™ RT PreMix(K-2101, Bioneer), AccuPower® DualStar™ qPCR PreMix(K-6110, Bioneer) and Exicycler™ 96 Real-Time Quantitative Thermal Block(A-2060)
• Analysis results of total RNA extracted from HeLa cell
Figure 5. Total RNA was extracted from HeLa cell (1 X 106 cells) and analyzed for quality of extracted RNA using LabChip GX (Caliper Life Science). As each subunit of rRNA is well observed, intact RNA was extracted without RNA degradation during total RNA extraction. Also, the average yield was 10 ㎍ and the average RQS was 9.5 or more.
• Results of real-time PCR using total RNA extracted from HeLa cell
Figure 6. After the total RNA extraction from HeLa cell (1 X 106 cells), it is results of real-time RT-PCR using AccuPower® RocketScrpt ™ RT PreMix (K-2101, Bioneer), AccuPower® DualStar ™ qPCR PreMix (K-6110, Bioneer) and Exicycler™ 96 Real-Time Quantitative Thermal Block (A-2060)
3Genomic DNA from cultured mammalian cell (HeLa)
- Sample volume: 1X106 cells
- Protocol number: 107
- Total prep time: about 1hr 30min.
- Average yield: 4-8 μg
Experimental Process
• Agarose gel analysis
Figure 7. Lanes 1, 3, 5, 7, 9, 11, 13, 15 were extracted with 1X106 cells of cultured HeLa cell and lanes 2, 4, 6, 8, 10, 12, 14, 16 were extracted with ddH2O as a negative control in DNA extraction. Note all samples have similar yields. Purity was also tested and was consistently between 1.8 and 2.0 (not shown).
4Genomic DNA from bacteria (E.coli)
- Sample volume: 1X109 cells
- Protocol number: 109
- Total prep time: about 1hr 40min.
- Average yield: 8-12 μg
Experimental Process
• Agarose gel analysis
Figure 8. Lanes 1, 3, 5, 7, 9, 11, 13, 15 were extracted with 1X109 cells of E.coli cells and lanes 2, 4, 6, 8, 10, 12, 14, 16 were extracted with ddH2O as a negative control in DNA extraction. Note all samples have similar yields. Purity was also tested and was consistently between 1.9 and 2.0 (not shown).
5Genomic DNA from tissue (bovine skeletal muscle)
- Sample volume: ~25 mg
- Protocol number: 102
- Total prep time: about 1hr 30min.
- Average yield: Up to 20 µg
Experimental Process
• Agarose gel analysis
Figure 9. Lanes 1, 3, 5, 7, 9, 11, 13, 15 were extracted with 25 mg of bovine tissues and lanes 2, 4, 6, 8, 10, 12, 14, 16 were extracted with ddH2O as a negative control in DNA extraction. Note all samples have similar yields. Purity was also tested and was consistently between 1.9 and 2.0 (not shown).
6Genomic DNA from plant tissue (spinach leaf)
- Sample volume: ~ 100 mg
- Protocol number: 104
- Total prep time: about 1 hr
- Average yield: Up to 5 µg
Experimental Process
• Agarose gel analysis
Figure 10. Lanes 1, 3, 5, 7, 9, 11, 13, 15 were extracted with 100 mg of spinach leaves and lanes 2, 4, 6, 8, 10, 12, 14, 16 were extracted with ddH2O as a negative control in DNA extraction. Note all samples have similar yields. Purity was also tested and was consistently between 1.9 and 2.0 (not shown).
- Product Info Attached File
B2B Trade
Price (FOB) | Negotiable | transportation | - |
---|---|---|---|
MOQ | Negotiable | Leadtime | Negotiable |
Payment Options | Negotiable | Shipping time | Negotiable |
- President
- PARK, HAN-OH
- Address
- 49-3, Munpyeong-dong, Daedoek-gu, Daejeon
- Product Category
- Pharmaceuticals
- No. of Total Employees
- 101-500
- Company introduction
-
Bioneer is a leading supplier of synthetic DNA, providing high-quality custom oligos at affordable prices. Recent improvements in oligonucleotide synthesis chemistry has led to the production of higher quality oligonucleotides at lower cost. In addition, we have implemented in-house production of raw materials along with our proprietary DNA synthesis system, called 384 parallel super DNA synthesizer, and BioRP oligo purification technology (patent pending). Furthermore, we have recently completed a state-of-the-art oligo manufacturing facility capable of producing over 45,000 oligos /day. Such oligo production capacity enables us to meet above and beyond the needs of our customers.
- Main Markets
-
Iran
Israel
Japan
U. Kingdom
U.S.A
- Main Product
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