Basic | Sample Capacity | 48x0.2ml |
Applicable Consumables | 0.2ml single tube, 8x0.2ml tube strip, 96-well plate |
PCR Volume Range | 20-120μL |
Working Temperature | 15-30°C |
Storage Temperature | -20-55°C |
Ambient Relative Humidity | ≤85% |
Dimensions and Weight | 466*310*273mm(W*D*H),17.5kg |
Power Supply | 220 V,50 Hz,865VA |
Temp. Control System | Heating/cooling Method | Semiconductor heating method, independent and intelligent temp. control over 4 zones |
Temperature Range | 4°C-100°C |
Ramp Rate | Heating: 4°C/S, Cooling: 4°C/S |
Temperature Accuracy | ≤0.5°C |
Temperature Uniformity | ≤±1°C |
Temperature Control technology | 4-zone independent temp. control combined with thermal compensation tech |
Gradient Temp. Function | Yes |
Gradient Temp. Columns | 8 |
Gradient Temp. Range | 1°C-32°C |
Gradient Temp. Zones | 4 |
Gradient Temp. Set Range | 30°C-100°C(Room temperature is lower than 28°C) |
Detection System | Excrtation Source | LED |
Detection Device | PD |
Light Propagation Medium | Dual-48 high temperature resistant optical fibers for Space |
Detection Channels | 4 |
Excitation Range | 1st Channel: 470nm+10nm 2nd Channel: 525nm±10nm
3rd Channel: 570nm+10nm 4th Channel: 620nm±10nm |
Detection Range | 1st Channel:520nm±10nm 2nd Channel:570nm±10nm
3rd Channel: 620nm±10nm 4th Channel: 670nm±10nm |
Dye Compatibility (name) | FAM/SYBR Green/Eva Green/LC Green/Fluorescein; VIC/HEX/TET/Cy3/JOE;ROX/Cy3.5/Texas Red; Cy5 etc |
Detection Sensitivity | ≥1 copy |
Confidence Coefficient | 99.90% |
Sensitivity | Allowed 1.5-fold in single reaction |
Sample Detection Repeatability | CV≤3% |
Linear Range | 1^0-10^9 copy |
Sample Linearity | ≥0.98 |
Software | Software Language | Chinese/English |
Control Method | Connect to PC for data analysis,USB, support LlMS/LIS system |
Software Function | Realtime monitoring, automatic identification and calculation of positive and negative
results, automatic establishmentof standard curve, absolute/relative quantification,
multiple quantification, melting curve, gene mutation, key methodgenotyping (faqman probe method),
Tim value determination, quality control graphic analysis ,PCR amplification efficiency, etc. |
Output | EXCEL/WORD/PDF |
| Medical Device Registration | CFDA No.20203220992 |
| Safety Compliances | CE/IS09001/IS013485 |
