Transcription Mediated Amplification (TMA) Component System
The most sensitive solution for HCV qualitative detection*

Transcription Mediated Amplification (TMA) Component System
 
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Target Capture System

Workstation Base Unit  
Capacity 100 Tubes (10TTUs)
Environment 15-30°C; ambient operating temperature
20-90% non-condensing ambient operating relative humidity
Dimensions 13* x 48 x 48cm (5 x 19 x 10in) H x W x D
*Requires 30.5cm (12in) above unit to maneuver the aspiration manifold.
Weight 9.6kg (21.2 lbs)
Dispense Station  
Injector Volumes
(Dispense Manifold)
1.0± 10% mL delivered. No splash back.
Dimensions 43 x 23 x 25cm (17 x 9 x 10in) H x W x D
Weight 2.5kg (5.5lbs)

 

Vacuum Trap  
Dimensions 47 x 38 x 18cm (17 x 9 x 10in) H x W x D
Weight 8.9kg (19.5lbs)

 

Luminometer HC+

Capacity                 250 tubes (25 TTUs)
Processing Time 100 Tubes in 75 Minutes
Dimensions 19.1 x 45.7 x 67.3cm (67.5 x 18 x 26.5 in) H x W x D
Weight 23 kg (50lbs)
Injector Volume 200µl ±10%, coefficient of variation <2%
Power 115 ±10% VAC(0.500A, Slow Blow MDL); 230 ±10% VAC (0.250A, T-Type); 50/60 Hz; 40 VA. Dual voltage switch. Use of a UPS/line conditioner is recommended (Included with the TMA Component System).
Environment 15-30°C; ambient operating temperature
10-90% non-condensing ambient operating relative humidity
Electrical Safety UL/CSA and CE Marked

 

TMA Computer System

CPU 166 MHz Pentium; 64MB RAM
Operating System Windows NT 4.0, Service PAck 5
Software TMA Data Reduction Software
Hard Drive 2.1 GB
External Drives CD-ROM and 3.5" floppy drives
Input/Output Ports Two RS-232 Serial Ports
Network 10baseT (Optional)
Monitor Color 15" SVGA; 800x600x256 color video resolution
Printer parallel printer supported by Windows NT (color or b/w)

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* The VERSANT HCV RNA Qualitative Assay (TMA) is the most sensitive assay for the detection of HCV currently approved by the U.S. FDA.