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LabTurbo Biotech Corporation
3f-1, No. 150, Section 4, Chen-De Rd.,
111052
Taipei
Taiwan
Taiwan
Telephone +886 22889 1136
Fax +886 22889 1146
Fax +886 22889 1146
Contact
Evan Lin
Sales manager
Joe Yu
Sales
Tina Tsai
Sales
Emily Chiang
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16 Nov 2020
Topic
all-day
Product presentation and inquiry
One by One consultation and Q&A
17 Nov 2020
Topic
all-day
Product presentation and inquiry
One by One consultation and Q&A
18 Nov 2020
Topic
all-day
Product presentation and inquiry
One by One consultation and Q&A
19 Nov 2020
Topic
all-day
Product presentation and inquiry
One by One consultation and Q&A
Our range of products
Product categories
- 03 Diagnostic tests
- 03.05 Infectious immunology testing
- 03.05.01 Bacteriology testing
Bacteriology testing
- 03 Diagnostic tests
- 03.06 Genetic testing, molecular diagnostics
- 03.06.01 DNA testing
DNA testing
- 03 Diagnostic tests
- 03.06 Genetic testing, molecular diagnostics
- 03.06.02 Molecular biomarkers
Molecular biomarkers
- 03 Diagnostic tests
- 03.06 Genetic testing, molecular diagnostics
- 03.06.03 Polymerase chain reaction (PCR)
Polymerase chain reaction (PCR)
Our products
Product category: DNA testing, Molecular biomarkers
LabTurbo AIO 48 SP-qPCR Automation System
High-Throughput, Speedy, Truly Walk-away
Sample-to-result Coronavirus SARS-CoV-2 detection
All-In-One(Sample-to-result) procedure: LabTurbo COVID-19 testing platform automates the whole detection procedure from sample to PCR results. Get 1 to 48 COVID testings done in 2 hours!
- Simple mode:
Throghput 1-48 in 2 hours - Simultaneously workflow mode:
Runing sample extraction and PCR at the same time
Only take 2 hours to finish first batch 48 samples, 48 samples PCR result per 1 hour after the first run. - Mass Rapid Transit Mode:
Operated by One AIO with two LabTurbo C48, 144 sample PCR result per 1 hour after the first run(2 hours)
Only take 1.32 square meter in lab
DIM: 66 x 72 x 170 cm (26 x 28 x 67 in)
Weight: 250 kg
Pipette Channel: 6 Channel
Pipette volume range: 5 -1000 ul
5-Channels for qPCR: FAM、HEX、Texas Red、CY5、CY5.5
Extraction Process time: 1-48 samples in an hour
qPCR process time (40cycle): 1- 1.5 hour
Sample throughput: 1-48 samples per run on extraction, 1-144 tests per run on PCR
Sample input volume: 0.3-3 ml
Elution volume: 50-200 ul
TFDA EUA Approval
Product category: DNA testing, Molecular biomarkers
LabTurbo 48 Compact System
Function: Sampling from Primary sample tube, Sample lysis, DNA/RNA Extraction, Simple PCR Setup(Optional), Self testing, liquid level detection, Auto-Worktable Clean And Recovery
DIM: 66 x 64 x 160 cm (26 x 26 x 63 in)
Weight: 200 kg
Pipette Channel: 6 Channel.
Pipette volume range: 5 -1000 ul
Process time: 90 mins
Sample throughput: 1-48 samples per run
Sample input volume: 0.3-3 ml
Elution volume: 50-200 ul
Product category: DNA testing, Molecular biomarkers
LabTurbo 24 Compact System
Function: Sampling from Primary sample tube, Sample lysis, DNA/RNA Extraction, Simple PCR Setup(Optional), Self testing, liquid level detection, Auto-Worktable Clean And Recovery
DIM: 66 x 53 x 82 cm (26 x 21 x 33 in)
Weight 80 kg
Pipette Channel: 6 Channel.
Pipette volume range: 5 -1000 ul
Process time: 70 mins
Sample throughput: 1-24 samples per run
Sample input volume: 0.3-3 ml
Elution volume: 50-200 ul
LabTurboTM AIO COVID-19 RNA Testing Kit(480)
LabTurboTM AIO COVID-19 RNA Testing Kit includes two products, Acov11240 and Acov13000. They contain oligonucleotide primers, dual-labeled hydrolysis probes, and control material used in RT-qPCR for the in vitro qualitative detection of SARS-CoV-2 (COVID-19) RNA in respiratory specimens. They are designed for assay and validation:
• Table 1. Detection Target in LabTurboTM AIO COVID-19 RNA Testing Kit Assay
Cat. No.: Acov11240
N gene(FAM)
E gene(HEX)
Endogenous IC(Cy5)
Cat. No.:Acov13000
RdRP(FAM)
Patient swab cell
COVID-19 Dye
The product, Kit No. Acov11240, is a multiplex RT-qPCR assay for N gene, E gene, and endogenous IC in the specimens. N gene is specifically used to validate SARS-CoV-2 (COVID-19) in specimens; the E gene is used to validate universal SARS-CoV RNA. RNase P (RP) is used as an endogenous Internal Control (IC) to validate successful specimen collection from individual patients. The Acov13000 kit is a singleplex RT-qPCR assay for the RdRP gene as a confirmatory validation for the presence of SARS-CoV-2 from specimens with negative N gene detection and positive E gene detection. Furthermore, thePositive Extraction Control (PEC) can validate the workflow and performance of the assay. The RNase-free water is used as the negative extraction control (NEC) to validate the reagent stability and monitor cross-contamination. Both PEC and NEC have to be validated in every batch of the assay. The positive control (PC) is used to validate the RT-qPCR performance if the PEC fails due to extraction; the negative control (NC) is used to confirm cross-contamination if the NEC fails due to extraction.
The assays could be completed using the fully automated instrument LabTurbo AIO SP-qPCR System (LabTurboTM AIO), or using the semi-automation LabTurbo 48 compact system (CE IVD), as an extractor, and with a RT-qPCR machine, such as the QuantStudioTM 5 Real-Time PCR Systems, manufactured by ThermoFisher. All systems can use the LabTurboTM Viral DNA/RNA Mini kit (LVX480-500) for nucleic acid extraction and the LabTurboTM AIO COVID-19 RNA Testing Kit (Acov11240 and Acov13000) for RT-qPCR assay.
• Table 1. Detection Target in LabTurboTM AIO COVID-19 RNA Testing Kit Assay
Cat. No.: Acov11240
N gene(FAM)
E gene(HEX)
Endogenous IC(Cy5)
Cat. No.:Acov13000
RdRP(FAM)
Patient swab cell
COVID-19 Dye
The product, Kit No. Acov11240, is a multiplex RT-qPCR assay for N gene, E gene, and endogenous IC in the specimens. N gene is specifically used to validate SARS-CoV-2 (COVID-19) in specimens; the E gene is used to validate universal SARS-CoV RNA. RNase P (RP) is used as an endogenous Internal Control (IC) to validate successful specimen collection from individual patients. The Acov13000 kit is a singleplex RT-qPCR assay for the RdRP gene as a confirmatory validation for the presence of SARS-CoV-2 from specimens with negative N gene detection and positive E gene detection. Furthermore, thePositive Extraction Control (PEC) can validate the workflow and performance of the assay. The RNase-free water is used as the negative extraction control (NEC) to validate the reagent stability and monitor cross-contamination. Both PEC and NEC have to be validated in every batch of the assay. The positive control (PC) is used to validate the RT-qPCR performance if the PEC fails due to extraction; the negative control (NC) is used to confirm cross-contamination if the NEC fails due to extraction.
The assays could be completed using the fully automated instrument LabTurbo AIO SP-qPCR System (LabTurboTM AIO), or using the semi-automation LabTurbo 48 compact system (CE IVD), as an extractor, and with a RT-qPCR machine, such as the QuantStudioTM 5 Real-Time PCR Systems, manufactured by ThermoFisher. All systems can use the LabTurboTM Viral DNA/RNA Mini kit (LVX480-500) for nucleic acid extraction and the LabTurboTM AIO COVID-19 RNA Testing Kit (Acov11240 and Acov13000) for RT-qPCR assay.
LabTurbo Extraction kit
LabTurbo Extraction kit can be applied to various application,
- Ready to use. Minimal preparation is needed
- Use the exact amount of reagents and consumables. No waste of kit.
- Reagents can be stored on the system for 3 months for ease of use
- Kit can be stored in room temperature for 1 year
Kit contains LabTurbo sample tubes, elution tubes, column sets,
reagents, and proteinase K. Filtered tips can be purchased separately.
Ethanol is to be provided by users.
Product category: DNA testing, Molecular biomarkers
LabTurbo Reaction (PCR) Setup System
Liquid-handling System
Fast & Precise PCR setup for 96 and 384-well plate
Size (cm): 66 x 53 x 70
Weight (kg): 60 (Bench-top)
Transfer volume: 2-50 ul
Master mix wells: up to 20
Sample wells: 1-96 wells
Pipette channels: 6(Sliding span 9-18 mm)
Cooling temperature: 10 ± 2 °C(at room temperature)
PCR plate format: 96 and 384 well plate
Throughput: 96 well transfer in 15 minutes / 384 well transfer in 35 minutes
About us
Company portrait
「LabTurbo」 was originally an automated nucleic acid department established by “Taigen Bioscience Co., Ltd." in 2000. For the past 20 years, it has focused on the development of nucleic acid application automation technology, product manufacturing and sales. It has successively developed more than 10 invention patents across Taiwan, the United States, China, Japan, South Korea, Germany and other countries, and began to deploy the global nucleic acid application market.
Based on the vigorous development of the global genetic testing market, 「 LabTurbo Biotech Co., Ltd.」was formally established in June 2019, and invested funds in the development of nucleic acid fully automated, full-process genetic testing systems, and strengthened the "AIO SP-qPCR" System Application Deepening" and "Global Market Layout".
LabTurbo products use the exclusive patented「flow membrane tube vacuum method」automatic nucleic acid extraction system, which has been adopted by the American Red Cross with ultra-high sensitivity. For four years, nearly 90,000 bags of blood transfusion of Lyme disease infected DNA Screening; the research results were published in the authoritative medical journal「The New England Journal of Medicine (NEJM)」and obtained the U.S. FDA medical materials certification. This result confirms that the company's branch automation products have reached international standards.
LabTurbo’s domestic customers cover nearly 40 institutions including hospitals at all levels, private inspection centers, universities, the Central Research Institute, the Food and Drug Administration of the Ministry of Health and Welfare, the Forensic Office of the Police Department, the Department of Disease Control, and the Animal Health Laboratory; The foreign customers are mainly the United States, and there are also product users in Israel, Singapore, and France. It is expected to continue to cultivate the global automated nucleic acid application market and expand the scope of automated genetic testing applications.
Based on the vigorous development of the global genetic testing market, 「 LabTurbo Biotech Co., Ltd.」was formally established in June 2019, and invested funds in the development of nucleic acid fully automated, full-process genetic testing systems, and strengthened the "AIO SP-qPCR" System Application Deepening" and "Global Market Layout".
LabTurbo products use the exclusive patented「flow membrane tube vacuum method」automatic nucleic acid extraction system, which has been adopted by the American Red Cross with ultra-high sensitivity. For four years, nearly 90,000 bags of blood transfusion of Lyme disease infected DNA Screening; the research results were published in the authoritative medical journal「The New England Journal of Medicine (NEJM)」and obtained the U.S. FDA medical materials certification. This result confirms that the company's branch automation products have reached international standards.
LabTurbo’s domestic customers cover nearly 40 institutions including hospitals at all levels, private inspection centers, universities, the Central Research Institute, the Food and Drug Administration of the Ministry of Health and Welfare, the Forensic Office of the Police Department, the Department of Disease Control, and the Animal Health Laboratory; The foreign customers are mainly the United States, and there are also product users in Israel, Singapore, and France. It is expected to continue to cultivate the global automated nucleic acid application market and expand the scope of automated genetic testing applications.
Company data
Export content
max. 75%
Number of employees
50-99
Area of business
- Laboratory equipment
- Diagnostics
