Ezplex Respiratory Pathogens Real-time PCR Kit is an in vitro diagnostic test for the qualitative detection of 19 respiratory viruses and 6 types of pneumonia-causing bacteria through nucleic acids isolated and extracted from human throat swabs using real-time polymerase chain reaction
Comprehensive Panel- One test can identify 19 respiratory viruses and 6 bacterial species simultaneously.
Sensitivity Detection of all targeted viruses and bacteria with high sensitivity.
Convenience Genetree Viewer analysis software available for users to conveniently produce test results.
Clinical Performance: Clinical testing confirmed the high sensitivity and specificity.
Stability: Shelf life of up to 12 months.
Analytical Specificity: Testing of 31 species of microorganisms showed no cross reactivity.
Ezple Respiratory Pathogens Real-time PCR Kit is an in vitro diagnostic test for the qualitative detection of 19 respiratory viruses and 6 types of pneumonia-causing bacteria through nucleic acids isolated and extracted from human throat swabs using real-time polymerase chain reaction.
This kit is intended for qualiativein vitro detection of Orf1ab and N genes of Novel Coronavirus 2019-nCoV which are found in throat swab,sputum and alveolar lavage fuid samples of suspected cases of pneumonia,suspected cases of clustering and other patients who need to carry out diagnosis or differential diagnosis of Novel Coronavirus 2019-nCoV infection.
* Detection of Sars-Cov-2 with reverse transcption Real time PCR ( TAT 2.0 hr )
* Amplify N gene and RdRp(orf1ab) gene of Sars-Cov2
AVAILABLE SAMPLE TYPE
* Sputum
* Oropharyngeal ( OP ) and nasopharyngeal ( NP ) swabs
SFTS Virus Real-time PCR Kit is an in vitro diagnostic test intended for the qualitative detection of the Dabie bandavirus that causes Severe Fever with thrombocytopenia Syndrome using nucleic acid RNA extracted from human blood or serum. Clinical evaluation performed with human blood specimens confirmed clinical accuracy. High reproducibility with similar results were confirmed various tests.
- In vitro diagnostics(IVD) Kits
- Designed for the qualitative detection of COVID-19 viral RNA
- Oropharyngeal swab, nasopharyngeal swab, sputum and bronchoalveolar lavage (BAL)
- Store at -25~ -15
Product description:
Detects the novel coronavirus.
COVID-19 using one-step real-time RT-PCR in a single tube.
The target genes for the detection of the virus are Orf1ab and N gene.
The sequence of primers and probes for the amplification were adapted from sources published by China CDC and WHO.
The kit includes primers and probe for the amplification of the human RNase P gene that serves as an internal positive control for the real-time RT-PCR.
Compatible real-time PCR machines: CFX96(Bio-Rad), ABI 7500/7500Fast(Thermo Fisher Scientific), SLAN-96S(Hongshi), Rotor-Gene Q(QIAGEN)
Ezplex�® SARS-CoV-2 G Kit, developed by SML Genetree, is a product that has received Emergency Use Authorization (EUA) from the U.S. Food and Drug Administration (FDA). This is an in vitro diagnostic test that qualitatively detects the nucleic acids of SARS-CoV-2 (RdRp and N genes) in sputum to aid in emergency screening for COVID-19. This product can be used for a large amount of screening tests because it can perform a pooling test, unlike the products that the existing domestic companies have approved for emergency use by the FDA. For the combined test, samples are collected in units of 5 people and tested. If positive, individual tests are performed. In the case of a negative test, all tests are performed in a negative way. In particular, since a large number of samples are tested at once, the test is only possible with high sensitivity and specificity compared to existing diagnostic kits. According to the FDA, it was confirmed that 100% agreement was achieved in the result comparison test of individual and collective tests, and it was the 20th in the world and the first Korean company to pass the test. Excellent clinical performance was demonstrated by confirming high sensitivity and specificity through clinical evaluation, and stability was confirmed for 12 months through long-term storage tests. In January 2021, it was officially approved by the Korean Ministry of Food and Drug Safety (MFDS).
Ezplex MTBC/NTM Real-time PCR Kit is an in vitro diagnostic test that simultaneously detects Mycobacterium tuberculosis complex (MTBC) and 20 types of nontuberculous mycobacteria (NTM).
Sensitivity : Multiple gene targets for MTBC and NTM.
Clinical Performance: Validated clinical performance.
Fast Results: Testing can be completed within 2 hours post extraction.
Ceylon cinnamon has been hailed as the "true cinnamon" or the "real cinnamon" that possesses outstanding health benefits especially for the diabetics and those challenged by obesity and high cholesterol issues. Unfortunately this cinnamon which is native to Sri Lanka and sourced from the plant Cinnamomum Zeylanicum
A highly valued culinary and medicinal spice. Price can be up to 10 times more than the Cassia/Chinese cinnamon.
Contains a small, negligible amount of coumarin, a naturally occurring blood-thinning substance. Recommended for regular use, e.g. for correcting blood sugar level.
Thin and paper-like textured bark that forms multiple layers when rolled up.
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Economical
Practical
Stable and accurate heating and temperature control system
Excellent optical system
Powerful comprehensive performance
Capacity
96x 0.2ml tubes (low profile and standard)
slides tube,
1x 96-well microplate
Dynamic range 1~1010 Copies
Applied probe
1st channel: FAM/ SYBR-Green
2nd channel: HEX, JOE, VIC, TET
3rd channel: ROX Texas -Red
4th channel: CY5
Test method four-fold fluorescence detection
Thermal cycle temperature control semiconductor thermoelectric module
Temperature Range 4.0�°C - 99.0�°C
Heating and cooling Rate â?¥1.5�°C/sec
Thermal Accuracy â?¤0.5�°C (at 90�°C)
Thermal Uniformity â?¤0.5�°C (at 90�°C)
Hot cover temperature range 50�°C - 108�°C
Optical detection excitation wavelength 300-800nm
Detection wavelength 500-800nm
Fluorescence repeatability CVâ?¤ 3%
Fluorescent linearity râ?¥0.99 coefficient of correlation
Software application genotyping by qualitative, absolute quantitative, standard solution curve, relative quantitative and endpoint method
Scanning method full plate, specified rank scanning
Data export format Excel, CVS
Custom report form support
The operating system Window 7/8/8.1/10
Minimum computer configuration Intel or AMD Dual-2.8GHz, more than 4G memory and 128GB
Power Supply AC 220V~, 50Hz, <800VA
Communication Ports RS232, USB
Size 490mmX355mmX284mm
Weight 20Kg
African swine fever virus (ASFV) real-time PCR test kit enables the safe detection
of African swine fever virus DNA in serum, blood, tissue, lymph nodes, spleen,
muscle from pigs and breeding environment samples within 40 minutes. The kit
consists of fluorescence PCR mix , positive control , negative control and lysis
solution for real-time PCR amplification of ASFV. Fluorescence PCR mix contains
primers, probes, enzyme and buffer for detection of the ASFV P72 gene. In addition,
the role of lysis solution is to simply process samples and release DNA.
COVID-19 Real Time RT-PCR Kit detects the novel corona virus, COVID-19 using one-step real-time RT-PCR in a single tube.
The target genes for the detection of the virus are Orf1 ab and N gene.
The kit includes primers and probe set targeting the human Rnase P gene that serves as an internal positive control for the real-time RT-PCR.
Ordering Info : 96 Tests/Kit (MOQ : 10 Kits)
Product Details:
Brand : TRIVITRON
Signal Signifies : Orthopox group, Monkeypox & Smallpox Virus
Test time : 1 hour
Compatible : Please visit Brochure
Storage : : - 20 between 2 C
Cat No : DVZ-30052 & DVZ-30053
Trivitron's Monkeypox Real-Time PCR kit is a multiplex RT-PCR Kit for the rapid qualitative in vitro detection of Monkeypox and Smallpox virus. The assay Kit can distinguish between smallpox and Monkeypox virus.
FEATURES
The kit is based upon Single Step RT-PCR, where both Reverse Transcription by Reverse Transcriptase and PCR by Taq Polymerase takes place in single tube.
Monkey Pox virus kit is developed using four colour fluorescence technology.
A signal from different channel signifies, presence of Orthopox group, Monkeypox & Smallpox virus respectively in the sample.
Assay validation through the additional human internal control gene.
Compatible with both dry swabs as well as sample swabs placed in VTM.
A total turnaround time of 1 hour
TECHNICAL SPECIFICATIONS
The kit has been validated on QuantStudio-5/3 and Bio-Rad CFX96, 384 and can also be used on applied Biosystems 7300/7500, Roche Diagnostics LightCycler 96/480, Qiagen Rotor-Gene Q, etc. (Instrument should be calibrated, maintained and used as per manufacturer recommendation).
Sample type: Swab samples collected from surface and/or exudate, roofs from more than one lesion, or lesion crusts.
Storage: -20 + 2 C
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