2X Real-Time PCR Master Mix including SYBR Green in Mixture 2X HRM Master mix
DESCRIPTION * 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
This product qualitatively confirms the presence or absence of a new coronavirus (2019-nCoV, COVID-19) using reverse-transcription Real Time Polymerase Chain Reaction in sputum, oropharyngeal and nasopharyngeal specimens. It is an in vitro diagnostic medical device.
Monkeypox Virus Real-time PCR Kit. PM for details.
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.
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.
Unit Price: USD 15 Target Region: RdRP, E gene, N gene Accuracy: 100% Recommended PCR: CFX96 Real Time PCR System (Bio Rad) DTprime DT-96 QIAGEN Rotor-Gene Q Box Size: Size: W 80 x D 80 x H 65 (mm) Weight: 45g / box Certification: Korea GMP (ISO 13485 2003) European CE
Test Covid19 with CE
Biocore 2019-nCoV Real Time PCR Kit - Brand: BIOCORE - Detailed information: 1.Type: RT-PCR 2. Reading Test Result: 1 hours 3. Accuracy: 95% 4. Storage: 2-30 â?? 5. Device reading: ***CFX96 ***SLAN-96P ***Applied Biosystems 7500 RT-PCR 6. MOQ: 10.000T (200Kit) 7. Packing: 100T / Kit 8. License: CE / GMP - Price: $13.00 / 1T - Payment: L/C or T/T
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.
Helicobacter pylori is a parasitic bacterium in the stomach that lives between the gastric mucosa and mucus. According to the WHO, more than half of the world's population has H. pylori and is the third leading cause of cancer-related deaths. In 1994, the WHO's IARC classified H. Pylori as a Class 1 carcinogen. The incidence of H. pylori in developing countries is the highest worldwide, highlighting the need for highly accurate and manageable testing. By 2025, the H. pylori testing market is expected to be worth 6 billion. Accordingly, SML Genetree has developed a reagent that can diagnose Helico-bacter pylori and Clarithromycin-resistant mutants (A2142G, A2143G) through DNA extracted from human hygienic tissue using Real-time Polymerase Chain Reaction. Since it contains multiple gene regions, Helico-bacter pylori and Clarithromycin-resistant mutations can be detected sensitively, and high reproducibility has been demonstrated through repeated tests by serially diluting various positive samples and standards. In addition, as a result of clinical evaluation on human sanitary inspection tissue by commissioning a large domestic consignment inspection institution, high sensitivity and specificity were confirmed, proving its excellent clinical performance.
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
Lowest detection line:200 copy/ml CE marks
25 tests per box
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.
Test Covid19 with CE
- 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).
