STANDARD M nCoV Real-Time Detection kit is used for identification and detection of novel coronavirus (2019-nCoV) ORF1ab (RdRp) gene and E gene in human nasopharyngeal swab, oropharyngeal swab, and sputum specimens using reverse transcription (RT) real-time PCR. This kit is helpful for the auxiliary diagnosis of 2019 novel coronavirus disease (COVID-19). The test results are for clinical reference only and cannot be used as a basis for confirming or excluding cases alone.
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SolGent DiaPlexQâ?¢ Novel Coronavirus (2019-nCoV) Detection Kit CE-IVD Real-Time OneStep RT-PCR based assay system for detection of 2019-nCoV CE-IVD DiaPlexQâ?¢ Novel Coronavirus(2019-nCoV) Detection Kit is CE-IVD reagent. It is screening kit to detect Novel Corona Virus as 2019-nCoV from isolated total RNA. Basic principal of this kit is Real-time PCR method, which is able to detect specific target gene into total RNA. One step RT-PCR contents are progressively apply for one tube RT(Reverse Transcription) reaction and PCR amplification. You can monitoring the nucleic acid amplification result based on real time condition through the amplification plot. The Control Template (2019-nCoV) is provide as positive control to assist the clinical sample data comparison analysis. - Detection target : 2019-nCoV ( COVID-19 ) - Target region : Orf1a, N gene - Detection technology : Real-Time OneStep RT-qPCR - Specimen type : Nasopharyngeal swab, Oropharyngeal swab, Sputum - Compatible instruments : CFX96â?¢ Real-Time PCR System (Bio-Rad), ABI 7500 / 7500 Fast Real-Time PCR System (Applied Biosystems) - PCR running time : ~ 120 mins - Simple & Rapid detection system: OneStep Multiplex RT-qPCR based detection - HotStart PCR: high-specificity - Reliable system: automatic PCR control (not Internal control) - Easy-to-use master mix: just adding template and Primer/Probe Mix - Positive control included (Plasmid)
STANDARD M nCoV Real-Time Detection kit is used for rapid identification and detection of novel coronavirus (2019-nCoV) nucleic acids in human nasopharyngeal swabs and throat swab samples. - One tube reaction for identification and detection of 2019-nCoV - One-step Real-Time RT-PCR - Provide all reagents required for PCR - Designed according to WHO interim guidance for laboratory testing for 2019 novel coronavirus (2019-nCoV) in humans" - nCoV primers/probes ORF1ab (RdRp) gene, E gene - Provide Internal controls - Test time : 90mins - Specimen : Nasopharyngeal swab, Oropharyngeal swab, Sputum - Applicable machine : CFX96. ABI7500 - CE, FDA EUA
iONEBIO Novel-CoV19 Real-time RT-LAMP-PCR Detection Kit Our In-vitro Diagnostic product enables precise and efficient detection of the Coronavirus disease (2019-nCoV), utilizing Real-time RT LAMP PCR Real-time Reverse-Transcription Loop-mediated isothermal Amplification PCR method on nasopharyngeal swab specimen of a suspected patient. - Detection target : 2019-nCoV ( COVID-19 ) - Target region : N gene - Detection technology : Real-Time RT -LAMP PCR (with OneStep) - Specimen type : Nasopharyngeal swab, Oropharyngeal swab, etc - PCR running time : 20 mins - Compatible PCR Device : CFX96TM Real-Time PCR System (Bio-Rad) Key Characteristics Rapid Detection System : Implementation of isothermal reaction method enables for 20-min test time SYBR green Application : Fluorometric Detection enables for High Specificity One step qRT-PCR system : en-bloc analysis without separate reverse-transcription process User-Friendly Diagnostic System: Analysis possible only with the RNA specimen Inclusion of Positive Control (Plasmid form) iONEBIOs RT-LAMP PCR Kit is groundbreaking rapid and accurate; thus is the most competitive diagnostic kit for COVID-19 available in the global market.
Contains : 1 test cassete, 1 Lysis Buffer, 1 Sterile Swab, 1 Bio-safety bag, 1 instruction of use
The HY-T COVID-19 Antigen Self-Test (Nasal Swab) is lateral flow assay designed for the qualitative detection of specific SARS-CoV-2 antigen in human anterior nasal swab specimen. It is intended to be used for the detection of SARS-CoV-2 virus infection. The results obtained should not be the sole determinant for clinical decision. The HY-T COVID-19 Antigen Self-Test (Nasal Swab) is intended for use for home self-testing. Platform: Immunochromatographic Assay Format: Cassette Detection Specific: SARS-CoV-2 antigen Specimen: Nasal swab Sensitivity: * 97.17% Specificity: * 100% Assay Time: 15-20 minutes Shelf Life: 18 months * Vs FDA Emergency Use Authorized real-time RT-PCR Suitable for: Individuals who wish to know their status on COVID-19 infection (symptomatic and asymptomatic regardless of their vaccination status)Individuals who have had close contact with COVID-19 positive patientsIndividuals with suspected exposure to coronavirusIndividuals who show symptoms related to COVID-19 (fever, dry cough, tiredness, sore throat,headache etc)Employees to perform regular testing to avoid workplace transmission Other appropriate and necessary screenings (such as International Entrance, cross-state, pre-employment screening, pre-admission to higher learning institutions etc.
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Avani was formed for the purpose of applying the proprietary oxygen enrichment technology to produce an exceptional smooth-tasting drinking water, which excels in purity and oxygen content. Avani with its exclusive purification process, is the only bottled water company known to produce water which so closely resembles the natural convectional rain water cycle. Avani then adds high levels of oxygen once found in natural water centuries ago. Avani adds higher oxygen content during the unique processing stage. The introduction of a premium-bottled water such as avani gives the consumer a thirst-quenching smooth, pure drink, which invigorates and combats potential illnesses. There is probably no other commercially produced drinking water which is as smooth, pure, safe and biologically beneficial as avani water. 335ml x 24 bottles per carton
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Format: Cassette Storage: 4-30�ºC Certificates: ISO13485 Specimen: Whole Bood,Serum / Plasma Read time: 10-15 Minutes Weight: 101g Sample rule Option 1: Offering existing samples Option 2: Customized samples based on customers' specifications Sample lead time 3-10days (depends on the style) Result: 15 Minutes Shipping mode 1.Sea shipment 2.Air shipment 3.Door to door parcel Intend to use 1.The New Coronavirus (Sars-CoV-2)Test is a rapid chromatographic immunoassay for the qualitative detection of Antibody(IgG) to coronavirus in human whole blood, serum or plasma specimens. 2.Common signs of coronavirus infection include respiratory symptoms, fever, cough, wheezing and dyspnea. In more severe cases, the infection can lead to pneumonia, severe acute respiratory syndrome, kidney failure and even death. Corona viruses can be excreted through respiratory secretions, transmitted through oral fluids, sneezing, contact, and through the air droplets spread. Positive:1. Two or three distinct lines appear. One line should always appear in the control line region (C), and another one or two apparent colored line(s) should appear in the test line region(s) (T1 and T2). 2. If a line appears on the quality control line, a line appears on the test line T1, and no sline appears on the test line T2, it indicates that IgG antibody is present in the sample and no IgM antibody is present. 3. If a line appears on the quality control line, a line appears on the test line T2, and no sline appears on the test line T1, it indicates that IgM antibody is present in the sample and no IgG antibody is present. Negative: One colored line appears in the control region (C). No Apparent colored lines appear in the test lines regions (T1 and T2). Invalid: Control line(C) fails to appear. Insufficient specimen volume or incorrect procedural technologies are the most likely reasons for control line failure. Review the procedure and repeat the test with a new test device. If the problem persists, discontinue using the test kit immediately and contact your local distributor. Note: The red line in the test line (T) can show different shades of color. However, even a very weak line should be judged as a positive result during the specified observation period, regardless of the color of the line.
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