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Find Verified Standard M N Cov Sd Biosensor Rt Detection Kit Suppliers, Manufacturers and Wholesalers

Jun-25-22
 
Cat No : 11NCo10. SD biosensor STANDARD M nCoV Real-Time Detection kit is used for identification and detectionof novel coronavirus (2019-nCoV) ORF1ab (RdRp) gene and E gene in humannasopharyngeal swab, oropharyngeal swab, and sputum specimens using reversetranscription (RT) real-time PCR. This kit is helpful for the auxiliary diagnosis of 2019novel coronavirus disease (COVID-19). The test results are for clinical referenceonly and cannot be used as a basis for confirming or excluding cases alone.
Jun-25-22
 
Cat. No : 601430050. Truenat COVID-19 Chip-based Real Time PCR Test is a semi quantitative detection of SARS CoV-2 RNA in human oropharyngeal and nasopharyngeal swab specimen and aids in detection and confirmation of SARS CoV-2 infection and diagnosis of COVID-19. The test detects the E and Orf1a genes of the virus.

Providing you the best range of Molbio Trueprep Auto Universal Cartridge Based Sample Prep Device, Molbio Trueprep AUTO Universal Cartridge Based Sample Prep Kit, Molbio Trueprep AUTO MTB Sample Pre Treatment Pack Kit, Molbio Trueprep AUTO Universal Sample Pre-treatment Pack and Molbio Trueprep AUTO Transport Medium for Swab Specimen Pack with effective & timely delivery.
Jun-25-22
 
The Acculaâ?¢ System from Thermo Fisher Scientific is a rapid diagnostic platform that combines the accuracy of RT-PCR with the simplicity, convenience, and procedural familiarity of traditional rapid immunoassays. The Acculaâ?¢ SARS-CoV-2 Test has received an Emergency Use Authorization (EUA) from the FDA for the detection of SARS-CoV-2 in Clinical Laboratory Improvement Amendments (CLIA) waived environments. Designed for use with the palm-sized Accula Dock, the Accula SARS-CoV-2 Test provides reliable, qualitative results in approximately 30 minutes
Jun-25-22
 
Pathodetect 2019- nCov Detectioin kit offer an in virto diagnostic real time PCR assay for qualitative detection of 2019 - Novel Coronavirus RNA in respiratory specimens and sera. The kit offer the universal detection of SARS- Like coronavirus and specific detection of 2019-nCOv.

Mylab Discovery solutions 2019-nCoV Detection Kit provides ready to use solution for detection of coronavirus using real time PCR technology. Detection is based on the amplification of a specific conserved RNA sequences of coronavirus and detection by Taqman probe-based chemistry. An Internal control is detected along with the coronavirus target controlling the extraction efficacy and possible PCR inhibition. The test is designed to use across wide range of PCR platforms. The recommended CDC protocol for coronavirus detection ensures that the kit leads to highly-specific and ultrasensitive results in short time.

KIT CONTENTS

Reagents for Nucleic acid extraction from respiratory/sera specimens
Reagents for Real time PCR
Inclusion of synthetic positive and negative controls
Jun-25-22
 
Cat No : RP10243X. Detection of COVID-19 specific target genes in a single tube- Reliable result with three target genes- Results within 1 hour and 50 minutes after extraction- Convenient work now on the automated MDx platform- Suitable for high-throughput- Providing whole process control for assay validity- Automated data interpretation with Seegene Viewer.
1284 Standard M N Cov Sd Biosensor Rt Detection Kit Suppliers
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Oct-11-22
 
Product Details:
Brand : Applied Biosystems
Model Name/Number : QuantStudio 7 Flex
Sample Capacity/Format 48 wells
Volume Thermal Block Sample : 0.2 mL
No of Channel : 4
Features:
Increased application versatility through the accomodation of 4 different block types
Compatible with over 8 million TaqMan�® assays for gene expression, genetic variation, gene regulation, or protein expression experiments
The intelligent design of the QuantStudioâ?¢ platform combined with Applied Biosystem instrument reliability and accuracy
Easy-to-use software, responsive touch-screen, automation capabilities, and effortless block exchange without the need for any tools
Oct-11-22
 
CFX Opus 96 Real-Time PCR Instrument 0.2 mL, 96 Wells

Product Details:
Brand BioRad
Model Name/Number CFX Opus 96
Sample Capacity/Format 96 wells
Multiplex analysis Up to 5 targets per well
Dimensions (W x D x H), cm/in 33x56x36 / 13x22x14
Cat No 12011319
Description
CFX Opus is the newest real-time PCR system in our robust CFX Family. The CFX Opus 96 Real-Time PCR System can analyze 96 wells and offers a number of new features:

More uniform thermal performance
Expanded connectivity Wi-Fi, ethernet, and USB
Cloud connectivity: Operate CFX Opus on our BR.io cloud platform or with desktop CFX Maestro Software
Network storage drive access for excellent data management
Shuttle optical system yields consistent optical measurements across your sample plate
SpecificationsThermal CyclerMaximum ramp rate, C/sec5Average ramp rate, C/sec3.3Heating and cooling methodPeltierLid, C30 110 Temperature Range, C4 100Accuracy, C ±0.2 of programmed target at 90 C Uniformity, C ±0.3 well-to-well after 10 sec of arrival at targetGradientOperational range, C30 100Programmable span, C1 24Optical DetectionExcitation6 filtered LEDs Detection6 filtered photodiodes Range of excitation wavelengths, nm450 684 Range of emission wavelengths, nm510 730Sensitivity
Detects 1 copy of target sequence in human genomic DNADynamic range10 orders of magnitudeScan TimeAll channels, sec12
FAM/SYBR Green only, sec3SoftwareOperating systemWindows 10Multiplex analysisUp to 5 targets per wellSystemSample capacity, wells96
Sample size, µl150 (10 50 recommended)
Communication interface USB 2.0
Electrical approvalsIEC, CE Dimensions (W x D x H), cm/in33x56x36 / 13x22x14Weight, kg/lb22/48
Oct-12-22
 
ThermoFisher Scientific Accula System Rapid & Reliable RT-PCR Test for Corona in 30mins

Product Details:
Number of Reactions(Preps)/Kit : 25
Brand : Thermo
Test Method : (SARS-CoV-2) RT-PCR
Sample Type : Nasal Swab
Test Time 30 min
The Accula System from Thermo Fisher Scientific is a rapid diagnostic platform that combines the accuracy of RT-PCR with the simplicity, convenience, and procedural familiarity of traditional rapid immunoassays. The Acculaâ?¢ SARS-CoV-2 Test has received an Emergency Use Authorization (EUA) from the FDA for the detection of SARS-CoV-2 in Clinical Laboratory Improvement Amendments (CLIA) waived environments. Designed for use with the palm-sized Accula Dock, the Accula SARS-CoV-2 Test provides reliable, qualitative results in approximately 30 minutes
Oct-12-22
 
Hi-PCR Coronavirus (COVID-19) Multiplex Probe PCR Kit

Product Details:
Number of Reactions(Preps)/Kit : 100 Rxns Per Box
Brand : HIMEDIA
Storage Temperature : -10 to -20 C
Detection : Probe Based
Target : E, N and RdRp gene.
Cat No : MBPCR243
Description
A ready to use Rt-PCR Kit for Detection of Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) causing coronavirus disease 2019 (COVID-19). SARS-CoV-2 is a coronavirus, subgenus Sarbecovirus, 150-200nm in diameter with a genome size of about 30
Used For
A ready to use Rt-PCR Kit for Detection of Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) causing coronavirus disease 2019 (COVID-19).
Oct-12-22
 
Product Details:
Number of Reactions(Preps) per Kit : 100
Brand : Seegene
ICMR(Govt) Approved : Yes
Test Method : (SARS-CoV-2) RT-PCR
Test Time : 2 Hours
Cat. No : RP10243X
-Detection of COVID-19 specific target genes in a single tube- Reliable result with three target genes- Results within 1 hour and 50 minutes after extraction- Convenient workow on the automated MDx platform- Suitable for high-throughput- Providing whole process control for assay validity- Automated data interpretation with Seegene Viewer

Additional Information:
Delivery Time: Immediate
Aug-28-21
Supplier From Chennai, Tamilnadu, India
Jun-25-22
 
Cat No : RK081-25. Ulta Covid-19 Ag test is a rapid Immunochromatographic assey for the qualitative detection of specific antigens to SAR-COV-2 present in human nasopharynx.
Jun-25-22
 
CAT No : RK055-25. STANDARD Q COVID-19 Ag is a rapid Immunochromatographic assay for the qualitative detection of specific antigens to SARS-CoV-2 present in human nasopharynx.

Qualitatively detects specific antigens to SARS-CoV-2 present in Human Nasopharynx.
The test should be used as an aid in early diagnosis of symptomatic cases in healthcare setting having ILI.
Validated by ICMR & AIIMS
Sensitivity of 84.38 % & Specificity of 100%
Sample Type- Human Nasopharyngeal swab (No other sample recommended)
Results in 15-30 mins
Jun-25-22
 
ImmunoQuick Covid-19 IgM/IgG Test :

Covid-19 or commonly known as Coronavirus is a viral infection involving a patients upper respiratory tract. It is highly contagious and causes a severe lung infection which can be severely debilitating and sometimes fatal. Our test detects two types of antibodies to Covid-19 which appear from 2 to 21 days after infection. It is an invaluable test to diagnose people who have been sick for a few days or those who have recovered.



Salient Features of the Product

It is rapid immunoassay for qualitative detection of Covid-19 IgM and IgG antibodiesin

Human Serum or Plasma or Whole Blood.

Results available in 15 minutes.

Sensitivity :: >96%

Specificity :: >99%

No cross reactivity observed.

Can be stored at 4 to 30C

Stable for 24 months.

Pack size :: 25 tests.
Jun-25-22
 
CAT No : 41FK51. The Panbio COVID-19 Antigen Self-Test is a single-use, in vitro (outside the body) visually read rapid immunoassay that uses a human nasal swab specimen for the qualitative detection of nucleocapsid protein SARS-CoV-2 antigen.
The test can determine if you have an active COVID-19 infection and you will know your test results in just 15 minutes
Only Proven High-Accuracy Self-Test in India
In clinical evaluations with self-test users, the Panbio COVID-19 Antigen Self-Test correctly identified 100% of negative samples and 95.2% of Positive Samples
Pregnancy had no impact on the performance of the test.
Sep-27-22
 
Genbody Influenza/ Covid - 19 Ag Triple,

Rapid immuno-diagnosis of influenza A, B & SARS-CoV Single test for 3 parameters: antigen test of influenza A,B & SARS-CoV-2 Easy to use, Simple Procedure, Quick resulting and high Accuracy.

Production information:

1.Specimen: nasopharyngeal swab or Viral transport medium (VTM)

2.No Cross-reaction with 27 kinds of other respiratory viruses.

3.No interference with 23 kinds of interfering substances.

4.Limit of detection (LoD):1.89x10 HA units/mL for influenza A, 4.1 x 10 HA units/ mL for influenza B, 1.78x10 TCID/mL for SARS-CoV-2.

5.Detection of SARS-CoV-2 Varients: alpha,beta,gamma, delta, omicron & stealth omicron.
Jun-25-22
 
Cat No: RK056-20. STANDARD Q COVID-19 IgM/IgG Combois a rapid Immunochromatographic assay for the qualitative dtection of specific antibodies to SARS-CoV-2 present in human Serum,Plasma or Whole Blood specimen.

Rapid testing for detection of IgM & IgG antibodies against SARS CoV-2
10 µl of specimen: Serum, Plasma & Whole Blood
Long term storage of 24 months at 2 - 30 C
Complementary to RT-PCR Test
Can be performed without extra equipment
Jun-25-22
 
Cat No: 41FK10. Panbio COVID-19 Ag Rapid Test Device is an in vitro diagnostic rapidtest for the qualitative detection of SARS-CoV-2 antigen (Ag) in humannasopharyngeal swab specimens from individuals who meet COVID-19clinical and / or epidemiological criteria. Panbio COVID-19 Ag RapidTest Device is for professional use only and is intended to be used asan aid in the diagnosis of SARS-CoV-2 infection.
Jun-25-22
 
Cat. No : 5513C. COVID-19 serology test.Cellex qSARS-CoV-2 IgG/IgM Rapid Test.qSARS-CoV-2 IgG/IgM Rapid Test Cassette.FDA Grants Emergency Authorization for First Rapid Antibody Test for COVID-19
Jun-25-22
 
Cat. No : F-NCOV-01G. STANDARD F COVID-19 Ag FIA is the fl uorescent immunoassay for the qualitative detection of specific nucleoprotein antigens to SARS-CoV-2 present in human nasopharynx. STANDARD F COVID-19 Ag FIA should be used with the STANDARD F Analyzers manufactured by SD BIOSENSOR. This test is for in vitro professional diagnostic use and intended as an aid to early diagnosis of SARS-CoV-2 infection in patient with clinical symptoms with SARS-CoV-2 infection.
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