Number of Reactions(Preps)/Kit 96 Wells
Brand CTK BioTech
Sample serum or plasma
Storage 2 - 8 C
Cat No : AE0510
INTENDED USE:
The TRUSTwell HCV IgG ELISA Kit is a solid phase enzyme linked immunosorbent assay for the qualitative detection of IgG to Hepatitis C virus (HCV) in human serum or plasma. It is intended for professional use only as an aid in the diagnosis of infection with HCV. Any reactive specimen with the TRUSTwell HCV IgG ELISA Kit must be confirmed with alternative testing method(s) and clinical findings.
TEST PRINCIPLE:
The TRUSTwell HCV IgG ELISA Kit is a solid phase enzyme linked immunosorbent assay based on the principle of the indirect EIA technique for the detection of the IgG to HCV in human serum or plasma. The TRUSTwell HCV IgG ELISA Kit is composed of two key components: 1) Solid microwells pre-coated with recombinant HCV antigens; 2) Liquid conjugates composed of mouse anti-human IgG conjugated with horse radish peroxidase (HRP-anti Human IgG conjugates). During the assay, the test specimen is first incubated with the coated microwells. The IgG anti HCV, if present in the specimen, bind to the antigens coated on the microwell surface. In the second incubation with the HRP-anti-human IgG conjugates, the IgG antibodies absorbed on the surface of microwell react to the HRP-anti-human IgG conjugates. Unbounded conjugates are then removed by washing. The presence of the complexed conjugates is shown by a blue color upon additional incubation with TMB substrate. The reaction is stopped with Stop Solution and absorbances are read using a spectrophotometer at 450 /620-690 nm.
Clinical Performance:
A total of 1108 patient specimens from susceptible subjects were tested by the TRUSTwell HCV IgG ELISA Kit.
Product Details:
Number of Reactions(Preps)/Ki : 25T
Brand : SD Biosensor
ICMR Approved : Yes
Result Time (Rapid Kits): 10-15 mins
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
Product Details:
Brand ; Genbody
ICMR Approved : Yes
Result Time (Rapid Kits) : 15 min
Packaging Size : 25 Test Kits /Box
CAT No : COVAG025
GenBody COVID-19 Ag is an immunochromatographic assay kit for the qualitative detection of SARS-CoV-2 antigen in nasopharyngeal and oropharyngeal swab from human.
Product Details:
Number of Reactions(Preps)/Kit :96
Brand : Abbott
ICMR Approved ; Yes
Test Method : (SARS-CoV-2) RT-PCR
Cat. No : 09N77-095
The Abbott RealTime SARS-C0V-2 assay is an Emergency Use Authorization (EUA) test authorized by the U.S. FDA for use by authorized laboratories, using real-time (RT) polymerase chain reaction (PCR) technology for the qualitative detection of nucleic acids from the SARS-CoV-2 virus and diagnosis of SARS-CoV-2 virus infection from individuals meeting CDC clinical and/or epidemiological testing criteria
Product Details:
Number of Reactions(Preps)/Kit : 250 Rxns Per Box
Brand : HiMedia
Storage Temperature : 15 DegreeC to 25 DegreeC
Elution Volume : 50 to 80 microliter
Cat. No : MB615
Description
This kit carries out efficient extraction of viral RNA from wide range of viral strains like Dengue, Chikungunya and viral pathogen of animals. Sample is first lysed under the highly denaturing conditions provided by Buffer HRL to inactivate RNases and to
Used For
HiPur Viral RNA Miniprep Purification Kit can be used for isolation of viral RNA from a wide variety of viruses, but performance may vary depending on virus type
Product Details:
Number of Reactions(Preps)/Kit : 100 T
Brand : RADI
Storage Temperature : -25 C to -15 C
Sample Material : RNA extracted from Nasopharyngeal and/or Oropharyngeal swab
Target : S gene, RdRP gene
Cat. No : RV008
The RADI COVID-19 Detection Kit is intended for the presumptive qualitative detection of specific nucleic acid sequences from the genome of the SARS-CoV-2 S gene and RdRP gene from the upper respiratory specimens such as Nasopharyngeal swab, Oropharyngeal swab.
Product Details:
Brand : RADI
Storage Temperature : -25 to -15 C
Sample Material : Human Skin Lesion, Crust or swab
Cat. No : RV015
Detection : Probe Based
Target : FAM,HEX and Cy5 gene
RayBiotech Monkeypox Virus (MPXV) PCR Nucleic Acid Detection Kit is a real-time PCR assay for the detection of MPXV DNA in a liquid sample. It uses a fluorescent probe with specific primer sets to detect the J2R gene specific for the genome of MPXV.
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
Product Details:
Number of Reactions(Preps)/Kit : 1000
Brand ; Thermofisher
Test Method : (SARS-CoV-2) RT-PCR
Sample Type : Nasal & Oral Swab
The Applied Biosystems TaqPath COVID-19 Combo Kit is a fast, highly sensitive multiplex diagnostic solution that contains the assays and controls needed for the real-time PCR detection of RNA from the SARS-CoV-2 virus.
Features of the newly developed multiplex diagnostic kit:
A complete workflow from viral RNA extraction from up to 94 specimens and genetic analysis using real-time PCR to diagnostic report generation in under 4 hours
Targeted specificity to 100% of currently available complete genomes for SARS-CoV-2
Assay targets spike (S) protein and nucleocapsid (N) protein regions having higher specificity and exhibiting lower risk for mutation
COVID-19 Interpretive Software, which automatically converts genetic analysis data into diagnosis, helping reduce risk of user interpretation error
The TaqPath COVID-19 Combo Kit consists of both the TaqPath RT-PCR COVID-19 Kit and the TaqPath COVID-19 Control Kit for simplified ordering. The kit can be used by clinical and public health laboratories to quickly evaluate up to 94 patient specimens in under 3 hours. The kit is approved for use with RNA extracted from nasopharyngeal swabs, nasopharyngeal aspirate (nasal aspirate), and bronchoalveolar lavage (BAL) from patients at risk of exposure to the SARS-CoV-2 virus or with signs and symptoms of COVID-19 (see product label for Intended Use Statement and product information). The TaqPath COVID-19 Combo Kit is a single, high-throughput (1,000 reactions) kit and is recommended for use with either the Applied Biosystems 7500 Fast Dx Real-Time PCR System or the 7500 Fast Real-Time PCR System (RUO version) and the associated Applied Biosystems COVID-19 Interpretive Software.
The TaqPath COVID-19 Combo Kit includes the following components:
TaqPath RT-PCR COVID-19 Kit
COVID-19 real-time PCR assay multiplexâ??multiplexed assays that contain three primer/probe sets specific to different SARS-CoV-2 genomic regions and primers/probes for bacteriophage MS2
MS2 phage controlâ??internal process control for nucleic acid extraction
TaqPath COVID-19 Controlâ??RNA control that contains targets specific to the SARS-CoV-2 genomic regions targeted by the assays
TaqPath COVID-19 Control Dilution Buffer dilution buffer for the IVT RNA control as defined in the IFU (information for use)
Product Details:
Number of Reactions(Preps)/Kit : 24 Test
Brand : Abbott
Result Time (Rapid Kits : 13 Min
Cat. No : 190-000
TECHNOLOGY ID NOW utilizes proven isothermal molecular technology in an intuitive platform, providing the fastest molecular results in the market.
EASE OF USE Simplifying the test process Designed for near-patient testing in a variety of environments* Assay kit contains necessary components for testing, including: 24 tests Swabs for sample collection Positive control swab Room-temperature storage eliminates need for refrigeration
Product Details:
Brand : SD Biosensor
Result Time (Rapid Kits) : 15-30 min
Packaging Size : 25 Test Kits/Box
CAT No : Q-NCOV-01G
STANDARD Q COVID-19 Antigen Test kit is chromatographic immunoassay for the qualitative detection of SARS CoV 2 nucleocapsid antigen present in human nasal sample.
Product Details:
Brand : Abbott
Model Name/Number : ID Now
Communication Interface : Bluetooth, USB
Scan time : 13 minutes
Usage : Molecular COVID-19 Test
Cat. No : NAT-000
ID NOW COVID-19SARS-COV-2 IN 13 MINUTES OR LESS*
The ID NOW platform combines the benefits of speed and accuracy for the fastest molecular results in the market.
The ID NOW COVID-19 test returns positive results in 13 minutes or less to enable immediate clinical decisions during the first patient visit.
The easy to use ID NOW platform is designed for near-patient, point-of-care use in a variety of healthcare settings.
Abbott BinaxNOW S. pneumoniae Antigen Card provides accurate, rapid identification of S. pneumoniae antigen in patients with pneumococcal pneumonia and pneumococcal meningitis with an easy-to-use technology, aiding physicians in providing rapid, focused therapy.
Cat No. 7D2543. By detecting early markers of Hepatitis B infection, the Alere Determineâ?¢ HBsAg helps to diagnose acute infection and confirm chronic infection - allowing healthcare professionals to initiate prompt and appropriate follow-up action for infected patients.
Rapid in-vitro qualitative ICT for detection of HBsAg
Sample Type: Serum/Plasma/Whole Blood
Sample Volume: 50�µL
Early marker of infection- helps in diagnosis
Facilitates appropriate follow-up of infected patients
Collection can be done by fingerprick or venipuncture
Clear, dependable results in 15 minutes
Quick Reference Card for the detection of HBsAg in
Cat No : 05FK80I40. The SD BIOLINE Malaria Ag P.f/Pv test is a rapid, qualitative and differential test for the detection of histidine-rich protein II (HRP-II) antigen of Plasmodium falciparum and Plasmodium lactate dehydrogenase (pLDH) of Plasmodium vivax in human whole blood.
Specomen: Whole blood
Time to result: 15 -30 minutes
Storage: 1-40 degree C for 24 months
Performance: Sensitivity: Pf-99.7%, Pv-95.5%
Specificity: 99.5 %
Optimal screening test for Plasmodium falciparum and Plasmodium vivax.
CAT No : 7D2343. A rapid in vitro qualitative immunoassay for detection of antibodies to the Human Immunodeficiency Virus Type 1 (HIV-1) and Type 2 (HIV-2)
Clear, dependable results in 15 minutes
Requires minimal training and no equipment
So easy it can be used at the lowest levels of health care service
The SD BIOLINE Dengue Duo kit is a rapid, an in-vitro immunochromatographic, one step assay designed to detect both dengue virus NS1 antigen and antibodies to Dengue virus (Dengue IgG/IgM) in human serum, plasma or whole blood. SD BIOLINE Dengue Duo rapid test contains two test devices (left side ; Dengue NS1 Ag test, right side ; Dengue IgG/IgM test). The SD BIOLINE Dengue Duo kit is intended only for an initial screening test and reactive samples should be confirmed by a supplemental assay such as RT-PCR, IgM / IgG ELISA or HI (Hemagglutination inhibition) test.
In primary infection with the dengue virus, IgG antibody appears a few days after IgM. In primary infections, IgG antibodies are produced at a lower level compared to IgM but will persist for many years after infection. In secondary infections, IgG response may rise quickly before or simultaneously with an IgM response and will become the predominant immunoglobulin isotype in secondary infections.
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