Cat. No : 9901-NCOV-01G. Reliable, rapid chromatographic immunoassay for the qualitative detection of specific antigens of SARS-CoV-2
The SARS-CoV-2 Rapid Antigen Test is a reliable, rapid chromatopgraphic immunoassay for the qualitative detection of specific antigens of SARS-CoV-2 present in the human nasopharynx.
This test is an aid in detecting antigen from the SARS-CoV-2 virus in individuals suspected of COVID-19. This product is strictly intended for professional use in laboratory and Point of Care environment.
Cat No : 195000. TheBinaxNOWTM COVID-19 Ag Card is a lateral flow immunoassay intended for the qualitative detection of nucleocapsid protein antigen from SARS-CoV-2 in direct anterior nasal (nares) swabs from individuals suspected of COVID-19 by their healthcare provider within the first seven days of symptom onset.
CAT No : R0063C. Utilizes recombinant chimeric dengue virus licensed from the US CDC
Detects all four dengue serotypes
Duo test format minimizes processing time
IgM detection indicates recent infection
IgG detection indicates recent or previous infections
Ag detection indicates a current infection Individually sealed foil pouches containing:
One cassette device
One desiccant
5 uL Capillary tubes (for Dengue IgG/IgM test)
Plastic droppers (for Dengue Ag test)
Sample diluent (REF SB-R0062, 5 mL/bottle)
One package insert (instruction for use)
Number of Reactions(Preps)/Kit : 10
Brand : CTK BioTech
Result Time (Rapid Kits) :15 min
Sample Type :Blood
Test Type Rapid Test
CAT No : R0092C
Single test for identifying acute infection and protective immunity by detecting and differentiating IgG and IgM anti-HAV
Indicates protective immunity by detecting HAV IgG titers â?¥70 mIU/mL
High confidence as it is traceable to the 2nd WHO International Standard for HAV, and IgM is in agreement with market leading ELISA test: Sensitivity: 94.8%; Specificity: 96.7%
Flexible specimen types including serum, plasma, or whole blood which allows testing at any time without special specimen preparation
Small sample volume (5 �µL) enables multiple testing on the same specimen without having to re-draw the patient.
Initial patient care action can begin during the patient's visit as test results are available in 15 minutes.
Easily transported, and can be stored for 24 months at 2-30oC
Individually sealed foil pouches containing:
One cassette device
One desiccant
5 Aul capillary tubes
Sample diluent (REF SB-R0092, 5 mL/bottle)
Package insert (instruction for use)
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Product Details:
Number of Reactions(Preps)/Kit:10T
Brand : CTK BioTech
Result Time (Rapid Kits): 15 min
Sample Type : Blood
Test Type : Rapid Test
CAT No : R0095C
Single test for identifying acute infection and protective immunity by detecting and differentiating IgG and IgM anti-HAV
Indicates protective immunity by detecting HAV IgG titers â?¥70 mIU/mL
High confidence as it is traceable to the 2nd WHO International Standard for HAV, and IgM is in agreement with market leading ELISA test: Sensitivity: 94.8%; Specificity: 96.7%
Flexible specimen types including serum, plasma, or whole blood which allows testing at any time without special specimen preparation
Small sample volume (5 �µL) enables multiple testing on the same specimen without having to re-draw the patient.
Initial patient care action can begin during the patientâ??s visit as test results are available in 15 minutes.
Easily transported, and can be stored for 24 months at 2-30oC
Individually sealed foil pouches containing:
One cassette device
One desiccant
5 AUL capillary tubes
Sample diluent (REF SB-R0092, 5 mL/bottle)
Package insert (instruction for use).
Product Details:
Number of Reactions(Preps)/Kit : 10
Brand : CTK BioTech
Result Time (Rapid Kits) : 20Min
Sample Material ; Serum / Plasma / Whole Blood
Cat. No : R0063c
The OnSite Dengue Ag rapid Test CE is a lateral flow chromatographic immunoassay for the qualitative detection of dengue NS1 antigen (DEN1, 2, 3, 4) in human serum, plasma or whole blood.
The test is designed to be used by professionals as a screening test and provides a preliminary test result to aid in the diagnosis of infection with dengue virus.
Any use or interpretation of this preliminary test result must also rely on other clinical findings and the professional judgment of health care providers. Alternative test method(s) should be considered to confirm the test result obtained by this device.
Recommended for use:
Any person presenting with clinical signs or symptoms within 9 days consistent with acute dengue infection or dengue fever including: high fever, severe headaches, severe pain behind the eyes, severe joint and muscle pain, fatigue, nausea, vomiting, and/or skin rash.
Dengue NS1 antigen is detectable in human blood from the first day after the onset of fever up to 9 days, which allows early detection and prompt treatment of infection with dengue virus.
As mild dengue fever symptoms can overlap with acute clinical manifestations of other arbovirus infections, such as Zika virus and chikungunya virus infections, correct diagnosis of dengue infection during early disease onset is critical for guiding clinical patient management.
Product Specification:
Individually sealed foil pouches containing:
One cassette device
One desiccant
Plastic droppers
Sample diluent (REF SB-R0063, 5 mL/bottle)
One package insert (instruction for use)
Number of Reactions(Preps)/Kit 30T
Brand CTK Biotech
Result Time (Rapid Kits) 20mins
Test Type Rapid Test
CAT No : R0234C
The OnSite Toxo IgG/IgM Combo Rapid Test is a lateral flow chromatographic immunoassay for the simultaneous detection and differentiation of IgG and IgM anti-Toxoplasma gondii (T. gondii) in human serum, plasma or whole blood.
Brand RAPHA
CAT No : N116A
Size 50 T
Result Time 5 Min
UNIQUE FEATURES:
EASY TO PERFORM: Rapid, One Step procedure. Test Procedure & interpretation of results printed on individual Pouch
HIGHER SENSITIVITY: Sensitivity of 20 mIU/mL of hCG hormone in Urine ensure the early detection of Pregnancy
FAST & ACCURATE RESULTS: Results within 5 minutes, Positive results just in 30 seconds
BIGGEST TEST WINDOW WIDTH: Test window width of 4mm ensure the clear background and better readability of the test results
USER FRIENDLY: Requires no external measurement system. Can be stored at Room Temperature (2 - 30C).
Product Details:
Number of Reactions(Preps)/Kit 30 T
Brand CTK BioTech
Result Time (Rapid Kits) 10 Min
Sample Material Plasma/Serum
Test Type Rapid test
Cat. No R0310C
The OnSite RF Rapid Test is a lateral flow immunoassay for the qualitative detection of all subtypes of rheumatoid factor (RF) in human serum, plasma or whole blood at a sensitivity of 8 IU/ml.
Product Features :
Rapid test to make RF detection simpler and quicker than Latex
Detects RF levels as low as 8 IU/mL
Detects all RF isotypes including IgM, IgG, and IgA
Simple procedure minimizes risk of operator error â?? no sample preparation required.
The results are ready in 10 minutes, which increases diagnostic efficiency.
The least complicated RF test- can be performed in any setting by any health care provider with simple training
Rapid test format allows room temperature shipping and storage.
Each kit contains:
Individually sealed foil pouches containing:
One cassette device
One desiccant
Capillary tubes (5 µL)
Sample Diluent ( REF SB-R0310, 5 mL/bottle )
One package insert (instruction for use)
Brand J.Mithra
Kit Type HIV Test Kit (Rapid) (Tri Dot)
Sensitivity 100% WHO Evaluation
Specificity 100% WHO Evaluation
Result Time Within 3 Minutes
Cat. No IR130100
Intended Use:The HIV TRI-DOT test is a visual, rapid, sensitive and accurate immunoassay for the differential detection of HIV-1 & HIV-2 antibodies (IgG,IgM & IgA) in human serum or plasma using HIV-1 & HIV-2 Antigens immobilized on an immunofiltration membrane. The test is a screening test for Anti HIV-1 and HIV-2 and is for in vitro diagnostic use only.
Salient Features:
Rapid visual test ,based on Flow Through Technology.
Differential detection of HIV-1 & HIV-2.
Detection of group O & subtype C.
Use of envelop antigens gp41& C terminus of gp120 for HIV-1 & gp36 for HIV-2.
100% sensitivity & 100% specificity as per WHO Evaluation.
Shelf life 24 months at 2-8C
Available in convenient pack sizes- 50 Tests and 100 Tests.
Results within 3 minutes.
No instrument required.
In built quality control dot.
Evaluations:
WHO Evaluation: Evaluation report from UNAIDS (WHO), CH-1211Geneva,Switzerland Aug 1999 the Sensitivity and Specificity of HIV TRI-DOT is 100 % .The panel used for evaluation of HIV TRI-DOT by Institute of Tropical Medicine, WHO Collaborating Centre in AIDS, Belgium also included HIV-O virus, which was found reactive with HIV TRI-DOT.
NIMHANS BANGALORE: Evaluation report from National HIV Reference Laboratories of Government of India , claiming Sensitivity and Specificity of HIV TRI-DOT to be 100 %.
CMC VELLORE: Evaluated by Department of Clinical Virology, Christian Medical College & Hospital, Vellore and published in JCM, vol. 38, Issue 2000,claiming 99.5% sensitivity and 99.9% specificity.
NARI PUNE: Evaluation Report from National AIDS Research Institute(NARI-Pune) claiming sensitivity & Specificity to be 100 %.
Approved by Drug Controller General of India( DCGI) for the usage in Blood Banks.
Product Details:
Number of Reactions(Preps)/Kit 25 T
Brand Premier
Result Time (Rapid Kits) 20 -30 MIN
Certified WHO Aproved
CAT No; PI13FRC25
First Response Malaria Antigen P.falciparum (HRP2) Card Test is intended to be performed by trained users (In either laboratory or point of care settings) as qualitative screening in vitro diagnostic test for detection of P. falciparum specific HRP2 antigen.
Sensitivity - 100%
Specificity - 100%
Rapid Result time within 20 - 30 Minutes.
Detects Histidine Rich protein(HRP2) of Plasmodium P.falciparum
Storage at 1 40 C.
Specimen Type- Whole Blood
Number of Reactions(Preps)/Kit 25 T
Brand Premier
Result Time (Rapid Kits) 20 - 30 Min
Certified WHO Approved
CAT No; PI19FRC25
First Response Malaria Ag. P.f. / P.v. Card Tests intended to be performed by trained users (In either laboratory or point of care settings) as qualitative screening in vitro diagnostic test for detection of P. falciparum and P. vivax.
Product specifications :
Sensitivity - 100%
Specificity -100%
Rapid Result time within 20 - 30 Minutes.
Detects P. falciparum and P. vivax.
Storage at 1 40 C.
Specimen Type- Whole Blood
Product Details:
Number of Reactions(Preps)/Kit 25 T
Brand Premier
Result Time (Rapid Kits) 20 - 30 Min
Certified WHO Aproved
CAT No; PI16FRC25
First Response Malaria Ag. pLDH/HRP2 Combo Card Test is intended to be performed by trained users (In either laboratory or point of care settings) as qualitative screening test for detection of P.falciparum, P. vivax, P. ovale and P. malariae.
100% - Specificity
100% - Sensitivity
Rapid Result time within 20 - 30 Minutes.
Storage at 1 40 C.
Detects P.falciparum, P. vivax, P. ovale and P. malariae.
Specimen - Whole Blood
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
Product Details:
Number of Reactions(Preps)/Kit 22 Test
Brand Abbott
Usage/Application Hospital
Cat. No 710-000
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.
Brand SD
Country of Origin Made in India
Specimen Serum
Shelf Life 24 Months
Temperature Storage 30 Degree Celsius
Sensitivity 97.6%
Specificity 98.0%
H.Pylori
Helicobacter pylori (H.pylori) is a spiral shaped bacterium and is found in the gastric mucous layer or adherent to epithelial lining of the stomach. H.pylori causes more than 90% of duodenal ulcers and up to 80% of gastric ulcers. Approximately two thirds of the world's population is infected with H.pylori. The immuno- chronomatographic techinques for the detection of antibodies specific to H.pylori has substantially resolved these problems.
General Information:
SD BIOLINE H.pylori test is a rapid test for the qualitative detection of antibodies of all isotypes (IgG, IgM, IgA etc) specific to Helicobacter pylori in human serum plasma or whole blood.
Detection of all isotype (IgG, IgM, IgA) antibodies against H.pylori
High Accuracy Sensitivity: 95.9%, Specificity: 89.6%
Specimen: Serum. Plasma, Whole blood
Material provided with this kit are as follows:
SD BIOLINE H.pylori test device multi-device
Assay diluent
Product Details:
Number of Reactions(Preps)/Kit 40
Brand Abon
Result Time (Rapid Kits) 15 mins
The Syphilis Rapid Test Cassette (Whole Blood/Serum/Plasma) is a rapid chromatographic immunoassay for the qualitative detection of antibodies (IgG and IgM) to Treponema Pallidum (TP) in whole blood, serum or plasma to aid in the diagnosis of Syphilis.
Product Details:
Number of Reactions(Preps)/Kit 25 T
Brand Abbott
Result Time (Rapid Kits) 15-20 Min
Cat. No 11FK50
Biolineâ?¢ DENGUE NS1 AgTEST FOR EARLY CLINICAL PHASE OF DENGUE INFECTION
Bioline Dengue NS1 Ag rapid test is an in vitro immunochromatographic assay designed to detect Dengue virus NS1 antigen in human serum, plasma or whole blood.
Product not available in all countries. Please check with your local sales representative regarding availability in your area.
Benefits:
Diagnosis of early acute dengue infection by detecting dengue NS1 antigen
Dengue NS1 antigen can be detected from 1 day after onset of fever
Specimen : Serum, plasma or whole blood (100l)
Test result : 15~20 minutes
Specification:
Sensitivity 92.4%, Specificity 98.4%
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