Number of Reactions(Preps)/Kit 30T
Brand CTK BioTech
ICMR Approved Yes
Result Time (Rapid Kits) 20min
CAT No : AR5001C
Details :
Utilizes Recombinant Orientia tsutsugamushi antigens.
Qualitative detection and differentiation of antibodies(IgG and IgM) against Orientia tsutsugamushi (Scrub typhus)
Compatible with Whole blood, Serum and Plasma.
Sensitivity: For IgG 95.4% and IgM 96.1%, Specificity: For IgG 96.8% and IgM 97.6%.
Results in 20 minutes.
Each kit contains:
Individually sealed foil pouches containing:
One cassette device
One desiccant
Detection buffer (tris-based buffered solution with preservatives)
Instructions 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.
Brand J.Mithra
Test Kit Type HBsAg Test Kit (Rapid)
Detects All the 11 subtype of HBsAg
Sensitivity 100% by WHO Evaluation
Specificity 100% by PATH USA Evaluation
Cat. No HB010100
Intended Use : Hepacard is visual, rapid, sensitive and accurate one step immunoassay for the qualitative detection of Hepatitis B surface antigen (HBsAg) in Human serum or plasma.The assay is intended to be used as an aid in the recognition and diagnosis of acute infections and chronic infectious carriers of the Hepatitis B Virus(HBV).
Salient Features:
Detects all the 11 subtype of HBsAg.
Antigen Sensitivity- 0.5 ng/ml.
No sample preparation required.
See through Device for easy result interpretation.
Shelf life-30 months at 2-30C.
WHO Evaluated with 100% Sensitivity.
Evaluations:
PATH USA: Sensitivity 100% and Specificity 100% .
DEPT. OF CLINICAL VIROLOGY, CMC VELLORE: Sensitivity 100% and Specificity 100%
Approved By Drug Controller General Of India( DCGI) For use In Blood Banks.
Product Details:
Usage/Application Hospital
Test for quantitative determination of albumin, creatinine and albumin/creatinine ratio (ACR) in human urine, used for early identification of renal disease in patients with diabetes and/or hypertension.
BENEFITSTIMELY TREATMENT CHANGES
The Afinion ACR (albumin, creatinine and albumin/creatinine ratio) detects microalbuminuria in human urine. Microalbuminuria is the first clinical sign of diabetic renal disease and cardiovascular disease. Simple testing for microalbuminuria is extremely efficient as an early indicator of renal failure.
SHORT ASSAY TIME IN 5 MINUTES
The Afinion ACR test gives you reliable results conveniently available when and where you need them.
Patient consultations can be carried out with confidence. The Afinion ACR Test Cartridge contains all reagents necessary for the measurement of albumin, creatinine and albumin/creatinine ratio.
Number of Reactions(Preps)/Kit : 96 wells
Brand : SD Biosensor
ICMR Approved : Yes
Result Time (Rapid Kits) : 1hr 40 mins
STANDARD E Dengue IgM ELISA analyzes IgM antibodies specific to Dengue virus in serum and plasma using enzyme linked immunosorbent assay.
Simple and easy to use - All necessary reagents included in the kit
Highest accuracy with all dengue serotypes(DEN1,2,3, and 4)
Performance
Sensitivity : 97.4% (77/79) / Specificity : 96.6% (346/358)
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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
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%
Number of Reactions(Preps)/Kit 100
Brand Alere
Usage/Application Hospital
Result Time (Rapid Kits) 15 mins
The irst and only FDA approved rapid point-of-care test that simultaneously andseparately detects HIV-1/2 antibodies and free HIV-1 p24 antigen on a single test strip.Determine Combo
Pack Size : 100 Test
Brand : 100 Test
Product Details:
Number of Reactions(Preps)/Kit 22T
Brand Abbott
Result Time (Rapid Kits) 15 Min
Cat. No 852-000
BinaxNOW Legionella Urinary Antigen Card is a rapid assay for the qualitative detection of Legionella pneumophila serogroup 1 antigen in urine samples from patients with symptoms of pneumonia. It is intended to aid in the presumptive diagnosis of Legionnaires disease caused by L. pneumophila serogroup 1 in conjunction with culture and other methods.
Sample Type: Urine
Time to Result: 15 minutes
Kit Size: 22 tests
Performance Data: Sensitivity/Specificity: 95%/95%
Product Details:
Brand Abbott
ICMR Approved Yes
Test Method Antigen Test
Result Time (Rapid Kits) 15 min
Packaging Size 25 Test Kits/Box
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
Product Details:
Brand : ABBOTT
ICMR Approved : Yes
Result Time (Rapid Kits) : 10-15 mins
Packaging Size: 1 T
CAT No : 41FK51
Certified CE certified
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.
Product Details:
Brand : Premier medicals
Result Time (Rapid Kits) : 15 min
Sample Type : Nasal Swab
Packaging Size : 25 Test Kits/Box
CAT No : SS03P25
Certified WHO Approved
Sure Status COVID-19 Antigen Card Test is a rapid chromatographic immunoassay for the qualitative detection of specific antigens to SARS-CoV-2 present in human nasopharynx
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