Product Details: Number of Reactions(Preps)/Kit : 25 Brand : CTK BioTech Result Time (Rapid Kits) ; 15 min Sample Type : Blood Test Type Rapid Test CAT No : R0162C Detects the specific antigens from either S. typhi or S. paratyphi Earlier detection results in faster treatment for disease eradication Works with a variety of specimen types including: fecal, blood culture Simple procedure minimizes operator error due to sample preparation Test result within 15 minutes allows medical professionals to take immediate action High level of reproducibility Test kits can be used and stored at room temperature Individually sealed foil pouches containing: One cassette device One desiccant Stool collection devices, each containing 1 mL Fecal Sample Extraction Buffer (REF SB-R0162) Sample diluent (REF SB-R0162-2, 5 mL/bottle) Plastic droppers Patient ID stickers One 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)
Product Details: 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.
Product Details: 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 10 T Brand CTK BioTech Test Type Rapid test Sample human serum, plasma, or whole blood Test time 10 Min Cat No : R0253C The OnSite TORCH Panel Rapid Test is a lateral flow chromatographic immunoassay for the qualitative detection and differentiation of antibodies (IgG and IgM) to Toxoplasma gondii (T. gondii), rubella virus, cytomegalovirus (CMV), herpes simplex virus 1 (HSV-1), and herpes simplex virus 2 (HSV-2) in human serum, plasma, or whole blood. This test is intended to be used by professionals as a screening test and provides a preliminary test result to aid in the diagnosis of infection with T. gondii, rubella virus, CMV, HSV-1 and HSV-2. Any interpretation or use of this preliminary test result must also rely on other clinical findings as well as on 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 consistent with TORCH infection. Women who are pregnant or who are planning to become pregnant Individuals with a compromised immune system The OnSite TORCH Panel Rapid Test detects and differentiates IgG and IgM antibodies for all 5 TORCH infections. In general, a negative test result indicates that the individual is at risk for acquiring a primary infection. A positive IgM result only indicates acute infection, a positive IgM and IgG test indicate acute, late phase infection, and a positive IgG test result only indicates past or chronic infection. The presence of IgM anti-rubella virus or high titers of IgG anti-rubella virus (> 200 IU/mL) are suggestive of acute rubella infection. Lower titers of IgG anti-rubella virus (â?¥ 10-15 IU/mL) are suggestive of previous exposure and protective immunity. An individual with an IgG anti-rubella virus titer less than 10-15 IU/mL is considered to be at risk of acquiring a rubella virus infection. The TORCH Panel Rapid test also differentiates between HSV-1 and HSV-2 antibodies using HSV-1 specific glycoprotein G1 and HSV-2 specific glycoprotein G2. Product Specification : Individually sealed foil pouches containing: One cassette device Two desiccants Plastic droppers Sample diluent (REF SB-R0253, 5 mL/bottle) One package insert (instruction for use)
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)
Product Details: 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
Product Details: 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: 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.
Product Details: 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)
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
Product Details: 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. Time to Result: 15 minutes Performance data: Urine Sensitivity/Specificity 86% / 94% CSF Sensitivity/Specificity 97% / 99% Ordering Information Cat No. Description Specimen Pack size 710000 Streptococcus Urine, CSF 22 Tests Pneumoniae Ag card
Product Details: Brand Roche Result Time (Rapid Kits) 15 min CAT No : 11621947196 Qualitative detection of troponin in anticoagulated (EDTA or heparin) venous whole blood Reaction time: 15 min. Positive result from a threshold (cut-off) of 100 ng/L Storage at 2 to 8 C Test can be used immediately after removal from the refrigerator Storage for 4 weeks at room temperature (15 to 25 C) Roche TROP T sensitive rapid assay is available in 5 and 10 pack sizes Content: 5 disposable test strips (individually sealed) 5 pipettes (150 L) disposable labels 1 package insert
Product Details: 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.
