Product Details: Number of Reactions(Preps)/Kit : 10T Brand : CTK BioTech Result Time (Rapid Kits) : 10 min Sample Type : Blood Test Type : Rapid test 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 auL 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)
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 : AR0151C Use of conserved antigens allows pan-filaria tests to be applicable Simple procedure provides alternative to diagnosis by blood smear Use serum, plasma or whole blood No restrictions on time of day for sample collection Each kit contains: Individually sealed foil pouches containing: One cassette device One desiccant Plastic droppers Sample diluent (1 bottle, 5 mL) One package insert (instruction for use)
Product Details: Number of Reactions(Preps)/Kit : 25T Brand : CTK BioTech Result Time (Rapid Kits) : 10 min Sample Type : Blood Test Type :Rapid Test CAT No : R2011C Designed to specifically detect low levels of fecal occult blood, hHB 25 ng/mL Higher accuracy, sensitivity and specificity than the Guaiac Test No dietary restrictions Clear, easy-to-interpret result Individually sealed foil pouches containing: One cassette test device One desiccant Stool collection devices, each containing 2 mL of extraction buffer (REF SB-R2011) Patient ID stickers One package insert (instruction for use)
Product Details: Number of Reactions(Preps)/Kit ; 25T Brand : CTK BioTech Result Time (Rapid Kits) : 10 min Sample Type : Blood Test Type : Rapid Test CAT No : R0192C Clinical accuracy: 96.7% sensitivity, 93.8% specificity Analytical sensitivity: 100% positive detection rate at 1 ng/mL of pylori lysate antigen in fecal specimens Cross reactivity: no cross reactivity with the following organisms at â?¥ 1 x 108 org/mL: Acinetobacter calcoaceticus, Neisseria gonorrheae, Adenovirus, Neisseria meningitides, Enterococcus faecalis, Proteus mirabilis, Escherichia coli, Proteus vulgaris Hauser, Gardnerella vaginalis, Pseudomonas aeruginosa, Geotrichum candidum, Rotavirus, Haemophilus influenza, Salmonella Paratyphi A, �±-haemolytics streptococcus, Salmonella Paratyphi B, �²-haemolytic streptococcus, Salmonella Paratyphi C, Klebsiella pneumonia, Salmonella typhi, Moraxella catarrhalis Interference: No interference was seen with 5 mg/mL Tums�® Antacid, 1:20 Pepto-Bismol�® Antacid, 5 mg/mL Tagamet�® Antacid, 5% Barium sulfate, 5 mg/mL Prilosec Antacid, 12.5% Hemoglobin (tarry stool), or 1:20 Mylanta�® Antacid Shelf life: 24 month Individually sealed foil pouches containing: One cassette device One desiccant Stool collection devices, each containing 2 mL extraction buffer Plastic droppers for transferring watery stool Package insert (instruction for use)
Product Details: 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)
Product Details: Number of Reactions(Preps)/Kit : 10 Brand : CTK BioTech Result Time (Rapid Kits): 15 min Sample Type : Blood Test Type Rapid Test CAT No : R0090C 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: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 : 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: 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 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
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
