We bring forth high quality Laboratory Testing Instruments, which are manufactured in compliance with industry standards. The Laboratory Testing Instruments offered by us, is highly appreciated among the clients owing to their high performance and longer working life .Further, the Instruments are offered in various specifications. Leaders in manufacturing and supplier of laboratory Testing Instruments : Overhead Lab Stirrer volt Model -3A(G), 4A(G), 6A(G). Overhead Lab Stirrer Model 3A,4A, 6A. Automatic Karl Fischer Hot Air Oven Digital. Vacuum Oven Round Digital ,Vacuum Oven Digital Rectangular,Hot Air Oven Top Motor Digital K. F. App. Precision Digital Melting /Boiling Point App. Autoclave , Autoclave Portable ,BOD Incubator,Environmental Chamber Digital Rate Test App Single State Water Still , Heating Mental Hot Plate Rectangular, Sieves Shaker, Bacteriological Incubator ,Water Bath Shaker pH Meter Digital Manual Temp. Comp. Mdl. pHM pH Meter digital Auto cum Manual Temp Comp. Mdl pHAM Muffle Furnace Digital , Oil. Bath Draining & Drying Rack, Digital Colony Counter, Orbital Shaker Incubator, Bulk Density App. Digital Antibiotic Zone Reader ,Digital Conductivity Meter, Griffin Flask Shaker, Rotary shaker Soxhlet Extraction Heater Hot Plate & Mantle Type IR Moisture Balance, Ultrasonic Bath ,Platform Shaker Constant Temp- Circulating Water Bath Hot Plate Round ,Tablet Hardness Taster Monsanto Rotary High Vacuum Pump Dissolution Apparatus Single & Three Stage Dissculution Rate Test Apparatus 6 test. Binocular Microscope Ford Flow Cup Viscometer Low Temp. Bath , Tablet Distigration Test , Friability Test Apparatus Viscometer Bath ,Deep Freezer Instrument Sterilizer , Leak Test Apparatus , Water Bath Thermostatic. Electric Bunsen Burner with Regulator Box Peristaltic Pump Water bath Dye Pots Multi Magnetic Stirrer Digital Tablet Disintegration, Hot Plate Magnetic Stirrer , Laboratory Centrifuge , Laminar Flow Tablet Hardness Tes
1. Requested Service Condition: 1.1. Ambient temperature: 0~20±2 1.2. Relative humidity: â?¤80% 1.3. Power supply: 220V±22Vï¼?50HZ 1.4. Should not be subject to severe vibration and mechanical shock 1.5. The air should not contain enough dust and impurities to erode device. 1.6. Should not be subject from strong electromagnetic interference. 1.7. Good ventilation 1.8. Grounding requirements: Ground resistance ï¼?1Ω
We have just achieved a major breakthrough in the development of dengue igg/igm antibody early test. Our new product is capable to detect the presence of dengue igm antibody in human serum within 3-5 days since primary infection (tested and verified with reference standard blood sample from usa cdc), while similar products currently found on the market can only detect it after at least 10-15 days. The significance of this achievement is that the new dengue igg/igm antibody early test now can diagnose dengue infection at a very early stage, which previously could only be done with a dengue ns1 antigen test. Type: immunoassay system Brand name: ntbio/oem/private label Place of origin: british columbia, canada Size: 60mm x 300mm Sensitivity: 95.3% Specificity: 95.0% Specimen: whole blood/serum/plasma .
Highest accuracy Fast result interpretation Cost effective Made with best choices of materials Type: immunoassay system Brand name: ntbio/oem/private label Place of origin: british columbia, canada Size: 60mm x 300mm Sensitivity: 94.3% Specificity: >98.9% Specimen: whole blood/serum/plasma .
Highest accuracy Fast result interpretation Cost effective Made with best choices of materials Type: immunoassay system Brand name: ntbio/oem/private label Place of origin: british columbia, canada Size: 60mm x 300mm Cut-off value: 1000 ng/ml Sensitivity: 99.5% Specificity: >99.7% Specimen: urine .
Intended use: Toxoplasma IGG/IGM rapid test is a rapid immunochromatographic test for the simultaneous detection of IGM and IGG antibodies to toxoplasma gondii in human serum/plasma. The test can be used as a screening test for toxoplasma infection and as an aid for differential diagnosis of the self limiting primary toxoplasma infections and the potentially fatal secondary toxoplasma infections in conjunction with other criteria. Test principle: The toxoplasma IGG/IGM rapid test is a lateral flow chromatographic immunoassay. The test cassette consists of: 1) A burgundy colored conjugate pad containing toxoplasma recombinant envelope antigens conjugated with colloid gold (toxoplasma conjugates) and rabbit igg-gold conjugates, 2) A nitrocellulose membrane strip containing two test bands (t1 and t2 bands) and a control band (c band). The t1 band is pre-coated with the antibody for the detection of IGM anti-toxoplasma, t2 band is coated with antibody for the detection of igg anti-toxoplasma, and the c band is pre-coated with goat anti rabbit IGG. Absence of any t bands (t1 and t2) suggests a negative result. The test contains an internal control (c band) which should exhibit a burgundy colored band of the immunocomplex of goat anti rabbit igg/rabbit igg-gold conjugate regardless of the color development on any of the t bands. Otherwise, the test result is invalid and the specimen must be retested with another device. Reagents and materials supplied : 1. Test cassette individually foil pouched with a desiccant. 2. Plastic dropper 3. Buffer 4. Package insert. Storage and stability: The kit must be stored at 2-30pc. Warning and precautions: 1. For in vitro diagnostic use only. Not for medicinal use. 2. Do not use beyond expiry date. 3. Read the instructions careful y before performing the test. 4. Handle all specimen as potential y infectious. 5. Follow standard biosafety guidelines for handling and disposal of potential y infective material.
H-fabp fast test kit (immunofluorescence assay) is intended for use together with getein1100 immunofluorescence quantitative analyzer (getein1100) or getein1600 immunofluorescence quantitative analyzer (getein1600) to quantitatively determine the concentrations of h-fabp in human serum, plasma, or whole blood specimens in point-of care and laboratory settings. H-fabp fast test kit (immunofluorescence assay) is intended for in vitro quantitative determination of heart-type fatty acid binding protein (h-fabp) in serum, plasma or whole blood. This test is used in the early diagnosis of ami and pulmonary embolism, and monitoring of chronic heart failure.
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Supplier: Hydraulic testing equipments for aggregate, asphalt, soil, concrete, cement, tensile strength testing machineries and laboratory equipments
Supplier: Laboratory testing, soil testing, materials testing, NDT/surveying instruments including total station and other relevant products