Product Details: Usage/Application Hospital Results 15 min SD BIOLINE TB Ag MPT64 Rapid is a rapid immune chromatographic identification test for the M. tuberculosis complex. M. tuberculosis has been known to secrete more than 33 different proteins. One of the predominant proteins, MPT64 was found in the culture fluid of only strains of the M. tuberculosis complex. Rapid discrimination between the M. tuberculosis complex and MOTT bacilli Identification of the M. tuberculosis complex in combination with culture systems Sample: Colony, Condensation fluid(Solid cultures) or Liquid cultures Interpretation time: 15minutes Detection limit: 105CFU/ml Ordering Information Cat No. Description Type Pack size 08FK50 SD TB Ag MPT64 Device 25 Test
Product Details: Usage/Application Hospital Tests Kit Filarial antigen Results 10 min The BinaxNOW Filariasis is an in vitro immunodiagnostic test used to detect Wuchereria bancrofti antigen in whole blood, serum, or plasma. The test employs an antibody specific for W. bancrofti. Accurate: Lymphatic filariasis does not always result in clinical symptoms so the most accurate way to diagnosis is using a blood test. Simple: The BinaxNOW Filariasis card test does not require laboratory facilities. Convenient: The test uses finger-prick blood taken at any time of the day without regard to nocturnicity of parasite. Traditionally testing was restricted to the hours of 10 pm and 2 am when the parasite appeared in the patientâ??s blood. Flexible: The test detects filarial antigen in whole blood, serum or plasma. Rapid: The test yields results in 10 minutes.
Product Details: Usage/Application Hospital Results 15-30 min Specimen Whole Blood Test Storage Room Temperature shelf life 24 months The Alere SD BIOLINE Malaria Ag P.f/Pan test is a rapid, qualitative and differential test for the detection of histidine-rich protein II (HRP-II) antigen of Plasmodium falciparum and common Plasmodium lactate dehydrogenase (pLDH) of Plasmodium species in human whole blood. Optimal screening test for P.falciparum and other Plasmodium species Ordering Information Cat No. Description Type Pack size 05FK63I01 SD Malaria Device 1 Test
Product Details: Usage/Application Hospital Time To Result 15 Min Method Rapid Shelf Life 24 Temperature 1-40C The SD BIOLINE Malaria Ag P.f/Pv test is a rapid, qualitative and differential test for the detection of histidine-rich protein II (HRP-II) antigen of Plasmodium falciparum and Plasmodium lactate dehydrogenase (pLDH) of Plasmodium vivax in human whole blood. Specomen: Whole blood Time to result: 15 -30 minutes Storage: 1-40 degree C for 24 months Performance: Sensitivity: Pf-99.7%, Pv-95.5% Specificity: 99.5 % Optimal screening test for Plasmodium falciparum and Plasmodium vivax Ordering Information Cat No. Description Type Pack size 05FK80I40 SD Malaria Device 40 Tests
Serachem India Private Ltd. have been successfully able to develop a transport media for CORONA virus by deactivating it. This means, now we don't have to be at risk while transporting the samples for testing to lab. Also, at present, as per the laid guidelines of ICMR Corona Virus testing can only be done in Biosafe Level-III laboratories. Which are very limited in no. Reason for the same is due to high level of security required in handling the virus. But now when we use STM Viral Transport Medium and Total Nucleic Acid Preservation System provides a rapid and simple method for the collection, preservation and shipping of swab samples in place of VTM (Viral Transport Medium) handling of the virus will be very safe and tests can now be conducted by any testing lab without posing a spread risk. This breakthrough will help in stopping the possible outbreak inside testing labs and hospitals and prevent a bigger disaster. Advantages of STM Viral Transport Medium: 1. No threat of exposure to live virus. 2. The Swab Preservative not only inactivates viruses but also prevents the growth of Gram-negative and Gram-positive bacteria and fungi allowing the resulting non-infectious samples to be handled and shipped safely. 3. The sample can be transported and preserved at room temperature for up to 3 days. (The sample does not get spoiled). 4. No need of having Biosafe Level -III safety norms in labs. 5. No chance of spreading of the virus in labs. 6. Safe for the institutions and their lab staff and medical staffs. 7. Testing facility can be increased exponentially. 8. More sample collection centres can be developed which will help in developing post outbreak strategies. 9. It has also been approved by ICMR. 10. Comes with two sterile Polyester Swabs with visible break point. 11. Price is almost same as VTM Kit. Two separately packed sterile synthetic fibre NYLON swabs with break point. 10-15 ml volume screw-cap, leak-proof self-standing tubes containing 2-3 ml viral transport medium (VTM) Vial has labeling stickers ï?? The pH is 7.3+ 0.3 and the osmolality in mOsm/Kg H20 500.00-600.00 The medium is stable at room temperature. STM meets European CE-IVD / US-FDA approved. Approved by ICMR.
Simple COvid-19 Test for home use .
Clarification of a possibly already occurred immune reaction of the body against SARS-CoV-2 by determination of the specific IgM and/or IgG immunoglobulins (Antigens: S1, S2 and N Proteins). Price-Details: 25% discount for government, clinics and medical facilities. Companies will only receive the discount if they can prove that they use the product for their own purposes and not for commercial purposes. Ask for special deal for 1,000,000 units and more. Performance: The rapid test has a very high accuracy because - unlike most rapid blood tests and laboratory tests - it uses 3 proteins (S1, S2 and N) to detect the antibodies (so-called trinity method). The significance of the rapid test increases during the course of the infection with the formation of antibodies in the blood (between day 4-11 in about 70% of patients). The overall sensitivity of the test (IgM/IgG) is 98.6% (> 1,100 clinical trials). The specificity of the test (reaction only to Covid19) is 99.5% (> 1,500 clinical trials). Please compare this with other tests! Advantages Quick result: The rapid test shows a significant result within 20 minutes. Test procedure: We provide a simple and fast test procedure with two drops of blood from the fingertip, from venous blood or from unfrozen serum. Certified Quality: The test is â??Made in Germany with CE conformity declaration and fulfils the FDA & WHO-requirements. What is included per unit: 1x Cassette (Polystyrene) 1x Support Pad (PVC 3.0 x 60 mm) 1x Cellulose Nitrate Membrane (Cellulose nitrate membrane coated with mouse, anti-human IgM and IgG antibodies) 1x Specimen Pad (Glass fiber / GF) 1x Liquid Absorption Pad (Cellulose acetate membrane) 1x Chemical Coupling Pad (Sealed glass fiber, coated with SARS-CoV-2 antigens and mouse IgG controls) 2g Desiccant (Molecular sieve desiccant) 1x, Aluminum Foil Package (12 x6.5 cm, three-layers of aluminum foil paper) 1x Tag (80 x 50 mm, single-sided plastic tag) 1x Sealable Bag (A sealable bag for disposal of the used cassette) 1x Lancet (Lancets for fingerstick whole blood only) 1x Plastic pipette (A transfer plastic pipette with the line mark of 50 ) 1x Squeezable plastic liquid dropper ampoule (Plastic ampoule containing dilution buffer 1) 1x Instructions for Use
COVID-19 Real Time RT-PCR Kit detects the novel corona virus, COVID-19 using one-step real-time RT-PCR in a single tube. The target genes for the detection of the virus are Orf1 ab and N gene. The kit includes primers and probe set targeting the human Rnase P gene that serves as an internal positive control for the real-time RT-PCR. Ordering Info : 96 Tests/Kit (MOQ : 10 Kits)
BioFACT Viral RNA/DNA Prep Kit is designed to isolate viral RNA/DNA from virous samples such as serum, plasma, cell-culture media, cell free body fluids and tissue. Highly purified viral RNA/DNA from Coronavirus(COVID-19), Adenovirus, Norovirus, Zikavirus, HCV, HIV and Yellow fiber virus can be isolated through the kit. -Isolation of pure viral RNA/DNA from virus samples -No carrier RNA required -Glass fiber membrane column based -Safety use : No phenol nor chloroform -Quantitative PCR (qPCR, qRT-PCR) -Pathogen detection -Poly-A detection -cDNA synthesis -Microarray -Northern blotting
COVID-19 Self Swab Test Kit is the first commercialized Black Gold Particle technology in the world (High Sensitivity & Specifity) -It's made as User friendly Dual Color System (Control Line: Red, Test Line: Black) -Rapid Test Time takes 5~8 Min. -It's intended to use for detection of SARS-CoV2 antigen -20 Tests / Kit (Box) -Tester indicates Negative(C: Red), Positive(C: Red & T: Black) and Invalid(No "C")
This kit is called CTM(Clinical Virus Transport Medium). CTM is intended for the collection and transport of clinical specimen containing Corona Virus and others. Collected Samples by each Nasopharyngeal Swab and Oropharyngeal Swab can be preserved in One Virus Transport Medium(CTM) simultaneously. -Nasopharyngeal Swab : Tilt the patient's head back slightly to straighten the passage from the front of the nose, and gently inset the swab along the base of the nose(not upwards) until it reaches the nasopharynx-gentle rotation of the swab for a few seconds may be helpful. -Oropharyngeal Swab : Press the tongue and extract the secretion from the back wall of pharynx.
1. Product Overview -EnSave is â??IMPROVER of COMBUSTION EFFICIENCY for INTERNAL COMBUSTION ENGINEâ?? operated by â??CATALYSTâ?? which is created from chemical reaction by rare earth element and precious metal such as platinum, lanthanum, &, etc. -EnSaveâ??s Catalytic Action acts to Enhance the Combustion Efficiency of the engine by leading close to perfect combustion. - As a result, EnSave realizes both â??FUEL SAVING and FUEMS SAVING - â??Double Effectâ?? at the same time, the Remarkable and Innovative Technology is under Patent Pending now. 2. Effectiveness 1) Improving Fuel Efficiency (5~20%): Save fuel cost & Profit-up 2) Engine Power up Higher Combustion Efficiency leads to Engine Power-up 3) Fumes Down: Makes Eco-friendly Green Car 4) Noise & Shaking Down: Driving Fatigue & Stress Down 5) Simple & Easy Installation: Just put EnSave into Air Cleaner Space, No A/S required
X-Perso Clean Protection Kit is ready to go. This is a product for everyone and a useful product. We are accepting new orders from Feb 2021 onwards. MOQ - 1 million pieces Monthly capacity 5 million pieces. This kit consist of following: a. 1 - 3Ply disposable mask. b. 1 - Pair of Plastic disposable gloves. c. 1 - Disinfectant Wipe d. 1 - 2ML Hand Sanitiser e. 1 - Facial wet wipe All products inside the kit are FDA and CE compliant. Payment terms - 50% advance payment for booking and remaining 50% at the time of supply.
Product Name: COVID-19 IgG/IgM TEST KIT(Colloidal Gold Method) HS code: 3002.15 Packing: 40Kits/Box; 36Box/Carton(1440pcs/Carton); Diluents: 2 bottles/Box. Carton size: 56*43*40CM Gross Weight: 15 KG/Carton.
1. Sample: Blood (Whole blood, Serum) 2. Measuring Time: 10~15 Minutes 3. Test Principle - Identification of COVID 19 antibody in blood COVID 19 IgG / IgM Rapid Test (WB / Serum / Plasma in human blood) is a fast chromatographic immunoassay for qualitative analysis of IgG and IgM antibodies to COVID 19. 4. Characteristics - Simplicity: No special equipment required and intuitive visual interpretation. - Rapid: Fast sampling with blood at the tip of the finger, results in 10~15 minutes. 5. Main Use - People with symptoms - Suspicious with or without mil d symptoms patient. - It is also used to test people in close contact with infected patients and those in quarantine.
The COVID-19 RT-PCR Peptide Nucleic Acid (PNA) KIT is a real-time reverse transcription (RT)-Polymerase chain reaction (PCR) assay intended for the qualitative detection of nucleic acid from SARS-CoV-2 in respiratory specimens such as nasopharyngeal swabs, oropharyngeal swabs, anterior nasal swabs, midturbinate nasal swabs, bronchoalveolar lavage (BAL), and nasopharyngeal wash/aspirates or nasal aspirates collected from individuals suspected of COVID-19 by their healthcare provider. Testing is limited to laboratories certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA), 42 U.S.C. 263a, to perform high complexity tests. Results are for the identification of SARS-CoV-2 RNA. The SARS-CoV-2 RNA is generally detectable in upper respiratory specimens during the acute phase of infection. Positive results are indicative of the presence of SARS-CoV-2 RNA; clinical correlation with patient history and other diagnostic information is necessary to determine patient infection status. Positive results do not rule out a bacterial infection or co-infection with other viruses. The agent detected may not be the definite cause of disease. Laboratories within the United States and its territories are required to report all positive results to the appropriate public health authorities. Negative results do not preclude SARS-CoV-2 infection and should not be used as the sole basis for patient management decisions. Negative results must be combined with clinical observations, patient history, and epidemiological information. The COVID-19 RT-PCR PNA KIT is intended for use by qualified and trained clinical laboratory personnel specifically instructed and trained in the techniques of real-time PCR and in vitro diagnostic procedures. The COVID-19 RT-PCR PNA KIT is only for use under the Food and Drug Administrations Emergency Use Authorization.
Unit Price: USD 15 Target Region: RdRP, E gene, N gene Accuracy: 100% Recommended PCR: CFX96 Real Time PCR System (Bio Rad) DTprime DT-96 QIAGEN Rotor-Gene Q Box Size: Size: W 80 x D 80 x H 65 (mm) Weight: 45g / box Certification: Korea GMP (ISO 13485 2003) European CE
Unit Price: USD 16 Target Region: RdRp, E gene Accuracy: 100% Recommended PCR: Roche Light Cycler 480 Qiagen Rotor-Gene Q plex HRM Applied Biosystems Quantstudio5 Applied Biosystems 7500 Real-Time PCR system Bio-RAD CFX96 Real-Time PCR Detection system Certification: ISO 13485 European CE Health Canada Saudi Arabia FDA
Unit Price: USD 10 Accuracy: 95% Box Size: L 22* W 13* D 7 cm Certificates EN ISO 13485:2016 Adopted Technical Standards IVD directive 98/79/EC, EN ISO13485:2016, EN ISO 14971:2012, EN ISO 18113 1:2011, EN 13975:2003 EN ISO 13612:2002, EN ISO 15223 1:2016, EN ISO 23640:2015 EN ISO 17511:2003
Unit Price: USD 20 Target Region: N gene Recommended PCR: CFX96 Real Time PCR System (Bio Rad) QauntStudio5 Real-time PCR QuantStudio3 Real-time PCR
