This antigen test is suitable for the qualitative detection of novel coronavirus in Saliva/Sputum/Stool/NP Swab/OP Swab samples (all methods in single test). Result in 15mins
NAME COVID-19 Nucleic Acid Detection Kit(PCR-fluorescent Probe) USE Diagnosis COVID-19 rapidly for public disease control Manual Biological cabinet, Appropriate real time PCR instrument, Appropriate nucleic acid extraction system or kit, Desktop centrifuge ( suitable for 96- well plate or 8-strip tube), Centrifuge with a rotor for 0.2ml reation tubes or plate. Vortex mixer, Adjustable piperres(with maximum capacity of 2 L, 10L, 50L, 100L, and 200L, respectively), Disposible pipette tips with filters, Disposable powder-free gloves, RNase FREE 1.5mL centrifuge tube, PCR reation tube / PCR reaction plate. Storage and Transportation Store in -20 - 5 and transport with carbon diaxide ice, avoid being repeated freezing and thawing. Expiration date 9 months * Please be noted the above is the price including the tax, NOT FOB.
The current test kit is based on specific antibody antigen reaction and immunoassay technique. The test card contains a gold labeled novel coronavirus N protein monoclonal antibody p re coated on the binding pad and a paired novel coronavirus N protein monoclonal antibodies fixed in the test line (T) and corresponding antibodies in the quality control line (C). During the test, the N protein in the specimen binds to the gold-labeled nove lcoronavirus N protein antibody pre-coated on the binding pad, and the conjugate moves upward under the capillary effect, and then is trapped by N protein monoclonal antibody conjugate fixed in the Test Line (T). The higher the N protein content in the specimen, the more conjugates are trapped, and the darker the color of the Test Line (T). If there is no novel coronavirus in the specimen or the virus content is below the detection limit, no colour appears in the Test Line (T). A purple red band will app ear in the Control Line (C) regardless of whether there is a virus in the specimen. The purple red band that appears in the Control Line (C) is the criteria for determining whether there is enough specimen and whether the chromatography process is normal.
The product is based on the principle of antigen-antibody reaction and immunoassay technique. The test device contains colloidal gold labeled SARS-CoV-2 recombinant protein, mouse-anti human IgG antibody immobilized in G test area, mouse-anti human IgM antibody immobilized in M test area and the corresponding antibody in quality control area (C). During the test, when the SARS-CoV-2 IgM antibody level in the sample is at or above the limit of detection of the test, the SARS-CoV-2 IgM antibody in the sample binds to the colloidal gold labeled SARS-CoV-2 recombinant protein which is pre-coated on a gold label pad. The conjugates migrate upward through capillary effect and would be captured by mouse-anti human IgM antibody immobilized in M test area subsequently and this produces a purple-red band appears in the M test area. When the SARS-CoV-2 IgG antibody level in the sample is at or above the limit of detection of the test, the SARS-CoV-2 IgG antibody in the sample binds to the colloidal gold labeled SARS-CoV-2 recombinant protein which is pre-coated on a gold label pad. Theconjugates migrate upward through capillary effect and would be captured by mouse-anti human IgG antibody immobilized in G test area subsequently and this produces a purple-red band appears in the G test area. If it is a negative sample, there is not a purple-red band appeared in the M and G test area. Regardless of the presence or absence of the SARS-CoV-2 antibody in the sample, a purple-red band will appear in the quality control area (C). The purple-red band in the quality control area (C) is a criterion for judging whether there is enough sample and whether the chromatography process is normal. It also serves as the internal control standard for reagents.
Super long life refrigeration sheet modified by special process; Precision temperature control technology ensures that the temperature fluctuation of each hole is less than 0.1 ; Ultra high sensitivity PMT system combined with precision optical system ensures accuracy; New automatic hot cover technology can effectively prevent reagent evaporation; Maximum 6 channels fluorescence detection, no cross interference between channels; Intelligent operating system, flexible program setting, comprehensive analysis and report function;
We hope everyone is doing their best to "be well informed about the COVID-19 virus, the disease it causes and how it spreads. Protect yourself and others from infection by washing your hands or using alcohol-based rub frequently and not touching your face." -WHO Affordable at-home COVID-19 testing. Results within minutes. A Leading POCT and IVD Enterprise In China! Attached to the Chinese Academy of Sciences! Quality Comes From Professionalism And Service Makes The Future We have a complete international after-sales processing system and provides 24 hours service. Any more questions please contact me! Covid-19 Antigen Rapid Test Kit (Colloidal gold) Covid-19 IgM/IgG Test Kit (Colloidal gold) Covid-19 IgM/IgG Test Kit (Rare earth nano fluorescence immunochromatography) ISO13485 certified Samples are available At-home testing Results within 15mins Accurate Simple Rapid Authorities approved Monthly productivity 15 million units #AmonMedCAS #ChineseAcademyofSciences #IVD #POCT #PCR #invitrodiagnostic #diagnostics #VdcConnect #healthcare #IgG #IgM #antibody #antigen #coronavirus #covid19 #Covid19testing #pruebacovid #laboratorio #nyccovid #covidathome #conciergetesting #clinical #lab #hospital #testkit #ISO13485 #rapidtest #biotecnologia #quimica #bioquimica
Product Features Easy Shorten window period in Antigen detection Flexible Saliva sample, Nasal/Throat swabs sample, VTM Simple Visual result interpreted, no instrument required Rapid Result interpreted in 15 minutes
Diagnostic Kit for IgM/IgG 2 in 1 Antibody to 2019-nCoV (Colloidal Gold) Test principle This diagnostic kit adopts the principle of colloidal gold immunochromatographic test strip to make qualitative test for 2019-nCoV IgM/IgG antibody in human serum, human plasma and whole blood samples. Purpose This diagnostic kit is used for making qualitative test for 2019-nCoV IgM/IgG antibody in human serum, human plasma and whole blood samples. It acts as an early-stage aided diagnostic kit for clinical patients infecting 2019-nCoV, yet it is not the only standard for clinical diagnose. Sample requirements This kit is suitable for human serum (EDTA anticoagulant, heparin anticoagulant, trisodium citrate dihydrate anticoagulant 1:9), human plasma and whole blood samples.
Purpose This test kit is used for making qualitative test for COVID-19 antigen in human nose swab and throat swab samples. It acts as an early-stage aided diagnostic kit for clinical patients infecting COVID-19, yet it does not stand for the basis for confirming COVID-19. Sample requirements When using sterile swab for collecting samples, polyester sponge swab with PP bar is recommended when collecting nose swab and throat swab. When collecting nose swab, the swab will be gently inserted into the nose palatine and stay for a moment, and then gradually rotate it until it is taken out. When collecting throat swab, the swab will be completely inserted into the throat from the mouth, then inspectors will wipe pharyngeal tonsil on both sides and posterior wall of pharynx with appropriate strength, and finally take the swab out. During this process, please avoid touching the tongue. After collecting the samples, please make processing with viral transport medium or sample diluent provided in the test kit as soon as possible, and complete test within five minutes. Test principle This test kit adopts the principle of high-specificity antigen-antibody reaction and colloidal gold labelling and immunochromatographic test strip techniques. The reagent contains COVID-19-NP antigen monoclonal antibody pre-fixed in film test area and COVID-19-NP antigen monoclonal antibody-colloidal go
hrough market research and government trading department internal documents, we have complied a covid-19 related products suppliers contract info. The data consists of product introduction (including description and certification) and main markets they export. Supplier�¢??s name and contact person phone number. All the contract person are the one who directly responsible for international selling, and the phone number is her/his direct mobile phone. 100% accurate and updated at the end of March 2020 The data consists of 6 categories 1. Diagnostic reagent supplier (eg. Covid-19 test kit etc.) 2. Medical equipment (like ventilators etc.) supplier 3. Chinese patent medicine supplier 4. AI-aid diagnostic system supplier 5. Temperature measuring device supplier (eg. Thermometer etc.) 6. Disinfection equipment (eg irradiation system and disinfection gel, hand wash etc.) 7. Protective clothing Each categories price: USD 100 Full package of seven categories: USD: 600
Bacterial Vaginosis Rapid Test Kit core Chromogenic Ingredient IBX-4041 IBX-4041 Testing vessel BV Blue active ingredient BVBlue active ingredient BVBlue substrates BV Blue substrates Chromogenic substrate IBX-4041 chromogenic substrate of sialidase enzyme Detection reagent for bacterial vaginosis (sialidase two-step method) Shenzhen BST Science & Technology Co., Ltd sells and exports chromogenic substrate of sialidase enzyme IBX-4041. Specification: Appearance: Light yellow solid powder Purity: 95% min Application: Two-step chromogenic substrates of neuraminidase (sialidase) BVBLUE Test Kit Component 1)BVBLUE Developer Solution: Water and Sodium hydroxide 2) BVBLUE Testing Vessel: Water, Potassium acetate, IBX-4041 (chromogenic substrate compound). IBX-4041 is the key ingredient of BVBLUE test kit, BVBLUE test is a rapid sialidase test for bacterial vaginosis. BVBLUE test method is currently the only test method approved by the FDA for testing Bacterial Vaginosis(BV), The BV BLUE Test contains a chromogenic substrate of sialidase enzyme, IBX-4041. BV Blue test is a commercially available test, it detects sialidase activity, an enzyme produced by BV-associated bacteria such as Gardnerella vaginalis, Bacteroides spp., Prevotella spp., and Mobiluncus spp. In the test procedure, a vaginal fluid sample is placed in the test vessel which contains a chromogenic substrate for sialidase. After incubation, a developer solution is added, and If the sample contained a high level of sialidase, a blue or green color is seen. Samples containing no sialidase, or low levels of this enzyme, will generate a yellow color in the reaction. The BV test has high specificity and sensitivity. The BVBlue test enables rapid detection of BV in a physician's office, and can thereby provide advantages over the Amsel methods and other methods requiring extensive laboratory testing. Advantage of BVBLUE Test Kit Compared to other diagnostic test methods for BV such as Amsel criteria, Nugent Gram-stain scoring system, Affirm�® Microbial Identification Test, BVBLUE Test Kit has following advantage: 1, BVBLUE Test is currently the only test method approved by the FDA for testing Bacterial Vaginosis(BV). 2, BVBLUE Test just take 10 minutes to 15 minutes to get the result. 3, High purity sialidase substrate with high specificity can reduce the occurrence of false positive. 4. Comparing with the gold standard, the coincidence rate is high, the relative sensitivity is 93%, and the specificity is 95%. 5. Easy to operate, do not need equipment. 6. The specimen does not need to pretreat.
REF - L031-11815 Format - Cassette 3.5 mm Finished or Bulk - Finished in kit box Kit Size - 25 Carton Size - 800 pouches (32 kits) Carton Size (mm) - 530*445*410 Gross weight per carton (kg) - 13.2 quantity per carton - 800 Carton # - 1,250.00 Order quantity (pcs) - 1,000,000 Order gross weight (kg) - 16500 Order total volume (cbm) - 120.873
REF - L031-125V5 Format - Cassette 3.5 mm Finished or Bulk - Finished in kit box Kit Size - 5 Carton Size - 600 pouches (120kits) Carton Size (mm) - 520*395*440 Gross weight per carton (kg) - 10.55 quantity per carton - 600 Carton # - 1,666.67 Order quantity (pcs) - 1,000,000 Order gross weight (kg) - 17583 Order total volume (cbm) - 150.627
Covid Test from PXY cooperation with public cooperation, CE certificated. Our products are designated by many European governments. PXY has invested in professional COVID test manufacturers, the COVID test kit we provide, SARS-CoV-2 Antigen Rapid Test Kit, the method used is Colloidal Gold Immunochromatography. Our rapid COVID test kit packed in Card-like format has the following advantage: * Non-invasive. Swabbed specimens from the nasopharynx or oropharyngeal; * Rapid, ONLY in 15 minutes can get the result; * Simple Operation. No more devices required; * High accuracy and stability. Gold-labeled SARS-CoV-2 N protein monoclonal antibodies immobilized on the test area, with corresponding antibodies in the quality control area;
Product Description The iHealth COVID-19 Antigen Rapid Test is a lateral flow assay intended for the qualitative detection of nucleocapsid protein antigen from SARS-CoV-2. This test is authorized for non-prescription home use with self-collected anterior nasal (nares) swab samples from individuals aged 15 years or older with symptoms of COVID-19 within the first 7 days of symptom onset. This test is also authorized for non-prescription home use with adult-collected nasal swab samples from individuals aged 2 years or older with symptoms of COVID-19 within the first 7 days of symptom onset. This test is also authorized for non-prescription home use with self-collected anterior nasal (nares) swab samples from individuals aged 15 years or older, or adult collected anterior nasal swab samples from individuals aged 2 years or older, with or without symptoms or other epidemiological reasons to suspect COVID-19 when tested twice over three days with at least 24 hours (and no more than 48 hours) between tests. Pricing: $5.5 PER KIT OF 2 TESTS MOQ: 1 pallet: 84 cartons / 7560 boxes / 15,120 tests Maximum Quantity: Please inquire Shipping Information: 90 Packs per Carton, 2 Tests per Pack 1 pallet: 84 cartons / 7560 boxes 1100 lbs Per pallet Single Package Dimensions (LxWxH) 6.18 x 3.19 x 0.71 Inches Single Package Weight (lb) 0.13 Carton Dimensions (LxWxH) 13.1 x 11.8 x 10.8 Inches Carton Weight (lb) 12.8
20 TESTS/KIT 30 TESTS/KIT SENSITIVITY:95.83% SPECIFICITY:98.5%
Contains : 1 test cassete, 1 Lysis Buffer, 1 Sterile Swab, 1 Bio-safety bag, 1 instruction of use
The One Step Microalbumin Test Cassette (Urine) is intended for the qualitative detection of human serum albumin (HSA) in human urine specimens, as a screening test and as an aid in the diagnosis of renal dysfunction. This assay provides only a preliminary result. Clinical expertise and professional judgment should be sought to further evaluate the result of the test.
The IgM rapid Test Cassette (Serum/Plasma) is a lateral flow chromatographic immunoassay for the qualitative detection of IgM antibodies in human serum to Rheumatoid Factor (RF) antigen. It is intended to be used as ascreening test and as an aid in the diagnosis of rheumatoid arthritis. Any reactive specimen with the RF IgM Rapid Test Cassette must be confirmed with alternative testing method(s) and clinical findings.
Monkeypox IgG/IgM Rapid Test Cassette (Whole Blood/Serum/Plasma) is a solid phase immunochromatographic assay for the rapid, qualitative and differential detection of IgG and IgM antibodies to monkeypox virus in human whole blood, serum or plasma. This test provides only a preliminary test result.
