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
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.
Our newly-developed monkeypox antigen rapid test kit by our R &D department is CE certificate
COV19/ FluA/ FluB Antigen Combo Rapid Test Kit (Colloidal Gold Method) Packing Specifications The kit is an in vitro immunochromatographic assay for the qualitative detection of Cov19, Influenza A and Influenza B virus antigens in human nasopharyngeal, oropharyngeal swab, and salvia samples. Cov19 is an acute respiratory infectious disease that humans are easily infected with. According to current epidemiological investigations, the incubation period is 1 to 14 days, mostly 3 to 7 days. The main symptoms are: fever, fatigue, dry cough, in a few cases can appear nasal congestion, sore throat, myalgia and diarrhea. Influenza, often called the flu is caused by the influenza virus. It is a highly contagious viral infection of the respiratory tract that can be spread by coughing or sneezing. Influenza outbreaks occur every fall and winter. There are influenza A, B and C viruses. Influenza A viruses are more prevalent than influenza B and Cand causes more severe illness. Cov19 infection and Influenza virus infection have similar symptoms, such as fever, cough, etc. This kit can simultaneously detect the antigens of the three viruses and provides an easy workflow, short turnaround time, and rapid diagnosis of Cov19, Influenza A and influenza B virus infections using nasopharyngeal, oropharyngeal swab or salvia samples. The kit is an immunochromatographic assay,based on double antibody sandwich method to detect Cov19 and Influenza A/B virus antigens. This method does not require expensive medical instruments and consumables. After adding the extracted specimen to the sample well on the test cassette, Cov19, Influenza A/B virus antigens in the sample will interact with the colloidal gold-labeled anti-CoV-2 and Influenza A/B antibodies on the conjugate pads. Then the conjugate pad will release re-solubilized conjugate onto the nitrocellulose membrane. The nitrocellulose membrane (NC membrane) diffuses it forward. As the sample moves along the device binding reagents situated on the nitrocellulose membrane bind to the target at the test line. If the sample contains a COV19 antigen, it will bind to the colloidal goldanti-CoV-2 Np monoclonal antibody, diffuse forward, and then react with the anti-CoV-2 Np monoclonal antibody immobilized on the NC membrane detection line (COV19 Test line). Similarly, if the specimen contains Influenza A/Influenza B antigens, the antigens will react with antibody-coated particles, the conjugate migrate laterally forward, and cause a colored lines (A, B linesrespectively).
Product Name Neutrophil Gelatinase-Associated Lipid Carrier Protein (NGAL)Test Kit (Immunofluorescence Chromatography) Purpose To detect the NGAL in human plasma/serum/whole blood in vitro quantitatively.For Professional Use only. Principles of Detection The NGAL Test is a fluorescent lateral flow immunoassay. The test consists of: 1) a conjugate pad containing NGAL antibody conjugated with fluorescent microspheres and a control antibody (goat anti-chicken IgY antibody) conjugated with fluorescence microspheres, 2) a nitrocellulose membrane strip containing a test line (T line) and a control line (C line). The T line is pre-coated with anotherNGAL antibody, and the C line is pre-coated with a control line antibody (chicken IgY antibody). NGAL concentration in specimen is positively correlated with the fluorescent density of the microspheres, after the measure and calculation of the quantitative fluorescence immunoassay analyzer, then the analyzer would calculate the concentration of NGAL according to the preset calibration curve in the machine and display the result, detection unit is ng/mL. C line should appear in any cases, which indicates the reaction system is effective. Reference range Reference value: 37-180ng/mL; The reference value is verified by referring to similar products on the market. Due to ethnic and regional differences, each laboratory can establish its own reference interval according to the actual situation.
Application For the detection of eye / nose / stool / rectal secretions or blood pathogens The most convenient and rapid diagnostic tool for canine distemper / canine parvovirus Feature High accuracy for monoclonal antibody capture target Good tools for antibody detection and disease diagnosis Easiest reagent to operate the test Quickly present the result Low testing cost Technical specification Technical Parameters for Rapid Canine Distemper Ag Test Kit Principle: colloidal gold lateral chromatography Test samples: eye / nasal secretions or blood Interpretation of time: 10-15 minutes Sensitivity: 98% Specificity: 97% Shelf life: 24 months Storage temperature: 4-28 Packing: 10 Test/ box Technical Parameters for Rapid Feline Parvovirus Ag Test Kit Principle: colloidal gold lateral chromatography Test samples: rectal / feces Interpretation of time: 10-15 minutes Sensitivity: 99% Specificity: 97% Shelf life: 24 months Storage temperature: 2-30 Packing: 10 Test / box
Antigen Detection Rapid Lateral Flow Test (latex bead-based) AIVD Biotech's Ag test is a lateral flow immunoassay intended for the qualitative detection of nucleocapsid protein (NP) antigen in direct nasal swabs from individuals suspected of infection. Description: This kit utilizes the principle of latex bead immunochromatography to qualitatively detect the Np antigen in human nasal swabs. Lateral flow immunochromatographic assay provides an easy workflow, short turnaround time, and rapid diagnosis of suspected patients. The test contains latex bead conjugate pad and a membrane strip pre-coated with antibodies specific to the antigen on the test lines (T). If novel NP antigen is present in the specimen, a visible band appears on the test lines (T) as antibody-antigen-antibody latex bead complex forms. The control line (C) is used for procedural control and should always appear if the test is performed correctly. This method does not require expensive medical instruments and consumables. Just take the specimen and add it to the sample well. If sample contains the antigen, it will interact with the latex bead-labeled anti- NP antibodies on the conjugate pad. Required components 1. A foil pouch with a desiccant and a single use test card, 1 piece 3. Sterile swab, 1 piece 3. Extraction buffer tube (1 ml), 1 tube. 4. Instructions for use, 1 piece. Storage conditions 1. Store at the dark place, room temperature 18~28C with low humidity. 2. After opening the foil bag, please use the test cassette within 30 mins. 3. Expiration period 12 month Specimen requirements: 1. Nasopharyngeal swab specimen. 2.Specimen should be tested as soon as possible upon collection. If the sample has to be stored, store the swab sample at room temperature for up to 1 hour or 2~8C for up to 4 hours prior to testing. Performance Characteristics A total of 365 samples from suspected patients were tested by the RT-qPCR test. Testing results are shown in the following table: PCR AIVD Antigen Rapid Test Kit Positive Negative Positive 59 8 Negative 6 292 Total: 65 300 Sensitivity: 90.7%; Specificity: 97.3%.
My company Marco&Micro test,based in china ,founded in 2010, is a leading manufacture of IVD manufacturers in China. We have successfully developed more than 200 detection test kits so far, like COVID-19 ,Tumor, Gene Test,Reproductive HIV, TP, ZIKA, Dengue, Malaria etc. Of course, OEM or ODM service are also available from us, also, worldwide distributors are very welcomed to discuss for win-win collaboration. whatsup:+8613814857410 sofia.zhang@hongweitest.com Our hot prevailing Covid19 product lines are: Antigen rapid test kits: saliva pen lollipop type rapid test kit Ag rapid test kit 3combo of covid19 and FluA&B rapid test Neutralizing Antibody Rapid Test Fast PCR test solution:sample release agent and Loyphilized pcr kit room temperature stock and delivery. extractor free, takes only 5mints to get RNA sample. All in one freeze-dried pcr kit ,decrease pipetting steps and lower contamination risk.
My company Marco&Micro test,based in china ,founded in 2010, is a leading manufacture of IVD manufacturers in China. We have successfully developed more than 200 detection test kits so far, like COVID-19 ,Tumor, Gene Test,Reproductive HIV, TP, ZIKA, Dengue, Malaria etc. Of course, OEM or ODM service are also available from us, also, worldwide distributors are very welcomed to discuss for win-win collaboration. whatsup:+8613814857410 sofia.zhang@hongweitest.com Our hot prevailing Covid19 product lines are: Antigen rapid test kits: saliva pen lollipop type rapid test kit Ag rapid test kit 3combo of covid19 and FluA&B rapid test Neutralizing Antibody Rapid Test Fast PCR test solution:sample release agent and Loyphilized pcr kit room temperature stock and delivery. extractor free, takes only 5mints to get RNA sample. All in one freeze-dried pcr kit ,decrease pipetting steps and lower contamination risk.
My company Marco&Micro test,based in china ,founded in 2010, is a leading manufacture of IVD manufacturers in China. We have successfully developed more than 200 detection test kits so far, like COVID-19 ,Tumor, Gene Test,Reproductive�¯�¼?HIV, TP, ZIKA, Dengue, Malaria etc. Of course, OEM or ODM service are also available from us, also, worldwide distributors are very welcomed to discuss for win-win collaboration. My whatsup:+8613814857410 sofia.zhang@hongweitest.com Our hot prevailing Covid19 product lines are: 1)Antigen rapid test kits: 2)saliva pen lollipop type rapid test kit 3)Ag rapid test kit 4)3combo of covid19 and FluA&B rapid test 5)Neutralizing Antibody Rapid Test Fast PCR test solution:sample release agent and Loyphilized pcr kit: 1)extractor-free sample releasing agent 2)3combo pcr liquid/loyphilized test of covid19 an 3) pcr pcr liquid/loyphilized test with target genes Orflab&N
Our products are directly from factories, Boson, H-Guard, Flow flex, etc.
We can provide 1.000.000 test kits (2 test pack) every week in Los Angeles. As of today (3/2/2022) we have stock available in LA, there are 850.000 tests left. The price is 8.8 USD. New stock arrives every Monday/Tuesday. If you would need a bigger qty, we can arrange direct delivery from CN on DDP terms. Operation procedure: 1) We sign the contract and issue an invoice for the buyer. 2) Buyer arrives at the warehouse (in LA) to inspect goods. 3) Buyer arrange payment and pick up product directly from the warehouse. If you are an intermediary, we can sign a commission contract. Contact details:
Multi-drug One Step 2-15 Urine Drug Test Cup (MOP, MET, KET, AMP, BAR, BUP, BZO, COC, COT, MDMA, THC, MTD, OPI, PCP, TCA)
A rapid, one step test for the qualitative detection of Amphetamines in human urine. For healthcare professionals including professionals at point of care sites For professional in vitro diagnostic use only. A drug-free urine pool was spiked with Amphetamine at the following concentrations: 0 ng/mL, 500 ng/mL, 750 ng/mL, 1,000 ng/mL, 1,250 ng/mL and 1,500 ng/mL. The result demonstrates >99% accuracy at 50% above and 50% below the cut-off concentration. The data are summarized below: AMP Concentration (ng/mL)Percent of CutoffnVisual Result NegativePositive 00%30300 500-50%30300 750-25%30237 1,000Cutoff30921 1,250+25%30129 1,500+50%30030
Dear Sir/Madam If you are someone who appreciated high quality,high cost-effective rapid test cassette, then I've got some helpful information with you. I am the sales manager of Avioq Bio-tech Co., Ltd. We are mainly engaged in the R&D, production, sales and services of in-vitro diagnose (IVD) reagents in biomedical field. We help many start-ups and well-known brands grow and expand business in their market.Let me know if you are interested on taking a look at our lastest catalogue. Email:
The kit is intended for the in vitro qualitative determination of Novel Coronavirus (2019-nCoV) IgG/IgM antibody in human serum, plasma or whole blood. Testing is limited to supplementary detection indicator for suspected nucleic acid negative results or in conjunction with nucleic acid detection in the diagnosis of suspected cases. It should not be used as the basis for diagnosis and exclusion of Novel Coronavirus Pneumonia.
