Indoleacetic acid oxidase Assay Kit
This kit is used to qualitatively detect the novel coronaviruses (SARS-CoV-2) antigen in human nasal throat swabs, oral throat swabs, posterior oropharyngeal saliva, sputum and stool samples.
Cat. No. - PB102-01 Packing - 1kit+C5:C53 Price - 20580
SARS-CoV-2 Antigen Assay Kit (Colloidal Gold Method) This kit is used for the qualitative detection of specific antigen against novel coronavirus (SARS-CoV-2) in human specimens (Nasal swabs, oropharyngeal swabs, lower respiratory tract samples). Principle This kit adopts colloidal gold-based flow-through, lateral-flow immunoassay and capture method to detect specific antigen against coronavirus in human specimens(Nasal swabs, oropharyngeal swabs.
The second brand in the world health organization test list Colloidal Gold Method This kit applies the principle lateral flow chromatographic immunoassay and uses capture method to detect specific IgM and IgG antibodies against novel coronavirus in human specimens (serum, plasma and venous whole blood).
Cat No : 09N77-095. The Abbott RealTime SARS-C0V-2 assay is an Emergency Use Authorization (EUA) test authorized by the U.S. FDA for use by authorized laboratories, using real-time (RT) polymerase chain reaction (PCR) technology for the qualitative detection of nucleic acids from the SARS-CoV-2 virus and diagnosis of SARS-CoV-2 virus infection from individuals meeting CDC clinical and/or epidemiological testing criteria.
Product Name: Surplex(R)-COVID-19 IgM/IgG Rapid test Product Description: Surplex(R)-COVID-19 IgM/IgG Rapid test is a serology test intended for the qualitative detection of IgM and IgG antibodies of the novel coronavirus (the SARS-COV-2 virus) in human serum, plasma or whole blood. It is CE marked and approved in Brazil (ANVISA approved). We are motivated to aggressively price our product and ready to send 20 tests (one box) to qualified buyers for evaluation, free of charge. Price of product: FOB USD $1.50 - $2.50 per test, volume dependent. Product origin : China. Key Specifications/Special Features : - Competitively priced and ready to ship in volume. - Currently shipping in volume to Brazil. - Highly accurate and specific - performance independently confirmed. - Results ready in 15 minutes. - Harmonization System (HS) Code: 382200. - We provide a full support during regulatory application. Minimum Order Size and Packaging details: MOQ: Flexible. Box of 20 or 50 test kits. Storage: 2-30C. Shelf Life: 10 months.
CareStart Covid-19 Antigen Test Kits-Rapid Test Kits Worldwide Shipping Lateral flow assay Detect SARS-CoV-2 nucleocapsid protein antigen Rapid results within 10-15 minutes Intended at POC setting (i.e., inpatient care settings) by medical professionals operating under a CLIA Certificate of Waiver, Certificate of Compliance, or Certificate of Accreditation For use under the Emergency Use Authorization (EUA) only For in vitro diagnostic use only For prescription use only For use with direct anterior nasal and nasopharyngeal swab specimens Clinical Performance 93.75% PPAa and 99.32% NPAb when used with a nasopharyngeal swab 87.18% PPAa and 100% NPAb when used with anterior nasal swab aPPA: Positive Percent Agreement, bNPA: Negative Percent Agreement.
Assay+ COVID-19 antigen rapid test is authorized with CE marker, the sensitivity is 90%, the specificity is 98.5%. Assay+ Covid 19 antigen rapid test is a lateral flow immunochromatographic assay intended for the qualitative detection of the nucleocapsid protein of SARS-CoV-2 from the nasopharyngeal swab from the suspected COVID-19 patients within five days of symptom onset. This test is an aid to differentiate Covid 19 virus infection from other respiratory tract infection caused by coronavirus 229E, NL63, OC43 and HKU1, or severe acute respiratory syndrome caused by SARS-CoV and MERS-CoV. The test should be performed in moderate, high or waived complexity tests. This test can also perform for the Point of Care (POC) purpose.
Global distributor: covid 19 igm/igg rapid test, covid 19 real time pcr assay, alk break apart fish probe kit, and warfarin genotyping assay.Global distributor
One Step Fecal Occult Blood (FOB) Rapid Test Cassette (Feces) Cat. No.: RH0301T INTENDED USE The One-Step Fecal Occult Blood (FOB) Diagnostic Kit is a qualitative detection of human occult blood in feces forself-testing. PRINCIPLE The One-Step Fecal Occult Blood (FOB) Diagnostic Kit is an immunochromatographic sandwich method, which employ two specific monoclonal antibodies to selectively identify hemoglobin in test samples. The result is very specific, and easier to interpret than those of guaiac-based test. The sensitivity is very high with the ability to detect 200ng/ml hemoglobin in feces. In addition, the accuracy of the test is not affected by interfering substances, and dietary restriction is not necessary. STORAGE The kits should be stored at temperature 4-30�°C, the sealed pouch for the duration of the shelf life (24 months). Do the test in 1 hour after open the pouch. WARNING AND PRECAUTIONS 1. For in vitro diagnostic use only. 2. Do not use kit beyond the expiration date. 3. Patient specimens may contain infectious agents and should be handled as though capable of transmitting disease. Wear disposable gloves throughout the specimen collection and assay procedures. 4. The test device should not be reused. REAGENTS AND MATERIALS PROVIDED 1. One pouched cassette with desiccant. 2. One operating Instruction MATERIALS REQUIRED BUT NOT PROVIDED 1. Clock or Timer SPECIMEN COLLECTION AND PREPARATION 1. Collect stool sample by using the sample collection device provided. 2. Unscrew the top of the sample collection device, take out the sample collection stick, and collect the sample by dipping the stick into 3 different places of the stool sample. 3. Put the sample collection stick back in the sample collection device and screw together tightly. 4. If the sample cannot be tested on the day of collection, store the stool sample at 4C. Bring the specimen to room temperature before testing. ASSAY PROCEDURE 1. Remove the test device from foil pouch by tearing along the notch. 2. Specimen collection. Please see also SAMPLE COLLECTION AND PREPARATION 3. Shake the sample collection device several times. 4. Holding the sample collection device upright, carefully unscrew the tip of collection device. 5. Squeeze 2-3 drops of the sample solution on the test sample pad. 6. Read the test results in 5 minutes. INTERPRETATION OF RESULTS Negative: Only one colored band appears on the control region (C). No colored band in the test region (T). Positive: In addition to the control band (C), a distinct colored band also appears in the test region (T). Invalid: If no bands appear, or a test band appears without a control band, the test should be repeated using a new test device.
The GENEDIA W COVID-19 Ag is an in vitro diagnostic single-use test and qualitative immunoassay to detect SARS-CoV-2 antigen in nasopharyngeal swab and sputum specimen from human. This assay is designed for professional personnel in laboratory and at point-of-care as an aid in screening patients suspected of being infected and asymptomatic patients. Allow wider testing with fast test time (10 minutes) Clinically proven data of asymptomatic patients available Separately packed extraction solution to minimize the possibility of contamination No additional instruments required Package Unit : 20 Tests/Kit Expiration Date : 24 Months (while sealed in the original aluminum foil pouch) GCMS manufactures COVID-19 antigen test kit, the GENEDIA W COVID-19 Ag which is listed on the EU common list, also with GMP and ISO certifications. GENEDIA W COVID-19 Ag is unaffected based on the in-silicon analysis of the mutations in the nucleocapsid (N gene) of Omicron viruses. Letter of statement is available upon your request. To get over COVID-19 pandemic, especially the recent Omicron breakout, currently we are doing big promotions for three kinds of COVID-19 Ag kit. All are in stock and available right away. 1. Nasopharyngeal 2. Nasal 3. Saliva The price is negotiable according to the amount of your order and shipping term. No MOQ is required but we prefer 1 pallet with 9,600 tests. (20 tests/kit, 30 kits/carton, 16 cartons/pallet)
Method:immunoturbidimetric two point end assay Form:liquid
Method:immunoturbidimetric two point end assay Form:liquid
Method:immunoturbidimetric two point end assay Form:liquid Bulk
Method:immunoturbidimetric two point end assay Form:liquid
Method:immunoturbidimetric two point end assay Form:liquid Bulk
INTENDED USE The Helicobacter-Pylori antigen rapid test kit (stool) is a rapid visual immunoassay for the qualitative detection of helicobacter pylori antigen in human stool specimens. This kit is used as an aid in the diagnosis of H. pylori infection. INTRODUCTION Helicobacter pylori (also known as Campylobacter pylori) as a spiral-shaped gram negative bacteria which infects the gastric mucosa. H. pylori to causes several gastro-enteric diseases such as non-ulcerous dyspepsia, gastric and duodenal ulcer, active gastritis and can even increase the risk of stomach adenocarcinoma. The epidemiologic study shows that more than 50% of the world's population is infected by H. pylori strains. Infection is more prevalent in developing countries. The lowest infection rate is 20%, and the highest infection rate can be 90% in developing countries. H. pylori strains is the major reason to cause chronic gastritis and gastric ulcers, 80%-90% chronic gastritis patients and 95%-100% gastric ulcers patients are infected by H. pylori strains. So the detection and treatment of H. pylori strains infection is very important. At present several invasive and non-invasive approaches are available to detect this infection state. Invasive methodologies require endoscopy of the gastric mucosa with histologic, cultural and urease investigation, which are expensive and require some time for diagnosis. Alternatively, non-invasive methods are available such as breath tests, which are extremely complicated and not highly selective, and classical ELISA and immunoblot assays. This Kit belongs to non-invasive approach.
Catalase(CAT) Assay Kit
Superoxide dismutase SOD.
