Quick Sars Test Results

Description: ELISA based test for quantitative detection of HDV-IgG hepatitis D IgG

Description: ELISA based test for quantitative detection of HPV (Human Papilloma Virus Antibody IgG)

Description: For the qualitative determination of IgG class antibodies against SARS Coronavirus in Human serum or plasma. It is intended for diagnosing and monitoring of patients related to infection by SARS Coronavirus.

Description: ELISA based test for quantitative detection of MV (Measles Virus Antibody IgG)

Description: ELISA based test for quantitative detection of TB (Mycobacterium Tuberculosis Antibody IgG)

Description: For rapid, direct determination of albumin concentrations in biological samples (e.g. serum, plasma, urine, etc). Key Features: Fast and sensitive. Use of 10 µL sample. Semi-quantitative measurement between 0-0.4 g/dL or 0-60 µM (undiluted) Albumin. Convenient. No sophisticated laboratory equipment required. Sample treatment and assay can be performed in under 15 minutes. Method: Visual. Samples: Serum, plasma, urine, etc. Species: All. Procedure: Assay takes approximately 15 min. Kit size: 10 tests.

Description: For rapid, direct determination of glucose concentrations in food and beverage samples as well as biological (e.g. urine, blood, etc.) samples. Key Features: Fast and sensitive. Use of 20 or 100 µL sample. Semi-quantitative measurement between 0-720 mg/L (undiluted) Glucose. Convenient. No expensive lab equipment needed. Sample treatment and assay can be performed in under 15 minutes. Method: Visual. Samples: Wine, beer, juice, etc. Species: All. Procedure: Assay takes approximately 15 min. Kit size: 10 tests.

Description: For rapid, direct determination of oxalate concentrations in biological samples. For Research Use Only (not for medical decisions). Key Features: Fast and sensitive. Use of 10 µL sample. Semi-quantitative measurement between 0-1.5 mg/dL or 0-170 µM (undiluted) Oxalate. Convenient. No expensive plate or cuvette readers required. Sample treatment and assay can be performed in under 10 minutes. Method: Visual. Samples: Serum, plasma, urine, fruits or vegetables, etc. Species: All. Procedure: Assay takes approximately 10 min. Kit size: 10 tests.

Description: For rapid, direct determination of pyruvate concentrations in food and beverage samples as well as biological samples. Key Features: Fast and sensitive. Use of 50, 100, or 400 µL sample. Semi-quantitative measurement between 0-131 mg/L (undiluted) Pyruvate. Convenient. No expensive plate or cuvette readers needed. Sample treatment and assay can be performed in under 15 minutes. Method: Visual. Samples: Wine, beer, biological samples, etc. Species: All. Procedure: Assay takes approximately 15 min. Kit size: 10 tests.

Description: For rapid, direct determination of Histamine concentrations in fish, wine, and other samples. Key Features: Fast and sensitive. Use of 500 mg of fish or 250 µL of sample. Semi-quantitative measurement between 0-200 ppm (undiluted) Histamine. Convenient. No expensive lab equipment needed. Sample treatment and assay can be performed in under 15 minutes. Method: Visual. Samples: Seafood, wine, juice, milk and dairy products, etc. Species: All. Procedure: Assay takes approximately 15 min. Kit size: 10 tests.

Description: For rapid, direct determination of urea concentrations in food and beverage samples as well as biological samples. Key Features: Fast and sensitive. Use of 20 µL sample. Semi-quantitative measurement between 0-1500 mg/L (undiluted) urea. Convenient. No expensive plate or cuvette readers needed. Sample treatment and assay can be performed in under 15 minutes. Method: Visual. Samples: Serum, plasma, urine, etc. Species: All. Procedure: Assay takes approximately 15 min. Kit size: 10 tests.

Description: For rapid, direct determination of malic acid concentrations in food and beverage samples as well as biological samples. Key Features: Fast and sensitive. Use of 20 or 100 µL sample. Semi-quantitative measurement between 0-500 mg/L (undiluted) malic acid. Convenient. No expensive lab equipment needed. Sample treatment and assay can be performed in under 15 minutes. Method: Visual. Samples: Wine, beer, milk, etc. Species: All. Procedure: Assay takes approximately 15 min. Kit size: 10 tests.

Description: For rapid, direct determination of L-Glutamate (monosodium glutamate or MSG) concentrations in food and beverage samples as well as biological samples. Key Features: Fast and sensitive. Use of 20 or 100 µL sample. Semi-quantitative measurement between 0-300 mg/L (undiluted) L-Glutamate. Convenient. No extra equipment required. Sample treatment and assay can be performed in under 15 minutes. Method: Visual. Samples: Soups, sauces, milk, etc. Species: All. Procedure: Assay takes approximately 15 min. Kit size: 10 tests.

Description: For rapid, direct determination of D-lactic acid concentrations in food and beverage samples as well as biological samples. Key Features: Fast and sensitive. Use of 20 or 100 µL sample. Semi-quantitative measurement between 0-180 mg/L (undiluted) D-lactic acid. Convenient. No expensive lab equipment needed. Sample treatment and assay can be performed in under 15 minutes. Method: Visual. Samples: Wine, beer, milk, etc. Species: All. Procedure: Assay takes approximately 15 min. Kit size: 10 tests.

Description: For rapid, direct determination of L-lactic acid concentrations in food and beverage samples as well as biological samples. Semi-quantitative measurement between 0-360 mg/L (undiluted) L-lactic acid. Convenient. No expensive lab equipment needed. Sample treatment and assay can be performed in under 15 minutes. Method: Visual. Samples: Wine, beer, milk, etc. Species: All. Procedure: Assay takes approximately 15 min. Kit size: 10 tests.

Description: This kit adopts the sandwich method and the technical principle of colloidal gold immunochromatography to qualitative determine the SARS-CoV-2 antigen. During the test, the sample is dropped into the sample well, and chromatography is performed under the capillary effect. The SARS-CoV-2 antigen in the sample combined with the colloidal goldlabeled SARS-CoV-2 monoclonal antibody I, and then spread to the test area. It is captured by another coated antibody (SARS-CoV-2 monoclonal antibody II), to form a complex and gather in the test area (T line). The quality control area is coated with the goat antimouse antibody, and the colloidal gold-labeled antibody is captured to form a complex and aggregate in the quality control area (C line). If the C line does not show color, it indicates that the result is invalid, and this sample needs to be tested again.

Description: This product is used for in vitro qualitative detection of SARS-CoV-2 antigen in human oropharyngeal swabs, nasal swabs and nasopharyngeal swabs. It is helpful as an aid in the screening of early mild, asymptomatic, or acute patients for identification of SARS-CoV-2 infection.

Description: The SARS-CoV-2 Rapid Antigen Test is a lateral fl ow rapid chromatographic immunoassay for the qualitative detection of nucleocapsid antigen to SARS-CoV-2 present in human nasal samples. This test is intended for use as an aid in detection of SARS-CoV-2 infection in individuals suspected of COVID-19 with clinical symptoms onset within 5 days. Results are for the identification of SARS-CoV-2 nucleocapsid antigen. Antigen is generally detectable in human nasal swab samples during the acute phase of infection. Positive results indicate the presence of viral antigens, but clinical correlation with patient history and other diagnostic information is necessary to determine infection status. Positive results do not rule out bacterial infection or co- infection with other viruses. The agent detected may not be the definite cause of disease. Negative results should be treated as presumptive, and do not rule out SARS-CoV-2 infection and should not be used as the sole basis for treatment or patient management decisions, including infection control decisions. Negative results should be considered in the context of a patient’s recent exposures, history and the presence of clinical signs and symptoms consistent with COVID-19, and confirmed with a molecular assay, if necessary, for patient management. The SARS-CoV-2 Rapid Antigen Test is intended for use in laboratory or POC settings by healthcare professionals, or self-collection under the supervision of a healthcare worke