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  • Novel Coronavirus (2019-nCoV) Antigen Testing Kit (Immunochromatography)
    Package specification Specification REF 1 Test /Box NRM-FT-154-1 5 Tests /Box NRM-FT-154-5 10 Tests /Box NRM-FT-154-10 25 Tests /Box NRM-FT-154-25 Subject Performance Parameter Product name Antigen Testing Kit Method colloidal gold Test Time 15 Minutes/Time Brand Name NORMAN Specimen NP/Throat Swab. Nasal Aspiration, Saliva Certification CE & ISO13485 approved, BFARM and PEi list Service OEM.ODM Test principle This kit is tested by immune chromatography. The sample will be under the capillary action to move forward along the test strip. If the sample contains SARS-CoV-2 antigen, the antigen nucleocapsid protein will be combined with a monoclonal antibody-coated particles. The immune complex will be captured with SARS-CoV-2 monoclonal antibody fixed on the membrane. If the test line shows colour, means positive; if the test line does not show any colour, means negative. The test card also contains a quality control line, whether the detection line is displayed or not, there will be coloured. If contains SARS-CoV-2antigen, the test line will be displayed a coloured line. Presence of this colored line indicates a positive result, while its absence indicates a negative result. To serve as a procedural control, a colored line will always appear at the control line region indicating that proper volume of specimen has been added and membrane wicking has occurred. If the control line does not appear, indicating the test result ismeaningless, this sample must be re-tested. Storage Sealed: The kit must be stored at 4-30℃, valid for 24 months. Keep dry. Opened: The test cassette must be used within 1 hour once its foil pouch is opened. Test procedure 1. Wash and dry your hand. Open the package and take out the test cassette. 2. Place the extraction tube on the tube holder of the box. The extract reagent R1 bottle is pressed vertically downward to allow the solution to drip freely into the extractor tube without touching the edge of the tube. Add 8 drops of Extract Reagent R1 to the extraction tube. 3. Put the swab specimen into the extraction tube, rotate the swab for about 15 seconds, and press the swab head against the tube wall to release the antigen in the swab. Squeeze the swab over the head to remove the swab so as to remove as much liquid as possible from the swab. Dispose of swabs into disposal bag. 4. Install the dripper on the extraction tube, put 2 drops into the sample hole of the test cassette, and start the timer. 5. Read the results in 20-30 minutes. Reading results after 30 minutes may be invalid. DE IFU - Novel Coronavirus (2019-nCoV) Antigen Testing Kit (Immunochromatography)-Self-testing

    Hot Tags : covid-19 self test kit covid-19 antigen test covid antigen test kit covid-19 home test kits antigen rapid test kit rapid test kit rapid antigen test kit

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  • 25OH Vitamin D test kit
    25OH Vitamin D total Kit (Immunofluorescence) is mainly for the in vitro quantitative measurement of 25-hydroxyvitamin D2 and D3 (25OH-D2 and 25OH-D3) in serum and plasma .

    Hot Tags : at home vitamin D test kit 25OH Vitamin D rapid test kit Vitamin D test kit Vitamin D blood test

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  • T4 Test Kit
    【Product Name】 Thyroxine (T4) Test Kit (Immunofluorescence) 【Package specifications】 25 Tests /Box 【Intended use】 This Thyroxine (T4) Test Kit is manly used for in vitro quantitative determination of total thyroxine (TT4) content in human serum. Thyroxine (T4) is a hormone synthesized and secreted by the thyroid gland, which plays an important role in the regulation mechanism. Thyroxine (T4) is combined with thyroglobulin and stored in the remnant cavity of thyroid follicles, secreted and released under the regulation of thyroid stimulating hormone (TSH), and participates in the circulation [1] . More than 99% of thyroxine (T4) in the serum is in the form of binding to thyroxine-binding globulin (TBG), albumin and other proteins.The concentration of transport protein in the serum is easily affected by exogenous and endogenous effects. Ignoring changes in the concentration of bound protein (such as pregnancy, taking estrogen or suffering from nephrotic syndrome, etc.) will lead to errors in the detection of thyroid metabolism. Results [2], [3]. Diseases in any part of the thyroid-pituitary hypothalamic system can cause excessive (hyperthyroidism) or insufficient (hypothyroidism) secretion of T4 or T3, Therefore, the determination of total thyroxine (T4) can be used for the diagnosis of primary and secondary hypothyroidism and the monitoring of thyroid stimulating hormone (TSH) suppression therapy [4] . At present, the commonly used detection methods in laboratories include enzyme-linked immunoassay, immunofluorescence, colloidal gold and chemiluminescence. 【Accessories required but not provided】 ♢ Immunofluorescence quantitative analyzer ♢ Reagent strip incubator 【Storage and stability】 Sealed: The kit must be stored at 4-30℃, valid for 24 months. The sample diluent must be stored at 4-30℃, valid for 24 months. Opened: The cartridge must be used within 1 hour once its foil pouch is opened. The sample diluent is valid for 1 month once it is opened.

    Hot Tags : thyroid hormone test kit t4 test kit diagnostic test get a rapid test poc diagnosis poc point of care

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  • Hemoglobin A1c (HbA1c) Kit (Immunofluorescence)
    Hemoglobin A1c (HbA1c) Kit (Immunofluorescence) is mainly for the in vitro quantitative determination of Hemoglobin A1c (HbA1c) content in human blood.

    Hot Tags : Hemoglobin ELISA Kit At Home HbA1c Test Kit A1C Test Kit HbA1c Reagent Kit hemoglobin A1c test

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  • cTnI CK-MB MYO Test Kit
    【Product Name】 Myocardial Infarction (MI) 3-in-1(cTnI/CK-MB/MYO) Test Kit (Immunofluorescence) 【Package specifications】 25 Tests /Box 【Intended use】 Myocardial Infarction (MI) 3-in-1 Test Kit (Immunofluorescence) is mainly for the in vitro quantitative determination of cardiac Troponin I (cTnI), Creatine Kinase-MB (CK-MB), Myoglobin (MYO) content in human serum. Cardiac Troponin I (cTnI) as one of the units of cardiac troponin (cTn), only exists in the atrial and ventricular myocytes, when myocardial cell membrane is complete, cTnI cannot penetrate the cell membrane into the blood circulation; when myocardial cells become necrosis due to ischemia or hypoxia, cTnI can enter the cytoplasm through damaged cell membrane, then enter the bloodstream, so cTnI can be used as an acute diagnostic index for acute myocardial infarction (AMI). As one of the three isoenzymes of creatine kinase (CK), CK-MB is mainly located in the myocardium, and has 20% activity of CK. CK-MB is an important index in the diagnosis of acute myocardial infarction (AMI), which is largely secreted into the blood when the AMI attacks, the concentration of CK-MB rises as early as 3 to 6 hours after onset, peaks at between 12 and 24 hours, and returns to normal after 3 days, if there are complications, serum CK-MB concentration will maintain at a high level, if AMI happens again, CK-MB will rise again. Myoglobin (MYO) is an oxygen-binding heme protein, mainly distributed in the cardiac and skeletal muscle. Myoglobin releases into the circulation as early as 2 to 3 hours after acute myocardial injury, peaks at between 9 and 12 hours, and returns to normal within 24 to 36 hours. It is recommended to sample and detect continuously for patients with acute coronary syndrome (ACS), because there is a delay between symptom appearing and blood releasing of protein makers. MYO negative is helpful to eliminate AMI, so myoglobin is one of the most important indexes for early diagnosis of AMI, and is widely used in the diagnosis of AMI, prognosis judgment and disease prediction. 【Accessories required but not provided】 ♢ Immunofluorescence quantitative analyzer ♢ Reagent strip incubator ♢ Pipette 【Storage and stability】 Sealed: The kit must be stored at 4-30℃, valid for 24 months. The sample diluent must be stored at 4-30℃, valid for 24 months. Opened: The cartridge must be used within 1 hour once its foil pouch is opened. The sample diluent is valid for 1 month once it is opened.

    Hot Tags : ASO/RF/CRP Test Kit blood diagnostics blood test solution test poct point of care testing point of care detection test reagent

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  • CRP/SAA Test Kit
    【Product Name】 C-reactive Protein/Serum Amyloid A (CRP/SAA) Test Kit (Immunofluorescence) 【Package specifications】 25 Tests /Box 【Intended use】 C-reactive Protein/Serum Amyloid A (CRP/SAA) Test Kit (Immunofluorescence) is mainly for the in vitro quantitative determination of C-reactive Protein and Serum Amyloid A (CRP/SAA) content in human serum. C-reactive protein (CRP) is an acute phase reaction protein, which is very low in healthy people and increases sharply when the body is infected and tissue damage. C-reactive protein is a marker of inflammation and tissue damage, and its elevation is associated with the degree of infection and can be used to detect routine inflammation and cardiovascular inflammation, providing information on the diagnosis, treatment and monitoring of inflammatory diseases. The common detection methods in Clinic are Turbidity method, Immunofluorescence method, colloidal gold method and Chemiluminescence method. Serum amyloid A (SAA) began to rise after an inflammatory reaction of about 8h, with a significant increase in SAA at the time of viral infection, while CRP did not rise in virus infection without bacterial infection or may have increased slightly within a narrow enclosure. Combined detection of SAA and CRP can make up for the difference of CRP level in virus infection without significant, which is beneficial to the early diagnosis of infectious diseases in children. The detection methods commonly used in SAA Clinic are turbidity method, Immunofluorescence method, colloidal gold method and Chemiluminescence method. 【Accessories required but not provided】 ♢Immunofluorescence quantitative analyzer ♢Reagent strip incubator 【Storage and stability】 Sealed: The kit must be stored at 4-30℃, valid for 24 months. The sample diluent must be stored at 4-30℃, valid for 24 months. Opened: The cartridge must be used within 1 hour once its foil pouch is opened. The sample diluent is valid for 1 month once it is opened.

    Hot Tags : crp home test kit blood test diagnosis blood poct

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  • ASO/RF/CRP Test Kit
    【Product Name】 Rheumatism Combo 3 in 1 (ASO/RF/CRP) Test Kit (Immunofluorescence) 【Package specifications】 25 Tests /Box 【Intended use】 Rheumatism Combo 3 in 1 (ASO/RF/CRP) Test Kit (Immunofluorescence) is mainly for the in vitro quantitative determination of ASO/RF/CRP content in human serum. Streptolysin O is one of several toxic extracellular enzymes produced by group A β - hemolytic streptococcus. The rise of anti streptolysin O titer is usually an indicator of a group β - hemolytic streptococcus infection recently, so it has become a routine indicator of diagnosis and treatment of acute rheumatic fever and acute glomerulonephritis. About 80-85% of people with recent streptococcal infection or its sequelae show an increased titer of antistreptolysin O. Rheumatoid factors are a heterogeneous group of autoantibodies directed against the antigenic determinants on the Fc‑region of IgG molecules. They are important in the diagnosis of rheumatoid arthritis, but can also be found in other inflammatory rheumatic diseases and in various non rheumatic diseases. They are also found in clinically healthy persons over 60 years of age. Despite these restrictions, the detection of rheumatoid factors is a diagnostic criterion of the American College of Rheumatology for classifying rheumatoid arthritis. The autoantibodies occur in all the immunoglobulin classes, although the usual analytical methods are limited to the detection of rheumatoid factors of the IgM type. C-reactive protein (CRP) is an acute phase reaction protein, which is very low in healthy people and increases sharply when the body is infected and tissue damage. C-reactive protein is a marker of inflammation and tissue damage, and its elevation is associated with the degree of infection and can be used to detect routine inflammation and cardiovascular inflammation, providing information on the diagnosis, treatment and monitoring of inflammatory diseases. 【Accessories required but not provided】 ♢ Immunofluorescence quantitative analyzer ♢ Reagent strip incubator ♢ Pipette 【Storage and stability】 Sealed: The kit must be stored at 4-30℃, valid for 24 months. The sample diluent must be stored at 4-30℃, valid for 24 months. Opened: The cartridge must be used within 1 hour once its foil pouch is opened. The sample diluent is valid for 1 month once it is opened.
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