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Novel Coronavirus (2019-nCoV) IgG/IgM Antibody Testing Kit (Colloidal Gold)

The cassette is used for the qualitative detection of novel coronavirus IgM and IgG antibodies in human whole blood, serum or plasma.

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FSH follicle stimulating hormone test kit

It is mainly used to quantitatively detect the content of follicle stimulating hormone (FSH) in human serum, plasma and whole blood in vitro.

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Thyroid-Stimulating-Hormone（TSH）Test Kit

Thyroid Stimulating Hormone (TSH) Kit (Immunofluorescence) is mainly for the in vitro quantitative determination of thyrotropin（TSH ) content in human serum

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Ferritin（Fer）Kit

Ferritin (Fer) Kit (Immunofluorescence) is mainly for the in vitro quantitative determination of Ferritin (Fer) content in human.

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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.

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25OH Vitamin D total Kit (Immunofluorescence)

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 .

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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

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Progesterone (PROG) Test Kit (Immunofluorescence)

【Product Name】 Progesterone (PROG) Test Kit (Immunofluorescence) 【Package specifications】 25 Tests /Box 【Intended use】 It is mainly used for quantitative determination of progesterone (PROG) in human serum, plasma and whole blood in vitro. Progesterone content is the main index to monitor female ovulation and placental function. Progesterone (PROG) is an important steroid hormone with a molecular weight of 314.5 Dalton. It is mainly produced by ovarian corpus luteum and placenta during pregnancy. The main function of progesterone is to ensure the implantation of uterine fertilized eggs and maintain pregnancy. During the follicular phase of the physiological cycle, the level of progesterone remained very low, while after reaching the luteal phase, the content of progesterone increased rapidly. If ovulation is abnormal, progesterone will decrease abnormally in the middle of luteal phase, leading to infertility and abortion. The abnormal increase of progesterone may be related to adrenocortical hyperfunction. The commonly used detection methods in clinic and laboratory include chemiluminescence, immunofluorescence and so on. 【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.

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C-reactive Protein/Serum Amyloid A (CRP/SAA) Test Kit (Immunofluorescence)

【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.

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