Test kit for self testing - Import export

Intended Use COVID-19 Test Kit (Colloidal Gold Method) is a solid phase immunochromatographic assay for the rapid, qualitativedetection of antigen to 2019 Novel Coronavirus in human nasal cavity. This test provides only a preliminary result forself-testing. Therefore, any reactive specimen with the COVID-19 Test Kit (Colloidal Gold Method) must be confirmedwith alternative testing method(s) and clinical findings. Features ·For self-testing use ·Results ready in 15 minutes ·Accurate diagnostic tool for active infection·Easy to administer and read results ·Affordable, no need for instrument, highly portable ·Enable testing on a massive scale COVID-19 Positive: lf the C and T band is present, the test indcates for the presence of COVID-19 (SARS-Cov-2) antigen in the specimen.The result is COVID-19 positive.

[Product Name] Generic Name: Alpha-fetoprotein (AFP) assay kit (ELISA) [Pack size]: 48 tests / kit, 96 tests / kit [Intended Use]: The Alpha-fetoprotein (AFP) assay kit is intended for quantitative determination of the Alpha-fetoprotein (AFP) concentration in human serum. [Introduction]: Alpha-fetoprotein (AFP) is a kind of embryonal single polypeptide which synthesized by embryo liver, yolk sac and gastrointestinal tract. Human AFP belongs to the alpha globulin, composed of 18 kinds of amino acids. The molecular weight of AFP is about 64 KD ~ 72 KD with a half-life of about 5d. Part of AFP can enter into the maternal blood circulation as amniotic fluid, AFP levels in body fluids of pregnant women all have a different enhanced. Normally, non-pregnancy women have lower concentration of serum AFP. Liver cancer is one of common reasons that induce abnormally increase of AFP.

[Product name] Bacterial Vaginosis Quick Test Kit (Sialidase Detection) [Packing size] 20 pcs/kit; 50 pcs/kit [Intended use] For qualitatively testing activity of neuraminidase in female’s vaginal fluid, only for auxiliary diagnosis of bacterial vaginosis. [Testing principle] Neuraminidase is one of pathogenic factors of bacterial vaginosis (BV). Activity of neuraminidase in vaginal fluid of BV women is significantly higher than that in vaginal fluid of normal women; there is no or only a small amount of neuraminidase in vaginal fluid of normal women. By testing for neuraminidase higher than normal level in the vaginal fluid, patients can be diagnosed whether have BV. This kit mainly contains bacterial neuraminidase-specific chromogenic substrate solution.

This kit is used for the quantitative determination of Luteinizing Hormone (LH) in human urine samples in vitro. Human luteinizing hormone (LH) is a kind of glycoprotein hormones secreted by the pituitary gland, exists in human blood and urine, its role is to stimulate the release of the ovaries mature eggs. LH in the middle of the menstrual secretion, sharply form LH peak, from the basic level of 5 ~ 20 miu/ml rapidly rising to the peak of 25 ~ 200 miu/ml.Urine LH concentration is usually about 36 ~ 48 hours before ovulation suddenly jumped sharply, in 14 ~ 28 hours peak, peak about 14 to 28 hours after theca burst, mature eggs. LH within two days after ovulation back to the basic level, to enter the luteal phase, luteal phase usually lasts for 14 days. Then, the new follicles began to development, into the next menstrual cycle, so the cycle, until the pregnancy. Women in the LH peak within 1 ~ 3 days after the most fertile.

The test kit is used for the quantitative determination of procalcitonin (PCT) in human serum, plasma or whole blood samples in vitro. Procalcitonin (PCT) is the prohormone of calcitonin (CT), which is generally less than 0.1 ng/mL in the blood of healthy people, and its secretion increases after being stimulated by pro-inflammatory responses, especially after bacterial infection. Procalcitonin is an important marker that can specifically distinguish bacterial infection from inflammatory response caused by other reasons. Viral infection, allergy, autoimmune disease and transplant rejection do not cause significant elevation of procalcitonin, while local bacterial infection can result in moderate elevation of procalcitonin concentrations. In some cases (neonatal, multiple trauma, burns, major surgery, prolonged or severe cardiogenic shock), the elevation of procalcitonin may not be related to infection and usually returns to normal values quickly.

[Intended use] HBsAg Test kit (Colloidal Gold) is used for qualitative detection of Hepatitis B surface Antigen in human serum or plasma samples. Hepatitis B surface Antigen (HBsAg) is the hepatitis b virus coat protein. It's not contagious, only the antigenicity. But it is usually accompanied by the presence of hepatitis b virus, so it is a sign of the hepatitis b virus infection. [Test principle] HBsAg Test kit (Colloidal Gold) uses colloidal gold immune chromatography technology to qualitative detection of Hepatitis B surface Antigen in human serum or plasma samples.

Monkeypox Virus Nucleic Acid Detection Kit (Fluorescence PCR) is used for the detection of nucleic acid from monkeypox virus in serum and human pustular or vesicular rash specimens from individuals suspected of monkeypox virus infectious. By specifically detecting the nucleic acid fragments of monkeypox virus, monkeypox virus can be quickly identified, which is suitable for rapid diagnosis of related diseases caused by monkeypox virus infection.

it is intend for qualitative determination of LH levels in women urine to predict ovulation time, so as to guide reproductive women to choose the optimal conception time or safe period contraception. Luteinizing Hormone(LH)Ovulation Test Kit based on the principle of colloidal gold labeling technique and immune chromatography of double-antibody sandwich method. During testing , the LH in urine specimen migrates via capillary action along the membrane to react with LH monoclonal antibody conjugated with nanoscale colloidal gold particles forming an antibody-antigen complex.

It is intend for qualitative determination of FSH levels in women urine. It provides some useful information for women who will prepare for pregnancy or focus on ovarian health, functions and fertility, also assists the diagnosis and treatment of pituitary and gonadal dysfunction. Follicle Stimulating Hormone(FSH) Test Kit (Colloidal Gold) is based on the principle of colloidal gold labeling technique and immune chromatography of double-antibody sandwich method. During testing, the FSH in urine specimen migrates via capillary action along the membrane to react with FSH monoclonal antibody conjugated with nanoscale colloidal gold particles forming an antibody-antigen complex.

The human chorionic gonadotropin (hCG) pregnancy test kit is a rapid, one-step lateral flow immunoassay for the qualitative delection of human chorionic gonadotropin (hCG) in urine to aid in the detection of pregnancy. The test utilizes a combination of antibodies including a monoclonal hCG antibody to selectively detect elevated levels of hCG in urine to aid in the early detection of pregnancy for self-testing. It obtained the result from the colored lines.

Monkeypox virus IgG/IgM Test Kit (Immunochromatography) is a solid phase immunochromatographic assay for the rapid, qualitative detection of IgG/IgM antibody to Monkeypox virus in human blood. This test provides only a preliminary test result. Therefore, any reactive specimen with the Monkeypox virus IgG/IgM Test Kit (Immunochromatography) must be confirmed with alternative testing method(s) and clinical findings.

IIntended Use Singclean Flu A/B Antigen Test Kit is an in vitro qualitative detection that uses colloidal goldimmunochromatography to test influenza A/B antigen in nasopharyngeal swab samples obtained from patients with signs and symptoms of respiratory infection in just 15 minutes. lt is designed to give rapid and reliable test results on the spot without any laboratory equipment. This allows early start of treatment,which helps reduce the duration and severity of the disease,Besides,detection of influenza reduces unnecessary use of antibiotics and aids in limiting thespread of the infection. Advantages a. Easy to operate: All components include in kit,no additional equipment orlaboratory resources required; b.Fast detection: 15 minutes to interpret the result after collecting specimen; c.Joint testing: Influenza A and B can both be tested in one reagent; d.Accurate，Rapid，Sensitive Positive: Positive influenza A and B:Line C, Line A and Line B allappeared.

The novel coronaviruses belong to the βgenus. COVID-19 is an acute respiratory infectious disease. People are generally susceptible. Currently, the patients infected by the novel coronavirus are the main source of infection: asymptomatic only infected people can also be an infectious source. Based on the current epidemiological investigation, the incubation period is 1 to 14 days, mostly 3 to 7 days. The main manifestations include fever, fatigue and dry cough. Nasal congestion, runny nose, sore throat, myalgia and diarrhea are found in a few cases.

The novel coronaviruses belong to the βgenus. COVID-19 is an acute respiratory infectious disease. People are generally susceptible. Currently, the patients infected by the novel coronavirus are the main source of infection: asymptomatic only infected people can also be an infectious source. Based on the current epidemiological investigation, the incubation period is 1 to 14 days, mostly 3 to 7 days. The main manifestations include fever, fatigue and dry cough. Nasal congestion, runny nose, sore throat, myalgia and diarrhea are found in a few cases.

The Sentebiolab Senteligo™️ SARS-CoV-2 (COVID-19) Multiplex qPCR Detection test includes a Primer-Probe set inside the Reaction Mix that contains primers and probes for human RNaseP and viral N1 and N2 regions. The internal control (primer/probe set for human RNaseP gene) is used to identify possible qPCR inhibition, confirm the integrity of the reagents, and verify the quality of RNA extraction from patient material. RNaseP primers and probes included in the kit recognize the human RNaseP gene. The primers and probes for viral N1 and N2 regions specifically identify two distinct regions on the nucleocapsid (N) gene of the SARS-CoV-2 virus. These primers and probes do not recognize the SARS-CoV virus, whose genetic structure is highly similar to SARS-CoV-2.

This product is a rapid, lateral flow immunoassay intended for the qualitative detection of SARS-CoV-2 nucleocapsid antigens from anterior nasal swabs that are self-collected by an individ-ual aged 18 years or older or are collected by an adult from an individual younger than 18 years old. This test is intended for use in individuals with symptoms or other epidemiological reasons to suspect a COVID-19 infection. This product is intended to be used as an aid in the diagnosis of SARS-CoV-2 infection

Easy to use with results in 15 minutes Reliable with a specificity of 99.2% and a sensitivity of 96.1% BfArM listed and evaluated by the PEI (Paul Ehrlich Institute). CE-certified as a self-test for self-use

Monkeypox virus Antigen Test Kit (Immunochromatography) is a solid phase immunochromatographic assay for the rapid, qualitative detection of antigen to Monkeypox virus in human body fluid. This test provides only a preliminary test result. Therefore, any reactive specimen with the Monkeypox virus Antigen Test Kit (Immunochromatography)must be confirmed with alternative testing method(s) and clinical findings.