SARS-CoV-2 Antigen Rapid Test Kit (Colloidal Gold Immunochromatography) Product Description SARS-COV2 Antigen Rapid Test Card contains a gold-labeled novel coronavirus N protein monoclonal antibody pre-coated on the bonding pad and a paired novel coronavirus N protein monoclonal antibodies �xed in the test line (T) and corresponding antibodies in the quality control line (C). SARS-COV2 Antigen Rapid Test Kit can detect the virus from the rst phase of infection (2-3 days before potential symptom onset) to the last phase of infection (7-10 days after potential symptom onset). Used to test COVID-19 antigen Card-like format detects the nucleocapsid (N) protein of the virus. Gold-labelled SARS-CoV-2 N protein monoclonal antibodies immobilized on the test area, with corresponding antibodies in the quality control area. Swabbed specimens from the nasopharynx or oropharyngeal, result in 15 minutes Product Features Non-invasive Simple to use Convenient, no devices required Rapid, get a result in 15 minutes Stable, with high accuracy Inexpensive, cost-efficiency Related News On 26th Jan 2021, report from PEI of an official test that The Federal Institute for Drugs and Medical Devices (Bundesinstitut fr Arzneimittel und Medizinprodukte, BfArM) authorized to perform, declared that Lepu Medical SARS-CoV-2 Antigen Rapid Test Kit has fulfilled all the minimum criteria for antigen tests conducted by PEI in consultation with the Robert Koch-Institut (RKI). In March 2021, German BfArM approved Lepu Medical SARS-CoV-2 antigen rapid test kit for home use. The test kit makes the coronavirus detection procedures rapid and easy.
covid 19 test kit
Product Name Human Chorionic Gonadotropin (HCG) Test Kit (Immunofluorescence Chromatography) Purpose To detect the content of HCG in human plasma/serum/whole blood in vitro quantitatively.For Professional Use only. Principles of Detection The HCG Test is a fluorescent lateral flow immunoassay. The test consists of: 1) a conjugate pad containing HCG antibody conjugated with fluorescent microspheres and a control antibody (goat anti-chicken IgY antibody) conjugated with fluorescence microspheres, 2) a nitrocellulose membrane strip containing a test line (T line) and a control line (C line). The T line is pre-coated with another HCG antibody, and the C line is pre-coated with a control line antibody (chicken IgY antibody). HCG concentration in specimen is positively correlated with the fluorescent density of the microspheres, after the measure and calculation of the quantitative fluorescence immunoassay analyzer, then the analyzer would calculate the concentration of HCG according to the preset calibration curve in the machine and display the result, detection unit is mIU/mL. C line should appear in any cases, which indicates the reaction system is effective. Storage conditions and shelf life Store in a sealed aluminum foil bag at 2 - 30 C. After unpacking the aluminum foil bag under temperature 20~30 C , humidity 35~65%, please use it immediately. Shelf life 18 months. Applicable instrument Avid fluorescent immunoanalyzer model: AI-IF 600
Product Name Triiodothyronine (T3) Test Kit (Immunofluorescence Chromatography) Purpose To detect the content of T3 in human plasma/serum/whole blood in vitro quantitatively.For Professional Use only. Principles of Detection The T3 Test is a fluorescent lateral flow immunoassay. The test consists of: 1) a conjugate pad containing T3 antibody conjugated with fluorescent microspheres and a control antibody (goat anti-chicken IgY antibody) conjugated with fluorescence microspheres, 2) a nitrocellulose membrane strip containing a test line (T line) and a control line (C line). The T line is pre-coated with another T3 antigen, and the C line is pre-coated with a control line antibody (chicken IgY antibody). T3 concentration in specimen is positively correlated with the fluorescent density of the microspheres, after the measure and calculation of the quantitative fluorescence immunoassay analyzer, then the analyzer would calculate the concentration of T3 according to the preset calibration curve in the machine and display the result, detection unit is nmol/mL. C line should appear in any cases, which indicates the reaction system is effective. Storage conditions and shelf life Store in a sealed aluminum foil bag at 2~30�°C. After unpacking the aluminum foil bag under temperature 20~30 �ºC , humidity 35~65%, please use it immediately. Shelf life 18 months. Reference range Reference value:The 95% concentrations of T3 in 239 non-stationary subjects without any obvious thyroid dysfunction ranged from 1.34 to 2.73nmol/L, with a median of 1.81nmol/L;The reference value has been verified with reference to similar products already on the market. Each laboratory can build own reference range according to actual situation.
Product Name C-reactive Protein(CRP)Test Kit (Immunofluorescence Chromatography) Purpose To detect the content of CRP in human plasma/serum/whole blood in vitro quantitatively.For Professional Use only. Principles of Detection The CRP Test is a fluorescent lateral flow immunoassay. The test consists of: 1) a conjugate pad containing CRP antibody conjugated with fluorescent microspheres and a control antibody (goat anti-rabbit IgG antibody) conjugated with fluorescence microspheres, 2) a nitrocellulose membrane strip containing a test line (T line) and a control line (C line). The T line is pre-coated with another CRP antibody, and the C line is pre-coated with a control line antibody (rabbit IgG antibody). CRP concentration in specimen is positively correlated with the fluorescent density of the microspheres, after the measure and calculation of the quantitative fluorescence immunoassay analyzer, then the analyzer would calculate the concentration of CRP according to the preset calibration curve in the machine and display the result, detection unit is mg/L. C line should appear in any cases, which indicates the reaction system is effective. Reference range Reference values:
Product Name Fecal Occult Blood(FOB)Test Kit (Colloidal Gold Method) Purpose To detect the content of FOB in human fecal in vitro qualitatively.For Professional Use only. Principles of Detection The FOB Rapid Test is a one-step chromatographic sandwich immunoassay. The test consists of: 1) a conjugate pad containing HB monoclonal antibody conjugated with colloidal gold. 2) a nitrocellulose membrane strip containing a test line (T line) and a control line (C line). The T line is pre-coated with another HB antibody, and the C line is pre-coated with a control line antibody (goat-anti-mouse IgG antibody). After addition of the sample, FOB will bind with a colloidal gold-labeled antibody on the conjugate release pad. The resulting complex flows over the nitrocellulose membrane where a specific capture reagent is pre-coated and a red line can be seen at the test zone (T). Unreacted colloidal gold-labeled antibodies in the sample are captured at the control zone (C). The intensity and speed at which the color develops depend on the FOB concentration in the sample. Reference range This kit can detect FOB at a minimum of 50ng/ml. Performance Characteristics 1. Critical value and repeatability: 1) The quality control substance of FOB with a concentration of 50ug/mL was detected for 20 times, and the positive coincidence rate was â?¥95%, and the color uniformity, and the reaction results were consistent. 2) The quality control substance of FOB with a concentration of 10ng/mL was detected for 20 times, and the negative coincidence rate was â?¥95%, and the color uniformity, and the reaction results were consistent. 2. Analysis specificity: 500ug/mL bovine HB,500ug/mL pork HB,500ug/ mL chicken HB,500ug/mL goat HB,2000ug/mL Horseradish Peroxidase specific quality control substance were all negative. 3.HOOK effect: human FOB positive quality control substance of 2000ug/mL was detected and the result was positive.
Product Name Glycosylated Hemoglobin(HbA1c)Test Kit (Immunofluorescence Chromatography) Purpose To detect the content of HbA1c in human whole blood in vitro quantitatively.For Professional Use only. Principles of Detection The HbA1c Test is a fluorescent lateral flow immunoassay. The test consists of: 1) a conjugate pad containing HbA1c antibody conjugated with fluorescent microspheres and a control antibody (goat anti-chicken IgY antibody) conjugated with fluorescence microspheres, 2) a nitrocellulose membrane strip containing a test line (T line) and a control line (C line). The T line is pre-coated with another HbA1c antibody, and the C line is pre-coated with a control line antibody (chicken IgY antibody). HbA1c concentration in specimen is positively correlated with the fluorescent density of the microspheres, after the measure and calculation of the quantitative fluorescence immunoassay analyzer, then the analyzer would calculate the concentration of HbA1c according to the preset calibration curve in the machine and display the result, detection unit is %units. C line should appear in any cases, which indicates the reaction system is effective. Storage conditions and shelf life Store in a sealed aluminum foil bag at 2~30�°C. After unpacking the aluminum foil bag under temperature 20~30 �ºC , humidity 35~65%, please use it immediately. Shelf life 18 months. Applicable instrument Avid fluorescent immunoanalyzer model: AI-IF 600 Manufacturer& After-Sales Company: Shenzhen Aivd Biotechnology Co., LTD. Address:C501,Building B5,China Merchants Guangming Science Park, #3009 Guanguang Road, Guangming District, Shenzhen,Guangdong Province, China Tel: 0755-26165742 Fax:0755-26401805 Specimen collection and preparation 1. Human whole blood samples can be used for this test. 2. Specimen collection:Collect blood specimen into a collection tube containing EDTA , evenly mixed before use. Do not use hemolyzed blood for testing. Whole blood specimens should be stored at 2-8�°C for no more than 4 hours if not test immediately. 3. Do not test patients' samples with severe hemolysis, lipemia and jaundice, all specimens should be treated as infectant. 4. Restore the specimen to 20-30�°C before the detection, cryopreserved specimen should be completely thawed, rewarmed and evenly mixed before use. Reference range Positive: reading value â?¥6%, a positive result. Negative: reading value 8%, poorly controlled blood glucose. The reference value is verified with reference to similar products that have been marketed. Due to ethnic and geographical differences, each laboratory can establish its own reference interval according to the actual situation.
his kit adopts the method of indirect competitive enzyme-linked immunoassay (ELISA) to detect Tylosin (TYL) in the sample such as poultry tissue, honey. Specification 96wells per kit
This kit adopts the method of indirect competitive enzyme-linked immunoassay (ELISA) to detect Aflatoxin B1 (AFB1) in the sample such as grains and feed.
This kit adopts the method of indirect competitive enzyme-linked immunoassay (ELISA) to detect Nitroimidazoles (NMZ) in the sample such as tissue, honey and eggs.
This kit adopts the method of indirect competitive enzyme-linked immunoassay (ELISA) to detect Tetracyclines (TCs) in the sample such as tissue, honey and eggs. Technique Data Kit Sensitivity: 0.05ppb (ng/mL) Reactive Mode: 37�ºC, 30min~30min~15min Detection Limits: Sample Detection Limits Tissue, liver, eggs 2ppb Honey 2ppb Urine 0.5ppb Milk 2ppb Milk powder 4ppb Cross-reaction rate: Tetracyclines..................â?¦.....100% Oxytetracycline ...............â?¦...107% Chlorotetracycline..................16.7% Doxycycline ..................â?¦.......4.2% Sample Recovery rate: Sample Recovery rate Tissue, liver, egg 75�±20% Honey 80�±20% Urine 80�±20% Milk, Milk powder 75�±20% Our products related to Bovine disease detection mainly include the following Zearalenone (ZON/ZEN) ELISA Kit Aflatoxin B1 (AFB1) ELISA Kit Deoxynivalenol � (DON) ELISA Kit Aflatoxin M1 (AFM1) ELISA Kit Total Aflatoxin � (AFT) ELISA Kit T2 Toxin (T2) ELISA Kit Fumonisin B1 � (FB1) ELISA Kit Ochratoxin A (OTA) ELISA Kit Shenzhen Finder Biotech Co., Ltd. is a a high-tech enterprise located in Shenzhen, China. Our company is engaged in rapid detection of food safety (such as residue detection of veterinary drugs, additives, hormones, mycotoxins), rapid diagnosis of animal diseases and related product development. There are hundreds of products. Secondly, the diagnostic kits and test cards for animal diseases mainly for livestock and poultry have been widely used in Animal Husbandry Government Department, scientific research institutions and universities, which provides a strong basis and guarantee for monitoring immunity and diagnosis.
New Arrival Pass Management Kiosk for Temperature Measurement & Face Recognition, Specially designed for COVID-19/Coronavirus. Introduction ONT-SV-1081D, pass management vertical module of temperature measurement & face recognition uses Rockchip RK3288 / RK3399 / Qualcomm MSM8953 high-performance hardware platform, equipped with industrial-class binocular camera, live face recognition technology and infrared thermal imaging module to support face-with-mask identify. It also supports expansion of various peripherals such as ID card readers, fingerprint readers, etc., which can be applied to gate passages and attendance system to achieve safe and efficient access control for personnel. Features 1. 8-inch IPS full-view LCD display. 2. Industrial-class appearance, waterproof and dustproof design which is stable and reliable. 3. Supports 30,000 face database. The 1: 1 comparison recognition rate is more than 99.7%, the 1: N comparison recognition rate is more than 96.7%@0.1% misrecognition rate, and the live detection accuracy rate is 98.3%@1% misrejection rate. Face recognition pass speed is less than 1 second. 4. Supports accurate face recognition and comparison while wearing a mask. 5. Using industrial-grade binocular wide dynamic camera, night infrared and LED dual photo flood lamp. 6. Support processors with strong performance: Rockchip RK3288 quad-core processor, Rockchip RK3399 six-core processor and Qualcomm MSM8953 octa-core processor. 7. Supports human body temperature detection and temperature display. The best temperature detection distance is 0.5 meters. The longest distance at which body temperature can be measured is 1 meter. The measurement error is plus or minus 0.5 â??. 8. It only takes a few seconds for detection, and supports automatic alarm for body temperature abnormality. 9. Attendance temperature measurement data is exported in real time. 10. Supports various peripheral expansions such as ID card reader, fingerprint reader, IC card reader, two-dimensional code reader, etc. 11. The documentation is complete and supports secondary development. 12. Support system level, APP offline level, APP + background network level multiple API docking.
Provides ultimate support to the lower lumbar region, abdomen and hip area to help provide relief of lower back pain and discomfort during pregnancy. Effectively prevents the formation of stretch marks by helping to avoid overstretching of the skin, but without restricting the baby's movement. Helps to correct physiological position of your baby at the late stage of pregnancy, hence prevents complications during pregnancy and labour. Helps relieve pressure on mother's organs caused by baby, allowing easier breathing, and less problems with bowels and water works. The support also encourages correct posture, relieving stress on the lower back caused by misalignment of the spine due to pregnancy. You will get into your normal shape after the birth more easily and quickly.
Mini alcohol breathalyzer With Bluetooth With mouthpieces Support transfer data to PC
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