Temperature Block Temperature Range: 0 - 105 Max. Heating Rate: 7 /s Max. Cooling Rate: 5 /s
Covid-19 Rapid Test Kit
Saliva Test Kit Painless testing plastic disposable Ag Rapid Detection Kit
Antibody Test Kits Hot Sale Medical Diagnostic Antigen Antibody Rapid Test Kits
Covid-19 Self Test Kit We are the authorized first vendor of ADTech! KFDA CE approved, FDA Pending Price : Negotiable Pre-Clinical Test Report Accuracy - In total samples 93.3% (14/15) - In positive samples 91.7% (11/12) 1. Pre-Clinical Test summary 1) Pre-clinical test is fulfilled by Domestic large clinical laboratory with ADTech COVID-19 IgM/IgG RAPID KIT 2) Tests are made by total 15 samples with 12 positive and 3 negative samples 3) Clinical Laboratory tested the sample with Immunofluorescence Analysis 2. Pre-clinical test result 1) Samples were tested by ADTech COVID-19 IgM/IgG RAPID KIT 2) Test result by ADTechs RAPID KIT - 4 negatives and 11 positives results in 15 samples 3) Comparison between Immunofluorescence analysis and ADTechs RAPID KIT - 14 test results are same(including negative and positive results) - 1 samples test result are different(Positive Negative by ADTech
Application Suspected case test in epidemic area Early test of fever clinic and CDC Screening of primary medical institutions Inspection of floating population in public areas Performance Characterisitics Sample tyep: nasal swab Time to result: 15-20 minutes Sensitivity: 97.70% Specificity: 99.84% Accuracy:98.97% Layperson study statistics 99.84% of non-professionals carried out the test without requiring assistance 99.82% of different types of results were interpreted correctly. Parameters: A Short Test Time: 15 mintues B Accuracy: More than 98.1% C Sensitivity: 96.4% Specificity: 100% D Easy operation: Nasal Swab E One Step solution F Lower cost with high efficiency G Package: 1 Test/Kit, 5 Tests/Kit, 25 Tests/Kit H It can detection for Omicron Virus Price and Minumum Quantity Price FOB in USD: 1.5Minimum Order Qty: 500000 Pieces Production Capacity: 100 Million Boxes Per WeekPackaging: 1,5,20,25,40,100,200 Pcs Per Box Sample: Available. Sample Cost Born By Buyer Product Model And Origin Brand: jwfModel: jwf01 Seller Code: Jwf Standards: Ce Competitive Advantages Lower cost with high efficiency Detection for omicron virus Easy operation Short test time Other Details Omicron covid test kit Covid test kit Omicron test card Covid test card
We supply various brands of Antigen Saliva and Nose test kit
We have 50mil indicaid covid test kit otg usa.
Malaria Antigen PF/PV Card Test
Covid -19 Test Kit (Colloidal Gold Method) For Self-testing Use (Nasal Swab) Top 10 In China Having Ce Mark For Rapid Covid - 19 Antigen Self-test Precise Rapid Sensitive For At-home Testing For Early Detection Able To Sell Across All Eu Member States
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:
COVID-19 Self Swab Test Kit is the first commercialized Black Gold Particle technology in the world (High Sensitivity & Specifity) -It's made as User friendly Dual Color System (Control Line: Red, Test Line: Black) -Rapid Test Time takes 5~8 Min. -It's intended to use for detection of SARS-CoV2 antigen -20 Tests / Kit (Box) -Tester indicates Negative(C: Red), Positive(C: Red & T: Black) and Invalid(No "C")
Ezplex HLA-B NGS typing Kit is an in vitro diagnostic test that detects and distinguishes allelic genes of HLA-B in human leukocyte antigens at high resolution using next-generation sequencing. Ezplex's unique amplicon approach simplifies the traditional complex NGS Library construction process and provides dedicated software optimized for HLA typing for easy analysis. The Ezplex HLA-B NGS typing Kit accurately reads the HLA-type Acuracy (95 percent Confidence Interval) in DRB1 Locus within a total of 35 hours from DNA extraction to NGS results analysis to help with pre-transplant testing.
We can provide various infectious diseases test kits as listed. Product name Cat. No. Specimen Packing Chlamydia Rapid Test Device ICH-502 Swab/urine Cassette: 10 or 40pcs/box or Customized HBsAg One Step Hepatitis B Surface Antigen Test Device IHBsg-302 Serum/plasma Cassette: 10 or 40pcs/box or Customized HBsAg Hepatitis B Surface Antigen Rapid Test Device IHBsg-402 Whole blood/serum/plasma Cassette: 10 or 40pcs/box or Customized HBsAg One Step Ultra Hepatitis B Surface Antigen Test Device IHBsg-302U Serum/plasma Cassette: 10 or 40pcs/box or Customized HCV Hepatitis C Virus Rapid Test Device IHC-302 Serum/plasma Cassette: 10 or 40pcs/box or Customized HCV Hepatitis C Virus Rapid Test Device IHC-402 Whole blood/serum/plasma Cassette: 10 or 40pcs/box or Customized HIV 1/2 Antibody Rapid Test Device IHI-402 Whole blood/serum/plasma Cassette: 10 or 40pcs/box or Customized H. Pylori Antigen Rapid Test Device IHPg-602 Feces Cassette: 10 or 40pcs/box or Customized H. Pylori Antibody Rapid Test Device IHPb-602 Serum/plasma Cassette: 10 or 40pcs/box or Customized Syphilis Ultra Rapid Test Device ISY-402U Whole blood/serum/plasma Cassette: 10 or 40pcs/box or Customized Dengue Fever Rapid Test Device IDE-402 Whole blood/serum/plasma Cassette: 10 or 40pcs/box or Customized Malaria P. f. /P. v. Rapid Test Device IMA-422 Whole blood Cassette: 10 or 40pcs/box or Customized
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 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.
HPV NGS Kit is an in vitro diagnostic test that simultaneously detects the genotype of human papillomavirus (HPV) using Next-Generation Sequencing technology (NGS). Automated workflows allow for fewer human errors and less hands-on time from library construction to analysis of results. HPV types are quickly identified by simultaneously analyzing up to 480 samples. NGS time is reduced to approximately 24 hours.
Corona virus diagnostic kit. Made in Korea. The minimum order quantity is 10,000ea.
Dental diagnostic kit All dentis use this kit --it include one dental handle with mirror , one probe and one tweezer Set of 3 pcs
