We are pleased to offer you Accu-Chek Performa 50 Test Strips as follows; Product Name: Accu-Chek Performa 50 Test Strips
Accu Chek Instant Strip
Accu Chek Guide
qualitative PCR thermal cycler, 48- or 96 wells, with- or without gradient.
Magnetic bead-based purification 1. High-quality nucleic acid can be obtained range from 10 min to 40min (up to different protocol). 2. High throughput: Can be integrated with magnetic rod method automatic instrument or pipetting method automatic instrument to carry out high throughput extraction experiment. 3.Safe and nontoxic: No toxic organic reagents such as phenol/chloroform are needed. 4.Complete removal of contaminants and PCR inhibitors for downstream experiments.
Real-time PCR test 96 Reactions/kit
The C-Reactive Protein Semi-Quantitative Rapid Test Device (Whole Blood/Serum/Plasma)is a rapid chromatographic immunoassay for semi-quantitative detection of C-Reactive Protein in whole blood, serum or plasma specimens to aid in evaluating risk of cardiovascular disease.
The CK-MB Rapid Test Cassette (Whole Blood/Serum/Plasma) is a rapid chromatographic immunoassay for the qualitative detection of human CK-MB in whole blood, serum or plasma as an aid in the diagnosis of myocardial infarction (MI).
Gut health is very important in order to maintain healthy life. The gut microbiome test which can be taken in the comfort of your home can reveal any imbalance in your gut flora. You can take corrective action to reduce your risk of diseases like Irritable Bowel Syndrome, diabetes, obesity, depression and hypertension caused by an unhealthy gut.
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.
New Sealed in Box 100 OneTouch Ultra Blue Test Strips Expiration: 10/2023
Newcastle Ag Rapid test Kit Features For rapid detection of Newcastle disease virus antigens Effective tool for disease detection and diagnosis The easiest operation and detection tools Quickly present the result Economic testing costs New castle Ab rapid test kit/Avian Influenza Ab rapid test kit Features Blocking method unlike other methods of rapid test kit, have a high coincidence rate with hemagglutination inhibition Convenient and fast detection tools: extremely simple operation, quick present results Economic testing costs: excellent testing tools, low prices. Parameters for Newcastle disease Ab rapid test kit Principle: blocking method colloidal gold lateral chromatography Test samples: serum Interpretation time: 20 minutes Sensitivity: 99% Specificity: 96% Shelf life: 24 months Storage temperature: 2-30 degrees Packing: 40 test /box Parameters for Avian Influenza Ab rapid test Kit Principle: blocking method colloidal gold lateral chromatography Test samples: serum Interpretation time: 20 minutes Sensitivity: 97% Specificity: 97% Shelf life: 24 months Storage temperature: 2-30 degrees Packing: 40 test/box Technical Parameters Principle: colloidal gold lateral chromatography Test samples: cloacal / laryngotracheal / stool Interpretation of time: 10-15 minutes Sensitivity:> 90% Specificity:> 90% Shelf life: 24 months Storage temperature: 2-30 â?? Packing: 20 pcs / box Minimum detection volume: 0.25HAU
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.
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.
On May 27th, 2022, Boson Rapid SARS-CoV-2 Antigen Test Card (Self-Testing) was authorized for marketing by Health Canada.Global Technology Foundation is a fully authorized independent distributor of Boson Biotechnology Co., Ltd. throughout North America. It has the ability to supply government and private buyers with a monthly supply of 30-40 million boxes. The quotation on this page is only for the USA .Sales, OTG supply, accept TT payment.The BOSONTM� Rapid SARS-CoV-2 Antigen Test Card (Home Test) has been sold to Europe, Southeast Asia, Australia, Canada and other countries, with excellent product quality and service. The test gained substantial popularity among users. The only supplier with the lowest price in North America for COVID-19 antigen test kits
The US Food and Drug Administration (FDA) granted Emergency Use Authorization for the BOSONTM Rapid SARS-CoV-2 Antigen Test Card (Home Test) on April 6, 2022. Global Technology Foundation is a fully authorized independent distributor of Boson Biotechnology Co., Ltd. throughout North America. It has the ability to supply government and private buyers with a monthly supply of 30-40 million boxes. The quotation on this page is only for the USA .Sales, DDP supply, accept TT payment.The BOSONTM� Rapid SARS-CoV-2 Antigen Test Card (Home Test) has been sold to Europe, Southeast Asia, Australia, Canada and other countries, with excellent product quality and service.  The test gained substantial popularity among users
