Namemifaresmart card Frequency13.56mhz Standardiso14443a Chipmifare classicâ® , ultralightâ® , desfireâ® Memory1k byte etc Dimensioncr80 standard Read/ write cycles100000 Reading distance1-10cm (depend on the reader and antenna) Application for access control system, ticketing system, id card, event tickets, etc Available craftsthermal printing number, , magnetic stripe, barcode, golden/silver hot-stamping, signature panel, series number printing, uv printing, uid number printing, laser engrave qr code etc. Samplesfree samples are available for testing Package1. Standard export packing: 200pcs/white box, 5000pcs/ctn. 2. G.W./n.W.: 35kg/34kg 3. Size of carton: 48*23*30cm 4. Packing way can according to your request
In vitro diagnostic products rapid test hcg pregnancy test, lh ovulation test, fsh test, fob test, hiv test, malaria test, dengue test, mop test, coc test.
Functions Functions Reading distance is more than 15 meters without affect from cars' anti-explosion metal film Directional.reception,interference-free.fromadjacentlanesDual-way machine code authentication; no interference when many readers work together. Signal strength can be adjusted automatically according to climate, Zero-interference from environment Fast identification without affect form vehicle speed Integrated design, simple layout After reading the cards, the reader will flicker and make sounds Two-layer water-proof structure; protection grade is IP66 Product Application Entry and Exit intelligent management parking system ETC Electronic Toll Collection System Non-stop counting system for vehicle Non-stop Attendance system for bus Electronic road test for driving system Technical Parameter Identification Distance Above 15 meters is adjustable and the best adjustment distance range is 5 meters from the railing. Identification Angle within 60 degree tapered region of reader's frontage Sending Channel 38K Receiving Channel 433M Reading Speed More than 60km/hr Communication Interface WieGand26\WieGand34\RS485 Communication Encryption Based on Bluetooth encryption algorithm Working Voltage +9 ~ +18V DC Working Temperature -40~80 degree Dimension 280*250*46(mm),Pole Bracket Ф60*12000mm Weight 4.5Kg Colour Grey\Grayish-black\Red orange(other colours as oredered)ïroviding ODM processing Packing List Host\Power\Connector\Instruction\Testing card
Canine parainfluenza virus(cpiv) is a highly contagious viral respiratory disease, which contributes to upper respiratory disease and infectious tracheobronchitis. Cpiv is often associated with other respiratory tract viruses. It will infect dogs of all ages that have not been vaccinated or previously infected, when young puppies will suffer more. With the one step cpiv ag test kit, cpiv can be easily and acurately diagnosed within 10 minutes without any complex lab procedure Principe: the kit is a solid phase chromatographic immunoassay using direct sandwich method. Specimens: respiratory tract secretions or serum Kit composition: 10 pouches, each containing one cpiv ag card with sucker and desiccant; 10 tubes with sample extraction buffer; 10 single packed swabs; one instruction for use
BOSON Rapid Antigen test card
Viral transport kit for covid 19, typhoid igm test. dengue ns1 kit, hcg pregnancy kits, molecular biology reagents, covid antigen kit etc.
Elisa Kits, Rapid Cards, Hematology Reagents,ivd Instrument Etc.
Overview Quick Details Place of Origin: China Brand Name: BATERSUARG Model Number: MSLCDV01 Properties: Diagnosis & Injection Product name: Canine Distemper Vires Test Card Application: Detect canine distemper virus Storage: Dry room temperature 2-30°C Warranty: 18 Months Material: CDV Aluminum Foil Bag Seal Supply Ability Supply Ability: 100000 Piece/Pieces per Day Packaging & Delivery Packaging Details Carton packing Port Shanghai, Tianjin Picture Example: package-img package-img Lead Time : Quantity(Pieces) 1 - 10000 >10000 Est. Time(days) 5 To be negotiated
13.56mhz HF RFID readers/writers, 13.56mhz oem RFID reader module, access control readers, RFID development kit, test board, RFID components, 13.56mhz rfid cards (mifare 1k/4k, iso15693 labels, id cards), key tags.OEM, ODM
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Rapid Test Kit, Rapid Diagnostic Device, HIV Test, HCV Test, HBSAG Test, HBSAB Test, HBEAG Test, HBEAB Test, HBCAB Test, HCG, LH, Dengue, Malaria, H, Pylori Ag Or AB, Rickettsia, TB, Syphilis, Rotavirus, Adenovirus, Hev, Doa, Psa, Fob, Afp, Cea.
SARS-CoV-2 IgG/IgM Rapid Test Kit Intended Use: To detect IgM and IgG antibodies against N and S protein of SARS-CoV-2 in whole blood, serum and plasma Product Format: 25 tests/kit Kit Contents: test card, diluent, capillary, lancet, and instruction for use. Storage/Stability: 2 C to 30C for 12 months.� eproducibility /Precision 100% Concordant across 3 lots with CV ±5% Performance Comparison (A) China Validation Test Positive Samples 100 / 102 Sensitivity: 98.04% Negative Samples 491/492 Specificity: 99.80% Overall Accuracy: 99.49% Performance Comparison (B) Positive Samples 23 / 25 Sensitivity: 92% Negative Samples 25 / 25 Specificity: 100% Overall Accuracy: 96%
When the epidemic is waiting for an opportunity again, to quickly control the spread of the virus, nucleic acid testing has become the only way to go, and it has also attracted attention from all walks of life. However, there are many factors that affect the results of nucleic acid testing, including sample collection location, collection method, storage and transportation process, nucleic acid extraction operation, and so on. Among them, the stability of the sample is a key link. How to quickly inactivate the virus and protect the viral nucleic acid from being degraded, maintaining the stability of the virus sample storage solution has become a top priority. Step 1: Break the shell and eliminate the "combat power" Like other RNA viruses, the results of the new coronavirus are simply composed of a protein shell wrapped in single-stranded nucleic acid-RNA. We can simply think of the RNA of the virus as the "brain" that gives orders, and the protein is the "limbs" that execute orders. The new coronavirus infects the human body and reproduces and causes symptoms. This process is mainly completed by the biologically active protein structure outside the virus. The inactivated virus preservation solution is mainly the virus modified by the nucleic acid extraction lysis solution; it is a powerful protein denaturant that can quickly dissolve the protein and cause the virus structure to be broken. When the clinical sample with the new coronavirus is mixed with the preservation solution, the virus in the sample is affected by the lysis solution, and the protein shell is quickly destroyed, and this damage is irreversible. At this time, the virus has lost its evil "minions" and no longer has the ability to infect people, thus ensuring the safety of contacts during sample transportation and processing. Step 2: Inhibit enzyme activity and escort the "ID card" After the shell is lysed, the RNA of the new coronavirus is free in the preservation solution. As a single-stranded macromolecule, the stability of RNA is not as immobile as double-stranded DNA. The RNase that exists everywhere in the natural environment is the culprit that causes RNA to hydrolyze and break. Therefore, it is generally considered that the viral RNA that has lost its outer shell protection is In addition to the inactivated virus storage solution, the virus preservation solution produced by Desheng also has a non-inactivated virus storage solution. It retains the protein coat of the virus and the viral nucleic acid DNA or RNA at the same time, so that the virus has the integrity of the protein epitope and nucleic acid in vitro. Of course, there is a certain risk of infectivity when operating errors. Long-term storage after sampling needs to keep strictly low temperature. Regardless of the virus preservation solution, we need to strictly operate, store or transport in accordance with the requirements when using it.
H-fabp fast test kit (immunofluorescence assay) is intended for use together with getein1100 immunofluorescence quantitative analyzer (getein1100) or getein1600 immunofluorescence quantitative analyzer (getein1600) to quantitatively determine the concentrations of h-fabp in human serum, plasma, or whole blood specimens in point-of care and laboratory settings. H-fabp fast test kit (immunofluorescence assay) is intended for in vitro quantitative determination of heart-type fatty acid binding protein (h-fabp) in serum, plasma or whole blood. This test is used in the early diagnosis of ami and pulmonary embolism, and monitoring of chronic heart failure.
The cardiac troponin i fast test kit (colloidal gold) is intended for use together with the fia8000 quantitative immunoassay analyzer (fia8000). The product employs colloidal gold immunochromatogrphy to determine ctni in human serum, plasma, or whole blood specimens. Two monoclonal antibodies are employed to identify ctni specifically, resulting in a purplish red streak appears on the test line. The color intensity of the test line increases in proportion to the concentrations of ctni. Then insert test card into the fia8000 quantitative immunoassay analyzer, the concentration of ctni is measured quantitatively and displayed on the screen. The result can be transmitted to the lab or hospital information system.
The One Step Test for NT-proBNP (colloidal gold) is intended for use together with the FIA8000 Quantitative Immunoassay Analyzer (FIA8000). The product employs colloidal gold immunochromatogrphy to determine NT-proBNP in human serum, plasma, or whole blood specimens. One monoclonal antibody and one polyclonal antibody are employed to identify NT-proBNP specifically, resulting in a purplish red streak appears on the test line. The color intensity of the test line increases in proportion to the concentrations of NT-proBNP. Then insert test card into the FIA8000 Quantitative Immunoassay Analyzer, the concentration of NT-proBNP is measured quantitatively and displayed on the screen. The result can be transmitted to the lab or hospital information system.
The One Step Test for PCT (colloidal gold) is intended for use together with the FIA8000 Quantitative Immunoassay Analyzer (FIA8000). The product employs colloidal gold immunochromatogrphy to determine PCT in human serum, plasma, or whole blood specimens. Two monoclonal antibodies are employed to identify PCT specifically, resulting in a purplish red streak appears on the test line. The color intensity of the test line increases in proportion to the concentrations of PCT. Then insert test card into the FIA8000 Quantitative Immunoassay Analyzer, the concentration of PCT is measured quantitatively and displayed on the screen. The result can be transmitted to the lab or hospital information system.
The One Step Test for NAGL (colloidal gold) is intended for use together with the FIA8000 Quantitative Immunoassay Analyzer (FIA8000). The product employs colloidal gold immunochromatogrphy to determine NGAL in human urine specimen. Monoclonal antibody and polyclonal antibody are employed to identify NGAL specifically, resulting in a purplish red streak appears on the test line. The color intensity of the test line increases in proportion to the concentrations of NGAL. Then insert test card into the FIA8000 Quantitative Immunoassay Analyzer, the concentration of NGAL is measured quantitatively and displayed on the screen. The result can be transmitted to the lab or hospital information system.
The One Step Test for B2-MG (colloidal gold) is intended for use together with the FIA8000 Quantitative Immunoassay Analyzer (FIA8000). The product employs colloidal gold immunochromatogrphy to determine B2-MG in human serum, plasma, or whole blood specimens. Two monoclonal antibodies are employed to identify B2-MG specifically, resulting in a purplish red streak appears on the test line. The color intensity of the test line increases in proportion to the concentrations of B2-MG. Then insert test card into the FIA8000 Quantitative Immunoassay Analyzer, the concentration of B2-MG is measured quantitatively and displayed on the screen. The result can be transmitted to the lab or hospital information system.
The One Step Test for mAlb (colloidal gold) is intended for use together with the FIA8000 Quantitative Immunoassay Analyzer (FIA8000). The product employs colloidal gold immunochromatogrphy to determine mAlb in human urine specimen. Polyclonal antibody and recombinant antigen are employed to identify mAlb specifically, resulting in a purplish red streak appears on the test line. The color intensity of the test line increases in proportion to the concentrations of mAlb. Then insert test card into the FIA8000 Quantitative Immunoassay Analyzer, the concentration of mAlb is measured quantitatively and displayed on the screen. The result can be transmitted to the lab or hospital information system.
