$1.15 for 10,000-99,000 pcs
$1.13 for 100,000-499,000 pcs
$1.11 for 500,000-1,000,000 pcs
Commission: $0.00
mark up: allowed - 50% Seller/50% buyer
Delivery: ExWork Beijing, China
Payment: 100% TT before loading
The PocRoc SARS-CoV-2 Antigen Rapid Test Kit (TRFIA) is an immunofluorescent sandwich assay. It can detect the virus with very high sensitivity and specificity.
When the sample is applied to the sample wells, SARS-CoV N protein and labeled antibody complexes are formed and travel up the strip. The labeled microsphere fluorescent probe reagent is used to form a visible red line with a matched UV flashlight.
The presence of SARS-CoV-2 will be indicated by a visible red test line (T) in the result window. The membrane is pre-coated with Chicken IgY on the control (C) line. Control (C) line appears in each result window when the sample has flowed through the strip.
The PocRoc SARS-CoV-2 Antigen Rapid Test Kit(Colloidal Gold)is used for qualitative detection of SARS-CoV-2 virus nucleocapsid protein, which is an important conserved structural protein of SARS-CoV-2 in human nasal/ oropharyngeal samples.
The detection of SARS-CoV-2 nucleocapsid protein antigen can be used to assist the diagnosis of novel coronavirus infection and is helpful for the early detection of novel coronavirus pneumonia infection in the latent period.
Rapid Antigen and Antibody test kit covid 19
Manufacturer: Shenzhen Lvshiyuan Biotechnology Co., Ltd / Green Spring Brand
The time required: 15 -20 minutes
Detect the virus 3 days after the infection
Accuracy: High
Specificity: High
Cost Saving : Low cost
Dr. Guard is space sterilization and deodorant using pure chlorine dioxide.
[Dr. Guard]
* Sterilization test against COVID-19 showed a high result of 99.99% effectiveness
* Registered as a disinfectant for general disinfection in the Central Defense Countermeasures Headquarters of Korean government
* Corona 19 self-disinfecting environment approved product
* Completed safety check test and the only product certified by the Ministry of Environment
* Registered with the FDA. Safety verification completed in WHO.
* With proven technical skills, Dr. Guard has been recognized for its effectiveness in removing germs and odors.
* Obtained certifications from honorable global health institutions such as CE, FDA, PFDA and KEMENKES
[ClO2 Chlorine Dioxide]
* Chlorine Dioxide (ClO2) is a World Health Organization (WHO) recognized safety class A-1 safety material.
As a sanitary disinfectant already in Korea under the Drinking Water Management Act of 1999. It is soluble in chlorine dioxide. This is because there is no problem even when used for drinking water.
* The fatal drawback is that it is difficult to commercialize because it vaporizes quickly and is not easy to manufacture in gaseous form. However, since the sterilizing and deodorizing power is strong, manufacturers have added additional additives (sulfur, surfactant, etc.) for long-term storage.
* So, to make pure chlorine dioxide, special and difficult differentiated technology is required. Dr. Guard is a pure chlorine dioxide product made by a purely Korean technology by an honest company.
[Germs that can be sterilized by Dr. guard]
COROPNA-19 virus, N1N1, Pneumococcus, Dermatophyte, Norovirus, Pseudomonas aeruginosa, Fungi, Salmonella typhi, Staphyococcus aureus, Legionella
[Applications of Dr. Guard]
Using pure silicon dioxide chlorine sterilizing and deodorizing agent, we use the best technology in producing Dr. Guard for variety of purposes.
Bedroom, Bathroom, Refrigerator, Kitchen
No alcohol, No cancerous agents, No preservatives
Air purification, Antivirul action
[How to use Dr. Guard]
The stick contains main solution�?� and an ample (secondary solution)
1. Bend central part of the stick.
2. Once the ample inside the stick cracks, shake it enough to mix the power with the solution well.
3. As it turns yellow, the active ingredients are released to the surface of the stick.
4. After 3~4 weeks of usage, dispose stick into normal trash bag once solution inside turns transparent.
NAME COVID-19 Nucleic Acid Detection Kit(PCR-fluorescent Probe)
USE Diagnosis COVID-19 rapidly for public disease control
Manual Biological cabinet, Appropriate real time PCR instrument, Appropriate nucleic acid extraction system or kit, Desktop centrifuge ( suitable for 96- well plate or 8-strip tube), Centrifuge with a rotor for 0.2ml reation tubes or plate. Vortex mixer, Adjustable piperres(with maximum capacity of 2 L, 10L, 50L, 100L, and 200L, respectively), Disposible pipette tips with filters, Disposable powder-free gloves, RNase FREE 1.5mL centrifuge tube, PCR reation tube / PCR reaction plate.
Storage and Transportation Store in -20 - 5 and transport with carbon diaxide ice, avoid being repeated freezing and thawing.
Expiration date 9 months
* Please be noted the above is the price including the tax, NOT FOB.
Diagnostic Kit for IgM/IgG 2 in 1 Antibody to 2019-nCoV (Colloidal Gold)
Test principle
This diagnostic kit adopts the principle of colloidal gold immunochromatographic test strip to make qualitative test for 2019-nCoV IgM/IgG antibody in human serum, human plasma and whole blood samples.
Purpose
This diagnostic kit is used for making qualitative test for 2019-nCoV IgM/IgG antibody in human serum, human plasma and whole blood samples. It acts as an early-stage aided diagnostic kit for clinical patients infecting 2019-nCoV, yet it is not the only standard for clinical diagnose.
Sample requirements
This kit is suitable for human serum (EDTA anticoagulant, heparin anticoagulant, trisodium citrate dihydrate anticoagulant 1:9), human plasma and whole blood samples.
Purpose
This test kit is used for making qualitative test for COVID-19 antigen in human nose swab and throat swab samples. It acts as an early-stage aided diagnostic kit for clinical patients infecting COVID-19, yet it does not stand for the basis for confirming COVID-19.
Sample requirements
When using sterile swab for collecting samples, polyester sponge swab with PP bar is recommended when collecting nose swab and throat swab. When collecting nose swab, the swab will be gently inserted into the nose palatine and stay for a moment, and then gradually rotate it until it is taken out. When collecting throat swab, the swab will be completely inserted into the throat from the mouth, then inspectors will wipe pharyngeal tonsil on both sides and posterior wall of pharynx with appropriate strength, and finally take the swab out. During this process, please avoid touching the tongue. After collecting the samples, please make processing with viral transport medium or sample diluent provided in the test kit as soon as possible, and complete test within five minutes.
Test principle
This test kit adopts the principle of high-specificity antigen-antibody reaction and colloidal gold labelling and immunochromatographic test strip techniques. The reagent contains COVID-19-NP antigen monoclonal antibody pre-fixed in film test area and COVID-19-NP antigen monoclonal antibody-colloidal go
hrough market research and government trading department internal documents, we have complied a covid-19 related products suppliers contract info.
The data consists of product introduction (including description and certification) and main markets they export. Supplier�¢??s name and contact person phone number. All the contract person are the one who directly responsible for international selling, and the phone number is her/his direct mobile phone. 100% accurate and updated at the end of March 2020
The data consists of 6 categories
1. Diagnostic reagent supplier (eg. Covid-19 test kit etc.)
2. Medical equipment (like ventilators etc.) supplier
3. Chinese patent medicine supplier
4. AI-aid diagnostic system supplier
5. Temperature measuring device supplier (eg. Thermometer etc.)
6. Disinfection equipment (eg irradiation system and disinfection gel, hand wash etc.)
7. Protective clothing
Each categories price: USD 100
Full package of seven categories: USD: 600
The Treponema pallidum Antibody Assay Kit (Colloidal Gold) is a lateral flow chromatographic immunoassay for the qualitative detection of antibodies (IgG, IgM and IgA) to Treponema pallidum (Tp) in human serum or plasma. It is intended to be used as a screening test and as an aid in the diagnosis of infection with Tp.
The test is a rapid colloidal gold immunochromatographic assay for the in vitro qualitative detection of the novel coronavirus(SARS-CoV-2), the influenza A virus (FluA) and the influenza B(FluB) antigen in human nasopharyngeal swab, oropharyngeal swab, nasal swab, and saliva samples from individuals suspected of respiratory viral infection.
