Cat No : 09N77-095. The Abbott RealTime SARS-C0V-2 assay is an Emergency Use Authorization (EUA) test authorized by the U.S. FDA for use by authorized laboratories, using real-time (RT) polymerase chain reaction (PCR) technology for the qualitative detection of nucleic acids from the SARS-CoV-2 virus and diagnosis of SARS-CoV-2 virus infection from individuals meeting CDC clinical and/or epidemiological testing criteria.
CAT No : 09FIL10D. Filariasis Ag Test Kit Contents: Test Device in a foil pouch with desiccant Disposable dropper Instruction for use
Covid-19 Diagnostic Kit(RT-PCR) Target gene ; 2 genes(Orf1ab,N) Real-time PCR machine ; ABI7500, CFX96,SLAN Kit component ; RT-PCR premix, Primer/Probe Mix, Positive control. Internal control ; Rnase P (house keeping RNA gene) PCR tube use ; one Lod ; 100 copies/reaction
Anti-Viral product-Pouch type-VASP-02 forming an invisible air sterilization covering by 1 meter Radius/2 meter Diameter sterilizing all kinds of viruses and bacterias
We are manufacturer in for PRP kit with using latest technology to provide the best quality with lowest price in the market. Please contact us for the PRP kits and we are looking for exclusive distributor in your country.
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
Product name Virus preservation solution Packaging specifications 1L/bottle 5L/bottle Product performance Non-inactivated type: it does not contain lysate, which can maintain the activity and integrity of pathogen, and can be used for virus culture and isolation. Inactivated type: it can split pathogen instantly and release nucleic acid, and the protective agent can prevent nucleic acid from degradation. Scope of use The virus preservation solution can be used for the collection, preservation and transportation of nasopharyngeal pathogen specimens such as new coronavirus, influenza, bird flu, hand-foot-mouth disease, measles and so on. Non-inactivated type: On the basis of Hank's, BSA (bovine serum albumin) amino acids, vitamins and other nutrients are added to maintain the virus' activity over a wide temperature range and maintain the originality of the sample to the greatest extent and can be used for virus nucleic acid extraction and detection, virus culture and isolation. Inactivated type: By fully mixing the collected samples with virus lysate and virus nucleic acid preservation solution, the virus in the samples can be inactivated, and the integrity of virus nucleic acid in the samples can be effectively guaranteed. The collected samples can be transported and preserved for a long time under normal temperature. The preserved viral RNA samples can be widely used for genetic testing, enzyme-linked immunoassay (ELISA), PCR testing, ect. Storage conditions and time Non-inactivated type: Store at 4-25 It shall be transported to the laboratory within 48 hours under 2-8 after sampling, or stored under - 70 Inactivated type: 30 days at normal temperature
Made in Korea, 2 type of Covid 19 test kit supply (1) The Q-Sens Covid-19 Detection kit V2 (RT-PCR test kit) - FOB Korea: 400$ US per kit (100 test/kit) - Certification: CE-IVD, KFDA - Using real time reverse transcription polymerase chain reaction (RT-PCR) technology. This product contains enzymes and reaction components required for cDNA synthesis and PCR amplification, so a RT-PCR reaction can be easily performed by one step of adding of RNA template to primer/probe mixture. - Targets: RdRp gene & E gene - Specimens: Nasopharyngeal swab, oropharyngeal swab and sputum from patients - Results within 2 hours - Packing: 100 tests / kit - Store at below -20C (2) The Q-Sens Covid 19 lgG/lgM rapid kit - FOB Korea: 390$ US per kit (100 test/kit) - Certification: CE-IVD, KFDA - Results within 10 min - Store at 2~30 C
CE certification PCR monkeypox test kit
CE certification PCR monkeypox test kit
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.
Unique sealing tube test strip series is the main breaking through the invention of amazing biotech, Which can diagnose all the three stages of the covid19 including Virus, antigen, and antibodies. Here we compare the screening method of different types of testing carried out for Covid-19 including nucleic acid, antigen-based, and antibody-based testing. The comparison is done on the basis of sampling specimen, earliest stage detection, time taken by each, Clinical significance of positive results, Specificity, Sensitivity, and technical difficulty. For nucleic acid testing, the specimen used must be nasopharyngeal swabs, sputum, buffer. For antigen specimen, the specimen must be nasopharyngeal swabs, sputum, buffer, urine. And for antibody-based testing, the specimen used must be plasma and serum. Similarly, the earliest stage detection for nucleic acid testing is after infection, and before symptoms arise. Antigen-based testing is also after infection before symptoms arise and antibody-based testing is One week after symptoms arise. The time taken to carry out the nucleic acid test is 60-180 mins, for antigen test is 10 to 15 minutes and for antibody test is 15 to 180 minutes. Product Detail PRINCIPLE Amazing COVID-19 Antigen Lockseal Tube Test Strip is based on sandwich lateral flow immunochromatographic assay highly sensitively detecting COVID-19 nucleocapsid protein in human nasopharyngeal, nasal secretion, saliva or/and serum specimens, having an invisible T (test) zone and C (control) zone. When the sample is applied into the test tube, the liquid will laterally flow on the surface of the test strip. If there is enough COVID-19 antigen in the sample, a visible T band will appear. The C band should always appear after a sample is applied, indicating a valid result. By this means, the device can accurately indicate the presence of COVID-19 antigen in the sample. Specification V.A: 20/24 kits X 1 pouch/box, 20/24 kits X 5/4 pouches/box V.B: 20/24 kits X 1 pouch/box, 20/24 kits X 5/4 pouches/box V.C: Duplex kits X 10/12 pouches/box, Duplex kits X 48/50 pouches/box V.D: Duplex kits/pouch/box
COVID-19 Ag/Ab Sealing Tube Twin Test Strip (Colloidal Gold) INTENDED USE: Amazing COVID-19 Ag/Ab Sealing Tube Twin Test Strip is a lateral flow immuno- chromatographic assay for the simultaneous rapid in vitro differential detection of COVID-19 nucleocapsid protein antigen and COVID-19 antibody (IgG/IgM). The kit has two strips. One strip is for the qualitative detection of COVID-19 nucleocapsid protein antigen in human nasopharyngeal, nasal secretion, saliva or/and serum specimens directly collected from individuals suspected of COVID-19 by their healthcare provider within the first seven days of symptom onset. Another strip is for the qualitative detection of COVID-19 antibody(IgG/IgM) in human serum, plasma (sodium citrate, sodium heparin, dipotassium EDTA), and whole blood (sodium citrate, sodium heparin, dipotassium EDTA or fingerstick whole blood) to aid identifying individuals with an adaptive immune response to COVID-19, indicating recent or prior infection and patients with suspected COVID-19 infection in conjunction with clinical presentation and the results of other laboratory tests. Results from the Amazing COVID-19 Ag/Ab(IgG/IgM) Sealing Tube Twin Test Strip should not be used as the sole basis for diagnosis. The kit is assistance for diagnostic and epidemiological investigation. These two strips are in the sealing tube to avoid potential biosecurity substances such as coronavirus from clinical samples, which will much help to avoid pathogen contamination and spreading to the operator and its environment. The kit is intended for use by medical professionals or trained operators who are proficient in performing tests and trained clinical laboratory personnel or individuals trained in point of care settings.
COVID-19 Ag/Ab(IgG/IgM) Sealing Tube Test Strip (Colloidal Gold):- INTENDED USE: Amazing COVID-19 Ag/Ab(IgG/IgM) and Influenza Ag(A/B) Sealing Tube Twin Test Strip is a lateral flow immunochromatographic assay for the simultaneous rapid in vitro differential detection of COVID-19 and Influenza virus. The kit has two strips. One is for the qualitative detection of COVID-19 nucleocapsid protein antigen and Influenza virus type A in human nasopharyngeal, nasal secretion, saliva or/and serum directly collected from individuals suspected of COVID-19 by their healthcare provider within the first seven days of symptom onset. Another is for the qualitative detection of COVID-19 antibody(IgG/IgM) in human serum, plasma (sodium citrate, sodium heparin, dipotassium EDTA) and whole blood (sodium citrate, sodium heparin, dipotassium EDTA or fingerstick whole blood) and Influenza virus type B in human nasopharyngeal, nasal secretion, saliva or/and serum specimens to aid identifying individuals with an adaptive immune response to COVID-19, indicating recent or prior infection and patients with suspected COVID-19 infection in conjunction with clinical presentation and the results of other laboratory tests. Results from the Amazing COVID-19 Ag/Ab(IgG/IgM) and Influenza Ag(A/B) Sealing Tube Twin Test Strip should not be used as the sole basis for diagnosis. The kit is assistance for diagnostic and epidemiological investigation. These two strips are in the sealing tube to avoid potential biosecurity substances such as coronavirus from clinical samples, which will much help to avoid pathogen contamination and spreading to the operator and its environment. The kit is intended for use by medical professionals or trained operators who are proficient in performing tests and trained clinical laboratory personnel or individuals trained in point of care settings.
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On March 23, Lepu SARS-CoV-2 Antigen Test Kit was granted special approval by the German Federal Institute for Drugs and Medical Devices (BfArM) for self-testing in Germany. This allows the users to apply tests at home with the aid of sample nasal swabs.
Non-invasive COVID TEST Simple to use Convenient, no devices required Rapid, get a result in 15 minutes Stable, with high accuracy Inexpensive, cost-efficiency
Place of Origin: China Brand Name: OEM Model Number: CL-GI0010 Disinfecting Type: Far Infrared Properties: DIAGNOSTIC Instruments, Medical Polymer Materials & Products Size: 1pc/box,non-sterile Stock: NO Shelf Life: 1years Material: 100% Nylon Quality Certification: ce Instrument classification: Class I Safety standard: None Product name: Disposable Pap Smear Kits Application: Gynaecologial Examination Certificate: CE/ISO13485 Package: 1pc/box, 400pcs/ctn
