HLA-DRB1 NGS typing Kit is an in vitro diagnostic test that detects and distinguishes allelic genes of HLA-DRB1 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-DRB1 NGS typing Kit accurately reads the HLA-type Acuracy % (95% Confidence Interval) in DRB1 Locus within a total of 35 hours from DNA extraction to NGS results analysis to help with pre-transplant testing.
HPV is a virus that causes papillomas (benign tumors), and about 200 types have been discovered so far. Some types of HPV are known to be the direct cause of cervical cancer, head and neck cancer, etc. In particular, in the case of cervical cancer, more than 99% of the causes are reported to be caused by HPV. If it is detected early, it is easy to treat, but if it is detected late, the 5-year survival rate is less than 15% even with treatment, so regular check-ups are very important. SML Genetree has developed the world's first Ezplex�® HPV NGS Kit to diagnose HPV using the NGS method. Unlike the existing methods that only detected up to 20 to 40 types and only positive-negative, NGS was introduced to provide positive results for 45 types of HPV (up to 100 types including for export) according to the amount of DNA detected in steps 1 to 3 Semi-quantitative inspection of the level is possible. It has a high level of automation that is close to full automatic. The time has been shortened so that up to 480 people can be analyzed within 16 hours with one analysis, and it is possible to distinguish HPV species that were difficult to distinguish precisely. Unlike the existing sequencing method, the NGS method has been highly evaluated for its potential as a precision medical technology that can dramatically reduce time and cost by analyzing numerous DNAs at high speed. As a result of clinical efficacy evaluation with more than 2500 clinical specimens in large domestic hospitals, it is a product with high sensitivity and specificity compared to existing tests.
Ezplex�® SARS-CoV-2 G Kit, developed by SML Genetree, is a product that has received Emergency Use Authorization (EUA) from the U.S. Food and Drug Administration (FDA). This is an in vitro diagnostic test that qualitatively detects the nucleic acids of SARS-CoV-2 (RdRp and N genes) in sputum to aid in emergency screening for COVID-19. This product can be used for a large amount of screening tests because it can perform a pooling test, unlike the products that the existing domestic companies have approved for emergency use by the FDA. For the combined test, samples are collected in units of 5 people and tested. If positive, individual tests are performed. In the case of a negative test, all tests are performed in a negative way. In particular, since a large number of samples are tested at once, the test is only possible with high sensitivity and specificity compared to existing diagnostic kits. According to the FDA, it was confirmed that 100% agreement was achieved in the result comparison test of individual and collective tests, and it was the 20th in the world and the first Korean company to pass the test. Excellent clinical performance was demonstrated by confirming high sensitivity and specificity through clinical evaluation, and stability was confirmed for 12 months through long-term storage tests. In January 2021, it was officially approved by the Korean Ministry of Food and Drug Safety (MFDS).
Ezplex MTBC/NTM Real-time PCR Kit is an in vitro diagnostic test that simultaneously detects Mycobacterium tuberculosis complex (MTBC) and 20 types of nontuberculous mycobacteria (NTM). Sensitivity : Multiple gene targets for MTBC and NTM. Clinical Performance: Validated clinical performance. Fast Results: Testing can be completed within 2 hours post extraction.
Ezplex Respiratory Pathogens Real-time PCR Kit is an in vitro diagnostic test for the qualitative detection of 19 respiratory viruses and 6 types of pneumonia-causing bacteria through nucleic acids isolated and extracted from human throat swabs using real-time polymerase chain reaction Comprehensive Panel- One test can identify 19 respiratory viruses and 6 bacterial species simultaneously. Sensitivity Detection of all targeted viruses and bacteria with high sensitivity. Convenience Genetree Viewer analysis software available for users to conveniently produce test results. Clinical Performance: Clinical testing confirmed the high sensitivity and specificity. Stability: Shelf life of up to 12 months. Analytical Specificity: Testing of 31 species of microorganisms showed no cross reactivity.
!!!!!!!!!!Buy 40000 Test will free one machine !!!!!!!! Economical Practical Stable and accurate heating and temperature control system Excellent optical system Powerful comprehensive performance Capacity 96x 0.2ml tubes (low profile and standard) slides tube, 1x 96-well microplate Dynamic range 1~1010 Copies Applied probe 1st channel: FAM/ SYBR-Green 2nd channel: HEX, JOE, VIC, TET 3rd channel: ROX Texas -Red 4th channel: CY5 Test method four-fold fluorescence detection Thermal cycle temperature control semiconductor thermoelectric module Temperature Range 4.0�°C - 99.0�°C Heating and cooling Rate â?¥1.5�°C/sec Thermal Accuracy â?¤0.5�°C (at 90�°C) Thermal Uniformity â?¤0.5�°C (at 90�°C) Hot cover temperature range 50�°C - 108�°C Optical detection excitation wavelength 300-800nm Detection wavelength 500-800nm Fluorescence repeatability CVâ?¤ 3% Fluorescent linearity râ?¥0.99 coefficient of correlation Software application genotyping by qualitative, absolute quantitative, standard solution curve, relative quantitative and endpoint method Scanning method full plate, specified rank scanning Data export format Excel, CVS Custom report form support The operating system Window 7/8/8.1/10 Minimum computer configuration Intel or AMD Dual-2.8GHz, more than 4G memory and 128GB Power Supply AC 220V~, 50Hz,
Monkeypox Virus Real-time PCR Kit. PM for details.
Real - Time OneStep RT-PCR based assay system for detection of 2019-nCoV (CE-IVD)
RTPCR testing kits are used for testing golden test processes to detect Covid19 viruses in patients.
OSANG An established PCR test kit that has had exceptional results both in the lab and in real world settings with major countries reporting sensitivity results. The PCR is the first Korean test kit to receive FDA, EUA, and CE approval, allowing this test kit to be sold globally without restrictions. We are able to secure ample volume reliably.
Intended Use Novel Coronavirus (2019-nCoV) Real-time RT-PCR Kit is a real-time RT-PCR test intended for the qualitative detection of nucleic acid from the 2019-nCoV in oropharyngeal swabs and bronchoalveolar lavage fluid collected form individuals suspected of COVID-19 by their healthcare provider. About SARS-CoV-2 Specific antibodies will be produced within days to weeks as the immune system makes immune defense against the SARS-CoV-2 infection. Total antibody detection is an aid in the diagnosis of patients with suspected SARS-CoV-2 infection in conjunction with clinical symptoms and result of other diagnostic methods. The test result should not be used as the sole basis for diagnosis and exclusion of SARS-CoV-2 infection. Total antibody may not be detected in the first few days of infection. SARS-CoV-2 neutralizing antibody is a protective soluble protein secreted by adaptive immunizing cells after inoculation with SARS-CoV-2 vaccine or infection with SARS-CoV-2. These antibodies can specific bind with virus RNA binding domain (RBD) to block the binding of RBD with angiotensin-converting enzyme 2 (ACE2) on human cells surface, thus prevent the virus or its genetic material into the human cell and virus infection. Benifits of the Kit 1) Room Temperature Transportation 2) Cost-Effective Shipping The shipping is at room temperature, with no need of cold chain shipping. 3) Highly Sensitive, Highly Specific Highly sensitive and highly specific for 2019-nCoV, reliable identification of COVID-19. 4) Environmentally Friendly The kit needs neither bulky packaging nor cold chain shipping. Contents A kit contains: Package specifications: 24 tests/kit, 48 tests/kit 1) 2019-nCoV-PCR Master Mix (Lyophilized Powder): 1 bottle/box 2) 2019-nCoV-PCR Positive Control (Lyophilized Powder):1 bottle/box 3) 2019-nCoV Diluent: 1 bottle/box 4) User Manual Note: Do not mix or interchange different batches of kits.
Novel Coronavirus (2019-nCoV) Real-time RT-PCR Kit is a real-time RT-PCR test intended for the qualitative detection of nucleic acid from the 2019-nCoV in oropharyngeal swabs and bronchoalveolar lavage fluid collected from individuals suspected of COVID-19 by their healthcare provider. A kit contains: Package specifications: 24 tests/kit, 48 tests/kit 1) 2019-nCoV-PCR Master Mix (Lyophilized Powder): 1 bottle/box 2) 2019-nCoV-PCR Positive Control (Lyophilized Powder):1 bottle/box 3) 2019-nCoV Diluent: 1 bottle/box 4) User Manual
OUR AUTHORIZED BIO TECH FATORY HAD QUICKLY TEST KIT (Saliva in 10 minutes 94.6-99.7% accurate, the world's most advanced, Europe, Canada, big seller) ANS PCR FROM SOUTH Korea Pls Send The Loi To Long Turn International Consulting Group Ltd
Product Description : The PaxView COVID -19 real-time RT-PCR Kit detects the novel coronavirus, COVID-19 using one-step real-time RT-PCR in a single tube intended for in vitro diagnostic use. The target genes for the detecton of the virus are Orf1ab and N gene. The sequence of primers and probes for the amplification were adapted from sources published by China CDC and WHO. The kit includes primers and probe set targeting the human RNase P gene that serves as an internal positive control for the real-time RT-PCR. Price of product ( USD price or FOB price) : 1no testing 20 USD 1kit testing = 96no testing 1kit = 96no * 24 USD = 2208 USD (base on Qty negociable) Product origin ; korea Key Specifications/Special Features : 1. with in 3hour testing result in come 2. One item 96person can check 3. 100% correct result coming then other method 4. It is same process in korea Minimum Order Size and Packgaing details : 50kit in box 500 x 460 x350 6kg MOQ : 500
UE had been striving to develop and enhance our products to empower anesthesiologists to convey a sense of expertise in all possible conditions, being fully aware that anesthesiologists race against time to save lives, and the primary step is tracheal intubation in a few precious seconds. UE integrates R&D, manufacturing, sales, and after-sales service. Our products are CE, FDA, South Korea KFDA, and CFDA approved and have complied with local regulatory requirements from different countries. Display 3" TFT LCD, 720x480 px Tilt and Rotation 0-110 tilt, 0-270 rotate Memory 32G, take> 400k photos, record 16 hrs of video Bettery Life 3.5 hrs on a full charge
RT PCR TEST KITS FOR COVID ARE AVAILABLE DIRECTLY FROM MANUFACTURERS IN SOUTH KOREA. No intermediaries. Please contact For quotes only if you are a buyer.
Dear sir we are korean trading company we supply the covid-19 test kit from korean factory we supply 1.RT-PCR test kit 2.Antibody test kit 3.Antigene test kit
Multiplex One Step RT-qPCR Probe Kit is a multiplex quantitative PCR kit based on RNA as template. In the process of the experiment, reverse transcription and quantitative PCR were carried out in the same tube, which simplified the experimental operation and reduced the risk of contamination. In this kit, the first strand cDNA was efficiently synthesized by heat-resistant Hifair V reverse transcriptase and quantitatively amplified by UNICON HotStart Taq DNA polymerase. The kit mainly contains optimized MP buffer, enzymes mix, etc. The buffer solution already contains Mg2+ and dNTP. In addition, the factors that can effectively inhibit the non-specific PCR amplification and improve the amplification efficiency of multiple qPCR reactions are added, which can ensure the amplification efficiency and carry out up to four reactions. Quantity: 100 T, 1000 T, 10000 T Applications: RT-qPCR, 4-plex reaction Sample Type: RNA template main enzyme: Hifair V Reverse Transcriptase,UNICON HotStart Taq DNA Polymerase Category: IVD PCR Research Area: RT-qPCR
Specification: 50T/kit or 100T/kit vial; 48T/kit or 96T/kit 0.1mL 8 strips/0.2mL 8 strips. Canine distemper virus(CDV) is caused by a single-stranded RNA virus of the family . The disease is highly contagious via inhalation. The distemper virus real time PCR detection kit is intended for the qualitative detection of Canine distemper virus in samples by using real time PCR systems.
RT-PCR direct Detection Kit is intended to be used to achieve direct detection of Severe acute respiratory syndrome coronavirus 2 viral RNA from nasal swabs, nasopharyngeal swabs and oropharyngeal swabs from patients with signs and symptoms of infection who are suspected of COVID-19. This product provides dual-detections of two independent genes of a single tube. gene and N gene is amplified and detected in FAM and HEX channel, respectively. An internal control is set with a Cy5 labeled probe using the RNase P gene of human as the target, to monitor the amplification effect of the detection system. Our nucleic acid detection reagent can be transported at room temperature by freeze-drying technology, and can be stored at low temperature for a long time for one and a half years, and maintain good effectiveness.
