Model: iScan
Manufacturer: Illumina / USA
Fully automated Micro-array System
– The iScan status indicator lights and scan bar on the front panel show the current status of the iScan: Power (blue) – Instrument is on; Ready (green check) – Instrument has been initialized and is ready to scan; Warning (amber triangle) – Instrument error has occurred
– The scanning system uses high-performance lasers, optics, and fully automated detection systems to provide extremely rapid scan times without sacrificing data quality, which helps to process complex data when running multiple samples
– With a high signal-to-noise ratio, high sensitivity, a low limit of detection, and a broad dynamic range, the iScan System can detect single copy number changes in gene expression and DNA methylation analysis
– The system uses microarray technology, the process of scanning and analyzing are carried out on the Beadchips.
– Beadchip is based on silicon particles with the size of 1-2 μm arranged in wells with a spacing of 5.7 μm between beads, each bead is covered by hundreds to thousands copies of specific oligonucleotides to generate a perfect hybridization environment in terms of large area, ensuring the highest hybridization yield.
– Ability to analyze high-quality data with high call rates (>99.9%), reducing the positive false and negative false.
– Normal Scan Function: manual loading
– Automatic Scan function: Automatic sample loading with robot
– Automatic Sample Running:
– The Beadchip tray allows to analyze four Beadchips simultaneously
– The system operates simultaneously ≥24 samples per run on a Beadchip
– Number of samples / run varies by chemical reagent kits and applications
– Scan time for each sample varies by specialized kits and applications
TaqMan Fast Advanced Master Mix cung cấp khả năng định lượng chính xác và độ tin cậy trong thời gian ngắn trên các nền tảng thiết bị qPCR.
Thiết kế cho các quy trình phát triển của bạn Hệ thống xử lý chất lỏng tốt nhất, dẫn đầu thị trường – được kết nối với các phần bổ sung theo đề xuất từ các khách hàng trên toàn cầu
Hệ thống tự động Biomek i7 được thiết kế để tối ưu quy trình và tăng thời gian “walk-away” ở các phòng lab công suất trung bình đến lớn.
Tách chiết DNA từ tế bào và máu toàn phần:
– Dễ dàng tách chiết DNA từ máu toàn phần, buffy coat, mẫu tăm bông, hoặc mẫu nuôi cấy tế bào.
– Quy trình k cần sử dụng Proteinase K và các chất biến tính cho mẫu dịch sinh hoặc và mẫu nuôi cấy tế bào.
Viral DNA and RNA from all biological fluids:
– Quick recovery of viral RNA from plasma, serum and other samples.
– Omits the use of organic denaturants and proteases.
– High-quality viral RNA is ready for RT-PCR, sequencing, etc.
Clean-up PCR and other enzymatic reactions in as little as 2 minutes:
– Clean and concentrate up to 5 μg DNA with ≥ 6 μl elution in as little as 2 minutes with 0 μl wash residue carryover.
– Column design allows DNA to be eluted at high concentrations into minimal volumes of water or TE buffer.
– Eluted DNA is well suited for use in PCR, DNA sequencing, DNA ligation, endonuclease digestion, RNA transcription, radiolabeling, arrays, etc.
Rapid purification of DNA from cells and whole blood:
– Easy purification of high-quality DNA from whole blood, buffy coat, swabs, or cultured cells.
– Protocol excludes the use of Proteinase K and organic denaturants for biofluid and cell samples.™ are fracture resistant and chemically insert.
The Health Statistics shows that there are 200,000 tuberculosis patients and 30,000 deaths every year in Vietnam. The main cause of human tuberculosis is M. Tuberculosis, also called as tuberculosis bacteria.
GeneProof Mycobacterium tuberculosis PCR Kit applies PCR technology to detect DNA of Mycobacterium tuberculosis in samples. The kit has CE-IVD certification for in vitro Diagnostic Use.
TruSight Exome Library Preparation Kit includes reagent sets for library preparation combined with exome enrichment to sequence genes on Next Generation Sequencing System of Illumina
TruSight Tumor 170 Kit includes library preparation reagent set and uses next-generation sequencing (NGS) technology to provide a comprehensive assessment of 170 genes that are commonly related to mutations in solid tumors and somatic variants.