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.

Thông tin sản phẩm

Designed for your evolving workflow priorities Representing the best of what made Biomek an industry leading liquid handler—combined with enhancements suggested by customers around the globe—the Biomek i7 Automated Workstation has been designed to optimize workflows and increase walk-away in mid- to high-throughput labs.

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.

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.

GeneProof Hepatitis C Virus (HCV) PCR Kit applies PCR technology to detect RNA of HCV virus in patient samples. The kit has CE-IVD certification for in vitro Diagnostic Use.

GeneProof Hepatitis B Virus (HBV) PCR Kit applies PCR technology to detect DNA of HBV virus in patient 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.