CDAMP® Hereditary Cancer 37 Panel Kit


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CDAMP® Hereditary Cancer 37 Panel Kit: pdf
CDAMP® Hereditary cancer 37 panel Kit Gene List: pdf
Product Infomation
Product Description: CDAMP® Hereditary Cancer 37 Panel Kit is specially designed for target enrichment and library preparation using a fast and simple workflow, in next generation sequencing (NGS) applications on Illumina platforms. The panel contains 1,447 amplicons covered a total of 37 genes associated with cancers of the breast, ovary, uterus, prostate, gastric and colorectal, etc. The panel can be used to detect inherited mutations. The Kit enables library preparation from as low as 10 ng genomic DNA per multiplex PCR reaction and allows a single library construction within 3 hours. This kit provides all required enzymes and buffers for Multiplex PCR Reaction, Purification, Indexing and Amplification. Magnetic beads can be used in library purification rapidly. The panel is optimized to deliver high specificity and highly uniform sequencing results. All Kit components are subjected to stringent quality control ensuring the consistency and reproducibility of library preparation.
Features: Ready-to-use and containing all necessary reagents for a rapid set-up. Fast and streamlined workflow enables library preparation in just 3 hours. Mutation detection on DNA amounts as low as 10 ng per multiplex PCR reaction. Optimized to deliver high specificity (≥95%) and high coverage uniformity (≥95%) sequencing results. All Kit components are subjected to stringent quality control ensuring the consistency and reproducibility of library preparation.
Enrichment Method: Amplicon sequencing
Number of Genes: 37
Target Size: 202kb
Amplicon Length : 105-299bp
Number of Primer Pools: 2
Sample Input Size : 10ng per pool for high quality gDNA; 20ng per pool for FFPE DNA
Species: human
Sample Type: Genomic DNA from whole blood, tissues, saliva, formalin-fixed paraffin-embedded (FFPE) tissues
Sequencing Platform: Illumina
Application: It is recommended to use this kit for: Germline mutations (Single nucleotide variations, insertions-deletions, structural rearrangement) Disease predisposition
Storage: All the components should be stored at -20℃.
* For Research Use Only. Not for use in diagnostic procedures.

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