Xiamen Spacegen Co., Ltd.

SPACEGENHuman Pan-Cancer Drive Gene Mutations Detection Kit

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Detection of 56 cancer-related genes, including 3000 COSMIC mutation loci. Guiding individualized diagnosis and treatment of pan-cancera
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Pan cancer driver gene mutation detection panel aims at the companion diagnostic genes approved by FDA and recommended by NCCN guidelines, covering 56 genes related to cancer treatment and prognosis, including 3000 cosmic mutation sites, so as to realize low-cost, high sensitivity and high-throughput gene detection of tumor tissue and circulating free DNA of cancer patients.

Cancer is a complex polygenic disease caused by the gradual accumulation of gene mutations. When the genes regulating cell growth are mutated or damaged, the cells lose control and proliferate and differentiate disorderly and infinitely, leading to the occurrence of malignant tumors.

Tumor precise diagnosis and treatment products provide important reference basis for precise drug treatment, molecular typing and efficacy evaluation by accurately analyzing the unique gene mutation information of each tumor patient.

Core Technology:RingCap®

Applicable Disease:Pan-cancer

Instruments Validated:Illumina,Ion Torrent, MGI, etc.

Sample Type:Tumor tissue,Peripheral Blood,Pleural effusion &Ascites

Qualification:ISO13485 certificate, CAP,CE marking

 Pack Size:16 Tests/Kit,32 Tests/Kit

It is suitable for a variety of solid tumors and some hematological tumors. It is mainly used to evaluate the drug sensitivity and prognosis of all tumor patients who need targeted therapy, to assist clinicians in selecting appropriate targeted drugs, and to guide the choice of systematic treatment of patients more comprehensively. At the same time, some genetic related information can be provided to assess family genetic risk.

1.Ease of Use : With patented RingCap® technology,Library preparation in  2 steps.

2.Fast Results :  The library  preparation  takes only 3.5 hours.

3.High Sensitivity: The kit allows the detection of 1% of specific gene mutations in 10 ng DNA samples and 20 copies/μL of fusion mutations in RNA samples.;

4.Comprehensive Coverage: 3000 kinds of cosmic mutation sites can be detected at one time.