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info@cd-genomics.com
info@cd-genomics.com
Our CD CNV Reference Mix is designed to address the genomic changes known as Copy Number Variations (CNV), including amplifications and losses, in comparison to a reference genome. Our CNV Reference Mix provides a single sample with three clinically-relevant CNVs, minimizing acquisition and sequencing costs while enabling laboratories to develop, optimize, and validate their assays for detecting a range of copy numbers, including amplifications.
CD CNV Reference Mix offers an extensive selection of essential genes associated with solid tumors, including 12 genes, AKT2, BRAF, EGFR, ERBB2, FGFR3, KIT, KRAS, MET, MYC, MYCN, NTRK1, PIK3CA, each represented with varying copies reflecting the diverse CNV landscape in these cancers.
Amount: 200 ng/each
Genes: AKT2, BRAF, EGFR, ERBB2, FGFR3, KIT, KRAS, MET, MYC, MYCN, NTRK1, PIK3CA
Copy Numbers: 3
Buffer: 1 mM Tris / 0.1 mM EDTA / 10 mM Potassium Chloride pH 8.0
FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC PROCEDURES.
| Method: | Validated Method: digital PCR |
| Concentration: | 10 ng/μL |
| Application: | Our CNV Reference Mix provides a single sample with three clinically-relevant CNVs, minimizing acquisition and sequencing costs while enabling laboratories to develop, optimize, and validate their assays for detecting a range of copy numbers, including amplifications. |
| Storage: | Store at -20°C |
Please submit a detailed description of your project. We will provide you with a customized project plan to meet your research requests. You can also send emails directly to info@cd-genomics.com for inquiries.
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