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Our Myeloid DNA NGS Reference Materials encompass 23 DNA variants associated with myeloid. These variants have been expertly designed to cover a range of allele frequencies (5%−15%) and critical mutation types, including Single Nucleotide Variants (SNV) and insertion deletions (INDELs). Our product employs high-sensitivity digital PCR detection for precise quantification of various variants. This ensures that your detection methods exhibit exceptional sensitivity and accuracy across different allele frequencies.
Number of Variants: 23
Allele Frequency: 5%−15%
Amount: 375 ng
Buffer: 1 mM Tris, 0.1 mM EDTA, 10 mM KCl, pH 8.0
FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC PROCEDURES.
Method: | Validated Method: ddPCR & NGS |
Concentration: | 15 ng/µL |
Application: | Assay Validation: Ensure the accuracy and sensitivity of liquid biopsy assays. LOD Determination: Precisely establish the limit of detection for your assays. Assay Development: Accelerate the development and optimization of myeloid assays. Research: Drive innovation in myeloid research with realistic patient sample simulations. Drug Development: Assess the performance of drug candidates in myeloid studies. |
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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