There are no known causes for multiple myeloma (MM). Understanding genetic variability — including mutation co-occurrence at the single-cell level — is vitally important for clinical researchers to break the cycle of treatment response, resistance and relapse. Uncover clonal evolution insights with precision, download the Tapestri Multiple Myeloma Panel today.
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Advance your understanding of the genetic heterogeneity underpinning multiple myeloma (MM) by targeting 16 genes with 60 amplicons for single-cell DNA sequencing using our Tapestri Multiple Myeloma Panel. Covering a combination of oncogenes and tumor suppressor genes, the Multiple Myeloma Panel is designed to cover some of the most commonly mutated genes associated with MM.
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Use Tapestri Designer to add or remove content from existing catalog panels and make this panel your own with content that is relevant to your research. Or start from scratch and upload your human (hg19) or mouse (mm10) targets using gene names, genomic coordinates, or SNV IDs. Target anywhere in the whole human or mouse genome and advance your research with targeted single-cell DNA sequencing.
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