The NEXTFLEX® Targeted NGS Hybridization Panel 1 simplifies the identification of relevant SNVs, indels, and CNVs in more than 75 genes related to endocrine and metabolic disorders, hemoglobinopathies, and primary immunodeficiencies.
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For research use only. Not for use in diagnostic procedures.
This complete library preparation solution can be used with DNA isolated from DBS, blood, and other sample types and is compatible with all Illumina® sequencing platforms. This kit contains enough material to prepare 16 DNA samples for NGS sequencing.
