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NEXTflex® Nephrotic Syndrome-1 Amplicon Panel for illumina Detayı

NEXTflex® Nephrotic Syndrome-1 Amplicon Panel for illumina

NEXTflex® Nephrotic Syndrome-1 Amplicon Panel for illumina-

Validated panel for the detection of mutation in the NPHS1, NPHS2, and WT1 genes with library prep reagents and 384 barcodes for Illumina® sequencing

  • 100% coverage of NPHS1, NPHS2, and WT1 exons and flanking intron-exon boundaries 
  • 97% uniformity of amplicons on 0.2x coverage; 100% of amplicons detected at >0.1X mean coverage
  • 384 unique barcodes available
  • Complete solution for targeted sequencing, including gene specific primers, PCR Master Mix, clean-up beads, and up to 384 barcodes
  • Low input - Only 20 ng DNA isolated from fresh or frozen samples required
http://www.biooscientific.com/NEXTflex-Nephrotic-Syndrome-1-Amplicon-Panel

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