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NEXTflex® Congenital Hyperinsulinism Amplicon Panel for illumina Detayı

NEXTflex® Congenital Hyperinsulinism Amplicon Panel for illumina

NEXTflex® Congenital Hyperinsulinism Amplicon Panel for illumina-

Validated panel for detection of the ABCC8, GLUD1, KCNJ11, GCK, HADH, HNF4A, INS, INSR, PDX1, SLC16A1 and UCP2 genes with library prep reagents and 384 barcodes for Illumina® sequencing

  • 100% coverage of ABCC8, GLUD1, KCNJ11, GCK, HADH, HNF4A, INS, INSR, PDX1, SLC16A1 and UCP2  

    exons and flanking intron-exon boundaries 

  • 98% 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-Congenital-Hyperinsulinism-Amplicon-Panel

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