CleanPlex® Organic Acidemia/Aciduria Panel

The CleanPlex® Organic Acidemia/Aciduria Panel is a pre-designed and made-to-order multiplex PCR / amplicon-based targeted sequencing assay for examining the germline variants or mutations across 65 genes associated with Organic Acidemia/Aciduria.

Product Description

The CleanPlex® Organic Acidemia/Aciduria Panel is a pre-designed and made-to-order multiplex PCR / amplicon-based targeted sequencing (NGS) assay designed to examine the germline variants or mutations across 65 genes associated with Organic Acidemia/Aciduria. The panel targets all the exonic regions of those genes and the flanking intronic sequences. Compatible with just 10 ng of DNA, sequencing-ready libraries can be prepared using a streamlined workflow in just 3 hours. The pre-designed panel is optimized in silico to deliver data with high on-target performance and high coverage uniformity to ensure efficient use of sequencing reads.

This product is made to order. Once we receive your order, we will synthesize the panel and the kit will contain CleanPlex Multiplex PCR Primers and CleanPlex Targeted Library Kit. CleanPlex Indexed PCR Primers and CleanMag® Magnetic Beads can be ordered separately to complete the workflow from input DNA to sequencing-ready NGS libraries.

Storage Temperature

Store at -20 °C.

For Research Use Only. Not for use in diagnostic procedures.

Gene List:
ABAT, ALDH5A1, ALDH7A1, AMT, ARHGEF9, ASNS, ATP1A3, CACNA1A, CACNA1B, CBS, CLTC, COMT, DBH, DDC, DHFR, DRD3, DRD4, DRD5, FOLR1, GABRA1, GABRB3, GABRD, GABRG2, GAD1, GCH1, GCSH, GLDC, GLRA1, GLRB, GLUL, GNAQ, GPHN, HTR1A, HTR2A, MAOA, MTHFD1, MTHFR, PC, PCBD1, PHGDH, PITX3, PNPO, PSAT1, PSPH, PTS, QDPR, SLC1A3, SLC25A22, SLC46A1, SLC6A1, SLC6A2, SLC6A3, SLC6A4, SLC6A5, SLC6A9, SNAP25, SNAP29, SNCA, SPR, STXBP1, SYN1, SYN2, SYP, TH, TPH2

References:
Pronicka E, et al New perspective in diagnostics of mitochondrial disorders: two years’ experience with whole-exome sequencing at a national paediatric centre. J Transl Med. 2016 Jun 12;14(1):174.

Wen W, et al. NGS in argininosuccinic aciduria detects a mutation (D145G) which drives alternative splicing of ASL: a case report study. BMC Med Genet. 2016 Feb 3;17:9.

Additional Information

Weight40 g
Dimensions10 x 7 x 5 cm
Pack Size (Reactions)

384