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入驻时间：2013-05-06
联系人：王荣
电话：010-67529703
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Email：SLBY800@163.COM

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CleanPlex® Comprehensive Neuropathy Panel

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产品名称：CleanPlex® Comprehensive Neuropathy Panel
产品型号：
产品展商：Paragon Genomics CleanPlex
产品文档：无相关文档
发布时间：2020-03-28
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简单介绍

The CleanPlex® Comprehensive Neuropathy 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 Comprehensive Neuropathy.

产品描述

Product Description

The CleanPlex® Comprehensive Neuropathy 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 Comprehensive Neuropathy. 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

Gene List:
AARS, AIFM1, ATL1, ATP7A, BICD2, BSCL2, DCTN1, DNAJB2, DNM2, DNMT1, DYNC1H1, EGR2, ELP1, FGD4, FIG4, GAN, GARS, GDAP1, GJB1, GNB4, HARS, HINT1, HSPB1, HSPB8, IGHMBP2, INF2, KIF1A, KIF5A, LITAF, LMNA, LRSAM1, MED25, MFN2, MORC2, MPZ, MTMR2, NDRG1, NEFL, NGF, NTRK1, PDK3, PLEKHG5, PMP22, PRPS1, PRX, RAB7A, REEP1, RETREG1, SBF1, SBF2, SCN11A, SCN9A, SH3TC2, SLC12A6, SLC52A2, SLC52A3, SLC5A7, SPTLC1, SPTLC2, TFG, TRIM2, TRPV4, TTR, WNK1, YARS

References:
Auer-Grumbach M. Hereditary sensory and autonomic neuropathies. Handb Clin Neurol. 2013;115:893-906.

Boyer O, et al. Mutations in INF2 are a major cause of autosomal dominant focal segmental glomerulosclerosis. J Am Soc Nephrol. 2011 Feb;22(2):239-45.

Rotthier A, et al. Genes for hereditary sensory and autonomic neuropathies: a genotype-phenotype correlation. Brain. 2009 Oct;132(Pt 10):2699-711.