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主营产品： Flexcell细胞力学和regenhu细胞3D生物打印机销售技术服务： 美国Flexcell品牌FX-5000T细胞牵张应力加载培养系统，FX-5K细胞显微牵张应力加载培养系统，Tissue Train三维细胞组织培养与测试系统，FX-5000C三维细胞组织压应力加载培养系统，STR-4000细胞流体剪切应力加载培养系统，德国cellastix品牌Optical Stretcher高通量单细胞牵引应变与分析系统 Regenhu品牌3D discovery细胞友好型3D生物打印机,piuma细胞纳米压痕测试分析、aresis多点力学测试光镊，MagneTherm细胞肿瘤电磁热疗测试分析系统
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CleanPlex® Hereditary Motor and Sensory Neuropathy (HMSN) Panel

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  • 产品名称：CleanPlex® Hereditary Motor and Sensory Neuropathy (HMSN) Panel
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  • 产品展商：Paragon Genomics CleanPlex
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简单介绍

CleanPlex® Hereditary Motor and Sensory Neuropathy (HMSN) 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 ge

产品描述

Product Description

CleanPlex®  Hereditary Motor and Sensory Neuropathy (HMSN) 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.

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