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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® Neurodegenerative Disorders1 Panel

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  • 产品名称:CleanPlex® Neurodegenerative Disorders1 Panel
  • 产品型号:
  • 产品展商:Paragon Genomics CleanPlex
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简单介绍

CleanPlex® Neurodegenerative Disorders1 Panel is a pre-designed and made-to-order multiplex PCR / amplicon-based targeted sequencing assay for examining the germline variants or mutations across

产品描述

Product Description

CleanPlex® Neurodegenerative Disorders1 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 32 genes associated with Alzheimer and Dementia Disease. 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: 
ABCA7, APOE, APP, C9ORF72, CHCHD10, CHMP2B, CSF1R, DCTN1, DNMT1, FUS, GRN, HNRNPA1, HNRNPA2B1, ITM2B, MAPT, NOTCH3, OPTN, PRNP, PSEN1, PSEN2, RNF216, SNCA, SNCB, SORL1, SQSTM1, TARDBP, TBK1, TREM2, TUBA4A, TYROBP, UBQLN2, VCP


References: 
Bertram L. Next Generation Sequencing in Alzheimer’s Disease. Systems Biology of Alzheimer’s Disease. Methods in Molecular Biology, vol 1303 (2016).

Goldman JS, et al. Alzheimer’s Disease and Frontotemporal Dementia: The Current State of Genetics and Genetic Testing Since the Advent of Next-Generation Sequencing. Mol Diagn Ther 22, 505–513 (2018).

Koriath C, et al. Predictors for a dementia gene mutation based on gene-panel next-generation sequencing of a large dementia referral series. Mol Psychiatry (2018)

Rongioletti M, et al. Excess Copper in Alzheimer Disease but Not in Frontotemporal Lobar Degeneration: Next-Generation Sequencing Study of ATP7B Gene in Patients Typified by High Copper, American Journal of Clinical Pathology. (2018);150(1):S65–S66.

Gámez-Valero A,et al. Exploratory study on microRNA profiles from plasma-derived extracellular vesicles in Alzheimer’s disease and dementia with Lewy bodies. Transl Neurodegener 8, 31 (2019)

Goldman JS, et al. Alzheimer’s Disease and Frontotemporal Dementia: The Current State of Genetics and Genetic Testing Since the Advent of Next-Generation Sequencing. Mol Diagn Ther 22, 505–513 (2018).

Batoletti-Stella A, et al. Identification of rare genetic cariants in Italian patients with dementia by targeted gene sequencing. Neurobiology of Aging. 2018;66:e23-180.e31

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