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主營(yíng)產(chǎn)品: Flexcell細(xì)胞力學(xué)和regenhu細(xì)胞3D生物打印機(jī)銷售技術(shù)服務(wù): 美國(guó)Flexcell品牌FX-5000T細(xì)胞牽張應(yīng)力加載培養(yǎng)系統(tǒng),F(xiàn)X-5K細(xì)胞顯微牽張應(yīng)力加載培養(yǎng)系統(tǒng),Tissue Train三維細(xì)胞組織培養(yǎng)與測(cè)試系統(tǒng),F(xiàn)X-5000C三維細(xì)胞組織壓應(yīng)力加載培養(yǎng)系統(tǒng),STR-4000細(xì)胞流體剪切應(yīng)力加載培養(yǎng)系統(tǒng),德國(guó)cellastix品牌Optical Stretcher高通量單細(xì)胞牽引應(yīng)變與分析系統(tǒng) Regenhu品牌3D discovery細(xì)胞友好型3D生物打印機(jī),piuma細(xì)胞納米壓痕測(cè)試分析、aresis多點(diǎn)力學(xué)測(cè)試光鑷,MagneTherm細(xì)胞腫瘤電磁熱療測(cè)試分析系統(tǒng)
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CleanPlex? Alzheimer’s disease Panel

  • 如果您對(duì)該產(chǎn)品感興趣的話,可以
  • 產(chǎn)品名稱:CleanPlex? Alzheimer’s disease Panel
  • 產(chǎn)品型號(hào):
  • 產(chǎn)品展商:Paragon Genomics CleanPlex
  • 產(chǎn)品文檔:無(wú)相關(guān)文檔
簡(jiǎn)單介紹

CleanPlex? Alzheimer’s disease Panel is a pre-designed and made-to-order multiplex PCR / amplicon-based targeted sequencing assay for examining the germline variants or mutations across

產(chǎn)品描述

Product Description

CleanPlex® Alzheimer’s disease 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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