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世聯博研(北京)科技有限公司 主營:Flexcell細胞力學和regenhu細胞3D生物打印機銷售技術服務: 美國Flexcell品牌FX-5000T細胞牽張應力加載培養系統,FX-5K細胞顯微牽張應力加載培養系統,Tissue Train三維細胞組織培養與測試系統,FX-5000C三維細胞組織壓應力加載培養系統,STR-4000細胞流體剪切應力加載培養系統,德國cellastix品牌Optical Stretcher高通量單細胞牽引應變與分析系統 Regenhu品牌3D discovery細胞友好型3D生物打印機,piuma細胞納米壓痕測試分析、aresis多點力學測試光鑷,MagneTherm細胞腫瘤電磁熱療測試分析系統
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主營產品: Flexcell細胞力學和regenhu細胞3D生物打印機銷售技術服務: 美國Flexcell品牌FX-5000T細胞牽張應力加載培養系統,FX-5K細胞顯微牽張應力加載培養系統,Tissue Train三維細胞組織培養與測試系統,FX-5000C三維細胞組織壓應力加載培養系統,STR-4000細胞流體剪切應力加載培養系統,德國cellastix品牌Optical Stretcher高通量單細胞牽引應變與分析系統 Regenhu品牌3D discovery細胞友好型3D生物打印機,piuma細胞納米壓痕測試分析、aresis多點力學測試光鑷,MagneTherm細胞腫瘤電磁熱療測試分析系統
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CleanPlex? Alzheimer and Dementia Disease Panel

  • 如果您對該產品感興趣的話,可以
  • 產品名稱:CleanPlex? Alzheimer and Dementia Disease Panel
  • 產品型號:
  • 產品展商:Paragon Genomics CleanPlex
  • 產品文檔:無相關文檔
簡單介紹

The CleanPlex? Alzheimer and Dementia 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 32 genes associated with Alzheimer and Dementia Disease.

產品描述

Product Description

The CleanPlex® Alzheimer and Dementia 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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