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Nx Gen Sequencing Dementia Test Cost

Original price was: 5,200 د.إ.Current price is: 4,680 د.إ.

-10%

The “Nx Gen Sequencing Dementia Test” is a cutting-edge diagnostic tool available at DNA Labs UAE, designed to identify genetic markers associated with dementia. Utilizing Next Generation Sequencing (NGS) technology, this test comprehensively scans the genome for mutations and variants that are known to increase the risk of developing dementia, including Alzheimer’s disease and other forms of cognitive decline. The test is priced at 4680 AED, reflecting the advanced technology and expertise required to perform the analysis. By providing a detailed genetic risk profile, the Nx Gen Sequencing Dementia Test offers individuals valuable insights into their genetic predisposition towards dementia, enabling early intervention strategies and personalized management plans to mitigate the impact of these conditions.

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  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
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Nx GEN SEQUENCING DEMENTIA Test – DNA Labs UAE

Are you concerned about dementia? DNA Labs UAE offers the Nx GEN SEQUENCING DEMENTIA Test, a cutting-edge genetic test that can provide valuable insights into the genetic basis of dementia. In this blog post, we will discuss the test components, cost, sample condition, report delivery, method, and more.

Test Details

The Nx GEN SEQUENCING DEMENTIA Test utilizes Next-generation sequencing (NGS), a high-throughput DNA sequencing technology. NGS allows for the rapid and efficient analysis of large amounts of genetic information, revolutionizing the field of genomics. This advanced technology has applications in disease diagnostics and personalized medicine.

When it comes to dementia, NGS can be used to identify genetic variations and mutations associated with the disease. By sequencing the entire genome or specific regions of interest, researchers can analyze the genetic makeup of individuals and compare it to known genetic markers for dementia. NGS can help identify rare genetic variants that may contribute to an individual’s risk of developing dementia.

NGS is particularly useful in identifying genetic mutations responsible for inherited forms of dementia, such as familial Alzheimer’s disease or frontotemporal dementia. Additionally, NGS can study the role of epigenetic modifications in dementia. Epigenetic changes, like DNA methylation or histone modifications, can influence gene expression and have been implicated in neurological disorders, including dementia. NGS provides a comprehensive view of the epigenome and helps identify specific epigenetic changes associated with dementia.

Overall, NGS holds great promise in advancing our understanding of the genetic basis of dementia. It may eventually lead to the development of more accurate diagnostic tests and targeted therapies for this devastating disease.

Test Components

The Nx GEN SEQUENCING DEMENTIA Test analyzes the following genetic components:

  • APOE
  • APP
  • CHMP2B
  • CSF1R
  • FUS
  • GRN
  • MAPT
  • PRNP
  • PSEN1
  • PSEN2
  • SORL1
  • TARDBP
  • TREM2
  • UBE3A
  • VCP

Price

The cost of the Nx GEN SEQUENCING DEMENTIA Test is 4680.0 AED.

Sample Condition

To perform the test, you need to submit 10 mL (5 mL minimum) of whole blood from 2 Lavender Top (EDTA) tubes. It is essential to ship the sample refrigerated and avoid freezing it. Additionally, a duly filled Whole Exome Sequencing Consent Form (Form 37) is mandatory.

Report Delivery

The sample is collected daily by 9 am, and the report will be delivered within 40 working days.

Method

The Nx GEN SEQUENCING DEMENTIA Test utilizes Next-generation sequencing (NGS) and Sanger sequencing methods to analyze the genetic information.

Test Type

The Nx GEN SEQUENCING DEMENTIA Test falls under the category of Genetic Disorders-Dementia.

Doctor and Test Department

The test is recommended by neurologists and falls under the Molecular Diagnostics department.

Pre Test Information

Before taking the Nx GEN SEQUENCING DEMENTIA Test, it is mandatory to fill out the Whole Exome Sequencing Consent Form (Form 37).

Take control of your health and gain valuable insights into the genetic basis of dementia with the Nx GEN SEQUENCING DEMENTIA Test offered by DNA Labs UAE. Stay informed and make informed decisions about your well-being.

Test Name Nx GEN SEQUENCING DEMENTIA Test
Components APOE, APP, CHMP2B, CSF1R, FUS, GRN, MAPT, PRNP, PSEN1, PSEN2, SORL1, TARDBP, TREM2, UBE3A, VCP
Price 4680.0 AED
Sample Condition Submit 10 mL (5 mL min.) whole blood from 2 Lavender Top (EDTA) tubes. Ship refrigerated. DO NOT FREEZE. Duly filled Whole Exome Sequencing Consent Form (Form 37) is mandatory.
Report Delivery Sample Daily by 9 am; Report 40 Working days
Method NGS, Sanger sequencing
Test type Genetic Disorders-Dementia
Doctor Neurologist
Test Department: MOLECULAR DIAGNOSTICS
Pre Test Information Duly filled Whole Exome Sequencing Consent Form (Form 37) is mandatory.
Test Details

Next-generation sequencing (NGS) is a high-throughput DNA sequencing technology that allows for the rapid and efficient analysis of large amounts of genetic information. It has revolutionized the field of genomics and has applications in various areas, including disease diagnostics and personalized medicine.

When it comes to dementia, NGS can be used to identify genetic variations and mutations that may be associated with the disease. By sequencing the entire genome or specific regions of interest, researchers can analyze the genetic makeup of individuals and compare it to known genetic markers for dementia.

NGS can help identify rare genetic variants that may contribute to an individual’s risk of developing dementia. It can also aid in the identification of genetic mutations that may be responsible for inherited forms of dementia, such as familial Alzheimer’s disease or frontotemporal dementia.

Furthermore, NGS can be used to study the role of epigenetic modifications in dementia. Epigenetic changes, such as DNA methylation or histone modifications, can influence gene expression and have been implicated in various neurological disorders, including dementia. NGS can provide a comprehensive view of the epigenome and help identify specific epigenetic changes associated with dementia.

Overall, NGS holds great promise in advancing our understanding of the genetic basis of dementia and may eventually lead to the development of more accurate diagnostic tests and targeted therapies for this devastating disease.