Microarray 60K AFCVS and Karyotyping and FISH Chromosome 21 Test sale cost 5200 AED
Lung Cancer Panel 3 EGFRALK1ROS1MET Test sale cost 6600 AED Lung Cancer Panel 3 EGFRALK1ROS1MET Test Cost 8,000 د.إ Original price was: 8,000 د.إ.6,600 د.إCurrent price is: 6,600 د.إ.
GATA2 Full-Length Gene Sequencing Chronic Neutropenia MonoMac Syndrome Mylodysplasia AML Test sale cost 2800 AED GATA2 Full-Length Gene Sequencing Chronic Neutropenia MonoMac Syndrome Mylodysplasia AML Test Cost 6,400 د.إ Original price was: 6,400 د.إ.2,800 د.إCurrent price is: 2,800 د.إ.
Sale!

Microarray 60K AFCVS and Karyotyping and FISH Chromosome 21 Test Cost

Original price was: 7,000 د.إ.Current price is: 5,200 د.إ.

-26%

Microarray 60K AFCVS, along with Karyotyping and FISH (Fluorescence In Situ Hybridization) for Chromosome 21, are advanced genetic tests designed to detect chromosomal abnormalities and genetic disorders. These tests are particularly crucial in prenatal diagnostics, cancer research, and for understanding genetic diseases.

The Microarray 60K AFCVS (Array-based Comparative Genomic Hybridization) is a comprehensive test that scans the entire genome for gains and losses of genetic material, providing detailed insights into numerous genetic conditions. It is capable of detecting abnormalities that are often missed by traditional cytogenetic techniques.

Karyotyping is a test that gives a complete picture of an individual’s chromosomes. It is used to look for abnormal numbers or structures of chromosomes, which can lead to genetic diseases. It’s particularly useful for diagnosing conditions like Down syndrome, where an extra copy of chromosome 21 is present.

FISH for Chromosome 21 is a more targeted approach, specifically designed to detect abnormalities in chromosome 21, including microdeletions or duplications that could lead to genetic disorders such as Down syndrome. This technique uses fluorescent probes that bind to specific parts of the chromosome, making it easier to visualize and analyze these regions under a microscope.

Offered at DNA Labs UAE, the combined test cost for these advanced genetic testing techniques is 5200 AED. This comprehensive suite of tests provides invaluable insights for individuals seeking detailed information about their genetic health, potential genetic disorders, or the genetic health of their unborn child. DNA Labs UAE is equipped with state-of-the-art technology and staffed by expert professionals to ensure accurate and reliable test results.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
Guaranteed Safe Checkout

Microarray 60K AFCVS and Karyotyping and FISH chromosome 21 Test

At DNA Labs UAE, we offer the Microarray 60K AFCVS and Karyotyping and FISH chromosome 21 Test for genetic analysis. This test is designed to identify any chromosomal abnormalities in fetal cells obtained from amniocentesis or chorionic villus sampling (CVS).

Test Components

  • Sterile Container/ Sterile Normal Saline Container

Price

5200.0 AED

Sample Condition

Amniotic fluid/ Chorionic villi

Report Delivery

7-9 days

Method

Microarray Agilent + Cell Culture + FISH

Test Type

Genetics

Doctor

Gynecologist

Test Department

Pre Test Information

Microarray 60K (AF/CVS) + Karyotyping + FISH chromosome 21 can be done with a Doctor’s prescription. Prescription is not applicable for surgery and pregnancy cases or people planning to travel abroad.

Test Details

Microarray 60K (AF/CVS) is a genetic test that analyzes a small sample of fetal cells obtained from either amniocentesis or chorionic villus sampling (CVS) to identify any chromosomal abnormalities. This test can detect a wide range of chromosomal disorders, including Down syndrome, Turner syndrome, and Edwards syndrome.

Karyotyping is another genetic test that examines the chromosomes in a sample of fetal cells to detect any abnormalities. This test involves growing the cells in a laboratory and staining them to visualize the chromosomes under a microscope. Karyotyping can detect larger chromosomal abnormalities, such as deletions, duplications, and translocations.

FISH (fluorescence in situ hybridization) chromosome 21 is a specific type of genetic test that uses fluorescent probes to identify any abnormalities on chromosome 21. This test is often used in conjunction with other genetic tests, such as microarray and karyotyping, to confirm a diagnosis of Down syndrome.

Together, these three tests provide a comprehensive evaluation of the fetal chromosomes and can help identify any genetic abnormalities that may affect the health of the developing fetus.

Test Name Microarray 60K AFCVS and Karyotyping and FISH chromosome 21 Test
Components Sterile Container/ Sterile Normal Saline Container
Price 5200.0 AED
Sample Condition Amniotic fluid\/ Chorionic villi
Report Delivery 7-9 days
Method Microarray Agilent]+ Cell Culture+ FISH
Test type Genetics
Doctor Gynecologist
Test Department:
Pre Test Information Microarray 60K (AF/CVS) + Karyotyping + FISH chromosome 21 can be done with a Doctors prescription. Prescription is not applicable for surgery and pregnancy cases or people planing to travel abroad.
Test Details

Microarray 60K (AF/CVS) is a genetic test that analyzes a small sample of fetal cells obtained from either amniocentesis or chorionic villus sampling (CVS) to identify any chromosomal abnormalities. This test can detect a wide range of chromosomal disorders, including Down syndrome, Turner syndrome, and Edwards syndrome.

Karyotyping is another genetic test that examines the chromosomes in a sample of fetal cells to detect any abnormalities. This test involves growing the cells in a laboratory and staining them to visualize the chromosomes under a microscope. Karyotyping can detect larger chromosomal abnormalities, such as deletions, duplications, and translocations.

FISH (fluorescence in situ hybridization) chromosome 21 is a specific type of genetic test that uses fluorescent probes to identify any abnormalities on chromosome 21. This test is often used in conjunction with other genetic tests, such as microarray and karyotyping, to confirm a diagnosis of Down syndrome.

Together, these three tests provide a comprehensive evaluation of the fetal chromosomes and can help identify any genetic abnormalities that may affect the health of the developing fetus.

SKU: TEST-800 Category:

Related products