QF PCR Panel 131821XY and Karyotyping Test sale cost 2400 AED
Methylenetetrahydrofolate Reductase MTHFR Factor V F5 Factor II F2 Test sale cost 2400 AED Methylenetetrahydrofolate Reductase MTHFR Factor V F5 Factor II F2 Test Cost 3,200 د.إ Original price was: 3,200 د.إ.2,400 د.إCurrent price is: 2,400 د.إ.
All PCR Panel Cytogenetics and PCR BCR-ABL TEL-AML1 MLL E2A Test sale cost 2300 AED All PCR Panel Cytogenetics and PCR BCR-ABL TEL-AML1 MLL E2A Test Cost 3,000 د.إ Original price was: 3,000 د.إ.2,300 د.إCurrent price is: 2,300 د.إ.
Sale!

QF PCR Panel 131821XY and Karyotyping Test Cost

Original price was: 3,200 د.إ.Current price is: 2,400 د.إ.

-25%

The QF PCR Panel 131821XY and Karyotyping Test is a comprehensive diagnostic tool used to detect genetic abnormalities and chromosomal disorders. Conducted at DNA Labs UAE, this test combines the precision of Quantitative Fluorescence Polymerase Chain Reaction (QF-PCR) with the broad scope of karyotyping analysis to offer a detailed examination of an individual’s genetic makeup.

The QF-PCR component specifically targets and amplifies small sections of DNA to detect chromosomal anomalies related to common conditions such as Down syndrome, Edwards syndrome, and Patau syndrome, as well as abnormalities in the sex chromosomes (XY). This technique is highly sensitive and can deliver results quickly, making it an invaluable tool for early diagnosis.

Karyotyping, on the other hand, provides a broader view by examining the entire set of chromosomes in a cell. This method can identify structural abnormalities, such as deletions, duplications, inversions, and translocations, that might be missed by more targeted approaches. It is particularly useful for diagnosing complex genetic disorders and for guiding treatment and management decisions.

The test is available at DNA Labs UAE, a leading facility in genetic testing, for a cost of 2400 AED. Given its comprehensive nature, the QF PCR Panel 131821XY and Karyotyping Test is an excellent choice for individuals seeking a thorough genetic analysis, whether for themselves or for their children. The combination of these two methods enhances the accuracy of diagnosis and provides a solid foundation for understanding and addressing genetic conditions.

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

QF PCR Panel 131821XY and Karyotyping Test

Cost: AED 2400.0

Test Details

The QF PCR panel [13, 18, 21, XY] refers to a genetic test that uses quantitative fluorescent polymerase chain reaction (QF PCR) to detect specific chromosomal abnormalities. In this case, the panel is designed to screen for trisomy 13 (also known as Patau syndrome), trisomy 18 (also known as Edwards syndrome), trisomy 21 (also known as Down syndrome), and to determine the sex chromosomes (XY) in a sample.

Karyotyping, on the other hand, is a different genetic test that involves examining the chromosomes of an individual to identify any structural or numerical abnormalities. It is a visual analysis of the chromosomes, typically performed using a microscope. Karyotyping can detect a wide range of chromosomal abnormalities, including deletions, duplications, translocations, and other rearrangements.

Both the QF PCR panel and karyotyping are commonly used in prenatal testing to screen for chromosomal abnormalities in fetuses. The QF PCR panel provides a rapid and accurate method for detecting specific abnormalities, while karyotyping offers a more comprehensive analysis of the entire set of chromosomes. These tests are often used together to provide a more comprehensive evaluation of the genetic health of the fetus.

Test Components

  • Sterile container
  • Sterile Normal Saline Container
  • EDTA & Sodium Heparin Vacutainer (2-3 ml. each)

Sample Condition

Amniotic fluid, Chorionic villi, Cord Blood

Report Delivery

1-2 days for QF PCR Panel 131821XY

12-15 days for Karyotyping Test

Method

Cell culture + Sanger Sequencing

Test Type

Genetics

Doctor

Gynecologist

Test Department

Pre Test Information

QF PCR Panel 13,18,21,XY + Karyotyping can be done with a Doctor’s prescription. Prescription is not applicable for surgery and pregnancy cases or people planning to travel abroad.

Test Name QF PCR Panel 131821XY and Karyotyping Test
Components Sterile container/ Sterile Normal Saline Container/ EDTA & Sodium Heparin Vacutainer (2-3 ml. each)
Price 2400.0 AED
Sample Condition Amniotic fluid\/ Chorionic villi\/ Cord Blood
Report Delivery 1-2 days/12-15 days
Method Cell culture + Sanger Sequencing
Test type Genetics
Doctor Gynecologist
Test Department:
Pre Test Information QF PCR Panel 13,18,21,XY] + Karyotyping can be done with a Doctors prescription. Prescription is not applicable for surgery and pregnancy cases or people planing to travel abroad.
Test Details

The QF PCR panel [13, 18, 21, XY] refers to a genetic test that uses quantitative fluorescent polymerase chain reaction (QF PCR) to detect specific chromosomal abnormalities. In this case, the panel is designed to screen for trisomy 13 (also known as Patau syndrome), trisomy 18 (also known as Edwards syndrome), trisomy 21 (also known as Down syndrome), and to determine the sex chromosomes (XY) in a sample.

Karyotyping, on the other hand, is a different genetic test that involves examining the chromosomes of an individual to identify any structural or numerical abnormalities. It is a visual analysis of the chromosomes, typically performed using a microscope. Karyotyping can detect a wide range of chromosomal abnormalities, including deletions, duplications, translocations, and other rearrangements.

Both the QF PCR panel and karyotyping are commonly used in prenatal testing to screen for chromosomal abnormalities in fetuses. The QF PCR panel provides a rapid and accurate method for detecting specific abnormalities, while karyotyping offers a more comprehensive analysis of the entire set of chromosomes. These tests are often used together to provide a more comprehensive evaluation of the genetic health of the fetus.

SKU: TEST-4809 Category:

Related products