Peripheral Blood for Karyotyping Single Test sale cost 750 AED
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Peripheral Blood for Karyotyping Single Test Cost

Original price was: 1,000 د.إ.Current price is: 750 د.إ.

-25%

Peripheral Blood for Karyotyping is a genetic test performed to examine the chromosomes in a sample of blood. This test is crucial for identifying chromosomal abnormalities that could lead to genetic disorders. By analyzing the size, shape, and number of chromosomes, healthcare providers can diagnose various conditions, such as Down syndrome, Klinefelter syndrome, and Turner syndrome, among others.

At DNA Labs UAE, the Peripheral Blood for Karyotyping Single Test is available for a cost of 750 AED. The lab utilizes state-of-the-art technology to ensure accurate and reliable results. The process involves collecting a small sample of the patient’s blood, which is then cultured in a lab to increase the number of cells available for analysis. Following this, the chromosomes are stained, visualized under a microscope, and analyzed by expert geneticists.

This test is recommended for individuals with suspected genetic disorders, couples with a history of miscarriages, or anyone advised by their healthcare provider to undergo genetic screening. With its commitment to precision and patient care, DNA Labs UAE provides a crucial service in the field of genetic diagnostics.

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  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
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Peripheral Blood for Karyotyping Single Test

At DNA Labs UAE, we offer the Peripheral Blood for Karyotyping Single Test at a cost of AED 750.0. This test is performed using Cell culture methodology and requires a sample of Peripheral blood in Sodium Heparin Vacutainer (2ml).

Test Details

Karyotyping is a laboratory technique used to analyze an individual’s chromosomes. It involves arranging and pairing the chromosomes to identify any structural or numerical abnormalities, such as missing or extra chromosomes. Peripheral blood is commonly used for karyotyping.

To obtain a sample for karyotyping, a healthcare professional will perform a venipuncture, which involves collecting a small amount of blood from a vein, usually in the arm. The collected blood sample is then sent to our laboratory where the white blood cells, specifically lymphocytes, are isolated.

The isolated cells are cultured and stimulated to divide, allowing for the chromosomes to be visualized and analyzed. The chromosomes are stained and examined under a microscope, and a karyotype is created by arranging the chromosomes in pairs based on their size, shape, and banding patterns.

This karyotype can then be analyzed for any abnormalities, helping in the diagnosis of various genetic disorders such as Down syndrome, Turner syndrome, or chromosomal translocations. It can also be used to determine the sex of an individual and assess the risk of certain genetic conditions.

Test Information

  • Test Name: Peripheral Blood for Karyotyping Single Test
  • Components: Sodium Heparin Vacutainer (2ml)
  • Price: 750.0 AED
  • Sample Condition: Blood, Blood Sodium Heparin
  • Report Delivery: 7-9 days
  • Method: Cell culture
  • Test Type: Genetics
  • Doctor: Gynecologist
  • Test Department:

Pre Test Information

For the Peripheral Blood for Karyotyping Single Test, the sample required is Peripheral blood in Sodium Heparin Vacutainer (2ml). Results can be expected within 7-9 days.

Test Name Peripheral blood for karyotyping SINGLE Test
Components Sodium Heparin Vacutainer (2ml)
Price 750.0 AED
Sample Condition Blood , Blood Sodium Heparin
Report Delivery 7-9 days
Method Cell culture
Test type Genetics
Doctor Gynecologist
Test Department:
Pre Test Information Peripheral blood for karyotyping (SINGLE)is performed using Cell culture methodology.Sample that have to be given is Peripheral blood in Sodium Heparin Vacutainer (2ml) for this test. You can expect results in 7-9 days
Test Details

Karyotyping is a laboratory technique used to analyze an individual’s chromosomes. It involves arranging and pairing the chromosomes to identify any structural abnormalities or numerical abnormalities, such as missing or extra chromosomes.

Peripheral blood is the blood that circulates through the veins and arteries, and it is commonly used for karyotyping. To obtain a sample for karyotyping, a healthcare professional will typically perform a venipuncture, which involves inserting a needle into a vein, usually in the arm, and collecting a small amount of blood into a tube.

Once the blood sample is collected, it is sent to a laboratory where the white blood cells are isolated. White blood cells, specifically lymphocytes, are used for karyotyping because they contain the complete set of chromosomes. The cells are then cultured and stimulated to divide, allowing for the chromosomes to be visualized and analyzed.

The chromosomes are stained and examined under a microscope, and a karyotype is created by arranging the chromosomes in pairs according to their size, shape, and banding patterns. This karyotype can then be analyzed for any abnormalities.

Karyotyping from peripheral blood is a commonly used technique in clinical genetics and can help diagnose various genetic disorders, such as Down syndrome, Turner syndrome, or chromosomal translocations. It can also be used to determine the sex of an individual and to assess the risk of certain genetic conditions.

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