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BCR-ABL Gene Rearrangement PCR Quantitative Test Cost

Original price was: 1,500 د.إ.Current price is: 1,350 د.إ.

-10%

The BCR-ABL Gene Rearrangement PCR Quantitative Test is a highly specialized diagnostic procedure used to detect the presence and quantify the amount of the BCR-ABL fusion gene in the blood or bone marrow. This genetic anomaly results from a chromosomal rearrangement between chromosome 9 and chromosome 22, known as the Philadelphia chromosome, which is a hallmark of chronic myeloid leukemia (CML) and, in some cases, acute lymphoblastic leukemia (ALL). The test employs Polymerase Chain Reaction (PCR) technology, a sensitive and precise method, to amplify traces of the BCR-ABL gene sequences for detailed analysis.

This test plays a crucial role in diagnosing CML and ALL, monitoring treatment response, and detecting minimal residual disease or relapse in patients. It helps clinicians tailor treatment strategies according to the genetic profile and disease progression of individual patients, improving the chances of successful outcomes.

In the United Arab Emirates, the BCR-ABL Gene Rearrangement PCR Quantitative Test is available at DNA Labs UAE, a leading diagnostic facility known for its advanced genetic testing services. The cost of the test is set at 1350 AED, reflecting the sophisticated technology and expertise required to perform this analysis. Patients and healthcare providers can rely on DNA Labs UAE for accurate and timely results, contributing to the effective management of leukemia cases.

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BCR-ABL GENE REARRANGEMENT PCR QUANTITATIVE Test

At DNA Labs UAE, we offer the BCR-ABL GENE REARRANGEMENT PCR QUANTITATIVE Test. This molecular diagnostic test is used to detect and quantify the presence of the BCR-ABL fusion gene in patients with certain types of leukemia, including chronic myeloid leukemia (CML) and a subset of acute lymphoblastic leukemia (ALL).

Test Details

The BCR-ABL gene rearrangement PCR quantitative test uses real-time PCR technology to amplify and detect the presence of the BCR-ABL fusion gene in a patient’s blood or bone marrow sample. This fusion gene is created when parts of the BCR gene on chromosome 22 and the ABL gene on chromosome 9 are rearranged. The resulting BCR-ABL tyrosine kinase protein is responsible for the uncontrolled growth and division of abnormal white blood cells seen in CML and some cases of ALL.

The test provides a quantitative measurement of the level of BCR-ABL gene expression, which can be used to monitor the response to treatment and assess the risk of disease progression. The results are reported as a ratio of BCR-ABL to a reference gene, such as ABL or GUS. A higher ratio indicates a higher level of BCR-ABL expression, which may indicate a more aggressive disease or a poor response to treatment. Conversely, a lower ratio indicates a lower level of BCR-ABL expression, which may indicate a better response to treatment or a lower risk of disease progression.

Test Components and Price

The BCR-ABL GENE REARRANGEMENT PCR QUANTITATIVE Test is priced at 1350.0 AED. The sample condition required is 5 mL (3 mL min.) of whole blood or bone marrow in 1 Lavender Top (EDTA) tube. The sample should be shipped refrigerated and should not be frozen. The report will be delivered daily by 9 am, and the results will be available on the same day.

Doctor and Test Department

This test is performed under the supervision of an Oncologist or Hematologist. The test is conducted in our Molecular Diagnostics department.

Pre Test Information

No special preparation is required before undergoing the BCR-ABL GENE REARRANGEMENT PCR QUANTITATIVE Test.

Importance of the Test

The BCR-ABL GENE REARRANGEMENT PCR QUANTITATIVE Test is an essential tool in the management of patients with CML and some cases of ALL. It is used for diagnosis, monitoring treatment response, guiding treatment decisions, and detecting minimal residual disease (MRD) – the presence of a small number of cancer cells that may remain after treatment.

Test Name BCR-ABL GENE REARRANGEMENT PCR QUANTITATIVE Test
Components
Price 1350.0 AED
Sample Condition 5 mL (3 mL min.) whole blood \/ Bonemarrowin 1 Lavender Top (EDTA)tube. Ship refrigerated. DO NOTFREEZE.
Report Delivery Sample Daily by 9 am; Report Same day
Method Real Time PCR
Test type Leukemia
Doctor Oncologist, Hematologist
Test Department: MOLECULAR DIAGNOSTICS
Pre Test Information No special preparation required
Test Details

The BCR-ABL gene rearrangement PCR quantitative test is a molecular diagnostic test used to detect and quantify the presence of the BCR-ABL fusion gene in patients with certain types of leukemia, specifically chronic myeloid leukemia (CML) and a subset of acute lymphoblastic leukemia (ALL).

The BCR-ABL fusion gene is created when parts of the BCR (breakpoint cluster region) gene on chromosome 22 and the ABL (Abelson) gene on chromosome 9 are rearranged. This fusion gene produces a protein called BCR-ABL tyrosine kinase, which is responsible for the uncontrolled growth and division of abnormal white blood cells seen in CML and some cases of ALL.

The BCR-ABL gene rearrangement PCR quantitative test uses polymerase chain reaction (PCR) technology to amplify and detect the presence of the BCR-ABL fusion gene in a patient’s blood or bone marrow sample. It provides a quantitative measurement of the level of BCR-ABL gene expression, which can be used to monitor the response to treatment and assess the risk of disease progression.

The test results are reported as a ratio of BCR-ABL to a reference gene, such as ABL or GUS. A higher ratio indicates a higher level of BCR-ABL expression, which may indicate a more aggressive disease or a poor response to treatment. Conversely, a lower ratio indicates a lower level of BCR-ABL expression, which may indicate a better response to treatment or a lower risk of disease progression.

The BCR-ABL gene rearrangement PCR quantitative test is an important tool in the management of patients with CML and some cases of ALL. It is used to diagnose these diseases, monitor treatment response, guide treatment decisions, and detect minimal residual disease (MRD) – the presence of a small number of cancer cells that may remain after treatment.