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JAK 2 Mutation Detection Qualitative PCR Test Cost

Original price was: 1,380 د.إ.Current price is: 1,240 د.إ.

-10%

The JAK2 Mutation Detection Qualitative PCR Test is a highly specialized diagnostic procedure aimed at identifying mutations in the JAK2 gene, which are often associated with certain types of blood cancers, including myeloproliferative neoplasms. This test employs the Polymerase Chain Reaction (PCR) technique, a cutting-edge method that amplifies the JAK2 gene segments, allowing for the precise detection of mutations in a qualitative manner.

Offered at DNA Labs UAE, a leading facility in genetic testing and diagnostics, the test is priced at 1240 AED. DNA Labs UAE is equipped with state-of-the-art technology and staffed by experts in the field of molecular genetics, ensuring high accuracy and reliability of test results. The test is crucial for the diagnosis and management of patients suspected of having hematological malignancies, as the presence of JAK2 mutations can significantly influence treatment decisions and prognostic assessments.

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JAK 2 MUTATION DETECTION QUALITATIVE PCR Test

Test Name: JAK 2 MUTATION DETECTION QUALITATIVE PCR Test

Components: 3 mL (2 mL min.) whole blood from 1 Lavender Top (EDTA) tube. Ship refrigerated. DO NOT FREEZE. Duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory.

Price: 1240.0 AED

Report Delivery: Sample Mon / Thu by 11 am; Report Wed / Sat

Method: Real Time PCR

Test Type: Cancer

Doctor: Oncologist

Test Department: MOLECULAR DIAGNOSTICS

Pre Test Information: Duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory.

Test Details

The JAK2 mutation detection qualitative PCR test is a laboratory test used to detect mutations in the JAK2 gene. This gene encodes a protein that plays a role in regulating the production and function of blood cells.

Mutations in the JAK2 gene, specifically the V617F mutation, have been associated with certain blood disorders, including polycythemia vera, essential thrombocythemia, and primary myelofibrosis. These disorders involve the overproduction of blood cells, leading to various symptoms and complications.

The qualitative PCR test is designed to identify the presence or absence of the JAK2 V617F mutation in a patient’s DNA sample. It involves amplifying a specific region of the JAK2 gene using polymerase chain reaction (PCR) technology and then analyzing the amplified DNA for the presence of the mutation.

If the JAK2 V617F mutation is detected in a patient’s DNA sample, it indicates that they have a higher risk of developing one of the associated blood disorders. This information can help guide further diagnostic and treatment decisions.

It is important to note that this test is a qualitative test, meaning it only provides a “yes” or “no” answer regarding the presence of the mutation. It does not provide information about the quantity or severity of the mutation.

The JAK2 mutation detection qualitative PCR test is typically performed in specialized laboratories and requires a blood or bone marrow sample from the patient. The results of the test are usually interpreted by a healthcare professional, such as a hematologist or oncologist, who can provide further guidance based on the findings.

Test Name JAK 2 MUTATION DETECTION QUALITATIVE PCR Test
Components
Price 1240.0 AED
Sample Condition 3 mL (2 mL min.) whole blood from 1 Lavender Top (EDTA) tube. Ship refrigerated. DO NOT FREEZE. Duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory.
Report Delivery Sample Mon / Thu by 11 am; Report Wed / Sat
Method Real Time PCR
Test type Cancer
Doctor Oncologist
Test Department: MOLECULAR DIAGNOSTICS
Pre Test Information Duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory.
Test Details

The JAK2 mutation detection qualitative PCR test is a laboratory test used to detect mutations in the JAK2 gene. This gene encodes a protein that plays a role in regulating the production and function of blood cells.

Mutations in the JAK2 gene, specifically the V617F mutation, have been associated with certain blood disorders, including polycythemia vera, essential thrombocythemia, and primary myelofibrosis. These disorders involve the overproduction of blood cells, leading to various symptoms and complications.

The qualitative PCR test is designed to identify the presence or absence of the JAK2 V617F mutation in a patient’s DNA sample. It involves amplifying a specific region of the JAK2 gene using polymerase chain reaction (PCR) technology and then analyzing the amplified DNA for the presence of the mutation.

If the JAK2 V617F mutation is detected in a patient’s DNA sample, it indicates that they have a higher risk of developing one of the associated blood disorders. This information can help guide further diagnostic and treatment decisions.

It is important to note that this test is a qualitative test, meaning it only provides a “yes” or “no” answer regarding the presence of the mutation. It does not provide information about the quantity or severity of the mutation.

The JAK2 mutation detection qualitative PCR test is typically performed in specialized laboratories and requires a blood or bone marrow sample from the patient. The results of the test are usually interpreted by a healthcare professional, such as a hematologist or oncologist, who can provide further guidance based on the findings.