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BRAF Mutation Analysis V600E Test Cost

Original price was: 2,400 د.إ.Current price is: 1,800 د.إ.

-25%

The BRAF Mutation Analysis V600E Test is a specialized diagnostic procedure aimed at detecting the V600E mutation within the BRAF gene. This mutation is significant because it is frequently associated with various types of cancer, including melanoma, thyroid cancer, and colorectal cancer. Identifying the presence of this mutation can help in tailoring the most effective treatment strategies for patients, as it often indicates responsiveness to specific targeted therapies.

Performed at DNA Labs UAE, a reputable facility known for its advanced genetic testing capabilities, this test offers a reliable means of genetic analysis. The process involves collecting a sample of the patient’s tissue or blood, which is then subjected to sophisticated molecular techniques to scrutinize the BRAF gene for the specific V600E mutation.

The cost of the BRAF Mutation Analysis V600E Test at DNA Labs UAE is 1800 AED. This price reflects the intricate technology and expertise required to accurately identify this genetic variation. For patients and healthcare providers, the test represents a crucial step in the journey towards personalized medicine, enabling more precise and effective cancer treatment plans based on an individual’s genetic makeup.

Description

BRAF Mutation Analysis V600E Test

Test Name: BRAF Mutation Analysis V600E Test

Components: Paraffin embedded tissue blocks

Price: 1800.0 AED

Sample Condition: Tumor tissue

Report Delivery: 7-8 days

Method: Sanger Sequencing

Test type: Genetics

Doctor: Gynecologist

Test Department:

Pre Test Information: BRAF Mutation Analysis (V600E) 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:

BRAF mutation analysis (V600E) is a molecular diagnostic test used to detect a specific mutation in the BRAF gene known as V600E. This mutation is commonly found in various types of cancer, including melanoma, colorectal cancer, and papillary thyroid cancer. The BRAF gene encodes a protein that plays a role in cell signaling pathways involved in cell growth and division. The V600E mutation leads to a constitutively activated BRAF protein, which can promote uncontrolled cell growth and tumor formation.

The analysis of the BRAF V600E mutation is typically performed using various molecular techniques, such as polymerase chain reaction (PCR) or DNA sequencing. These techniques can detect the presence of the mutation in a patient’s tumor tissue or blood sample.

The results of the BRAF mutation analysis can help guide treatment decisions for patients with cancer. For example, the presence of the V600E mutation in melanoma patients can indicate eligibility for targeted therapies, such as BRAF inhibitors.

Overall, BRAF mutation analysis (V600E) is an important tool in personalized medicine, allowing for the identification of specific genetic alterations that can inform treatment decisions and improve patient outcomes.

Test Name	BRAF Mutation Analysis V600E Test
Components	Paraffin embedded tissue blocks
Price	1800.0 AED
Sample Condition	Tumor tissue
Report Delivery	7-8 days
Method	Sanger Sequencing
Test type	Genetics
Doctor	Gynecologist
Test Department:
Pre Test Information	BRAF Mutation Analysis (V600E) can be done with a Doctors prescription. Prescription is not applicable for surgery and pregnancy cases or people planing to travel abroad.
Test Details	BRAF mutation analysis (V600E) is a molecular diagnostic test used to detect a specific mutation in the BRAF gene known as V600E. This mutation is commonly found in various types of cancer, including melanoma, colorectal cancer, and papillary thyroid cancer. The BRAF gene encodes a protein that plays a role in cell signaling pathways involved in cell growth and division. The V600E mutation leads to a constitutively activated BRAF protein, which can promote uncontrolled cell growth and tumor formation. The analysis of the BRAF V600E mutation is typically performed using various molecular techniques, such as polymerase chain reaction (PCR) or DNA sequencing. These techniques can detect the presence of the mutation in a patient’s tumor tissue or blood sample. The results of the BRAF mutation analysis can help guide treatment decisions for patients with cancer. For example, the presence of the V600E mutation in melanoma patients can indicate eligibility for targeted therapies, such as BRAF inhibitors. Overall, BRAF mutation analysis (V600E) is an important tool in personalized medicine, allowing for the identification of specific genetic alterations that can inform treatment decisions and improve patient outcomes.