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NRAS Mutation Analysis Codons 12 and 13 Test Cost

Original price was: 2,800 د.إ.Current price is: 2,100 د.إ.

-25%

The NRAS Mutation Analysis Codons 12 and 13 Test is a specialized genetic test performed to detect mutations in codons 12 and 13 of the NRAS gene. These mutations are significant because they can play a critical role in the development and progression of various types of cancer, including melanoma, colorectal cancer, and others. Identifying these mutations can help in determining prognosis, guiding treatment decisions, and potentially targeting therapies more effectively.

This test is carried out at DNA Labs UAE, a reputable facility known for its advanced genetic testing services. The process involves analyzing a sample of DNA, usually extracted from a blood sample or a biopsy of the tumor tissue, to look for specific alterations in the NRAS gene that could drive cancer growth.

The cost of the NRAS Mutation Analysis Codons 12 and 13 Test at DNA Labs UAE is set at 2100 AED. This price reflects the sophisticated technology and expertise required to accurately identify these genetic mutations. For patients and healthcare providers, this test represents a valuable tool in the arsenal against cancer, offering insights that can significantly impact treatment planning and outcomes.

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NRAS Mutation Analysis codons 12 and 13 Test

Welcome to DNA Labs UAE, your trusted genetic lab. In this blog, we will discuss the NRAS Mutation Analysis codons 12 and 13 Test, including its cost, symptoms, diagnosis, and more.

Test Details

The NRAS gene is a proto-oncogene that codes for a protein involved in cell signaling pathways. Mutations in this gene can lead to the activation of the NRAS protein, which can contribute to the development of various cancers, including melanoma, colorectal cancer, and thyroid cancer. Codons 12 and 13 of the NRAS gene are hotspots for mutations.

The most common mutation in these codons is a substitution of the amino acid glycine for aspartic acid (G12D) or cysteine (G12C). Other mutations at these codons include substitutions of glycine for valine (G12V), serine (G12S), or arginine (G12R).

NRAS mutation analysis involves testing for the presence of these mutations in tumor samples. This analysis can be done using various techniques, including polymerase chain reaction (PCR) and DNA sequencing.

By identifying NRAS mutations, healthcare providers can determine the most appropriate treatment options for patients with cancer, as certain targeted therapies are available for individuals with specific NRAS mutations.

Test Components

  • Paraffin embedded tissue blocks

Price

The cost of the NRAS Mutation Analysis codons 12 and 13 Test is 2100.0 AED.

Sample Condition

Tumor tissue

Report Delivery

The report will be delivered within 7-8 days.

Method

Sanger Sequencing

Test Type

Genetics

Doctor

Gynecologist

Test Department

Pre Test Information

Pre Test Information

NRAS Mutation Analysis (codons 12 & 13) can be done with a doctor’s prescription. Prescription is not applicable for surgery and pregnancy cases or people planning to travel abroad.

Thank you for choosing DNA Labs UAE for your genetic testing needs. If you have any further questions or would like to schedule an appointment, please contact us.

Test Name NRAS Mutation Analysis codons 12 and 13 Test
Components Paraffin embedded tissue blocks
Price 2100.0 AED
Sample Condition Tumor tissue
Report Delivery 7-8 days
Method Sanger Sequencing
Test type Genetics
Doctor Gynecologist
Test Department:
Pre Test Information NRAS Mutation Analysis (codons 12 & 13) 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 NRAS gene is a proto-oncogene that codes for a protein involved in cell signaling pathways. Mutations in this gene can lead to the activation of the NRAS protein, which can contribute to the development of various cancers, including melanoma, colorectal cancer, and thyroid cancer.

Codons 12 and 13 of the NRAS gene are hotspots for mutations. The most common mutation in these codons is a substitution of the amino acid glycine for aspartic acid (G12D) or cysteine (G12C). Other mutations at these codons include substitutions of glycine for valine (G12V), serine (G12S), or arginine (G12R).

NRAS mutation analysis involves testing for the presence of these mutations in tumor samples. This analysis can be done using various techniques, including polymerase chain reaction (PCR) and DNA sequencing. By identifying NRAS mutations, healthcare providers can determine the most appropriate treatment options for patients with cancer, as certain targeted therapies are available for individuals with specific NRAS mutations.