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FISH – 14q32.3 or LSI IGH Gene Breakapart Test Cost

Original price was: 1,120 د.إ.Current price is: 1,010 د.إ.

-10%

The FISH – 14q32.3 or LSI IGH Gene Breakapart Test is a sophisticated diagnostic procedure utilized to detect chromosomal abnormalities, specifically translocations involving the immunoglobulin heavy chain (IGH) gene located at the 14q32.3 locus. This test is particularly relevant in the diagnosis and management of various hematologic malignancies, such as multiple myeloma and certain types of non-Hodgkin lymphoma, where the rearrangement of the IGH gene plays a critical role in the disease’s pathogenesis.

Fluorescence in situ hybridization (FISH) technology is employed in this test, allowing for the visualization of genetic abnormalities at a molecular level. This technique uses fluorescent probes that bind to specific DNA sequences of interest, in this case, the IGH gene, enabling the detection of gene rearrangements that may not be visible through conventional cytogenetic methods.

Conducted at DNA Labs UAE, a leading facility in genetic testing and analysis, the test offers a high level of accuracy and reliability. The cost of the FISH – 14q32.3 or LSI IGH Gene Breakapart Test is 1010 AED. This investment is invaluable for patients requiring precise diagnosis and treatment planning for conditions associated with the IGH gene rearrangements, providing crucial information that can guide therapeutic decisions and potentially improve patient outcomes.

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FISH – 14q32.3 OR LSI IGH GENE BREAKAPART Test

At DNA Labs UAE, we offer the FISH – 14q32.3 OR LSI IGH GENE BREAKAPART Test to detect genetic abnormalities in certain types of cancer. This laboratory test is specifically designed for lymphomas and leukemias and utilizes fluorescence in situ hybridization (FISH) technology.

Test Details

The FISH – 14q32.3 OR LSI IGH GENE BREAKAPART Test is a valuable tool in cancer diagnostics. It helps detect rearrangements or translocations involving the 14q32.3 region or the IGH (immunoglobulin heavy chain) gene. These abnormalities can lead to the development and progression of cancer.

Test Components

  • Price: 1010.0 AED
  • Sample Condition: 5 mL (3 mL min.) whole blood OR 4 mL (2 mL min.) Bone Marrow from 2 Green Top (Sodium Heparin) tubes. Ship at 18-22°C. DO NOT FREEZE.
  • Requisition Form: Duly filled Chromosome & FISH analysis Requisition Form (Form 17) is mandatory.

Report Delivery

Sample Daily by 4 pm; Report 4 days

Method

FISH (Fluorescence in situ hybridization)

Test Type

Leukemia

Doctor

Oncologist, Hematologist

Test Department

Cytogenetics

Pre Test Information

Duly filled Chromosome & FISH analysis Requisition Form (Form 17) is mandatory.

About the FISH – 14q32.3 OR LSI IGH GENE BREAKAPART Test

The FISH – 14q32.3 or LSI IGH gene breakapart test is a laboratory test used to detect genetic abnormalities in certain types of cancer, specifically lymphomas and leukemias. It is a type of fluorescence in situ hybridization (FISH) test that looks for rearrangements or translocations involving the 14q32.3 region or the IGH (immunoglobulin heavy chain) gene.

In normal cells, the IGH gene is located on chromosome 14q32.3 and plays a role in the production of antibodies. However, in some cancer cells, there may be rearrangements or translocations involving this gene. These genetic abnormalities can lead to the formation of abnormal proteins or overexpression of certain genes, which can contribute to the development and progression of cancer.

The FISH – 14q32.3 or LSI IGH gene breakapart test uses fluorescently labeled DNA probes that specifically bind to the 14q32.3 region or the IGH gene. By visualizing the fluorescence pattern under a microscope, the test can determine if there are any abnormalities in the location or structure of the IGH gene. The presence of a break or rearrangement in the gene can help diagnose specific types of lymphomas or leukemias, such as Burkitt lymphoma or multiple myeloma.

Overall, the FISH – 14q32.3 or LSI IGH gene breakapart test is a valuable tool in cancer diagnostics, providing important information about the genetic alterations present in certain types of cancer cells. This information can help guide treatment decisions and prognosis for patients.

Test Name FISH – 14q32.3 OR LSI IGH GENE BREAKAPART Test
Components
Price 1010.0 AED
Sample Condition 5 mL (3 mL min.) whole blood OR 4 mL (2 mL min.) Bone Marrow from 2 Green Top (Sodium Heparin) tubes. Ship at 18-22?\u00f8C. DO NOT FREEZE. Duly filled Chromosome & FISH analysis Requisition Form (Form 17) is mandatory.
Report Delivery Sample Daily by 4 pm; Report 4 days
Method FISH
Test type Leukemia
Doctor Oncologist, Hematologist
Test Department: CYTOGENETICS
Pre Test Information Duly filled Chromosome & FISH analysis Requisition Form (Form 17) is mandatory.
Test Details

The FISH – 14q32.3 or LSI IGH gene breakapart test is a laboratory test used to detect genetic abnormalities in certain types of cancer, specifically lymphomas and leukemias. It is a type of fluorescence in situ hybridization (FISH) test that looks for rearrangements or translocations involving the 14q32.3 region or the IGH (immunoglobulin heavy chain) gene.

In normal cells, the IGH gene is located on chromosome 14q32.3 and plays a role in the production of antibodies. However, in some cancer cells, there may be rearrangements or translocations involving this gene. These genetic abnormalities can lead to the formation of abnormal proteins or overexpression of certain genes, which can contribute to the development and progression of cancer.

The FISH – 14q32.3 or LSI IGH gene breakapart test uses fluorescently labeled DNA probes that specifically bind to the 14q32.3 region or the IGH gene. By visualizing the fluorescence pattern under a microscope, the test can determine if there are any abnormalities in the location or structure of the IGH gene. The presence of a break or rearrangement in the gene can help diagnose specific types of lymphomas or leukemias, such as Burkitt lymphoma or multiple myeloma.

Overall, the FISH – 14q32.3 or LSI IGH gene breakapart test is a valuable tool in cancer diagnostics, providing important information about the genetic alterations present in certain types of cancer cells. This information can help guide treatment decisions and prognosis for patients.