FISH – t1114 OR LSI IGHCCNDI Test
Test Cost: AED 1200.0
Test Components:
- 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.
- Duly filled Chromosome & FISH analysis Requisition Form (Form 17) is mandatory.
Report Delivery: Sample Daily by 4 pm; Report 4 Working days
Method: FISH
Test Type: Lymphoma
Doctor: Oncologist, Hematologist
Test Department: CYTOGENETICS
Pre Test Information: Duly filled Chromosome & FISH analysis Requisition Form (Form 17) is mandatory.
Test Details:
The FISH (Fluorescence In Situ Hybridization) t(1114) test is a genetic test used to detect a specific chromosomal abnormality called t(11;14)(q13;q32). This abnormality is commonly found in multiple myeloma, a type of blood cancer. The FISH test uses fluorescent probes that bind to specific regions of chromosomes to identify the presence of this abnormality.
On the other hand, the LSI IGH/CCND1 test is also a genetic test used to detect a different chromosomal abnormality called t(14;18)(q32;q21). This abnormality is often associated with certain types of non-Hodgkin lymphoma, particularly follicular lymphoma. The LSI IGH/CCND1 test uses fluorescent probes to identify the fusion of the IGH (immunoglobulin heavy chain) gene on chromosome 14 with the CCND1 (cyclin D1) gene on chromosome 11.
Both tests are important in diagnosing and monitoring certain types of blood cancers, but they detect different chromosomal abnormalities in different types of cancer. The FISH t(1114) test is used for multiple myeloma, while the LSI IGH/CCND1 test is used for follicular lymphoma.
Test Name | FISH – t1114 OR LSI IGHCCNDI Test |
---|---|
Components | |
Price | 1200.0 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 Working days |
Method | FISH |
Test type | Lymphoma |
Doctor | Oncologist, Hematologist |
Test Department: | CYTOGENETICS |
Pre Test Information | Duly filled Chromosome & FISH analysis Requisition Form (Form 17) is mandatory. |
Test Details | The FISH (Fluorescence In Situ Hybridization) t(1114) test is a genetic test used to detect a specific chromosomal abnormality called t(11;14)(q13;q32). This abnormality is commonly found in multiple myeloma, a type of blood cancer. The FISH test uses fluorescent probes that bind to specific regions of chromosomes to identify the presence of this abnormality. On the other hand, the LSI IGH/CCND1 test is also a genetic test used to detect a different chromosomal abnormality called t(14;18)(q32;q21). This abnormality is often associated with certain types of non-Hodgkin lymphoma, particularly follicular lymphoma. The LSI IGH/CCND1 test uses fluorescent probes to identify the fusion of the IGH (immunoglobulin heavy chain) gene on chromosome 14 with the CCND1 (cyclin D1) gene on chromosome 11. Both tests are important in diagnosing and monitoring certain types of blood cancers, but they detect different chromosomal abnormalities in different types of cancer. The FISH t(1114) test is used for multiple myeloma, while the LSI IGH/CCND1 test is used for follicular lymphoma. |