Test Directory

TCR Gene Clonality

Containers - Adult

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Red Cap Tube EDTA KE 2.7ml
Volume Range

​5ml peripheral blood, bone marrow specimen or FFPE tissue

Additive per Container

​EDTA

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FFPE block / H&E slide / Pathology report

Laboratory Site

WGH
Crewe Road South
Edinburgh
EH4 2XU
Telephone: 0131 537 1000

Transport arrangements

Blood and bone marrow specimens should ideally arrive within 24 hours of collection (maximum of 48 hours).  There is no time limit for FFPE samples.  Samples should be sent to the following address:

Western General Hospital

Haematology/Biochemistry Combined Reception

Immunophenotyping Laboratory

Crewe Road

Edinburgh

EH4 2XU​

 

See also Specimen transportation.

Sample storage arrangements

Samples should be stored at room temperature. See specimen requirements.

How to request

Please refer to our detailed requesting ​instructions.  The HMDS request form can be located here.​

 

 

Requests for testing FFPE tissue should be sent to the Molecular Pathology Service at RIE with a completed HMDS test request form.

Availability

Monday - Friday 9am-5pm

Anticipated turnaround

Results should be expected within 14 days. See results.

Static information/disclaimer

This test is accredited to ISO 15189:2012

General additional information

TCR gene rearrangement studies include assessment of TCRB and TCRG gene loci. The TCRD gene rearrangement clonality assay is usually not performed, but is available where required (e.g. hepatosplenic T-cell lymphoma). Please see testing for more information.

TCR gene rearrangement assessment is undertaken using the BIOMED‐2 designed assays, with a standard PCR protocol and primer sets designed to target the TCRG, TCRB and TCRD loci. Clonality assessment is a useful tool to aid with the diagnosis of T cell lymphoproliferative disorders. However, the results should always be interpreted in conjunction with morphology, immunophenotyping and/or immunohistochemistry results as well as the clinical findings.

This assay is not suitable for the assessment of low level minimal residual disease in acute leukaemia or lympoproliferative neoplasms.

For details on the interpretation of results, please see Langerak et al., Leukemia 2012; 26:2159-2171

For clinical advice on appropriate investigations and advice for the interpretation of test results, please see contact us​.