b'Gel & Capillary | CE-IVD Assays T-Cell Receptor Gamma GeneGel and CapillaryAssays T-Cell Receptor Gamma GeneGel and CapillaryAssays Rearrangement Assay 2.0Rearrangement Assay 2.0IdentiClone T-Cell Receptor Gamma GeneRearrangement Assay 2.0ReagentsControls Concentration Units in Assay Units in Assay MegaKitAssay Description Performance Characteristics5% TCRG Positive Control DNA 50 g/mL 1 x 50 L tube 5 x 50 L tubeThe IdentiClone T-Cell Receptor Gamma Gene Rearrangement AssayTo assess the performance of the TCRG 2.0 Assay, testing wasTCRG Negative Control DNA 50 g/mL 1 x 50 L tube 5 x 50 L tube2.0 is an in vitro diagnostic product intended for PCR-based detectionperformed on cell lines with known clonal rearrangements followed byMaster Mixes Target Units in Assay Units in Assay MegaKitof clonal T-cell receptor gamma chain gene rearrangements intesting on previously sequenced clinical samples.TCRG - 6FAM V1-V11 + J1/J2, JP, JP1/JP2 1 x 1500 L tube 10 x 1500 L tubespatients with suspect lymphoproliferations.When used in combination with the provided TCRG AlgorithmSpecimen Control Size Ladder Multiple Genes 1 x 1500 L tube 10 x 1500 L tubesSpecifically, the T-Cell Receptor Gamma Gene Rearrangement Assayworksheet, the assay was capable of detecting DNA from 6 control 2.0 can be used to identify clonality in suspect lymphoproliferations. cell lines (200 ng/L) diluted into polyclonal tonsil DNA (200 ng/L) at 5% (v/v).Summary and Explanation of the TestFurthermore, the performance of the TCRG 2.0 Assay was evaluatedOrdering Informationon clinical samples for which the T-cell receptor gamma geneCatalog # Products QuantityRearrangements of the antigen receptor genes occur during ontogenyrearrangement status had been identified by Roche 454 sequencing.in B- and T-lymphocytes. These gene rearrangements generateFor the 7 samples that had been identified as clonal by sequencing,9-207-0101 IdentiCloneT-Cell Receptor Gamma Gene Rearrangement Assay 2.0 - ABI Fluorescence Detection 33 reactionsproducts that are unique in length and sequence. Polymerase chainthe TCRG 2.0 assay had 100% concordance. For the 12 samples9-207-0111 IdentiClone T-Cell Receptor Gamma Gene Rearrangement Assay MegaKit 2.0 - ABI Fluorescence Detection 330 reactionsreaction (PCR) assays can be used to identify lymphocyte populationsthat were either negative for a clonal event or were oligoclonal, derived from a single cell by detecting the unique V-J geneconcordance of the TCRG 2.0 assay was 75%. Sample types includedThese are in vitro diagnostic products, and are not available for sale or use within North America.rearrangements present within these antigen receptor loci. 1 peripheral blood, bone marrow, and formalin-fixed, paraffin This assay allows for amplification of the TRG region with fluorescentembedded (FFPE) tissue. labeled primers, yielding products that can be grouped under aAlways interpret the results of molecular clonality tests in the contextsingle Gaussian distribution when separated by size using capillaryof clinical, histological and immunophenotypic data.electrophoresis. In addition, the product size facilitates increased success when testing FFPE samples. The included analysis algorithm aids in the interpretation of data and identification of significant clonalReferencespeaks. Presence or absence of molecular clonality can support the differential diagnosis of reactive lesions and certain B- and T-cell1. Miller JE, Wilson SS, Jaye DJ, and Kronenberg M. Mol. Diag. 1999,malignancies, provided that the results are interpreted in the context4(2):101-117. of all available clinical, histological, and immunophenotypic data. 2. Armand, Marine et al. HemaSphere, 2019;3:3.This assay was developed by Invivoscribe.The performance of this assay was reviewed and validated by the EuroClonality/BIOMED-2 Group. 2Figure Legend: Simple representation of the organization of the T-cell receptor gamma gene on chromosome 7p14. Black arrows represent the relative positions of primers that target the variable region genes and the downstream joining region gene segments that are involved in rearrangements in T-cell lymphomas. The downstream primers are fluorescently labeled through the incorporation of a 6FAM fluorophore. The amplicon products generated from these rearrangements are detected by capillary electrophoresis.72Invivoscribe 2021|73'