Additional file 12: of Mobilization of retrotransposons as a cause of chromosomal diversification and rapid speciation: the case for the Antarctic teleost genus Trematomus

Specific qPCR primer pairs. For “Methods section”. Sum up of specific primers (primer sequence, fragment size (bp), region of amplification, Tm of amplification (°C)) used to amplify single copy genes RAG1 and Rhodopsin, and DIRS1, Gypsy and Copia retrotransposons in nototheniid genomes for TE copy...

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Bibliographic Details
Main Authors: J. Auvinet, P. Graça, L. Belkadi, L. Petit, E. Bonnivard, A. Dettaï, W. Detrich, C. Ozouf-Costaz, D. Higuet
Format: Text
Language:unknown
Published: figshare 2018
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Online Access:https://dx.doi.org/10.6084/m9.figshare.6234677.v1
https://springernature.figshare.com/articles/Additional_file_12_of_Mobilization_of_retrotransposons_as_a_cause_of_chromosomal_diversification_and_rapid_speciation_the_case_for_the_Antarctic_teleost_genus_Trematomus/6234677/1
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Summary:Specific qPCR primer pairs. For “Methods section”. Sum up of specific primers (primer sequence, fragment size (bp), region of amplification, Tm of amplification (°C)) used to amplify single copy genes RAG1 and Rhodopsin, and DIRS1, Gypsy and Copia retrotransposons in nototheniid genomes for TE copy number quantification. (PDF 149 kb)