BH3 profiling toolkit

Our BH3 mimetic toolkit measures early drug-induced changes in proapoptotic signaling, revealing shifts in antiapoptotic dependencies. It helps to identify novel drug targets and predictive biomarkers, and offers to assess cellular fate across diverse experimental settings.

DNA-RNA immunoprecipitation sequencing (DRIP-seq)

DRIP-seq maps DNA-RNA hybrids (R-loops) across the genome to study their roles in gene regulation and genome stability. It helps reveal mechanisms of transcription, DNA repair, and chromatin organization, providing insights relevant to disease and potential therapeutic strategies.

Okazaki fragments sequencing (OK-seq)

OK-seq enables researchers to map the genome-wide locations of proteins involved in DNA replication and replication fork directionality. By unraveling the spatial organization of replication machinery and Okazaki fragments, OK-seq offers insights into the coordination and regulation of DNA synthesis during genome replication. This approach provides information for understanding genome stability and cellular proliferation.

Global run-on sequencing (GRO-seq)

GRO-seq allows researchers to map the locations of actively transcribing RNA polymerases and nascent RNA molecules to study the regulation and coordination of gene expression. This technique facilitates the identification of transcriptional enhancers, promoters, and regulatory elements, shedding light on the orchestration of cellular processes and the molecular basis of disease.

Mouse Model for lymphoid neoplasms – DLBCL

Explore our mouse models designed respectively for the study of DLBCL, Burkitt Lymphoma, Amyloid light-chain amylosis, Multiple Myeloma, or Fanconi Syndrom, Light and heavy chain deposition disease. These models enable the identification of novel therapeutic targets as well as the evaluation of drug efficacy and toxicity.

Immunoglobulin repertoire sequencing (Ig-Rep-Seq)

Immunoglobulin Repertoire Sequencing (Ig-Rep-Seq) deciphers the antibody diversity and immune responseat the single-cell level. This method can be used to study lymphoid malignancies, track immune responses, and guide cancer immunotherapy development.

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