Solid tumor

NGS analysis of relevant regions related to Acute Lymphoblastic Leukemia.

NGS panel for the study of fusions, point mutations and expression levels in lymphomes.

NGS panel for the study of fusions, point mutations and expression levels in several types of myeloid diseases.

NGS kits for the study and investigation of gene fusions.

NGS assay for the study of 31 genes involved in thyroid and lung cancer

NGS panels for AML, MPN, MDS and some Lymphoid malignancy markers

NGS assays associated with solid tumors

NGS panel for the study of 23 key genes associated with Chronic Lymphocytic Leukemia (CLL), including the biomarkers outlined in international guidelines (TP53 and somatic hypermutation).

Prognostic and predictive molecular in vitro test to determine the risk of recurrence and the absolute benefit of chemotherapy over the next 15 and 10 years, respectively, in patients with ER+/HER2- primary breast cancer.

NGS assay for the study of 17 genes involved in lung cancer.

NGS kit for the study of solid tumors associated genes.

NGS assays associated with soft tissue cancers.

Spatial study of the expression of over 1,800 genes involved in tumour biology, tumour microenvironment and immune response.

The GeoMx® Immune Pathways Panel is designed to profile key aspects of tumor biology, the tumor microenvironment, and the immune response, with spatial resolution from distinct regions of interest with a single tissue section.   This panel allows you to profile the expression of 84 RNA targets covering several pathways. You will be able to:   Profile the global immune response Assess microenvironment immune activity  Quantify tumor reactivity Measure the 18-gene Tumor Inflammation Signature (TIS) known to be associated with response to PD-1/PD-L1 inhibitor pathway blockade  Furthermore, it can be customized with up to 10 additional targets of interest.  The GeoMx® Immune…

Comprehensive spatial study of cellular biology, with full coverage of protein coding genes, and application in several fields: oncology, immunology, neuroscience, developmental biology...

NGS assay for the analysis of 32 genes associated with common solid tumors from circulating tumor DNA (ctDNA)

NGS assay to study 28 genes commonly associated with solid tumor type cancers from circulating cell-free tumor DNA (ccfDNA/cfDNA/ctDNA).

The most comprehensive tumor test to determine Homologous Recombination Deficiency (HDR) Status by studying the BRCA genes in patients with ovarian cancer.

Study of the individual’s immune response to transplanted tissue.

Comprehensive study of the immune response, optimized for immuno-oncology research, including essential genes for the tumor biology and the tumoral microenvironment.

Comprehensive study of genes involved in the tumoral immune evasion and the response to immunotherapy, including essential genes for the tumoral microenvironment and the immune response.

Comprehensive study of genes involved in major cancer pathways, including essential genes for the tumor biology, the tumoral microenvironment and the immune response.

Comprehensive study of genes involved in processes and mechanisms related to cancer progression, including essential genes for tumor biology, the tumoral microenvironment and the immune response.

Comprehensive study of dysfunctional cell signaling in cancer, including essential genes for the tumor biology, the tumoral microenvironment and the immune response.

Automatic extractor of genetic material

The Oncodeep kit from OncoDNA offers a comprehensive solution for identifying mutations, variants, and fusions in the somatic line of genes associated with solid tumors through Next-Generation Sequencing (NGS). Designed by oncology experts, this kit includes the most relevant and complete gene panel in the field of cancer, consisting of 638 genes, which allows for…

Panel de NGS para el estudio de 23 genes relevantes en la Leucemia Linfocítica Crónica (LLC), incluyendo los biomarcadores descritos en las guías internacionales (TP53 e hipermutación somática)

Kits de Secuenciación masiva para análisis de múltiples genes implicados en distintas enfermedades.

Pretreatment of the patient's serum for detection of antibodies against blood group antigens

Introduction The SRSLY NGS Library Prep Kit from ClaretBio offers an efficient and simplified solution for library preparation using a technology based on single-stranded DNA through a ligation method. Unlike traditional library preparations, which are based on double-stranded DNA, SRSLY kits allow the entire DNA of the initial sample to be transformed into a sequenceable…