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DNA services
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Comprehensive Array-CGH Service – aberrations and variations
Based on Agilent’s Microarray platform, Miltenyi Biotec offers a comprehensive service for array-CGH (comparative genomic hybridization). Screening for chromosomal aberrations, such as amplification or deletion, has become a major factor in genetic analysis, whole-genome association studies and clinical diagnostics. CGH can be used to study genomic variations, like copy-number variations (CNV), and enables the identification and characterization of various chromosomal imbalances that cause diseases. This helps to identify new oncogenes, tumor suppressor genes, drug targets, and biomarkers.
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Agilent CGH Microarray Services - genome-wide coverage on a single microarray
Based on Agilent’s Microarray platform, Miltenyi Biotec offers a comprehensive service for array-CGH (comparative genomic hybridization), enabling the study of copy-number variations in any region of the genome. Agilent's CGH microarray platform allows the identification and characterization of chromosomal imbalances in cancer and genetic disorders. Agilent CGH microarrays are high-resolution tools for genome-wide DNA variation profiling with comprehensive probe coverage spanning both coding and non-coding regions. Agilent offers a large number of CGH microarrays for a variety of species. For a complete list of DNA microarrays please click here. In addition, Custom High-Definition CGH Microarrays can be designed from a database of about eight million in silico-validated CGH probes, spaced at 400 bp on average, to focus on specific genomic regions. Choose your region of interest to design a customized microarray tailored to your research needs, leveraging pre-designed CGH probes that cover both exonic, intronic, and intergenic regions of the genome.
Just send ready extracted DNA or, if you wish, your sample as fresh or FFPE tissue and use our DNA Extraction Service or FFPE Sample Preparation Service for subsequent CGH studies.
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