Genomics, the study of genomes, includes functional genomics, evolutionary genomics and comparative genomics. There are many genomic technologies such as DNA sequencing of whole genomes, computational biology and bioinformatics. DNA and nucleic acids must be isolated and concentrated from cells for analysis with kits, automated analyzers and software. Other useful technologies for studying genomics include PCR, microarrays and electrophoresis.
Agilent™s Model Organism ChIP-on-chip Microarrays provides researchers with clear insight into species research through traditional chromatin immunoprecipitation (ChIP) pull-down coupled with powerful DNA microarray location analysis. Beyond embryonic and adult development gene regulation, Agilent™s ChIP-on-chip model systems effectively elucidates the vital biological processes. Probe number depends on species 4x44k and…
Agilent™s Model Organism ChIP-on-chip Microarrays provides researchers with clear insight into species research through traditional chromatin immunoprecipitation (ChIP) pull-down coupled with powerful DNA microarray location analysis. Beyond embryonic and adult development gene regulation, Agilent™s ChIP-on-chip model systems effectively elucidates the vital biological processes. Probe number depends on species 4x44k and…
The Agilent SurePrint G3 ISCA v2 CGH 4x180K Microarray dual-color chromosomal microarray contains 60-mer high-quality probes. The ISCA CGH microarray is an effective tool for targeted genome-wide DNA copy number variation profiling without reducing amplification or complexity.
The SurePrint G3 ISCA v2 CGH 8x60K dual-color chromosomal microarray contains 60-mer high-quality probes. The ISCA CGH microarray is an effective tool for targeted genome-wide DNA copy number variation profiling without amplification or complexity reduction.
The Agilent Human Genome CGH Microarray is a high-resolution tool for genome-wide DNA copy number variation profiling without amplification or complexity reduction. Comprehensive probe coverage is enhanced with emphasis on known genes, promoters, miRNAs, pseudoautosomal, and telomeric regions. Coding and non-coding human sequences represented Probes annotated against NCBI Build 37 (UCSC hg19, February 2009) Probes on t…
The Agilent Human Genome CGH Microarray is a high-resolution tool for genome-wide DNA copy number variation profiling without amplification or complexity reduction. Comprehensive probe coverage is enhanced with emphasis on known genes, promoters, miRNAs, pseudoautosomal, and telomeric regions. Coding and non-coding human sequences represented Probes annotated against NCBI Build 37 (UCSC hg19, February 2009) Probes on t…
The Agilent Model Organism Genome CGH Microarray brings optimal clarity to comparative genomic hybridization by enabling researchers to perform ultra high resolution, genome-wide DNA variation profiling without amplification or complexity reduction. Coding and non-coding sequences represented Format-dependent overall median probe spacing Probes annotated against indicated sources 0.5g total genomic DNA input require…
The Agilent Model Organism Genome CGH Microarray brings optimal clarity to comparative genomic hybridization by enabling researchers to perform ultra high resolution, genome-wide DNA variation profiling without amplification or complexity reduction. Coding and non-coding sequences represented Format-dependent overall median probe spacing Probes annotated against indicated sources 0.5g total genomic DNA input require…
The Agilent Model Organism Genome CGH Microarray brings optimal clarity to comparative genomic hybridization by enabling researchers to perform ultra high resolution, genome-wide DNA variation profiling without amplification or complexity reduction. Coding and non-coding sequences represented Format-dependent overall median probe spacing Probes annotated against indicated sources 0.5g total genomic DNA input require…
The Agilent Model Organism Genome CGH Microarray brings optimal clarity to comparative genomic hybridization by enabling researchers to perform ultra high resolution, genome-wide DNA variation profiling without amplification or complexity reduction. Coding and non-coding sequences represented Format-dependent overall median probe spacing Probes annotated against indicated sources 0.5g total genomic DNA input require…
