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CP-Select CB Columns for MTBE

Agilent Technologies

Agilent J&W CP-Select CB for MTBE provides guaranteed analysis of MTBE in reformulated gasolines, with reproducible results. It has unique selectivity for ease-of-use with MTBE. The column's broad dynamic range for MTBE quantification delivers the highest productivity for increasingly demanding volatiles applications. 

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Refinery Gas Analyzers

Agilent Technologies

Refinery gas analyzers are an integral part of any refinery lab and provide valuable information that allow refiners to monitor and optimize catalytic and other processes, establish market value of a gas when sold to the chemical industry, and enable the study of gaseous products from process under study or development.

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GC/MS Forensic Toxicology Analyzer 

Agilent Technologies

GC/MS methods are widely used for forensic toxicology, especially for the screening of large numbers of target compounds in complex matrices. Full-scan EI methods offer many advantages for broad-range screening, such as an unlimited number of targets, full-spectrum identity confirmation, and library searching for identification of non-targets. Technologies such as Capillary Flow Technology backflushing, Deconvolution Reporting…

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Custom CGH Microarrays

Agilent Technologies

The Agilent Custom CGH+SNP Microarray product line uses Agilent’s SurePrint technology to design and print user-defined CGH+SNP microarrays. Using Agilent’s eArray free application, users can design their own CGH+SNP microarrays to detect copy number changes and copy neutral aberrations, such as loss of heterozygosity (LOH) and uniparental disomy (UPD), on the same array.

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Custom CGH+SNP Microarrays

Agilent Technologies

The Agilent Custom CGH+SNP Microarray product line uses Agilent’s SurePrint technology to design and print user-defined CGH+SNP microarrays. Using Agilent’s eArray free application, users can design their own CGH+SNP microarrays to detect copy number changes and copy neutral aberrations, such as loss of heterozygosity (LOH) and uniparental disomy (UPD), on the same array.

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