Agilent Manuals

Agilent's Multiple Affinity Removal System is a polyclonal antibody-based system that rapidly depletes multiple high-abundance proteins in serum, plasma or CSF. The system was launched in August 2003 and remains the leading technology in this market.

GC-ICP-MS technology helps solve the problem of low detection limits for siloxanes in biogas usage. It has low detection limits and high sensitivity. The technology allows for accurate quantification of any volatile Si containing compound based on the response of a single standard compound.

The Agilent 1200 Series RRLC system is designed for conventional LC with long columns of large internal diameter as well as for ultra-fast or rapid resolution LC with narrow bore column of about 2.1 mm id. Using a 600 bar, 2-position/6-port valve provides for switching between optimized conditions for both types of analysis.

This document introduces the performance characteristics of the Agilent 1120 Compact LC, including high precision time and area, precise gradient formation and excellent signal-to-noise ratio

This document introduces GCRMA usage.

This document introduces RMA (Robust Multi-array Analysis) method, which is used to normalize and summarize probe-level intensity measurements from Affymetrix Gene Chips ®.

This guide will step you through the process of importing Agilent miRNA data and setting up the experiment for analysis in GeneSpring GX 9.0.

The document describes that the Dionex Chromeleon® 6.80 control software with service pack 3 and driver update 2c is able to fully support an Agilent 1200 Series Rapid Resolution LC (RRLC) system, except for some special functions. After installing the Chromeleon software and respective drivers, the Agilent 1200 Series RRLC system can be easily installed and configured, supports all important module parameters, evaluates raw data, including three-dimensional (3D) and two-dimensional (2D) data and spectra from Agilent ultraviolet (UV) detectors, supports maintenance and diagnostics with the Agilent Lab Monitor & Diagnostic software, can be quickly accessed using the Agilent 1200 Series instant pilot handheld controller, and executes some basic diagnostic/maintenance tasks from within Chromeleon.

DRS A.04 G1716AA is the latest revision, introduced in 2008, with features such as automatic, high-precision, and multi-functionality. It can automatically detect chemicals that violate the Chemical Weapons Convention, identify compounds at low concentration levels in complex matrices, and use retention time as a qualifier.

This document introduces the retention time locking (RTL) technology, which allows for the consistency of retention times on different instruments, simplifying method development and transfer.

This document compares the Agilent Quick Amp and Low RNA Input Linear Amplification Kits and shows that both kits are equivalent when used for gene expression profiling.

A key step in metabolomics research is the identification of metabolites. Searching accurate-mass LC/MS data against metabolite databases is a powerful technique for identifying metabolites. Due to the presence of isobaric masses such as compound isomers and diastereomers, database searching by mass alone is generally insufficient for positive identification. Public databases do not contain retention time information and thus there is no way to resolve the issue of isobaric masses. However, with Agilent Technologies’ METLIN Personal metabolite database, empirically derived, method-specific retention times (RTs) can be added to compounds in the database, creating an accurate-mass retention time (AMRT) database. Retention times then provide a second match criterion orthogonal to, and independent of, compound mass. Searching an AMRT database provides a narrower, more focused list of possible metabolite identities. This technical note discusses the addition of retention times to the METLIN Personal metabolite database and provides a faster batch approach for creating an AMRT database.

Describes the role of gas chromatography (GC) column quality control test probes (QC test probes), including ensuring that the columns have been properly deactivated, contain the correct amount of stationary phase, and have the same relative retention as the last column purchased.

This document introduces a new method for protein detection on the Agilent 2100 bioanalyzer based on fluorescent labeling. The method has high sensitivity, a large linear dynamic range, can detect impurities, and is fast and reliable.