Shimadzu's triple quadrupole LC/MS/MS system combines world-leading LC performance with advanced mass spectrometry technologies to create a unique system approach to ultrafast mass spectrometry detection. It features a scan speed of 15,000 u/sec and ability to perform 500 different MRM measurements, as well as easy maintenance for greater uptime and usability.
Ideally suited as a front-end for LC/MS and LC/MS/MS systems, the SIL-30ACMP achieves an ultrafast injection performance while maintaining the ultralow carryover performance for which Shimadzu autosamplers are known. In addition to exceptional speed and reproducibility, up to 6 microplates can be loaded, enabling a maximum of 2304 samples to be analyzed continuously.
The Perfinity Workstation is a multi-column apparatus that automates protein separations and mass spec sample preparation. It enables users to start with serum and in10 minutes have peptides ready for LC/MS analysis. In addition, the system generates CV values of less than 10 percent and realizes a significant reduction in cost/sample.
The next generation of triple quad mass spectrometry, Shimadzu’s LCMS-8030 features the fastest MRM transition times available today (1 msec) for up to 500 MRM transitions/second, unsurpassed polarity switching speed, less cross-talk, accelerated workflows, and easier operation. Shimadzu’s LCMS-8030: The world’s fastest tandem quadrupole LC/MS/MS system.
I am working at department of biophysics, Panjab University, Chandigarh, India as a senior Research Fellow. I often use the UV spectrophotometer from Shimadzu for various biochemical assays which require detection of optical densities at...
Whether your protein of interest is large or small, a monomer or multimer, hydrophoboic or hydrophilic, you can analyze it using HPLC. And whether your analysis...
The BioSpec-mini UV-Visible Spectrophotometer from Shimadzu is designed to meet the everyday needs of a molecular biology laboratory. This spectrophotometer is designed to measure and analyze...
Prominence UFLC has been designed to achieve
Ultra-Fast HPLC by utilizing the Prominence
hardware series. In this respect, we are successful
in demonstrating high speed and separation performance
without resorting to high pressure, while providing high
reliability and expandability not available with other fast
LC systems.
The traditional method for quantification and assessment of purity of DNA samples is spectrophotometric measurement at 260 and 280nm (1). It is generally accepted that a sample of pure, double-stranded DNA of 50 µg/mL will have an absorbance at 260nm of 1.0 and that the ratio of absorbance at 260 and 280nm of this sample will be greater than 1.8 (2). If a sample has an A260 / A280 of less than 1.8, it is usually considered to be contaminated by protein. In such measurements, there is frequently little consideration given to the resolution or bandwidth of the spectrophotometer used for the measurements.
It could be said that spectroscopy-based applications fall into two broad categories: Analytical determinations and routine quality control of sample preparations. The Shimadzu UV-1700 spectrophotometer is suitable...
The UV-1700 ParmaSpec is a sensitive, reliable instrument for accurate detection of various substances, including biological samples. The 1 nm bandwidth makes it competent for higher resolution than the UV-160A (which has a 2 nm bandwidth). The UV-1700 contains a 20 W halogen lamp and deuterium lamp with a wavelength range of 190 to 1100 nm. The instrument is compact...
The Shimadzu LCMS-IT-TOF incorporates the higher MS stages available with an ion trap and the high resolution and mass accuracy of a time-of-flight (TOF) mass spectrometer, leading to the only mass spectrometer in the field that allows for excellent mass accuracy for both parent and fragment ions (up to MS10).
In a speech presenting the 1952 Nobel Prize in Chemistry, Nobel laureate Arne Tiselius cited the invention of partition chromatography as key to the development of advanced chromatographic methods for biology, chemistry, and medicine. These advancements sparked a chromatography explosion in the latter half of the century. With the introduction of HPLC in the mid-1960s, liquid chromatography techniques such as ion exchange separation became more widely used for biomolecular applications...