 |
|
|
[24] |
 |
[6] |
 |
[34] |
 |
[49] |
 |
[68] |
 |
[6] |
 |
[1] |
 |
[4] |
 |
[10] |
 |
[35] |
 |
[18] |
 |
[47] |
 |
[29] |
 |
[18] |
 |
[13] |
 |
[1] |
 |
[42] |
 |
[17] |
 |
[43] |
 |
[12] |
 |
[11] |
 |
 |
|
|
[68] |
 |
| |
Laboratory News Directory is not responsible for the content of external internet sites |
|
Millipore (UK) Ltd
|
| |
Millipore (UK) Ltd
Address: Units 3 & 5, The Courtyards, Hatters Lane, Watford, Hertfordshire, UK WD18 8YH
Tel: 08709004645 Fax:
08709004644 Web: www.millipore.com Email:
H2O@millipore.com Contact: MW
Company Profile Millipore Bioscience is a market leader in fluid separation and purification technologies. Millipore technologies are used in a diverse range of applications from protein sample preparation and vaccine sterilization to monoclonal antibody production. Millipore also offers a diverse range of water purification systems, designed to respond to laboratory needs for purified water. Purified water quality can be critical in analytical applications such as HPLC, ICP-MS and TOC analysis, or in molecular biological applications, such as cell culture or electrophoresis. Millipore’s water purification systems employ a variety of complementary technologies (reverse osmosis, electrodeionization, activated carbon adsorption, microfiltration, ultrafiltration, UV photo-oxidation, etc.) to optimise water quality for specific application needs, with systems available producing several litres to those producing several thousand litres per day |  |
Products from Millipore (UK) Ltd |
|   |
RNA-protein binding
Millipore Corporation has launched its new Magna RIP RNAbinding protein immunoprecipitation (RIP) kit, which is the first to provide a complete solution for the entire RIP workflow. With this kit, any researcher, even those inexperienced in RNA purification, can investigate the dynamics of ribonucleoprotein assembly as it occurs inside the cell. Cells respond to stimuli by altering gene expression, and RNA-protein complexes drive almost all processes regulating gene expression at the posttranscriptional level, including splicing, nuclear export, mRNA stability, and translation. Therefore, understanding gene regulation depends on characterising the changes in RNA binding in these various processes. Traditionally, RNA-protein interactions have been identified by screening libraries in yeast, bacteria, or by in vitro selection, all confounded by system limitations, biases, or artifacts. In contrast, data obtained from RIP show increased biological relevance, enabling researchers to achieve their goals more quickly.
Request information for this product
Date added: 01 October 2009 |
|
|