Blue Stream Laboratories to use Agilent's Proteomics Technology for Protein Analysis
News Apr 13, 2007
Agilent Technologies has announced that Blue Stream Laboratories Inc. has chosen to equip its protein characterization lab with Agilent's proteomics tools. Blue Stream's management chose Agilent's products after conducting an in-depth cost-benefit evaluation of instruments offered by Agilent and its chief competitors.
Blue Stream Laboratories specializes in recombinant glycoprotein, peptide and small molecule product characterization, lot release, and stability programs required for pharmaceutical and biopharmaceutical product development.
At the heart of Blue Stream's lab setup is Agilent's HPLC-chip technology, a form of liquid chromatography (LC) separation. When combined with Agilent's 6340 ion trap mass spectrometer (MS) equipped with electron transfer dissociation (EDT), it is effective in identifying proteins and post-translational modifications.
Blue Stream's laboratory also features an Agilent 6210 time-of-flight (TOF) mass spectrometer equipped with both MALDI and electrospray capabilities. In the mix as well are supporting software and a services package.
"These Agilent instruments are helping to establish Blue Stream Laboratories as one of the premier contract research laboratories in the biologics product development and testing space," explained Blue Stream's President and Co-Founder Michael Kouchakdjian, Ph.D.
"To our knowledge, Blue Stream is the first commercial lab to use the combination of Agilent's HPLC chip with its ion trap mass spectrometer with ETD. This unique combination is particularly useful for complex protein characterization studies and will support our growing protein biomarker validation program," he continued.
"There were many factors that went into our decision," commented Blue Stream Chief Scientific/Operating Officer Mario DiPaola, Ph.D. "With two distinct but complementary Agilent instruments, we can better service our clients and substantially increase our productivity. Agilent offered us a terrific breadth of portfolio, high reliability and a comprehensive services package."
As genome editing technologies advance toward clinical therapies, they are raising hopes of a completely new way to treat disease. However, challenges need to be addressed before potential treatments can be widely used in patients. To tackle these challenges, the National Institutes of Health has launched the Somatic Cell Genome Editing program, which has awarded multiple grants including more than $3.6 million to assess the safety of genome editing in human cells and tissues.