Safety: Parker Balston gas generators completely eliminate the safety hazards involved with handling high-pressure gas cylinders. Enjoy hassle-free automation with no tanks to charge and no downtime.
Reliability: Thousands of laboratories worldwide have Parker Balston gas generators in routine use. Parker Balston gas generators are recommended and used by major instrument manufacturers. We offer the best technology at an affordable price from the brand you trust.
Quality: Each Parker Balston gas generator is manufactured under a strict total quality management program. We have a world-class ISO 9001-certified manufacturing facility in the United States. All Parker Balston gas generators are backed by a complete satisfaction guarantee. Parker offers preventative maintenance, extended warranties, and field repair programs for all laboratory gas generators, as well as a network of highly specialized sales, application, and technical support people.
Products: Hydrogen gas generators produce 99.99999% pure hydrogen for gas chromatographs. Zero air generators produce zero grade air for gas chromatographs. UHP nitrogen generators produce 99.9999% pure nitrogen for GCs or ICP spectrometers. FT-IR gas generators produce dry, CO2-free purge gas for FT-IR spectrometers. Pure air and nitrogen generators produce dry, ultrapure compressed gas for laboratory instruments, including LC–MS instruments.
Parker Hannifin manufactures all gas generators in Haverhill, Massachusetts. Parker has over 50,000 generators installed globally and distribution points worldwide.
Parker Hannifin Corporation Gas Separation and Filtration Division
4087 Walden Avenue
Lancaster, NY 14086
TELEPHONE
(978) 858-0505
FAX
(978) 556-7501
WEB SITEwww.labgasgenerators.com
NUMBER OF EMPLOYEES
55,000
YEAR FOUNDED
1924
FT-IR Analysis of pH and Xylitol Driven Conformational Changes of Ovalbumin–Amide VI Band Study
November 21st 2024This study uses Fourier transform infrared (FT-IR) spectroscopy to analyze how the globular protein ovalbumin's secondary structures transition under varying pH conditions in the presence of the cosolvent xylitol, highlighting the role of noncovalent interactions in these conformational changes.