The largest database of trusted experimental protocols

G1956b single quadrupole mass spectrometer

Manufactured by Agilent Technologies
Sourced in United States

The G1956B is a single quadrupole mass spectrometer manufactured by Agilent Technologies. It is designed to analyze the molecular composition of samples by ionizing, separating, and detecting ions based on their mass-to-charge ratio. The instrument provides accurate mass measurements and can be used for a variety of analytical applications.

Automatically generated - may contain errors

2 protocols using g1956b single quadrupole mass spectrometer

1

Advanced Spectroscopic Analysis of Compounds

Check if the same lab product or an alternative is used in the 5 most similar protocols
Optical rotations were measured using a Perkin-Elmer model 343 polarimeter (Perkin-Elmer Inc., Waltham, MA, USA). UV and ECD spectra were recorded on an Applied Photophysics Chirascan spectrometer (Applied Photophysics Ltd., Surrey, UK). IR spectra were measured using a Nicolet 5700 FT-IR microscope spectrometer (FT-IR microscope transmission) (Thermo Electron Corp., Madison, WI, USA). NMR spectra were acquired on a AVANCE III HD 600 MHz spectrometers (Bruker Corp., Karlsruhe, Germany) in CDCl3 with tetramethylsilane as an internal reference. ESIMS data were obtained using an Agilent 1100 LC/MSD with a G1956B single quadrupole mass spectrometer (Agilent Technologies, Ltd., Santa Clara, CA, USA). HRESIMS data were recorded using a Thermo LTQ Orbitrap XL mass spectrometer (Thermo Fisher Scientific, Waltham, MA, USA). Flash chromatography was performed on an Ez Purifier (Suzhou Lisure Science Co., Ltd., Suzhou, China). Column chromatography was carried out using silica gel (Qingdao Marine Chemical Inc, Qingdao, China) and Toyopearl gel HW-40F (Tosoh Co., Tokyo, Japan). HPLC separation was performed with a Shimadzu LC-20AP binary pump (Shimadzu Co., Kyoto, Japan) equipped with an SPD-M20A diode array detector using a Shiseido Capcell C18 MGII preparative (20 mm × 250 mm) or semi-preparative (10 mm × 250 mm) column.
+ Open protocol
+ Expand
2

Extraction and Quantification of Metabolites

Check if the same lab product or an alternative is used in the 5 most similar protocols
Cell culture media was extracted with 10% acetic acid in 2:20:30 water/isopropanol/hexane as described by Levison et al.61 (link) The hexane layer was evaporated to dryness and reconstituted in 85% methanol in water. Targeted detection was performed by the NHLBI Biochemistry Core using an Agilent 1100 HPLC coupled to an Agilent G1956B single-quadrupole mass spectrometer. The sample was injected into a Zorbax XDB-Phenyl, 2 μM x 50 mm column (Agilent) with an injection volume of 5 μM. The mobile phase consisted of (A) 0.1% formic acid in dH2O and (B) 0.1% formic acid in acetonitrile.
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!