scholarly journals Urinary amino acid analysis: A comparison of iTRAQ®–LC–MS/MS, GC–MS, and amino acid analyzer

2009 ◽  
Vol 877 (20-21) ◽  
pp. 1838-1846 ◽  
Author(s):  
Hannelore Kaspar ◽  
Katja Dettmer ◽  
Queenie Chan ◽  
Scott Daniels ◽  
Subodh Nimkar ◽  
...  
1993 ◽  
Vol 218 (1) ◽  
pp. 113-116 ◽  
Author(s):  
Mary A. Preece ◽  
Ian J. Sewell ◽  
Jacqueline A. Taylor ◽  
Anne Green

2019 ◽  
Author(s):  
Amanda Blake

This protocol describes the deproteinization process that all canine and feline serum and plasma research samples undergo prior to amino acid analysis with a Biochrom 30+ Amino Acid Analyzer at the Gastrointestinal Lab, Texas A&M University. L-norleucine is used as an internal standard.


2012 ◽  
Vol 413 (9-10) ◽  
pp. 953-954
Author(s):  
D. Kavanagh ◽  
M. Holmes ◽  
M. Appleton ◽  
K. Bartlett

2014 ◽  
Vol 10 (6) ◽  
pp. 1441-1449 ◽  
Author(s):  
Yuanyuan Zhang ◽  
Xian Zhou ◽  
Chao Li ◽  
Jianfang Wu ◽  
John E. Kuo ◽  
...  

This study assessed the feasibility of radiation injury early triage based on urinary amino acid analysis.


1975 ◽  
Vol 21 (13) ◽  
pp. 1970-1975 ◽  
Author(s):  
Henri Dirren ◽  
Arthur B Robinson ◽  
Linus Pauling

Abstract The urinary amino acid profiles of 79 young women and 72 young men were studied with an automated high-pressure amino acid analyzer. A nonparametric statistical analysis was applied for detecting profile differences related to sex and other variables. A strong sex-related pattern was confirmed and its power for sex determination was evaluated. For the women, profile differences related to the use of oral contraceptives were also discovered and evaluated. No correlation with the menstrual cycle was detected.


1991 ◽  
Vol 56 (4) ◽  
pp. 923-932
Author(s):  
Jana Stejskalová ◽  
Pavel Stopka ◽  
Zdeněk Pavlíček

The ESR spectra of peroxidase systems of methaemoglobin-ascorbic acid-hydrogen peroxide and methaemoglobin-haptoglobin complex-ascorbic acid-hydrogen peroxide have been measured in the acetate buffer of pH 4.5. For the system with methaemoglobin an asymmetrical signal with g ~ 2 has been observed which is interpreted as the perpendicular region of anisotropic spectrum of superoxide radical. On the other hand, for the system with methaemoglobin-haptoglobin complex the observed signal with g ~ 2 is symmetrical and is interpreted as a signal of delocalized electron. After realization of three repeatedly induced peroxidase processes the ESR signal of the perpendicular part of anisotropic spectrum of superoxide radical is distinctly diminished, whereas the signal of delocalized electron remains practically unchanged. An amino acid analysis of methaemoglobin along with results of the ESR measurements make it possible to derive a hypothesis about the role of haptoglobin in increasing of the peroxidase activity of methaemoglobin.


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