Identification of active deubiquitinases in the chicken tissues

PROTEOMICS ◽  
2021 ◽  
pp. 2100122
Author(s):  
Bindu Nanduri ◽  
Cathy R. Gresham ◽  
Gary Jones ◽  
Richard H. Bailey ◽  
Mariola J Edelmann
Keyword(s):  
2014 ◽  
Vol 116 (5) ◽  
pp. 702-707 ◽  
Author(s):  
Yoshihiro Nishimura ◽  
Hiroyuki Tanaka ◽  
Tetsuo Ishida ◽  
Shinji Imai ◽  
Yoshitaka Matsusue ◽  
...  

2012 ◽  
Vol 29 (6) ◽  
pp. 918-924 ◽  
Author(s):  
Yumei Zhang ◽  
Yufeng Du ◽  
Jun Yin ◽  
Chengyun Hu ◽  
Xie Liu ◽  
...  

1982 ◽  
Vol 92 (1) ◽  
pp. 23-27 ◽  
Author(s):  
E C Beyer ◽  
S H Barondes

Two lactose-binding lectins from chicken tissues, chicken-lactose-lectin-1 (CLL-1) and chicken-lactose-lectin-11 (CLL-11) were quantified with a radioimmunoassay in extracts of a number of developing and adult chicken tissues. Both lectins could be measured in the same extract without separation, because they showed not significant immunological cross-reactivity. Many embryonic and adult tissues, including brain, heart, intestine, kidney, liver, lung, muscle, pancreas, and spleen, contained one or both lectins, although their concentrations differed markedly. For example, embryonic muscle, the richest source of CLL-1 contained only traces of CLL-11 whereas embryonic kidney, a very rich source of CLL-11 contained substantial CLL-1. In both muscle and kidney, lectin levels in adulthood were much lower than in the embryonic state. In contrast, CLL-1 in liver and CLL-11 in intestine were 10-fold to 30-fold more concentrated in the adult than in the 15-d embryo. CLL-1 and CLL-11 from several tissues were purified by affinity chromatography and their identity in the various tissues was confirmed by polyacrylamide gel electrophoresis, isoelectric focusing, and peptide mapping. The results suggest that these lectins might have different functions in the many developing and adult tissues in which they are found.


1980 ◽  
Vol 63 (6) ◽  
pp. 1211-1214
Author(s):  
Etsuko Suzuki ◽  
Mihoko Matsuda ◽  
Atsushi Momose ◽  
Masaya Namekata

Abstract A sensitive and specific gas-liquid chromatographic (GLC) method has been developed for determining low levels of clopidol in chicken tissues. Clopidol is extracted from the tissues with methanol, and cleaned up on an alumina column and an anion exchange resin column with 0.1% acetic acid–methanol as eluate. Clopidol is methylated with diazomethane, and then determined by GLC. 2,4-Dinitro-l-chlorobenzene is used as an internal standard. The method is applicable to levels as low as 2 ppb in chicken tissues. Recoveries of 2–20 ppb clopidol added to tissues averaged 87% for muscle, 84% for liver, 80% for kidney, and 76% for fat.


1974 ◽  
Vol 57 (4) ◽  
pp. 914-918
Author(s):  
E Leroy Bjerke ◽  
James L Herman

Abstract Ten collaborators participated in a study of an improved method for determining residues of the coccidiostat clopidol (3,5-dichloro-2,6- dimethyl-4-pyridinol) in chicken tissues and eggs. Tissues are extracted with methanol and the extract is cleaned up with columns of alumina and anion exchange resin. After methylation with diazomethane reagent, clopidol methyl ether is determined by gas chromatography with electron capture detection. The method is applicable to levels as low as 0.1 ppm in chicken tissues and 0.05 ppm in eggs. Results from 9 collaborators gave an average recovery of 84% from muscle, 90% from liver, and 84% from eggs. Results from an unknown sample of each substrate were excellent. The method has been adopted as official first action.


2014 ◽  
Vol 58 (4) ◽  
pp. 573-579 ◽  
Author(s):  
Anna Gajda ◽  
Andrzej Posyniak ◽  
Grzegorz Tomczyk

Abstract For the purpose of quantitative determination of doxycycline (DC) residues in tissues, a sensitive liquid chromatography - tandem mass spectrometry (LC-MS/MS) method was developed. The method was used to determine DC residues in chicken tissues (breast and thigh muscle, liver and kidney) after oral administration with drinking water to five-weak-old broiler chickens. The DC was administered for five consecutive days at a therapeutic dose of 10 mg/kg b.w. once a day. The tissues were collected after 6 h, 24 h, 7 d, and 8 d. The method was validated and the decision limit was established for muscle - 109.2 μg/kg, for liver - 326.1 μg/kg, and for kidney - 634.0 μg/kg. The detection limit was 2 μg/kg and the limit of quantification was 5 μg/kg. In a short period after ceasing the treatment, the detected concentrations of DC were much higher than the established maximum residue limit values. The highest residue concentrations of DC were observed in the kidney, followed by the liver and muscle. The lowest concentration of DC was determined in tight muscle.


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