Capillary isoelectric focusing of microorganisms in the pH range 2–5 in a dynamically modified FS capillary with UV detection

2006 ◽  
Vol 385 (5) ◽  
pp. 840-846 ◽  
Author(s):  
Marie Horká ◽  
Filip Růžička ◽  
Veronika Holá ◽  
Karel Šlais
2006 ◽  
Vol 841 (1-2) ◽  
pp. 152-159 ◽  
Author(s):  
Marie Horká ◽  
Filip Růžička ◽  
Jaroslav Horký ◽  
Veronika Holá ◽  
Karel Šlais

2015 ◽  
Vol 48 (15) ◽  
pp. 1011
Author(s):  
Atefeh Sadat Zarabadi ◽  
Seyedeh Maryam Vasefi ◽  
Tiemin Huang ◽  
John G. Mielke

1973 ◽  
Vol 73 (3) ◽  
pp. 483-488 ◽  
Author(s):  
F. Adlkofer ◽  
H. Schleusener ◽  
L. Uher ◽  
A. Ananos ◽  
C. Brammeier

ABSTRACT Crude IgG of sera from 3 patients with Graves' disease, which contained LATS-activity and/or thyroid antibodies, was fractionated by isoelectric focusing in a pH-range between 6.0 to 10.0. LATS-activity was found in IgG-subfractions from pH 7.5 to 9.5, thyroglobulin antibodies and thyroid microsomal antibodies from pH 6.0 to 10.0. It was not possible to separate LATS-activity from the thyroid antibodies by this technique. The results indicate that LATS and the thyroid antibodies are heterogeneous and of polyclonal origin.


2016 ◽  
Vol 146 (3) ◽  
pp. 361-368 ◽  
Author(s):  
Toon Schiemsky ◽  
Caroline Brusselmans ◽  
Elke Nackers ◽  
Pieter Vermeersch ◽  
Koen Poesen ◽  
...  

2021 ◽  
Vol 67 (1) ◽  
Author(s):  
Mariko Takano ◽  
Masaya Nakamura ◽  
Masanobu Tabata

AbstractWe performed an analysis using isoelectric focusing to comprehensively clarify the isozyme composition of laccase derived from Japanese lacquer tree, Toxicodendron vernicifluum. When water extracts of acetone powder obtained from lacquer were subjected to isoelectric focusing, five bands within pI 7.35–9.30 and nine bands within pI 3.50–5.25 were detected using Coomassie staining. Similarly, laccase activity staining using guaiacol showed five bands within pI 7.35–9.30 and three bands within pI 3.50–4.25. However, laccase activity staining using gallic acid showed remarkable staining within pI 3.50–5.85, whereas staining was very weak within pI 7.35–9.30. When the water extracts of acetone powder were fractionated into the fractions containing bands within pI 7.35–9.30 and pI 3.50–5.85 by SP-Sepharose column chromatography, the former had a blue color and the latter a yellow color. The laccase activity was measured for each of the fractions in buffer solution in the pH range of 2.5–8.0. When syringaldazine, guaiacol, and 2,6-dimethoxyphenol were used as substrates, the yellow fraction showed considerably higher activity than the blue fraction for pH 5.5–7.5. When 3-methylcatechol and 4-methylcatechol were used as substrates, the yellow fraction showed higher activity for pH 4.5–6.5, and the blue fraction showed higher activity for pH 7.0–8.0. When 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) was used as the substrate, both fractions showed maximum activity at optimum pH of 3.0–4.0. Conventionally, in research on blue laccase derived from lacquer, the non-blue fraction corresponding to the yellow fraction lower than pI 6 has been removed during the purification process and thus has not been analyzed. Our results indicated that yellow laccase was present in the non-blue components of lacquer and that it may play a role in urushiol polymerization with previously reported blue laccase.


2001 ◽  
Vol 917 (1-2) ◽  
pp. 147-158 ◽  
Author(s):  
A.M Lasdun ◽  
R.R Kurumbail ◽  
N.K Leimgruber ◽  
A.S Rathore

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