Detailed Information on Publication Record
2006
Capillary isoelectric focusing of proteins and microorganisms in dynamically modified fused silica with UV detection.
HORKÁ, Marie, Filip RŮŽIČKA, Jaroslav HORKÝ, Veronika HOLÁ, Karel ŠLAIS et. al.Basic information
Original name
Capillary isoelectric focusing of proteins and microorganisms in dynamically modified fused silica with UV detection.
Name in Czech
CIEF proteinů a mikroorganizmů v dynamicky modifikované křemičité kapiláře s UV detekcí.
Authors
HORKÁ, Marie (203 Czech Republic), Filip RŮŽIČKA (203 Czech Republic, guarantor), Jaroslav HORKÝ (203 Czech Republic), Veronika HOLÁ (203 Czech Republic) and Karel ŠLAIS (203 Czech Republic)
Edition
Journal of Chromatography B, Amsterdam, The Netherlands, Elsevier, 2006, 1570-0232
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
30300 3.3 Health sciences
Country of publisher
Netherlands
Confidentiality degree
není předmětem státního či obchodního tajemství
Impact factor
Impact factor: 2.647
RIV identification code
RIV/00216224:14110/06:00016449
Organization unit
Faculty of Medicine
UT WoS
000240393200017
Keywords (in Czech)
kapilární izoelektrická fokusace; proteiny; mikroorganizmy; dynamická modifikace; UV detekce
Keywords in English
capillary isoelectric focusing; proteins; microorganisms; dynamically modified fused silica; UV detection.
Tags
Tags
International impact, Reviewed
Změněno: 25/6/2009 09:24, prof. MUDr. Filip Růžička, Ph.D.
V originále
We suggest a method for the reproducible and efficient capillary isoelectric focusing of proteins and microorganisms in the pH gradient 3-10. The method involves the segmental injection of the simple ampholytes, the solution of the selected electrolytes, and the sample mixture of bioanalytes and carrier ampholytes to the fused silica capillaries dynamically modified by poly(ethylene glycol), PEG 4000, which is added to the catholyte, the anolyte and injected solutions. In order to receive the reproducible results, the capillaries were rinsed by the mixture of acetone/ethanol between analyses. For the tracing of the pH gradients the low-molecular-mass pI markers were used. The simple proteins and the mixed cultures of microorganisms, Saccharomyces cerevisiae CCM 8191, Escherichia coli CCM 3954, Candida albicans CCM 8180, Candida parapsilosis, Candida krusei, Staphylococcus aureus, Streptococcus agalactiae CCM 6187, Enterococcus faecalis CCM 4224, Staphylococcus epidermidis CCM 4418 and Stenotrophomonas maltophilia, were focused and separated by the method suggested. The minimum detectable number of microbial cells was 5x10(2) to 1x10(3) with on-column UV detection at 280 nm.
In Czech
Navržená CIEF metoda umožňuje citlivě a reprodukovatelně v gradientu pH 3-10 detekovat a identifikovat proteiny i mikroorganizmy a to jak z čistých kultur, tak ze směsí.
Links
IAA4031302, research and development project |
|