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Preparativeseparationof immunoglobulins from bovine colostrum by continuous divergent-flow electrophoresis

Identifikátory výsledku

  • Kód výsledku v IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68081715%3A_____%2F23%3A00562904" target="_blank" >RIV/68081715:_____/23:00562904 - isvavai.cz</a>

  • Výsledek na webu

    <a href="https://hdl.handle.net/11104/0335073" target="_blank" >https://hdl.handle.net/11104/0335073</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1002/jssc.202200679" target="_blank" >10.1002/jssc.202200679</a>

Alternativní jazyky

  • Jazyk výsledku

    angličtina

  • Název v původním jazyce

    Preparativeseparationof immunoglobulins from bovine colostrum by continuous divergent-flow electrophoresis

  • Popis výsledku v původním jazyce

    Immunoglobulins in bovine colostrum were separated and fractionated from other proteins using method and instrumentation developed in our laboratory. The proposed separation was based on bidirectional isotachophoresis/moving boundary electrophoresis with electrofocusing of the analytes in pH gradient from 3.9 to 10.1. The preparative instrumentation included the trapezoidal non-woven fabric that served as separation space with divergent continuous flow. The defatted and casein precipitate free colostrum supernatant was loaded directly into instrument without any additional colostrum pre-preparation. Immunoglobulin G that was fractionated from other immune proteins such as bovine serum albumin, β-lactoglobulin and α-lactalbumin, was continuously collected in separated fractions over 3 hours. The fractions were further processed, and isolated immunoglobulin G in the liquid fractions was confirmed by sodium dodecyl sulphate-polyacrylamide gel electrophoresis and by re-focusing in gel isoelectric focusing. Separated immunoglobulin G was detected in seven fractions by sodium dodecyl sulphate-polyacrylamide gel electrophoresis with gradually decreased concentration in the fractions. Re-focusing of the proteins in the fractions by gel isoelectric focusing revealed multiple separated zones of immunoglobulin G with the pI values covering the range from 5.4 to 7.2. Each fraction contained the distinct zones with gradually increased pI values and decreased concentrations from fraction to fraction.

  • Název v anglickém jazyce

    Preparativeseparationof immunoglobulins from bovine colostrum by continuous divergent-flow electrophoresis

  • Popis výsledku anglicky

    Immunoglobulins in bovine colostrum were separated and fractionated from other proteins using method and instrumentation developed in our laboratory. The proposed separation was based on bidirectional isotachophoresis/moving boundary electrophoresis with electrofocusing of the analytes in pH gradient from 3.9 to 10.1. The preparative instrumentation included the trapezoidal non-woven fabric that served as separation space with divergent continuous flow. The defatted and casein precipitate free colostrum supernatant was loaded directly into instrument without any additional colostrum pre-preparation. Immunoglobulin G that was fractionated from other immune proteins such as bovine serum albumin, β-lactoglobulin and α-lactalbumin, was continuously collected in separated fractions over 3 hours. The fractions were further processed, and isolated immunoglobulin G in the liquid fractions was confirmed by sodium dodecyl sulphate-polyacrylamide gel electrophoresis and by re-focusing in gel isoelectric focusing. Separated immunoglobulin G was detected in seven fractions by sodium dodecyl sulphate-polyacrylamide gel electrophoresis with gradually decreased concentration in the fractions. Re-focusing of the proteins in the fractions by gel isoelectric focusing revealed multiple separated zones of immunoglobulin G with the pI values covering the range from 5.4 to 7.2. Each fraction contained the distinct zones with gradually increased pI values and decreased concentrations from fraction to fraction.

Klasifikace

  • Druh

    J<sub>imp</sub> - Článek v periodiku v databázi Web of Science

  • CEP obor

  • OECD FORD obor

    10406 - Analytical chemistry

Návaznosti výsledku

  • Projekt

  • Návaznosti

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Ostatní

  • Rok uplatnění

    2023

  • Kód důvěrnosti údajů

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Údaje specifické pro druh výsledku

  • Název periodika

    Journal of Separation Science

  • ISSN

    1615-9306

  • e-ISSN

    1615-9314

  • Svazek periodika

    46

  • Číslo periodika v rámci svazku

    1

  • Stát vydavatele periodika

    DE - Spolková republika Německo

  • Počet stran výsledku

    10

  • Strana od-do

    2200679

  • Kód UT WoS článku

    000876663100001

  • EID výsledku v databázi Scopus

    2-s2.0-85141364876