Pregled bibliografske jedinice broj: 56457
An improved method for electrophoretic determination of bone and liver isoenzymes of alakaline phosphatase
An improved method for electrophoretic determination of bone and liver isoenzymes of alakaline phosphatase // Clinical Chemistry and Laboratory Medicine / Siest, Gerard ; Dominiczak, Marek H (ur.).
Berlin : New York: Walter de Gruyter, 1999. (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 56457 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
An improved method for electrophoretic determination of bone and liver isoenzymes of alakaline phosphatase
Autori
Sokolić, Božica ; Čepelak, Ivana ; Galović, Ružica ; Dodig, Slavica ; Kunović, Branka
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Clinical Chemistry and Laboratory Medicine
/ Siest, Gerard ; Dominiczak, Marek H - Berlin : New York : Walter de Gruyter, 1999
Skup
IFCC-WorldLab, 17th International and 13th European Congress of Clinical Chemistry and Laboratory Medicine
Mjesto i datum
Firenca, Italija, 06.06.1999. - 11.06.1999
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
electrophoresis; alkaline phosphatase; isoenzymes
Sažetak
We describe a simple method for separation and quantification of the bone and liver isoenzymes of alkaline phosphatase (AP). Bone isoenzyme is clearly separated from the liver one by specific binding to wheat-germ lectin and subsequently retarded during electrophoretic separation.
We modified lectin-affinity electrophoresis on cellogel membranes described by Rosalki and Foo (1984). Barbital buffer pH=9.2 and electrophoresis temperature of 25 C are giving the best resolution. Visualisation using Fast Violet B salt is suitable for densitometric quantification. Using method of Hausamen et al. (1967) we determined total AP and quantified bone and liver AP by heat-inactivation, also.
Precision in series (CV≤5%), reproducibility (CV≤5%) and correlation with heat-inactivation method (r=0.87, r=0.84 for bone and liver isoenzymes, respectively) were found for lectin-affinity electrophoresis. We established referent values in sera from healthy people: 87 adults (age 21-81: 42 men, 45 women) and 21 children (age 1-14). Total AP and bone and liver isoenzymes (mean±1.96SD U/l) for men (142.5±45.5, 69.6±37.8, 72.9±26.7, respectively), women (122.3±40.5, 66.2±33.5, 56.2±23.9, respectively) and children (467.0±172.7, 397.3±137.4, 70.0±58.8, respectively) were determined. We examined differences in total and isoenzymes activities related to age of subjects.
Lectin-affinity electrophoresis is a rapid, precise, reproducible and suitable method for use in the diagnostic laboratory.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti
POVEZANOST RADA
Projekti:
006311
Ustanove:
Farmaceutsko-biokemijski fakultet, Zagreb
Profili:
Slavica Dodig
(autor)
Božica Sokolić
(autor)
Branka Kunović
(autor)
Ivana Čepelak
(autor)
Ružica Galović Rengel
(autor)