Hydrolyses of alpha-naphthyl acetate, beta-naphthyl acetate, and acetyl-DL-phenylalanine beta-naphthyl ester
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
Standard
Hydrolyses of alpha-naphthyl acetate, beta-naphthyl acetate, and acetyl-DL-phenylalanine beta-naphthyl ester. / Kirkeby, S; Moe, D.
I: Acta Histochemica, Bind 72, Nr. 2, 1983, s. 225-31.Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
Harvard
APA
Vancouver
Author
Bibtex
}
RIS
TY - JOUR
T1 - Hydrolyses of alpha-naphthyl acetate, beta-naphthyl acetate, and acetyl-DL-phenylalanine beta-naphthyl ester
AU - Kirkeby, S
AU - Moe, D
N1 - Keywords: Animals; Carboxylic Ester Hydrolases; Esterases; Histocytochemistry; Hydrogen-Ion Concentration; Hydrolysis; Kidney; Male; Mice; Mice, Inbred BALB C; Naphthols; Spectrophotometry
PY - 1983
Y1 - 1983
N2 - Using simultaneous coupling azo dye techniques kidney enzymes active against alpha-naphthyl acetate, beta-naphthyl acetate, and acetyl-DL-phenylalanine beta-naphthyl ester are characterized. The enzymes show identical distribution in the section. The banding patterns in zymograms are the same after incubation with the different substrates. The enzymes might, however, be separated by difference in pH optimum, initial velocity and sensitivity to inhibitors and activators.
AB - Using simultaneous coupling azo dye techniques kidney enzymes active against alpha-naphthyl acetate, beta-naphthyl acetate, and acetyl-DL-phenylalanine beta-naphthyl ester are characterized. The enzymes show identical distribution in the section. The banding patterns in zymograms are the same after incubation with the different substrates. The enzymes might, however, be separated by difference in pH optimum, initial velocity and sensitivity to inhibitors and activators.
M3 - Journal article
C2 - 6410665
VL - 72
SP - 225
EP - 231
JO - Acta Histochemica
JF - Acta Histochemica
SN - 0065-1281
IS - 2
ER -
ID: 10209547