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fontinalis/protease

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ArtiklidKliinilistes uuringutesPatendid
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Natural anti-proteases (alpha 1-protease inhibitor (alpha 1-PI; alpha 1-antitrypsin) and alpha 2-macroglobulin (alpha 2-M)) were found in the blood of rainbow trout, Oncorhynchus mykiss and brook charr, Salvelinus fontinalis. The alpha 2-M inhibited Cryptobia salmositica proteases and was
A 2.4-kilobase (kb) clone (kallikrein trout #14; KT-14) was isolated from a brook trout ovulatory cDNA library. KT-14 contains an open reading frame (ORF) of 768 base pairs (bp), presumably encoding a protein of 255 amino acids. The KT-14 cDNA also contains a 711 -bp 5' untranslated region and a
Proteolytic activity was demonstrated in the follicle wall surrounding oocytes of brook trout (Salvelinus fontinalis) by an assay system that incorporated protein substrates into sodium dodecyl sulfate-polyacrylamide gel electrophoresis (substrate-SDS-PAGE). At least six proteolytic enzymes (78, 70,
Proteolytic activity was measured in the follicle wall surrounding oocytes from brook trout (Salvelinus fontinalis) and yellow perch (Perca flavescens) by use of two different protease assays: sodium dodecyl sulfate-polyacrylamide gel electrophoresis (substrate-SDS-PAGE) and a chromogenic synthetic

Selenium and its species in the aquatic moss Fontinalis antipyretica.

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The ability of the widely distributed aquatic moss Fontinalis antipyretica to take up Se from water was studied. Nine locations in the Notranjska region (Slovenia) with different land use in the catchment were sampled for water and moss in the year 2010 in spring, summer and autumn. The
The presence of 17α,20β-dihydroxy-4-pregnen-3-one (17α,20β-DHP) oocyte receptor activity has been demonstrated in brook troutSalvelinus fontinalis. Scatchard analyses of the cytosol fraction during various terminal stages of oocyte maturation gave a high equilibrium association constant (Ka) value
Using stage-specific subtractive cDNA cloning, a 0.8-kilobase (kb) cDNA (TOP-1; trout ovulatory protein-1) was previously obtained that hybridized only with ovarian RNA and was highly up-regulated at the time of ovulation. In the present study, a 1.4-kb cDNA (TOP-2; trout ovulatory protein-2) was
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