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    Wyświetlanie 1-3 z 3
    Tytuł:
    Quantification of triazine herbicides using chloroplasts in conjunction with thin-layer chromatography
    Autorzy:
    Broszat, M.
    Ernst, H.
    Spangenberg, B.
    Powiązania:
    https://bibliotekanauki.pl/articles/363070.pdf
    Data publikacji:
    2011
    Wydawca:
    Uniwersytet Warmińsko-Mazurski w Olsztynie
    Tematy:
    połączone analizy bioefektywne
    derywatyzacja
    HPTLC
    liniowy zakres kalibracji
    kwantyfikacja
    TLC
    herbicydy triazynowe
    video densytometria
    bioeffective-linked analysis
    derivatization
    linear calibration range
    quantification
    triazine herbicides
    videodensitometry
    Opis:
    We present a video-densitometric quantification method for the triazine herbicides atraton, terbumeton, simazine, atrazine and terbutylazine. Triazine herbicides were separated on silica gel using methyl-t-butyl ether, cyclohexane (1+1, v/v) as mobile phase. The quantification was based on a bioeffective-linked analysis using chloroplast and 2,6-dichlorophenolindophenol. Within 1-2 minutes HILL-reaction inhibitor substances show blue-grey zones on a pale yellowgreen background. To increase the contrast, the moist plate can be dipped into a solution of PEG-600 (10% PEG-600 in methanol) for 2s. Measurements were carried out using a 16 bit ST-1603ME CCD camera with 1.56 megapixels (from Santa Barbara Instrument Group, Inc., Santa Barbara, USA). A white LED was used for illumination purposes. The range of linearity covers more than one magnitude using the (1/R) - 1 expression data transformation. The method can be used for herbicide screenings in environmental samples, because not spectral sensitivity but herbicide activity is measured. The separation method is cheap, fast and reliable.
    Źródło:
    Environmental Biotechnology; 2011, 7, 2; 47-52
    1734-4964
    Pojawia się w:
    Environmental Biotechnology
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Relative quantification of CYP1A gene expression in whitefish (Coregonus lavaretus) exposed to benzo[a]pyrene
    Autorzy:
    Brzuzan, P.
    Jurczyk, Ł.
    Łuczyński, M. K.
    Góra, M.
    Powiązania:
    https://bibliotekanauki.pl/articles/363188.pdf
    Data publikacji:
    2005
    Wydawca:
    Uniwersytet Warmińsko-Mazurski w Olsztynie
    Tematy:
    ekspresja genu CYP1A
    sieja
    benzo(a)piren
    real-time PCR
    benzo(a)pyrene
    Coregonus lavaretus
    CYP1A gene expression
    RealTime PCR
    relative quantification
    Opis:
    The expression of CYP1A (cytochrome P4501A) can be induced by a number of aromatic compounds in teleost fishes. We developed a real-time PCR assay for measuring relative quantities (RQ) of CYP1A mRNA in whitefish (Coregonus lavaretus). To test for the usefulness of the assay we performed a treatment study, using benzo[a]pyrene (B[a]P) a model CYP1A inducer. Primers for the CYP1A gene were adapted from the literature, whereas those for [beta]-actin (endogenous control) were designed from a region that was found to be conserved among salmonid [beta]-actin genes. A group of hatchery raised whitefish, with an average body mass of 15 g and total length of 12 cm were given an intraperitoneal injection (10 mg/kg) of B[a]P in corn oil (2 mg B[a]P/ml corn oil) or corn oil alone (Control). After 48 h, whitefish liver, head kidney and brains were collected for mRNA isolation and analysis. In all three tissues sampled, CYP1A mRNA was affected by treatment with B[a]P. Head kidney tissue showed the greatest induction potential (RQ=11.00) from base levels (RQ=1.00), followed by liver (RQ=9.45), and brain (RQ=3.76). These results demonstrated that CYP1A was highly inducible by B[a]P in whitefish head kidney and liver, and to some extent, in brain tissue. The approach presented here has the advantage of providing rapid and accurate measures of CYP1A induction in various tissues of fish responding to PAH contaminant exposure.
    Źródło:
    Environmental Biotechnology; 2005, 1, 1; 11-15
    1734-4964
    Pojawia się w:
    Environmental Biotechnology
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Cyclopenta[c]phenanthrene induction of CYP1A in brain of rainbow trout (Oncorhynchus mykiss)
    Autorzy:
    Brzuzan, P.
    Woźny, M.
    Łuczyński, M. K.
    Góra, M.
    Ciesielski, S.
    Kuźmiński, H.
    Powiązania:
    https://bibliotekanauki.pl/articles/363272.pdf
    Data publikacji:
    2007
    Wydawca:
    Uniwersytet Warmińsko-Mazurski w Olsztynie
    Tematy:
    benzo(a)piren
    mózg
    CYP1A
    cyklopenta[c]fenantren
    absolutna kwantyfikacja mRNA
    pstrąg tęczowy
    benzo(a)pyrene
    brain
    cyclopenta[c]phenanthrene
    mRNA absolute quantification
    rainbow trout
    Opis:
    We assessed the effects of cyclopenta[c]phenanthrene (CP[c]Ph) and benzo[a]pyrene (B[a]P; positive control) on CYP1A gene expression in brain of juvenile rainbow trout (Oncorhynchus mykiss) using the quantitative reverse transcription polymerase chain reaction (Q-RT-PCR). A group of hatchery raised rainbow trout, with an average body mass of 49.4 g and total length of 15.5 cm were given an intraperitoneal injection (10 mg*kg-1) of either CP[c]Ph or B[a]P in corn oil (2 mg*mi-1 corn oil) or corn oil alone (control). After 24 and 48 h, trout brains were collected for mRNA isolation and analysis. After 24 hours of the exposure, only B[a]P-treated rainbow trout had 10-fold higher number of CYP1A transcripts (mean = 3.63*106 transcripts*µg-1 total RNA) than control fish (3.24*105 transcripts*µg-1 total RNA; Tukey test, P<0.05). After 48 hrs, significantly higher levels of CYP1A expression (Tukey test, P<0.001) were found in either CP[c]Ph- or B[a]P- induced group (1.45*106 and 6.92*106 transcriptsźµg-1 total RNA, respectively) over a control group (mean=1.41*105 transcripts*µg-1 total RNA). The finding that CYP1A in brain tissue was inducible by CP[c]Ph, a polycyclic aromatic hydrocarbon (PAH) of different than B[a]P planar characteristics, may further validate the use of rainbow trout brain CYP1A mRNA levels as a biomarker of PAH exposure.
    Źródło:
    Environmental Biotechnology; 2007, 3, 1; 10-14
    1734-4964
    Pojawia się w:
    Environmental Biotechnology
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
      Wyświetlanie 1-3 z 3

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