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log10  (ATCC)


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    ATCC log10
    Log10, supplied by ATCC, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/64310/Ceriporiopsis+rivulosa+(Berkeley+et+Curtis)+Gilbertson+et+Ryvarden/pm28361404-163-28-60
    Average 90 stars, based on 1 article reviews
    log10 - by Bioz Stars, 2026-11
    90/100 stars

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    Related Articles

    Concentration Assay:

    Article Title: Antibacterial mode of action of violacein from Chromobacterium violaceum UTM5 against Staphylococcus aureus and methicillin-resistant Staphylococcus aureus (MRSA).
    Article Snippet: Violacein, violet pigment produced by Chromobacterium violaceum, has attracted much attention recently due to its pharmacological properties including antibacterial activity.. The present study investigated possible antibacterial mode of action of violacein from C. violaceum UTM5 against Staphylococcus aureus and methicillin-resistant S. aureus (MRSA) strains.. Violet fraction was obtained by cultivatingC. violaceumUTM5 in liquid pineapple waste medium, extracted, and fractionated using ethyl acetate and vacuum liquid chromatography technique.

    Activity Assay:

    Article Title: Antibacterial mode of action of violacein from Chromobacterium violaceum UTM5 against Staphylococcus aureus and methicillin-resistant Staphylococcus aureus (MRSA).
    Article Snippet: Violacein, violet pigment produced by Chromobacterium violaceum, has attracted much attention recently due to its pharmacological properties including antibacterial activity.. The present study investigated possible antibacterial mode of action of violacein from C. violaceum UTM5 against Staphylococcus aureus and methicillin-resistant S. aureus (MRSA) strains.. Violet fraction was obtained by cultivatingC. violaceumUTM5 in liquid pineapple waste medium, extracted, and fractionated using ethyl acetate and vacuum liquid chromatography technique.

    Incubation:

    Article Title: Antibacterial mode of action of violacein from Chromobacterium violaceum UTM5 against Staphylococcus aureus and methicillin-resistant Staphylococcus aureus (MRSA).
    Article Snippet: Violacein, violet pigment produced by Chromobacterium violaceum, has attracted much attention recently due to its pharmacological properties including antibacterial activity.. The present study investigated possible antibacterial mode of action of violacein from C. violaceum UTM5 against Staphylococcus aureus and methicillin-resistant S. aureus (MRSA) strains.. Violet fraction was obtained by cultivatingC. violaceumUTM5 in liquid pineapple waste medium, extracted, and fractionated using ethyl acetate and vacuum liquid chromatography technique.



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    SST-mediated effects on calcium signaling and downstream mediators. ( A ). The intracellular level of Ca 2+ was assessed using the Fluo-4 calcium indicator. Cells treated with Aβ 1-42 resulted in an increased Ca 2+ influx compared to the SST or untreated control. Cells treated with Aβ 1-42 in the presence of SST resulted in a noticeable inhibition of the Ca 2+ influx compared to the cells treated with Aβ 1-42 alone. B. Representative Western blot displaying the changes in the expression of calpain, CDK5, and p35/25 expression in cells treated with Aβ 1-42 in the presence or absence of SST. ( C – E ). Histograms represent the densitometry analysis of the Western blot shown in ( B ). Data represent the mean ± SD of three independent experiments. * p < 0.05 against respective control, Two-way ANOVA with Bonferroni post-hoc tests.

    Journal: Biomedicines

    Article Title: Somatostatin Ameliorates β-Amyloid-Induced Cytotoxicity via the Regulation of CRMP2 Phosphorylation and Calcium Homeostasis in SH-SY5Y Cells

    doi: 10.3390/biomedicines9010027

    Figure Lengend Snippet: SST-mediated effects on calcium signaling and downstream mediators. ( A ). The intracellular level of Ca 2+ was assessed using the Fluo-4 calcium indicator. Cells treated with Aβ 1-42 resulted in an increased Ca 2+ influx compared to the SST or untreated control. Cells treated with Aβ 1-42 in the presence of SST resulted in a noticeable inhibition of the Ca 2+ influx compared to the cells treated with Aβ 1-42 alone. B. Representative Western blot displaying the changes in the expression of calpain, CDK5, and p35/25 expression in cells treated with Aβ 1-42 in the presence or absence of SST. ( C – E ). Histograms represent the densitometry analysis of the Western blot shown in ( B ). Data represent the mean ± SD of three independent experiments. * p < 0.05 against respective control, Two-way ANOVA with Bonferroni post-hoc tests.

    Article Snippet: Other antibodies used were mouse monoclonal CDK5 (1:2000; Cat# 05-364; Millipore) and rabbit monoclonal p35/25 (1:250; Cat# 64310; Cell Signaling).

    Techniques: Control, Inhibition, Western Blot, Expressing