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test organisms enterococcus faecalis  (ATCC)


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    Structured Review

    ATCC test organisms enterococcus faecalis
    A box plot of the log 10 -transformed colony-forming unit (CFU) values of <t>Enterococcus</t> <t>faecalis</t> , Streptococcus mutans , and Candida albicans in untreated samples (negative controls), laser-treated samples (test groups 4 mm/s, 2 mm/s, and 1 mm/s), and positive controls treated with chlorhexidine digluconate (CHX). Data source .
    Test Organisms Enterococcus Faecalis, supplied by ATCC, used in various techniques. Bioz Stars score: 98/100, based on 1392 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/test organisms enterococcus faecalis/product/ATCC
    Average 98 stars, based on 1392 article reviews
    test organisms enterococcus faecalis - by Bioz Stars, 2026-03
    98/100 stars

    Images

    1) Product Images from "Evaluation of the Inactivation of Microorganisms by a Blue Laser (445 nm)—An In Vitro Study"

    Article Title: Evaluation of the Inactivation of Microorganisms by a Blue Laser (445 nm)—An In Vitro Study

    Journal: Antibiotics

    doi: 10.3390/antibiotics15020137

    A box plot of the log 10 -transformed colony-forming unit (CFU) values of Enterococcus faecalis , Streptococcus mutans , and Candida albicans in untreated samples (negative controls), laser-treated samples (test groups 4 mm/s, 2 mm/s, and 1 mm/s), and positive controls treated with chlorhexidine digluconate (CHX). Data source .
    Figure Legend Snippet: A box plot of the log 10 -transformed colony-forming unit (CFU) values of Enterococcus faecalis , Streptococcus mutans , and Candida albicans in untreated samples (negative controls), laser-treated samples (test groups 4 mm/s, 2 mm/s, and 1 mm/s), and positive controls treated with chlorhexidine digluconate (CHX). Data source .

    Techniques Used: Transformation Assay

    Testing of the carrier solutions: phosphate buffered saline (PBS), deionised H 2 O, potassium phosphate buffer (KPO 4 ), sodium potassium phosphate buffer (NaKPO 4 ) and Tris-buffered saline with hydrochloric acid (Tris-HCl) by applying the microorganisms to the ceramic test specimens, vital staining using MTT, and subsequent microscopic evaluation of the microbial converted blue formazan. Tris-HCl reduced the viability slightly for Enterococcus faecalis and strongly for Streptococcus mutans . Sodium potassium phosphate buffer was not suitable for any of the test organisms. PBS was also not optimal for this test setup, with clearly recognisable salt crystals forming. Stable viability results were shown with the H 2 O (deionised) solution for Candida albicans and Enterococcus faecalis and with the potassium phosphate buffer solution for Streptococcus mutans . Figure source .
    Figure Legend Snippet: Testing of the carrier solutions: phosphate buffered saline (PBS), deionised H 2 O, potassium phosphate buffer (KPO 4 ), sodium potassium phosphate buffer (NaKPO 4 ) and Tris-buffered saline with hydrochloric acid (Tris-HCl) by applying the microorganisms to the ceramic test specimens, vital staining using MTT, and subsequent microscopic evaluation of the microbial converted blue formazan. Tris-HCl reduced the viability slightly for Enterococcus faecalis and strongly for Streptococcus mutans . Sodium potassium phosphate buffer was not suitable for any of the test organisms. PBS was also not optimal for this test setup, with clearly recognisable salt crystals forming. Stable viability results were shown with the H 2 O (deionised) solution for Candida albicans and Enterococcus faecalis and with the potassium phosphate buffer solution for Streptococcus mutans . Figure source .

    Techniques Used: Saline, Staining



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    Image Search Results


    A box plot of the log 10 -transformed colony-forming unit (CFU) values of Enterococcus faecalis , Streptococcus mutans , and Candida albicans in untreated samples (negative controls), laser-treated samples (test groups 4 mm/s, 2 mm/s, and 1 mm/s), and positive controls treated with chlorhexidine digluconate (CHX). Data source .

    Journal: Antibiotics

    Article Title: Evaluation of the Inactivation of Microorganisms by a Blue Laser (445 nm)—An In Vitro Study

    doi: 10.3390/antibiotics15020137

    Figure Lengend Snippet: A box plot of the log 10 -transformed colony-forming unit (CFU) values of Enterococcus faecalis , Streptococcus mutans , and Candida albicans in untreated samples (negative controls), laser-treated samples (test groups 4 mm/s, 2 mm/s, and 1 mm/s), and positive controls treated with chlorhexidine digluconate (CHX). Data source .

    Article Snippet: The test organisms Enterococcus faecalis (ATCC ® 29212TM) , Streptococcus mutans (DSM 20523/ATCC ® 25175TM), and Candida albicans (SC5314/ATCC MYA-2876D-5TM) were used for the main experiments: two Gram positive bacteria and one fungus as representatives of important dental pathogens.

    Techniques: Transformation Assay

    Testing of the carrier solutions: phosphate buffered saline (PBS), deionised H 2 O, potassium phosphate buffer (KPO 4 ), sodium potassium phosphate buffer (NaKPO 4 ) and Tris-buffered saline with hydrochloric acid (Tris-HCl) by applying the microorganisms to the ceramic test specimens, vital staining using MTT, and subsequent microscopic evaluation of the microbial converted blue formazan. Tris-HCl reduced the viability slightly for Enterococcus faecalis and strongly for Streptococcus mutans . Sodium potassium phosphate buffer was not suitable for any of the test organisms. PBS was also not optimal for this test setup, with clearly recognisable salt crystals forming. Stable viability results were shown with the H 2 O (deionised) solution for Candida albicans and Enterococcus faecalis and with the potassium phosphate buffer solution for Streptococcus mutans . Figure source .

    Journal: Antibiotics

    Article Title: Evaluation of the Inactivation of Microorganisms by a Blue Laser (445 nm)—An In Vitro Study

    doi: 10.3390/antibiotics15020137

    Figure Lengend Snippet: Testing of the carrier solutions: phosphate buffered saline (PBS), deionised H 2 O, potassium phosphate buffer (KPO 4 ), sodium potassium phosphate buffer (NaKPO 4 ) and Tris-buffered saline with hydrochloric acid (Tris-HCl) by applying the microorganisms to the ceramic test specimens, vital staining using MTT, and subsequent microscopic evaluation of the microbial converted blue formazan. Tris-HCl reduced the viability slightly for Enterococcus faecalis and strongly for Streptococcus mutans . Sodium potassium phosphate buffer was not suitable for any of the test organisms. PBS was also not optimal for this test setup, with clearly recognisable salt crystals forming. Stable viability results were shown with the H 2 O (deionised) solution for Candida albicans and Enterococcus faecalis and with the potassium phosphate buffer solution for Streptococcus mutans . Figure source .

    Article Snippet: The test organisms Enterococcus faecalis (ATCC ® 29212TM) , Streptococcus mutans (DSM 20523/ATCC ® 25175TM), and Candida albicans (SC5314/ATCC MYA-2876D-5TM) were used for the main experiments: two Gram positive bacteria and one fungus as representatives of important dental pathogens.

    Techniques: Saline, Staining