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Sarstedt microtest plates
Microtest Plates, supplied by Sarstedt, used in various techniques. Bioz Stars score: 85/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/microtest plates/product/Sarstedt
Average 85 stars, based on 1 article reviews
Price from $9.99 to $1999.99
microtest plates - by Bioz Stars, 2020-07
85/100 stars

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Staining:

Article Title: Differential protein expression in Colletotrichum acutatum: changes associated with reactive oxygen species and nitrogen starvation implicated in pathogenicity on strawberry
Article Snippet: .. For measurement of ROS upon nutritional induction, 80 µL conidia (105 conidia/mL) were resuspended in Reg medium or in water containing 5 m m of one of the various nitrogen‐containing compounds tested (glutamine, urea, nitrate, nitrite or ammonium sulphate), and allowed to germinate in Microtest plates (Sarstedt, Inc., Newton, NC) for various times within a 16‐h period, before staining for 1 h with the H2 DCFDA probe. .. Fluorescence levels were then measured by fluorometry (Microplate Fluorescence Reader FL600; BIO‐TEK, Winooski, VT).

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  • 91
    Sarstedt 96 well flat bottom microtiter plates
    Plasma assisted deposition on (A) <t>96-well</t> <t>microtiter</t> plates, (B) steel coupons.
    96 Well Flat Bottom Microtiter Plates, supplied by Sarstedt, used in various techniques. Bioz Stars score: 91/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/96 well flat bottom microtiter plates/product/Sarstedt
    Average 91 stars, based on 2 article reviews
    Price from $9.99 to $1999.99
    96 well flat bottom microtiter plates - by Bioz Stars, 2020-07
    91/100 stars
      Buy from Supplier

    92
    Sarstedt microtiter plates
    Growth curve analysis of P. aeruginosa PA-01 (A) in the presence of nisin (1/4×, 1/10× MIC) and polymyxin B (1/2×, 1/5×, 1/10× MIC) and combinations thereof as carried out in 96 well <t>microtiter</t> plates, followed by crystal violet (CV) staining for the detection of biofilm formation (B) and P. aeruginosa PA-01 (C) in the presence of nisin (1/4×, 1/10× MIC) and colistin (1/2×, 1/5×, 1/10× MIC) and combinations thereof, followed by CV staining (D) . The means and standard deviations of triplicate determinations are presented. Asterisks indicate statistically significant differences (Student’s t-test) between peptide and antibiotic combinations used at similar concentration ( ∗∗∗ p
    Microtiter Plates, supplied by Sarstedt, used in various techniques. Bioz Stars score: 92/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/microtiter plates/product/Sarstedt
    Average 92 stars, based on 4 article reviews
    Price from $9.99 to $1999.99
    microtiter plates - by Bioz Stars, 2020-07
    92/100 stars
      Buy from Supplier

    91
    Sarstedt microtiter plate growth phenotype analysis
    (A) The evolutionarily conserved GA catabolic pathway in filamentous fungi as proposed by Martens‐Uzunova and Schaap 5 . GA is converted in pyruvate and glycerol by consecutive action of GaaA, GaaB, GaaC, and GaaD enzymes. Growth profile of the reference strain ( MA 249.1) and GA catabolic pathway deletion mutants ∆gaaA , ∆gaaB , ∆gaaC, and ∆gaaD (B) on solid MM without any carbon source, or with 50 m m monomeric or 1% polymeric carbon sources after 7 days at 30 °C, and (C) in <t>microtiter</t> plate in liquid medium with 50 m m GA at 30 °C. Error bars represent standard deviation of six biological replicates.
    Microtiter Plate Growth Phenotype Analysis, supplied by Sarstedt, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/microtiter plate growth phenotype analysis/product/Sarstedt
    Average 91 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    microtiter plate growth phenotype analysis - by Bioz Stars, 2020-07
    91/100 stars
      Buy from Supplier

    Image Search Results


    Plasma assisted deposition on (A) 96-well microtiter plates, (B) steel coupons.

    Journal: Frontiers in Cellular and Infection Microbiology

    Article Title: Efficacy of Cold Plasma for Direct Deposition of Antibiotics as a Novel Approach for Localized Delivery and Retention of Effect

    doi: 10.3389/fcimb.2019.00428

    Figure Lengend Snippet: Plasma assisted deposition on (A) 96-well microtiter plates, (B) steel coupons.

    Article Snippet: A concentration gradient of antibiotic was created in 96-well flat bottom microtiter plates (Sarstedt, Nümbrecht, Germany) −100 μl of antibiotic in MHB in concentration two times higher than the highest concentration used in the experiment was added into the wells in the first row, while 50 μl of MHB with no antibiotic was added into the remaining wells.

    Techniques:

    Growth curve analysis of P. aeruginosa PA-01 (A) in the presence of nisin (1/4×, 1/10× MIC) and polymyxin B (1/2×, 1/5×, 1/10× MIC) and combinations thereof as carried out in 96 well microtiter plates, followed by crystal violet (CV) staining for the detection of biofilm formation (B) and P. aeruginosa PA-01 (C) in the presence of nisin (1/4×, 1/10× MIC) and colistin (1/2×, 1/5×, 1/10× MIC) and combinations thereof, followed by CV staining (D) . The means and standard deviations of triplicate determinations are presented. Asterisks indicate statistically significant differences (Student’s t-test) between peptide and antibiotic combinations used at similar concentration ( ∗∗∗ p

    Journal: Frontiers in Microbiology

    Article Title: Synergistic Nisin-Polymyxin Combinations for the Control of Pseudomonas Biofilm Formation

    doi: 10.3389/fmicb.2016.01713

    Figure Lengend Snippet: Growth curve analysis of P. aeruginosa PA-01 (A) in the presence of nisin (1/4×, 1/10× MIC) and polymyxin B (1/2×, 1/5×, 1/10× MIC) and combinations thereof as carried out in 96 well microtiter plates, followed by crystal violet (CV) staining for the detection of biofilm formation (B) and P. aeruginosa PA-01 (C) in the presence of nisin (1/4×, 1/10× MIC) and colistin (1/2×, 1/5×, 1/10× MIC) and combinations thereof, followed by CV staining (D) . The means and standard deviations of triplicate determinations are presented. Asterisks indicate statistically significant differences (Student’s t-test) between peptide and antibiotic combinations used at similar concentration ( ∗∗∗ p

    Article Snippet: Growth Curve Experiments For growth experiments, overnight cultures were transferred (107 cfu ml-1 in a volume of 1.0 ml.) into LB supplemented with the relevant concentration of nisin A and antibiotic/peptide combinations, and subsequently 0.2 ml was transferred to 96 well microtiter plates (Sarstedt).

    Techniques: Staining, Concentration Assay

    (A) The evolutionarily conserved GA catabolic pathway in filamentous fungi as proposed by Martens‐Uzunova and Schaap 5 . GA is converted in pyruvate and glycerol by consecutive action of GaaA, GaaB, GaaC, and GaaD enzymes. Growth profile of the reference strain ( MA 249.1) and GA catabolic pathway deletion mutants ∆gaaA , ∆gaaB , ∆gaaC, and ∆gaaD (B) on solid MM without any carbon source, or with 50 m m monomeric or 1% polymeric carbon sources after 7 days at 30 °C, and (C) in microtiter plate in liquid medium with 50 m m GA at 30 °C. Error bars represent standard deviation of six biological replicates.

    Journal: Febs Letters

    Article Title: The pathway intermediate 2‐keto‐3‐deoxy‐L‐galactonate mediates the induction of genes involved in D‐galacturonic acid utilization in Aspergillus niger

    doi: 10.1002/1873-3468.12654

    Figure Lengend Snippet: (A) The evolutionarily conserved GA catabolic pathway in filamentous fungi as proposed by Martens‐Uzunova and Schaap 5 . GA is converted in pyruvate and glycerol by consecutive action of GaaA, GaaB, GaaC, and GaaD enzymes. Growth profile of the reference strain ( MA 249.1) and GA catabolic pathway deletion mutants ∆gaaA , ∆gaaB , ∆gaaC, and ∆gaaD (B) on solid MM without any carbon source, or with 50 m m monomeric or 1% polymeric carbon sources after 7 days at 30 °C, and (C) in microtiter plate in liquid medium with 50 m m GA at 30 °C. Error bars represent standard deviation of six biological replicates.

    Article Snippet: For microtiter plate growth phenotype analysis, wells in a 96‐well, flat bottom plate (Sarstedt AG & Co., Nümbrecht, Germany) were filled with 180 μL MM (pH 5.8) containing 55 mm GA as the sole carbon source, and 20 μL freshly harvested spores (7.5 × 105 spores·mL−1 ).

    Techniques: Standard Deviation