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s epidermidis rp62a atcc35984 rp62a strain  (ATCC)


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    Structured Review

    ATCC s epidermidis rp62a atcc35984 rp62a strain
    S Epidermidis Rp62a Atcc35984 Rp62a Strain, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1656 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/staphylococcus+epidermidis+rp62a/Staphylococcus+epidermidis/pm41599690-161-14-21
    Average 99 stars, based on 1656 article reviews
    s epidermidis rp62a atcc35984 rp62a strain - by Bioz Stars, 2026-10
    99/100 stars

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    Related Articles

    Analogues:

    Article Title: Antimicrobial Activity of Short Analogues of the Marine Peptide EeCentrocin 1: Synthesis of Lipopeptides and Head-to-Tail Cyclic Peptides and Mechanism of Action Studies.
    Article Snippet: Danijela Simonovic, Hymonti Dey, Natascha Johansen, Trude Anderssen, Ida K. Ø. Hansen, Hege Devold, Terje Vasskog, Hans-Matti Blencke, Frode Jacobsen Øyen, Elizabeth G. Aarag Fredheim, Tor Haug, Morten B. Strøm 1 Department of Pharmacy, Faculty of Health Sciences, UiT the Arctic University of Norway, NO-9037 Tromsø, NORWAY.. 2 The Norwegian College of Fishery Science, Faculty of Biosciences, Fisheries and Economics, UiT the Arctic University of Norway, NO9037 Tromsø, NORWAY.. # Authors contributed equally.

    Activity Assay:

    Article Title: Antimicrobial Activity of Short Analogues of the Marine Peptide EeCentrocin 1: Synthesis of Lipopeptides and Head-to-Tail Cyclic Peptides and Mechanism of Action Studies.
    Article Snippet: Danijela Simonovic, Hymonti Dey, Natascha Johansen, Trude Anderssen, Ida K. Ø. Hansen, Hege Devold, Terje Vasskog, Hans-Matti Blencke, Frode Jacobsen Øyen, Elizabeth G. Aarag Fredheim, Tor Haug, Morten B. Strøm 1 Department of Pharmacy, Faculty of Health Sciences, UiT the Arctic University of Norway, NO-9037 Tromsø, NORWAY.. 2 The Norwegian College of Fishery Science, Faculty of Biosciences, Fisheries and Economics, UiT the Arctic University of Norway, NO9037 Tromsø, NORWAY.. # Authors contributed equally.

    Sequencing:

    Article Title: An unprecedented small RNA-riboswitch interaction controls expression of a bifunctional pump that is essential for Staphylococcus aureus infection
    Article Snippet: To complement mutant strains, mntY , mnrS-mntY , mnrW-ykoY, mswM-yybP , and mntE coding sequences were amplified using indicated primers (Table S3B) and cloned under the control of a constitutive BlaZ-derived promoter as described in Menendez-Gil et al . All constructs were verified by DNA sequencing (Eurofins). .. A list of putative targets has been obtained using CopraRNA (default parameters) and the sequence of isrR genes from Staphylococcus aureus strain HG001 isolate RN1 (NZ_CP018205), Staphylococcus epidermidis RP62A (NC_002976), Staphylococcus epidermidis ATCC 12228 (NC_004461), Staphylococcus haemolyticus JCSC1435 (NC_007168), Staphylococcus aureus subsp. aureus NCTC 8325 (NC_007795), Staphylococcus pseudintermedius ED99 (NC_017568), Staphylococcus warneri SG1 (NC_020164.1), Staphylococcus pasteuri SP1 (NC_022737), Staphylococcus capitis subsp. capitis strain AYP1020 (NZ_CP007601), Staphylococcus aureus strain CA12 (NZ_CP007672), Staphylococcus xylosus strain SMQ-121 (NZ_CP008724), Staphylococcus schleiferi strain 1360-13 (NZ_CP009470), Staphylococcus aureus strain MS4 (NZ_CP009828), Staphylococcus aureus strain ZJ5499 (NZ_CP011685), Staphylococcus sp. AntiMn-1 (NZ_CP012968), Staphylococcus equorum strain KS1039 (NZ_CP013114), Staphylococcus lugdunensis strain K93G (NZ_CP017069), Staphylococcus succinus strain 14BME20 (NZ_CP018199), Staphylococcus capitis strain FDAARGOS_378 (NZ_CP023966), Staphylococcus simiae strain NCTC13838 (NZ_LT906460). ..

    Bacteria:

    Article Title: Intensification of extraction process through IVDV pretreatment from Eryngium creticum leaves and stems: Maximizing yields and assessing biological activities
    Article Snippet: Mueller Hinton Broth (MHB), Tryptic Soy Broth (TSB) and Brain Heart Agar (BHA) were obtained from HIMEDIA (Mumbai, India). .. Bacteria used in this study included Staphylococcus aureus (ATCC 49619) and Staphylococcus epidermidis RP62A (ATCC 35984), both Gram-positive strains, and Escherichia coli (ATCC 35218) and Pseudomonas aeruginosa (ATCC 27853), both Gram-negative strains. ..

    other:

    Article Title: Discovery of GuaB inhibitors with efficacy against Acinetobacter baumannii infection
    Article Snippet: Strains used in MIC testing of GuaBi were S. aureus (USA300 NRS384), Staphylococcus epidermidis RP62A (ATCC35984), Mycobacterium avium (ATCC25291), Mycobacterium tuberculosis H37Rv (ATCC27294), Mycobacterium smegmatis (mc2-155 (ATCC700084), Enterococcus faecium (ATCC700221), Enterococcus faecalis (ATCC47077), Bacillus subtilis (Ward’s Bioscience 85W1640), Pseudomonas aeruginosa PAO1 (ATCC-BAA-47), Stenotrophomonas maltophilia (ATCC700267), Burkholderia cepacia (ATCC25416), Burkholderia thailandensis E264 (ATCC700388), Escherichia coli UPEC CFT073 (ATCC700928), Citrobacter werkmanii (ATCC51114), Serratia marcescens (ATCC29021), Enterobacter cloacae (ATCC222), Enterobacter aerogenes (ATCC13048), Klebsiella pneumoniae (ATCC 43816), and Proteus mirabilis (ATCC29906).

    Article Title: A comprehensive comparison of biofilm formation and capsule production for bacterial survival on hospital surfaces.
    Article Snippet: Other well-known biofilm-producing bacterial strains, including Staphylococcus aureus ATCC 25923, Staphylococcus epidermidis RP62A, and Pseudomonas aeruginosa PAO1 were also included to verify the importance of biofilm formation in bacterial survival in the hospital environments (Table 1).



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    Average physical properties of cells and cell clusters detached from S. epidermidis biofilms after matrix-targeted biofilm disruption. (A) Average concentration of cells detached from biofilms. Statistical significance determined by one-way ANOVA with Dunnett’s T3 multiple comparisons tests (**P ≤ 0.01). (B-E) Average (B) number of cells per cluster, (C) Euclidian diameter, (D) anisotropy index, and (E) asphericity of cell clusters detached from S. epidermidis <t>RP62A</t> biofilms with no treatment or treated with NaIO 4 , Proteinase K, DNase I, or pH 10 TSB G with statistical significance determined by non-parametric Kruskal-Wallis tests with Dunn’s multiple comparison tests (*P ≤ 0.05, **P ≤ 0.01, ***P ≤ 0.001, ****P ≤ 0.0001).
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    ATCC r s aureus atcc 25923 s epidermidis rp62a s aureus atcc 43300b e
    Average physical properties of cells and cell clusters detached from S. epidermidis biofilms after matrix-targeted biofilm disruption. (A) Average concentration of cells detached from biofilms. Statistical significance determined by one-way ANOVA with Dunnett’s T3 multiple comparisons tests (**P ≤ 0.01). (B-E) Average (B) number of cells per cluster, (C) Euclidian diameter, (D) anisotropy index, and (E) asphericity of cell clusters detached from S. epidermidis <t>RP62A</t> biofilms with no treatment or treated with NaIO 4 , Proteinase K, DNase I, or pH 10 TSB G with statistical significance determined by non-parametric Kruskal-Wallis tests with Dunn’s multiple comparison tests (*P ≤ 0.05, **P ≤ 0.01, ***P ≤ 0.001, ****P ≤ 0.0001).
    R S Aureus Atcc 25923 S Epidermidis Rp62a S Aureus Atcc 43300b E, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ATCC staphylococcus epidermidis rp62a reference strain
    Average physical properties of cells and cell clusters detached from S. epidermidis biofilms after matrix-targeted biofilm disruption. (A) Average concentration of cells detached from biofilms. Statistical significance determined by one-way ANOVA with Dunnett’s T3 multiple comparisons tests (**P ≤ 0.01). (B-E) Average (B) number of cells per cluster, (C) Euclidian diameter, (D) anisotropy index, and (E) asphericity of cell clusters detached from S. epidermidis <t>RP62A</t> biofilms with no treatment or treated with NaIO 4 , Proteinase K, DNase I, or pH 10 TSB G with statistical significance determined by non-parametric Kruskal-Wallis tests with Dunn’s multiple comparison tests (*P ≤ 0.05, **P ≤ 0.01, ***P ≤ 0.001, ****P ≤ 0.0001).
    Staphylococcus Epidermidis Rp62a Reference Strain, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    rp62a  (ATCC)
    97
    ATCC rp62a
    Average physical properties of cells and cell clusters detached from S. epidermidis biofilms after matrix-targeted biofilm disruption. (A) Average concentration of cells detached from biofilms. Statistical significance determined by one-way ANOVA with Dunnett’s T3 multiple comparisons tests (**P ≤ 0.01). (B-E) Average (B) number of cells per cluster, (C) Euclidian diameter, (D) anisotropy index, and (E) asphericity of cell clusters detached from S. epidermidis <t>RP62A</t> biofilms with no treatment or treated with NaIO 4 , Proteinase K, DNase I, or pH 10 TSB G with statistical significance determined by non-parametric Kruskal-Wallis tests with Dunn’s multiple comparison tests (*P ≤ 0.05, **P ≤ 0.01, ***P ≤ 0.001, ****P ≤ 0.0001).
    Rp62a, supplied by ATCC, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ATCC s epidermis rp62a
    Average physical properties of cells and cell clusters detached from S. epidermidis biofilms after matrix-targeted biofilm disruption. (A) Average concentration of cells detached from biofilms. Statistical significance determined by one-way ANOVA with Dunnett’s T3 multiple comparisons tests (**P ≤ 0.01). (B-E) Average (B) number of cells per cluster, (C) Euclidian diameter, (D) anisotropy index, and (E) asphericity of cell clusters detached from S. epidermidis <t>RP62A</t> biofilms with no treatment or treated with NaIO 4 , Proteinase K, DNase I, or pH 10 TSB G with statistical significance determined by non-parametric Kruskal-Wallis tests with Dunn’s multiple comparison tests (*P ≤ 0.05, **P ≤ 0.01, ***P ≤ 0.001, ****P ≤ 0.0001).
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    Image Search Results


    Average physical properties of cells and cell clusters detached from S. epidermidis biofilms after matrix-targeted biofilm disruption. (A) Average concentration of cells detached from biofilms. Statistical significance determined by one-way ANOVA with Dunnett’s T3 multiple comparisons tests (**P ≤ 0.01). (B-E) Average (B) number of cells per cluster, (C) Euclidian diameter, (D) anisotropy index, and (E) asphericity of cell clusters detached from S. epidermidis RP62A biofilms with no treatment or treated with NaIO 4 , Proteinase K, DNase I, or pH 10 TSB G with statistical significance determined by non-parametric Kruskal-Wallis tests with Dunn’s multiple comparison tests (*P ≤ 0.05, **P ≤ 0.01, ***P ≤ 0.001, ****P ≤ 0.0001).

    Journal: bioRxiv

    Article Title: Biophysical properties and phenotypes of cell clusters detached from Staphylococcus epidermidis biofilms after matrix-targeted disruption

    doi: 10.64898/2026.01.28.701379

    Figure Lengend Snippet: Average physical properties of cells and cell clusters detached from S. epidermidis biofilms after matrix-targeted biofilm disruption. (A) Average concentration of cells detached from biofilms. Statistical significance determined by one-way ANOVA with Dunnett’s T3 multiple comparisons tests (**P ≤ 0.01). (B-E) Average (B) number of cells per cluster, (C) Euclidian diameter, (D) anisotropy index, and (E) asphericity of cell clusters detached from S. epidermidis RP62A biofilms with no treatment or treated with NaIO 4 , Proteinase K, DNase I, or pH 10 TSB G with statistical significance determined by non-parametric Kruskal-Wallis tests with Dunn’s multiple comparison tests (*P ≤ 0.05, **P ≤ 0.01, ***P ≤ 0.001, ****P ≤ 0.0001).

    Article Snippet: S. epidermidis RP62A (ATCC 35984), a PIA-dependent biofilm forming strain was used as the primary model organism.

    Techniques: Disruption, Concentration Assay, Comparison

    k- means clustering of the biophysical properties of cellular clusters detached from S. epidermidis RP62A biofilms. (A) Two-dimensional t-distributed stochastic neighbor embedding (t-SNE) visualization of the five distinct biofilm detached cell phenotypes. (B) Projections of 3D CLSM images (left column) and renderings (right column) of representative bacterial cell clusters for each biofilm-detached cell cluster phenotype. Scale bars = 2 µm. Phenotype 1 (purple circle) contains small, oblate clusters, Phenotype 2 (blue square) contains mid-sized, oblate clusters, Phenotype 3 (green inverse triangle) contains large, oblate clusters, Phenotype 4 (orange triangle) contains small, spherical clusters, and Phenotype 5 (pink diamond) contains small, prolate clusters.

    Journal: bioRxiv

    Article Title: Biophysical properties and phenotypes of cell clusters detached from Staphylococcus epidermidis biofilms after matrix-targeted disruption

    doi: 10.64898/2026.01.28.701379

    Figure Lengend Snippet: k- means clustering of the biophysical properties of cellular clusters detached from S. epidermidis RP62A biofilms. (A) Two-dimensional t-distributed stochastic neighbor embedding (t-SNE) visualization of the five distinct biofilm detached cell phenotypes. (B) Projections of 3D CLSM images (left column) and renderings (right column) of representative bacterial cell clusters for each biofilm-detached cell cluster phenotype. Scale bars = 2 µm. Phenotype 1 (purple circle) contains small, oblate clusters, Phenotype 2 (blue square) contains mid-sized, oblate clusters, Phenotype 3 (green inverse triangle) contains large, oblate clusters, Phenotype 4 (orange triangle) contains small, spherical clusters, and Phenotype 5 (pink diamond) contains small, prolate clusters.

    Article Snippet: S. epidermidis RP62A (ATCC 35984), a PIA-dependent biofilm forming strain was used as the primary model organism.

    Techniques:

    Journal: bioRxiv

    Article Title: Biophysical properties and phenotypes of cell clusters detached from Staphylococcus epidermidis biofilms after matrix-targeted disruption

    doi: 10.64898/2026.01.28.701379

    Figure Lengend Snippet:

    Article Snippet: S. epidermidis RP62A (ATCC 35984), a PIA-dependent biofilm forming strain was used as the primary model organism.

    Techniques:

    Relative abundance of S. epidermidis biofilm detached cells after matrix-targeted biofilm disruption across different growth conditions and strains. Relative abundance of biofilm detached cells, where the concentration or absorbance (OD 600 ) of cells detached from biofilms after treatment is normalized to the untreated condition, for: (A) S. epidermidis RP62A biofilms grown in flow at a shear stress of 0.1 Pa or statically in a 96-well plate, and (B) eight S. epidermidis strains: RP62A, 1457, P2, P6, P12, P18, P37 and P47 grown in a 96-well plate. Statistical significance is determined by two-way ANOVA with Dunnett’s T3 multiple comparison tests (*P ≤ 0.05, **P ≤ 0.01, ***P ≤ 0.001, ****P ≤ 0.0001).

    Journal: bioRxiv

    Article Title: Biophysical properties and phenotypes of cell clusters detached from Staphylococcus epidermidis biofilms after matrix-targeted disruption

    doi: 10.64898/2026.01.28.701379

    Figure Lengend Snippet: Relative abundance of S. epidermidis biofilm detached cells after matrix-targeted biofilm disruption across different growth conditions and strains. Relative abundance of biofilm detached cells, where the concentration or absorbance (OD 600 ) of cells detached from biofilms after treatment is normalized to the untreated condition, for: (A) S. epidermidis RP62A biofilms grown in flow at a shear stress of 0.1 Pa or statically in a 96-well plate, and (B) eight S. epidermidis strains: RP62A, 1457, P2, P6, P12, P18, P37 and P47 grown in a 96-well plate. Statistical significance is determined by two-way ANOVA with Dunnett’s T3 multiple comparison tests (*P ≤ 0.05, **P ≤ 0.01, ***P ≤ 0.001, ****P ≤ 0.0001).

    Article Snippet: S. epidermidis RP62A (ATCC 35984), a PIA-dependent biofilm forming strain was used as the primary model organism.

    Techniques: Disruption, Concentration Assay, Shear, Comparison