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s pullorum atcc  (ATCC)


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    Structured Review

    ATCC s pullorum atcc
    S Pullorum Atcc, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 29 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/s+pullorum+atcc/Salmonella+enterica+subsp%2E+enterica+(ex+Kauffmann+and+Edwards)+Le+Minor+and+Popoff+serovar+Pullorum/pm41493571-71-118-122
    Average 93 stars, based on 29 article reviews
    s pullorum atcc - by Bioz Stars, 2026-09
    93/100 stars

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    Related Articles

    Incubation:

    Article Title: Unravelling the genomic and functional potential of bacteriophages against non-typhoidal Salmonella Enteritidis and Salmonella Typhimurium.
    Article Snippet: consumption of contaminated foods.. It can easily adapt to a wide range of hosts and rapidly spread via both animalderived and non-animal-derived foods, such as dairy products, Chicken and eggs, meat products, seafood, sprouts, fresh fruits and vegetables (Buyrukoglu et al. 2024; Rakover 2025).. S. enterica serovars Enteritidis and Typhimurium are the most common NTS serovars, accounting for half of all salmonellosis (Katz et al. 2024).

    Isolation:

    Article Title: Unravelling the genomic and functional potential of bacteriophages against non-typhoidal Salmonella Enteritidis and Salmonella Typhimurium.
    Article Snippet: consumption of contaminated foods.. It can easily adapt to a wide range of hosts and rapidly spread via both animalderived and non-animal-derived foods, such as dairy products, Chicken and eggs, meat products, seafood, sprouts, fresh fruits and vegetables (Buyrukoglu et al. 2024; Rakover 2025).. S. enterica serovars Enteritidis and Typhimurium are the most common NTS serovars, accounting for half of all salmonellosis (Katz et al. 2024).



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    S Pullorum Atcc, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ATCC s enteritidis atcc 9120
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    ATCC s enterica
    Antibacterial activity characterization of 3×amyloid β-peptide-HA-6×His. (A) Inhibition zone assays of 3×amyloid β-peptide-HA-6×His against Gram-positive strains S. aureus (ATCC 25923), <t>L.</t> <t>monocytogenes</t> (ATCC 21633), B. subtilis L300-1, B. subtilis LZ13-4, and Gram-negative strains Escherichia coli O157 (ATCC 35150), S. <t>enterica</t> (ATCC 10398), E. coli (ATCC 10305), and E. sakazakii (ATCC 29544). The conditions tested were: (1) 3×amyloid β-peptide-HA-6×His (1×MIC) in buffer solution (50 mM Tris/HCl), (2) gentamicin (50 µg/ml) as a positive control, (3) Tris/HCl buffer alone as a negative control, and (4) C. reinhardtii CC-125 cell lysate as an additional negative control. Gram-positive and Gram-negative bacteria are indicated as Gram + and Gram − , respectively. (B) The inhibition zone diameters (in mm) generated by 3×amyloid β-peptide-HA-6×His (1×MIC) were measured for eight bacterial strains and compared to those produced by gentamicin (50 µg/ml). Data are presented as mean ± standard deviation from three independent experiments. Statistical significance is indicated as follows: p < 0.05 (*), p < 0.01 (), p < 0.001 (*), while n.s. denotes non-significant results.
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    ATCC s pullorum strain atcc 9120
    Antibacterial activity characterization of 3×amyloid β-peptide-HA-6×His. (A) Inhibition zone assays of 3×amyloid β-peptide-HA-6×His against Gram-positive strains S. aureus (ATCC 25923), <t>L.</t> <t>monocytogenes</t> (ATCC 21633), B. subtilis L300-1, B. subtilis LZ13-4, and Gram-negative strains Escherichia coli O157 (ATCC 35150), S. <t>enterica</t> (ATCC 10398), E. coli (ATCC 10305), and E. sakazakii (ATCC 29544). The conditions tested were: (1) 3×amyloid β-peptide-HA-6×His (1×MIC) in buffer solution (50 mM Tris/HCl), (2) gentamicin (50 µg/ml) as a positive control, (3) Tris/HCl buffer alone as a negative control, and (4) C. reinhardtii CC-125 cell lysate as an additional negative control. Gram-positive and Gram-negative bacteria are indicated as Gram + and Gram − , respectively. (B) The inhibition zone diameters (in mm) generated by 3×amyloid β-peptide-HA-6×His (1×MIC) were measured for eight bacterial strains and compared to those produced by gentamicin (50 µg/ml). Data are presented as mean ± standard deviation from three independent experiments. Statistical significance is indicated as follows: p < 0.05 (*), p < 0.01 (), p < 0.001 (*), while n.s. denotes non-significant results.
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    https://www.bioz.com/product/s+pullorum+atcc/Salmonella+enterica+subsp%2E+enterica+(ex+Kauffmann+and+Edwards)+Le+Minor+and+Popoff+serovar+Pullorum/10__1016_slash_j__ifset__2025__104127-103-15-18
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    ATCC s pullorum atcc 9120
    Antibacterial activity characterization of 3×amyloid β-peptide-HA-6×His. (A) Inhibition zone assays of 3×amyloid β-peptide-HA-6×His against Gram-positive strains S. aureus (ATCC 25923), <t>L.</t> <t>monocytogenes</t> (ATCC 21633), B. subtilis L300-1, B. subtilis LZ13-4, and Gram-negative strains Escherichia coli O157 (ATCC 35150), S. <t>enterica</t> (ATCC 10398), E. coli (ATCC 10305), and E. sakazakii (ATCC 29544). The conditions tested were: (1) 3×amyloid β-peptide-HA-6×His (1×MIC) in buffer solution (50 mM Tris/HCl), (2) gentamicin (50 µg/ml) as a positive control, (3) Tris/HCl buffer alone as a negative control, and (4) C. reinhardtii CC-125 cell lysate as an additional negative control. Gram-positive and Gram-negative bacteria are indicated as Gram + and Gram − , respectively. (B) The inhibition zone diameters (in mm) generated by 3×amyloid β-peptide-HA-6×His (1×MIC) were measured for eight bacterial strains and compared to those produced by gentamicin (50 µg/ml). Data are presented as mean ± standard deviation from three independent experiments. Statistical significance is indicated as follows: p < 0.05 (*), p < 0.01 (), p < 0.001 (*), while n.s. denotes non-significant results.
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    https://www.bioz.com/product/s+pullorum+atcc/Salmonella+enterica%3B+subsp%2E+enterica%3B+serovar+Pullorum/10__1016_slash_j__ifset__2025__104127-55-1-3
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    ATCC s pullorum atcc 10398
    Antibacterial activity characterization of 3×amyloid β-peptide-HA-6×His. (A) Inhibition zone assays of 3×amyloid β-peptide-HA-6×His against Gram-positive strains S. aureus (ATCC 25923), <t>L.</t> <t>monocytogenes</t> (ATCC 21633), B. subtilis L300-1, B. subtilis LZ13-4, and Gram-negative strains Escherichia coli O157 (ATCC 35150), S. <t>enterica</t> (ATCC 10398), E. coli (ATCC 10305), and E. sakazakii (ATCC 29544). The conditions tested were: (1) 3×amyloid β-peptide-HA-6×His (1×MIC) in buffer solution (50 mM Tris/HCl), (2) gentamicin (50 µg/ml) as a positive control, (3) Tris/HCl buffer alone as a negative control, and (4) C. reinhardtii CC-125 cell lysate as an additional negative control. Gram-positive and Gram-negative bacteria are indicated as Gram + and Gram − , respectively. (B) The inhibition zone diameters (in mm) generated by 3×amyloid β-peptide-HA-6×His (1×MIC) were measured for eight bacterial strains and compared to those produced by gentamicin (50 µg/ml). Data are presented as mean ± standard deviation from three independent experiments. Statistical significance is indicated as follows: p < 0.05 (*), p < 0.01 (), p < 0.001 (*), while n.s. denotes non-significant results.
    S Pullorum Atcc 10398, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ATCC s pullorum atcc 13036
    Antibacterial activity characterization of 3×amyloid β-peptide-HA-6×His. (A) Inhibition zone assays of 3×amyloid β-peptide-HA-6×His against Gram-positive strains S. aureus (ATCC 25923), <t>L.</t> <t>monocytogenes</t> (ATCC 21633), B. subtilis L300-1, B. subtilis LZ13-4, and Gram-negative strains Escherichia coli O157 (ATCC 35150), S. <t>enterica</t> (ATCC 10398), E. coli (ATCC 10305), and E. sakazakii (ATCC 29544). The conditions tested were: (1) 3×amyloid β-peptide-HA-6×His (1×MIC) in buffer solution (50 mM Tris/HCl), (2) gentamicin (50 µg/ml) as a positive control, (3) Tris/HCl buffer alone as a negative control, and (4) C. reinhardtii CC-125 cell lysate as an additional negative control. Gram-positive and Gram-negative bacteria are indicated as Gram + and Gram − , respectively. (B) The inhibition zone diameters (in mm) generated by 3×amyloid β-peptide-HA-6×His (1×MIC) were measured for eight bacterial strains and compared to those produced by gentamicin (50 µg/ml). Data are presented as mean ± standard deviation from three independent experiments. Statistical significance is indicated as follows: p < 0.05 (*), p < 0.01 (), p < 0.001 (*), while n.s. denotes non-significant results.
    S Pullorum Atcc 13036, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/s+pullorum+atcc/Salmonella+enterica%3B+subsp%2E+enterica%3B+serovar+Pullorum/pmc12543498-60-4-6
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    ATCC s pullorum str atcc 9120
    Antibacterial activity characterization of 3×amyloid β-peptide-HA-6×His. (A) Inhibition zone assays of 3×amyloid β-peptide-HA-6×His against Gram-positive strains S. aureus (ATCC 25923), <t>L.</t> <t>monocytogenes</t> (ATCC 21633), B. subtilis L300-1, B. subtilis LZ13-4, and Gram-negative strains Escherichia coli O157 (ATCC 35150), S. <t>enterica</t> (ATCC 10398), E. coli (ATCC 10305), and E. sakazakii (ATCC 29544). The conditions tested were: (1) 3×amyloid β-peptide-HA-6×His (1×MIC) in buffer solution (50 mM Tris/HCl), (2) gentamicin (50 µg/ml) as a positive control, (3) Tris/HCl buffer alone as a negative control, and (4) C. reinhardtii CC-125 cell lysate as an additional negative control. Gram-positive and Gram-negative bacteria are indicated as Gram + and Gram − , respectively. (B) The inhibition zone diameters (in mm) generated by 3×amyloid β-peptide-HA-6×His (1×MIC) were measured for eight bacterial strains and compared to those produced by gentamicin (50 µg/ml). Data are presented as mean ± standard deviation from three independent experiments. Statistical significance is indicated as follows: p < 0.05 (*), p < 0.01 (), p < 0.001 (*), while n.s. denotes non-significant results.
    S Pullorum Str Atcc 9120, supplied by ATCC, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/s+pullorum+atcc/Salmonella+enterica%3B+subsp%2E+enterica%3B+serovar+Pullorum/pmc11078800-25-0-3
    Average 94 stars, based on 1 article reviews
    s pullorum str atcc 9120 - by Bioz Stars, 2026-09
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    Antibacterial activity characterization of 3×amyloid β-peptide-HA-6×His. (A) Inhibition zone assays of 3×amyloid β-peptide-HA-6×His against Gram-positive strains S. aureus (ATCC 25923), L. monocytogenes (ATCC 21633), B. subtilis L300-1, B. subtilis LZ13-4, and Gram-negative strains Escherichia coli O157 (ATCC 35150), S. enterica (ATCC 10398), E. coli (ATCC 10305), and E. sakazakii (ATCC 29544). The conditions tested were: (1) 3×amyloid β-peptide-HA-6×His (1×MIC) in buffer solution (50 mM Tris/HCl), (2) gentamicin (50 µg/ml) as a positive control, (3) Tris/HCl buffer alone as a negative control, and (4) C. reinhardtii CC-125 cell lysate as an additional negative control. Gram-positive and Gram-negative bacteria are indicated as Gram + and Gram − , respectively. (B) The inhibition zone diameters (in mm) generated by 3×amyloid β-peptide-HA-6×His (1×MIC) were measured for eight bacterial strains and compared to those produced by gentamicin (50 µg/ml). Data are presented as mean ± standard deviation from three independent experiments. Statistical significance is indicated as follows: p < 0.05 (*), p < 0.01 (), p < 0.001 (*), while n.s. denotes non-significant results.

    Journal: Scientific Reports

    Article Title: Amyloid β-peptide multimer expressed in green algae efficiently inhibits bacteria growth by disrupting cell membrane permeability

    doi: 10.1038/s41598-025-16109-y

    Figure Lengend Snippet: Antibacterial activity characterization of 3×amyloid β-peptide-HA-6×His. (A) Inhibition zone assays of 3×amyloid β-peptide-HA-6×His against Gram-positive strains S. aureus (ATCC 25923), L. monocytogenes (ATCC 21633), B. subtilis L300-1, B. subtilis LZ13-4, and Gram-negative strains Escherichia coli O157 (ATCC 35150), S. enterica (ATCC 10398), E. coli (ATCC 10305), and E. sakazakii (ATCC 29544). The conditions tested were: (1) 3×amyloid β-peptide-HA-6×His (1×MIC) in buffer solution (50 mM Tris/HCl), (2) gentamicin (50 µg/ml) as a positive control, (3) Tris/HCl buffer alone as a negative control, and (4) C. reinhardtii CC-125 cell lysate as an additional negative control. Gram-positive and Gram-negative bacteria are indicated as Gram + and Gram − , respectively. (B) The inhibition zone diameters (in mm) generated by 3×amyloid β-peptide-HA-6×His (1×MIC) were measured for eight bacterial strains and compared to those produced by gentamicin (50 µg/ml). Data are presented as mean ± standard deviation from three independent experiments. Statistical significance is indicated as follows: p < 0.05 (*), p < 0.01 (), p < 0.001 (*), while n.s. denotes non-significant results.

    Article Snippet: For the assays, bacterial strains including E. coli (ATCC 10305), S. aureus (ATCC 25923), L. monocytogenes (ATCC 21633), E. coli O157 (ATCC 35150), B. subtilis L300-1, S. enterica ( ATCC 10398), E. sakazakii (ATCC 29544) and B. subtilis LZ13-4 were cultured in LB medium at 37 °C until reaching a OD 600 of 1.

    Techniques: Activity Assay, Inhibition, Positive Control, Negative Control, Bacteria, Generated, Produced, Standard Deviation

    Determination of biochemical stability of 3×amyloid β-peptide-HA-6×His. (A-C) SEC profiles of 3×amyloid β-peptide-HA-6×His under various temperature (4, 25, 37, 60, and 90 °C) for 1 h (A), pH conditions (pH 2, 4, 6, 8, and 10) for 4 h (B) and against proteolytic degradation by proteinase K, papain, trypsin, and pepsin after 2 h incubation (C). (D-F) The antimicrobial efficacy of 3×amyloid β-peptide-HA-6×His against the Gram-positive and Gram-negative bacteria strains after incubation at various temperatures (D), pH conditions (E), and against proteolytic degradation by proteinase (F). For all panels, error bars indicate standard deviation. S. aureus (ATCC 25923) and L. monocytogenes (ATCC 21633) (left panel) stand for Gram-positive bacteria and E. coli O157 (ATCC 35150) and S. enterica (ATCC 10398) (right panel) stand for Gram-negative bacteria.

    Journal: Scientific Reports

    Article Title: Amyloid β-peptide multimer expressed in green algae efficiently inhibits bacteria growth by disrupting cell membrane permeability

    doi: 10.1038/s41598-025-16109-y

    Figure Lengend Snippet: Determination of biochemical stability of 3×amyloid β-peptide-HA-6×His. (A-C) SEC profiles of 3×amyloid β-peptide-HA-6×His under various temperature (4, 25, 37, 60, and 90 °C) for 1 h (A), pH conditions (pH 2, 4, 6, 8, and 10) for 4 h (B) and against proteolytic degradation by proteinase K, papain, trypsin, and pepsin after 2 h incubation (C). (D-F) The antimicrobial efficacy of 3×amyloid β-peptide-HA-6×His against the Gram-positive and Gram-negative bacteria strains after incubation at various temperatures (D), pH conditions (E), and against proteolytic degradation by proteinase (F). For all panels, error bars indicate standard deviation. S. aureus (ATCC 25923) and L. monocytogenes (ATCC 21633) (left panel) stand for Gram-positive bacteria and E. coli O157 (ATCC 35150) and S. enterica (ATCC 10398) (right panel) stand for Gram-negative bacteria.

    Article Snippet: For the assays, bacterial strains including E. coli (ATCC 10305), S. aureus (ATCC 25923), L. monocytogenes (ATCC 21633), E. coli O157 (ATCC 35150), B. subtilis L300-1, S. enterica ( ATCC 10398), E. sakazakii (ATCC 29544) and B. subtilis LZ13-4 were cultured in LB medium at 37 °C until reaching a OD 600 of 1.

    Techniques: Incubation, Bacteria, Standard Deviation

    Antibacterial mechanisms of 3×amyloid β-peptide-HA-6×His. (A) Fluorescence microscopy images showing PI uptake by Gram-positive bacteria and Gram-negative bacteria E. coli O157 (ATCC 35150) and S. enterica (ATCC 10398) after treatment with 1×MIC, 2×MIC and 3×MIC concentrations of 3×amyloid β-peptide-HA-6×His. Bacterial cells treated with PBS served as negative controls. Representative phase contrast (PC) images are presented. Scale bar: 5 μm. (B) SEM analysis of morphological changes in the Gram-positive bacteria and the Gram-negative bacteria following treatment with 3×amyloid β-peptide-HA-6×His (3×MIC). PBS served as a negative control. Red arrows indicate areas of altered cell morphology. Scale bar: 5 μm. For both panels, Gram + and Gram − refer to Gram-positive and Gram-negative bacteria, respectively.

    Journal: Scientific Reports

    Article Title: Amyloid β-peptide multimer expressed in green algae efficiently inhibits bacteria growth by disrupting cell membrane permeability

    doi: 10.1038/s41598-025-16109-y

    Figure Lengend Snippet: Antibacterial mechanisms of 3×amyloid β-peptide-HA-6×His. (A) Fluorescence microscopy images showing PI uptake by Gram-positive bacteria and Gram-negative bacteria E. coli O157 (ATCC 35150) and S. enterica (ATCC 10398) after treatment with 1×MIC, 2×MIC and 3×MIC concentrations of 3×amyloid β-peptide-HA-6×His. Bacterial cells treated with PBS served as negative controls. Representative phase contrast (PC) images are presented. Scale bar: 5 μm. (B) SEM analysis of morphological changes in the Gram-positive bacteria and the Gram-negative bacteria following treatment with 3×amyloid β-peptide-HA-6×His (3×MIC). PBS served as a negative control. Red arrows indicate areas of altered cell morphology. Scale bar: 5 μm. For both panels, Gram + and Gram − refer to Gram-positive and Gram-negative bacteria, respectively.

    Article Snippet: For the assays, bacterial strains including E. coli (ATCC 10305), S. aureus (ATCC 25923), L. monocytogenes (ATCC 21633), E. coli O157 (ATCC 35150), B. subtilis L300-1, S. enterica ( ATCC 10398), E. sakazakii (ATCC 29544) and B. subtilis LZ13-4 were cultured in LB medium at 37 °C until reaching a OD 600 of 1.

    Techniques: Fluorescence, Microscopy, Bacteria, Negative Control