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lb agar plates  (Thermo Fisher)


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    Structured Review

    Thermo Fisher lb agar plates
    Lb Agar Plates, supplied by Thermo Fisher, 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/agar+plate/Kanamycin+monosulfate/pm42176792-240-31-39
    Average 94 stars, based on 1 article reviews
    lb agar plates - by Bioz Stars, 2026-10
    94/100 stars

    Images

    Related Articles

    Incubation:

    Article Title: An Oxygen-Releasing Mouthwash Reduces Porphyromonas gingivalis Biofilm and Suppresses fimA and hagA Expression
    Article Snippet: P. gingivalis derived from ATCC 33277 (Microbiologics, Kwik-stik, 0912) was activated and grown on a Brucella blood agar supplemented with hemin and vitamin K (Watin Biolife) according to the manufacturer’s instructions. .. The agar plate was placed onto a maintained atmosphere using an anaerobic jar (Thermo Scientific, Oxoid Anaerojar, Basingstoke) and gas-generating sachets (Thermo Scientific, Oxoid AnaeroGen 2.5 L, Basingstoke) and incubated for 5 days at 37°C. .. A modified tryptic soy broth (mTSB) (ATCC Medium 2722) was prepared for all assays.

    Article Title: Monitoring of Staphylococcus epidermidis biofilm formation on platelet storage bag surfaces
    Article Snippet: An agar plate was inoculated from a frozen culture of S. epidermidis ATCC 35984 and incubated at 37 ± 1 ̊C for 24 hours. .. A fresh culture was then obtained by inoculating 10 ml of TSB with a few colonies from the agar plate, followed by overnight incubation at 37 ± 1 ̊C with continuous agitation at 250 rotations per minute (rpm) (Thermo Scientific, MaxQ 4000 orbital shaker). ..

    Article Title: Synthesis, Characterization, and Anti-Listerial Activity of Chitosan-Stabilized Selenium Nanoparticles.
    Article Snippet: The antibacterial efficacy of chitosan (C) stabilized selenium nanoparticles (C-SeNPs) against Listeria monocytogenes (LM) was assessed.. In addition, the physicochemical properties of C-SeNPs, including particle size, morphology, surface charge, optical behavior, elemental composition, and crystallinity were systematically characterized using transmission electron microscopy (TEM), scanning electron microscopy (SEM), dynamic light scattering (DLS), zeta potential analysis, X-ray diffraction (XRD), inductively coupled plasma–optical emission spectroscopy (ICP-OES), energy-dispersive X-ray spectroscopy (EDX), UV–visible spectroscopy, and fluorescence spectroscopy.. Based on ICP-OES analysis, elemental selenium (Se0 ) content in the C-SeNPs was 29.80 ± 0.35 mg/L.

    Article Title: An Oxygen-Releasing Mouthwash Reduces Porphyromonas gingivalis Biofilm and Suppresses fimA and hagA Expression.
    Article Snippet: .. Bacterial strain and culture conditions P. gingivalis derived from ATCC 33277 (Microbiologics, Kwikstik, 0912) was activated and grown on a Brucella blood agar supplemented with hemin and vitamin K (Watin Biolife) according to the manufacturer’s instructions.30 The agar plate was placed onto a maintained atmosphere using an anaerobic jar (Thermo Scientific, Oxoid Anaerojar, Basingstoke) and gas-generating sachets (Thermo Scientific, Oxoid AnaeroGen 2.5 L, Basingstoke) and incubated for 5 days at 37° C. A modified tryptic soy broth (mTSB) (ATCC Medium 2722) was prepared for all assays. .. All bacterial broths were incubated in an Excella E24 incubator shaker (New Brunswick Scientific) at 37°C and 140 rpm.

    Article Title: Genomic Drivers of Biofilm Formation in Salmonella Enteritidis and S . Kentucky from Poultry Production
    Article Snippet: To activate the cultures, a loopful of the frozen culture was streaked onto Xylose Lysine Deoxycholate (XLD) agar plates (Hardy Diagnostics Inc., Santa Maria, CA, USA) and incubated at 37 °C overnight to obtain isolated colonies. .. A single colony of each bacterial isolate was transferred and inoculated from the overnight agar plate into a 10 mL sterile Lennox Broth no-salt (LN-NS (10 g tryptone (VWR Chemicals LLC, Solon, OH, USA) +5 g yeast extract (Thermo Fisher Scientific, Sasingstoke, UK) in 1 L distilled water and incubated at 37 °C overnight. ..

    Sterility:

    Article Title: A Vibrio-susceptibility class of antimicrobial peptide Ajapocin via membranolytic pattern to combat "non-cholera" pathogens in vivo infection models.
    Article Snippet: Pathogenic “non-cholera” Vibrio species of Vibrio parahaemolyticus (V. parahaemolyticus) and Vibrio vulnificus (V. vulnificus) frequently pose a serious threat to aquaculture security and public health by causing infectious diseases.. In this study, we reported the discovery of a marine-sourced antimicrobial peptide (AMP) called Ajapocin, which identified through a sequence optimization strategy.. Ajapocin exhibited potent activity against V. parahaemolyticus and V. vulnificus pathogens, with minimum inhibitory concentrations (MICs) of 6–12 μM—comparable to the clinical agent Polymyxin B (PMB).

    Article Title: Genomic Drivers of Biofilm Formation in Salmonella Enteritidis and S . Kentucky from Poultry Production
    Article Snippet: To activate the cultures, a loopful of the frozen culture was streaked onto Xylose Lysine Deoxycholate (XLD) agar plates (Hardy Diagnostics Inc., Santa Maria, CA, USA) and incubated at 37 °C overnight to obtain isolated colonies. .. A single colony of each bacterial isolate was transferred and inoculated from the overnight agar plate into a 10 mL sterile Lennox Broth no-salt (LN-NS (10 g tryptone (VWR Chemicals LLC, Solon, OH, USA) +5 g yeast extract (Thermo Fisher Scientific, Sasingstoke, UK) in 1 L distilled water and incubated at 37 °C overnight. ..

    Article Title: Evaluation of the Preoperative Antiseptic Efficacy of Ozone on Dog Skin in Comparison with Traditional Methods.
    Article Snippet: .. For further microbiological analysis, 2 mL of sterile saline solution was added to each test tube and sown by streak plate method onto Petri dishes containing Agar Plate Count medium (Oxoid®, Milan, Italy). ..

    Derivative Assay:

    Article Title: An Oxygen-Releasing Mouthwash Reduces Porphyromonas gingivalis Biofilm and Suppresses fimA and hagA Expression.
    Article Snippet: .. Bacterial strain and culture conditions P. gingivalis derived from ATCC 33277 (Microbiologics, Kwikstik, 0912) was activated and grown on a Brucella blood agar supplemented with hemin and vitamin K (Watin Biolife) according to the manufacturer’s instructions.30 The agar plate was placed onto a maintained atmosphere using an anaerobic jar (Thermo Scientific, Oxoid Anaerojar, Basingstoke) and gas-generating sachets (Thermo Scientific, Oxoid AnaeroGen 2.5 L, Basingstoke) and incubated for 5 days at 37° C. A modified tryptic soy broth (mTSB) (ATCC Medium 2722) was prepared for all assays. .. All bacterial broths were incubated in an Excella E24 incubator shaker (New Brunswick Scientific) at 37°C and 140 rpm.

    Modification:

    Article Title: An Oxygen-Releasing Mouthwash Reduces Porphyromonas gingivalis Biofilm and Suppresses fimA and hagA Expression.
    Article Snippet: .. Bacterial strain and culture conditions P. gingivalis derived from ATCC 33277 (Microbiologics, Kwikstik, 0912) was activated and grown on a Brucella blood agar supplemented with hemin and vitamin K (Watin Biolife) according to the manufacturer’s instructions.30 The agar plate was placed onto a maintained atmosphere using an anaerobic jar (Thermo Scientific, Oxoid Anaerojar, Basingstoke) and gas-generating sachets (Thermo Scientific, Oxoid AnaeroGen 2.5 L, Basingstoke) and incubated for 5 days at 37° C. A modified tryptic soy broth (mTSB) (ATCC Medium 2722) was prepared for all assays. .. All bacterial broths were incubated in an Excella E24 incubator shaker (New Brunswick Scientific) at 37°C and 140 rpm.

    Saline:

    Article Title: Evaluation of the Preoperative Antiseptic Efficacy of Ozone on Dog Skin in Comparison with Traditional Methods.
    Article Snippet: .. For further microbiological analysis, 2 mL of sterile saline solution was added to each test tube and sown by streak plate method onto Petri dishes containing Agar Plate Count medium (Oxoid®, Milan, Italy). ..

    other:

    Article Title: Human spinal cord organoids recapitulate developmental and disease-associated oligodendrocyte lineage signatures
    Article Snippet: Slides, 2D culture plates, and live cultures were imaged on a Leica Stellaris 5 confocal microscope.



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    Thermo Fisher lb agar plate
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    Image Search Results


    Isolation, characterization, and phenotypic analysis of HCC tumor-resident S. epidermidis (A) Summary of viable bacterial species isolated from the T and PT tissues of four HCC patients. Species identification was confirmed by 16S/18S rRNA sequencing and MALDI-TOF mass spectrometry. (B) FISH images showing the spatial localization of S. epidermidis within HCC tumor tissue. Green signals correspond to the S. epidermidis- specific or E. cloacae -specific probe, red signals correspond to the K. pneumoniae- specific probe, while blue signals represent the cell nuclei stained with DAPI. Scale bars, 20 μm. (C) Comparison of detection methods for S. epidermidis across the four patient samples. Positive detection by either culture-based isolation or FISH is indicated. (D) Colony morphologies of GX-1 and GX3-2 compared with those of the reference strain ATCC 12228 on Columbia blood agar plates after 24 h of incubation. (E) SEM images revealing the ultrastructures of GX-1, GX3-2, and ATCC 12228 strains. The arrows highlight the raised granular structures on the surface of the clinical isolates. Scale bars, 500 nm. (F) Growth curves of the GX-1, GX3-2, and ATCC 12228 strains cultured in BHI medium. The optical density (OD) was measured at 600 nm over 24 h. (G) Representative growth inhibition curves for S. epidermidis GX3-2. Bacterial growth, measured by OD 600 , is plotted against serially diluted concentrations of various antibiotics. The data are presented as the mean ± SEM from three independent experiments.

    Journal: iScience

    Article Title: A tumor-resident Staphylococcus epidermidis strain exhibits genomic and metabolic traits driving hepatocellular carcinoma progression

    doi: 10.1016/j.isci.2026.116084

    Figure Lengend Snippet: Isolation, characterization, and phenotypic analysis of HCC tumor-resident S. epidermidis (A) Summary of viable bacterial species isolated from the T and PT tissues of four HCC patients. Species identification was confirmed by 16S/18S rRNA sequencing and MALDI-TOF mass spectrometry. (B) FISH images showing the spatial localization of S. epidermidis within HCC tumor tissue. Green signals correspond to the S. epidermidis- specific or E. cloacae -specific probe, red signals correspond to the K. pneumoniae- specific probe, while blue signals represent the cell nuclei stained with DAPI. Scale bars, 20 μm. (C) Comparison of detection methods for S. epidermidis across the four patient samples. Positive detection by either culture-based isolation or FISH is indicated. (D) Colony morphologies of GX-1 and GX3-2 compared with those of the reference strain ATCC 12228 on Columbia blood agar plates after 24 h of incubation. (E) SEM images revealing the ultrastructures of GX-1, GX3-2, and ATCC 12228 strains. The arrows highlight the raised granular structures on the surface of the clinical isolates. Scale bars, 500 nm. (F) Growth curves of the GX-1, GX3-2, and ATCC 12228 strains cultured in BHI medium. The optical density (OD) was measured at 600 nm over 24 h. (G) Representative growth inhibition curves for S. epidermidis GX3-2. Bacterial growth, measured by OD 600 , is plotted against serially diluted concentrations of various antibiotics. The data are presented as the mean ± SEM from three independent experiments.

    Article Snippet: Positive detection by either culture-based isolation or FISH is indicated. (D) Colony morphologies of GX-1 and GX3-2 compared with those of the reference strain ATCC 12228 on Columbia blood agar plates after 24 h of incubation. (E) SEM images revealing the ultrastructures of GX-1, GX3-2, and ATCC 12228 strains.

    Techniques: Isolation, Sequencing, Mass Spectrometry, Staining, Comparison, Incubation, Cell Culture, Inhibition