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cell basal media  (ATCC)


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    Structured Review

    ATCC cell basal media
    Cell Basal Media, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 308 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/cell basal media/product/ATCC
    Average 96 stars, based on 308 article reviews
    cell basal media - by Bioz Stars, 2026-03
    96/100 stars

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    Citrullinated and Homocitrullinated Proteins/Peptides are Present in DBA/1J Metatarsophalangeal Joints. A) Representative hematoxylin + eosin (H&E) at 80× magnification and immunofluorescent micrographs at 20× magnification of joints from DBA/1J mice immunized with bovine type II collagen (arthritic: N = 9; non-arthritic: N = 10) or PBS (N = 9). Scale bars represent 500 μm. Max projections of Z-stacks show nuclei <t>(DAPI;</t> blue), citrullinated proteins/peptides (CitP; green), and homocitrullinated proteins/peptides (HomoCitP; red). Corrected total fluorescence intensity for B) CitP and C) HomoCitP in three joint structures: bone marrow, synovium, and cartilage. Graphs show the median [IQR], with each symbol representing an individual mouse. Statistical analysis was performed using Kruskal-Wallis with Dunn's multiple comparisons test, and the resulting p-values were p = 0.0046, p = 0.0084, p = 0.4076, p = 0.0143, p = 0.0136, and p = 0.1733 respectively, with p-values for pairwise comparisons indicated on the graphs. ns: not significant.
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    Citrullinated and Homocitrullinated Proteins/Peptides are Present in DBA/1J Metatarsophalangeal Joints. A) Representative hematoxylin + eosin (H&E) at 80× magnification and immunofluorescent micrographs at 20× magnification of joints from DBA/1J mice immunized with bovine type II collagen (arthritic: N = 9; non-arthritic: N = 10) or PBS (N = 9). Scale bars represent 500 μm. Max projections of Z-stacks show nuclei <t>(DAPI;</t> blue), citrullinated proteins/peptides (CitP; green), and homocitrullinated proteins/peptides (HomoCitP; red). Corrected total fluorescence intensity for B) CitP and C) HomoCitP in three joint structures: bone marrow, synovium, and cartilage. Graphs show the median [IQR], with each symbol representing an individual mouse. Statistical analysis was performed using Kruskal-Wallis with Dunn's multiple comparisons test, and the resulting p-values were p = 0.0046, p = 0.0084, p = 0.4076, p = 0.0143, p = 0.0136, and p = 0.1733 respectively, with p-values for pairwise comparisons indicated on the graphs. ns: not significant.
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    Citrullinated and Homocitrullinated Proteins/Peptides are Present in DBA/1J Metatarsophalangeal Joints. A) Representative hematoxylin + eosin (H&E) at 80× magnification and immunofluorescent micrographs at 20× magnification of joints from DBA/1J mice immunized with bovine type II collagen (arthritic: N = 9; non-arthritic: N = 10) or PBS (N = 9). Scale bars represent 500 μm. Max projections of Z-stacks show nuclei <t>(DAPI;</t> blue), citrullinated proteins/peptides (CitP; green), and homocitrullinated proteins/peptides (HomoCitP; red). Corrected total fluorescence intensity for B) CitP and C) HomoCitP in three joint structures: bone marrow, synovium, and cartilage. Graphs show the median [IQR], with each symbol representing an individual mouse. Statistical analysis was performed using Kruskal-Wallis with Dunn's multiple comparisons test, and the resulting p-values were p = 0.0046, p = 0.0084, p = 0.4076, p = 0.0143, p = 0.0136, and p = 0.1733 respectively, with p-values for pairwise comparisons indicated on the graphs. ns: not significant.
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    Citrullinated and Homocitrullinated Proteins/Peptides are Present in DBA/1J Metatarsophalangeal Joints. A) Representative hematoxylin + eosin (H&E) at 80× magnification and immunofluorescent micrographs at 20× magnification of joints from DBA/1J mice immunized with bovine type II collagen (arthritic: N = 9; non-arthritic: N = 10) or PBS (N = 9). Scale bars represent 500 μm. Max projections of Z-stacks show nuclei <t>(DAPI;</t> blue), citrullinated proteins/peptides (CitP; green), and homocitrullinated proteins/peptides (HomoCitP; red). Corrected total fluorescence intensity for B) CitP and C) HomoCitP in three joint structures: bone marrow, synovium, and cartilage. Graphs show the median [IQR], with each symbol representing an individual mouse. Statistical analysis was performed using Kruskal-Wallis with Dunn's multiple comparisons test, and the resulting p-values were p = 0.0046, p = 0.0084, p = 0.4076, p = 0.0143, p = 0.0136, and p = 0.1733 respectively, with p-values for pairwise comparisons indicated on the graphs. ns: not significant.
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    95
    Teknova mops minimal medium
    Growth analyses of <t>C.</t> <t>japonicus</t> strains grown in <t>MOPS</t> defined media supplemented with 0.5% (w/v) of (A) mannobiose, (B) mannotriose, (C) mannosyl‐glucose, (D) cellobiose, (E) glucomannan, (F) carob galactomannan, (G) guar galactomannan, or (H) linear mannan. Notably, panels A—D were grown on a separate microplate from panels E—F and are shown together for ease of visualization. Growth analyses were conducted using an EPOCH2 microplate reader (Biotek) in biological triplicate for 48 h. Error bars depict standard deviation but are too small to be observed in some graphs. Complete growth statistics are available in Table .
    Mops Minimal Medium, supplied by Teknova, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    Citrullinated and Homocitrullinated Proteins/Peptides are Present in DBA/1J Metatarsophalangeal Joints. A) Representative hematoxylin + eosin (H&E) at 80× magnification and immunofluorescent micrographs at 20× magnification of joints from DBA/1J mice immunized with bovine type II collagen (arthritic: N = 9; non-arthritic: N = 10) or PBS (N = 9). Scale bars represent 500 μm. Max projections of Z-stacks show nuclei (DAPI; blue), citrullinated proteins/peptides (CitP; green), and homocitrullinated proteins/peptides (HomoCitP; red). Corrected total fluorescence intensity for B) CitP and C) HomoCitP in three joint structures: bone marrow, synovium, and cartilage. Graphs show the median [IQR], with each symbol representing an individual mouse. Statistical analysis was performed using Kruskal-Wallis with Dunn's multiple comparisons test, and the resulting p-values were p = 0.0046, p = 0.0084, p = 0.4076, p = 0.0143, p = 0.0136, and p = 0.1733 respectively, with p-values for pairwise comparisons indicated on the graphs. ns: not significant.

    Journal: Journal of Translational Autoimmunity

    Article Title: T cell proliferative response to a homocitrullinated peptide correlates with joint pathology in collagen induced arthritis

    doi: 10.1016/j.jtauto.2025.100345

    Figure Lengend Snippet: Citrullinated and Homocitrullinated Proteins/Peptides are Present in DBA/1J Metatarsophalangeal Joints. A) Representative hematoxylin + eosin (H&E) at 80× magnification and immunofluorescent micrographs at 20× magnification of joints from DBA/1J mice immunized with bovine type II collagen (arthritic: N = 9; non-arthritic: N = 10) or PBS (N = 9). Scale bars represent 500 μm. Max projections of Z-stacks show nuclei (DAPI; blue), citrullinated proteins/peptides (CitP; green), and homocitrullinated proteins/peptides (HomoCitP; red). Corrected total fluorescence intensity for B) CitP and C) HomoCitP in three joint structures: bone marrow, synovium, and cartilage. Graphs show the median [IQR], with each symbol representing an individual mouse. Statistical analysis was performed using Kruskal-Wallis with Dunn's multiple comparisons test, and the resulting p-values were p = 0.0046, p = 0.0084, p = 0.4076, p = 0.0143, p = 0.0136, and p = 0.1733 respectively, with p-values for pairwise comparisons indicated on the graphs. ns: not significant.

    Article Snippet: Following application of TrueView autofluorescence quencher, slides were mounted using Vectashield Vibrance Antifade mounting media with DAPI (SP-8500-15; Vector Laboratories; USA) and air dried for 2 h before imaging on the Nikon Ti2-E microscope.

    Techniques: Fluorescence

    Growth analyses of C. japonicus strains grown in MOPS defined media supplemented with 0.5% (w/v) of (A) mannobiose, (B) mannotriose, (C) mannosyl‐glucose, (D) cellobiose, (E) glucomannan, (F) carob galactomannan, (G) guar galactomannan, or (H) linear mannan. Notably, panels A—D were grown on a separate microplate from panels E—F and are shown together for ease of visualization. Growth analyses were conducted using an EPOCH2 microplate reader (Biotek) in biological triplicate for 48 h. Error bars depict standard deviation but are too small to be observed in some graphs. Complete growth statistics are available in Table .

    Journal: Molecular Microbiology

    Article Title: Late Stage Mannan Metabolism in Cellvibrio japonicus Requires the Combined Action of a Mannosyl‐Glucose Phosphorylase and a Mannobiose Epimerase

    doi: 10.1111/mmi.70043

    Figure Lengend Snippet: Growth analyses of C. japonicus strains grown in MOPS defined media supplemented with 0.5% (w/v) of (A) mannobiose, (B) mannotriose, (C) mannosyl‐glucose, (D) cellobiose, (E) glucomannan, (F) carob galactomannan, (G) guar galactomannan, or (H) linear mannan. Notably, panels A—D were grown on a separate microplate from panels E—F and are shown together for ease of visualization. Growth analyses were conducted using an EPOCH2 microplate reader (Biotek) in biological triplicate for 48 h. Error bars depict standard deviation but are too small to be observed in some graphs. Complete growth statistics are available in Table .

    Article Snippet: C. japonicus strains were cultured in MOPS minimal medium from TekNova (cat. no. M2106), supplemented with 1.32 mM phosphate and 0.2% (w/v) glucose.

    Techniques: Standard Deviation

    Growth analyses of C. japonicus single gene deletions, intermediate strains, and double ectopic complementation strains grown in MOPS defined media supplemented with 0.5% (w/v) of either (A) mannobiose, (B) mannotriose, (C) glucomannan, (D) carob galactomannan, (E) guar galactomannan, or (F) linear mannan. Panels A, B, and F were grown on a separate microplate from Panels C, D, and E, and are shown here together for ease of visualization. Growth analyses were conducted using an EPOCH2 microplate reader (Biotek) in biological triplicate for 48 h. Error bars depict standard deviation but are too small to be observed in many of the graphs. Complete growth statistics are available in Table .

    Journal: Molecular Microbiology

    Article Title: Late Stage Mannan Metabolism in Cellvibrio japonicus Requires the Combined Action of a Mannosyl‐Glucose Phosphorylase and a Mannobiose Epimerase

    doi: 10.1111/mmi.70043

    Figure Lengend Snippet: Growth analyses of C. japonicus single gene deletions, intermediate strains, and double ectopic complementation strains grown in MOPS defined media supplemented with 0.5% (w/v) of either (A) mannobiose, (B) mannotriose, (C) glucomannan, (D) carob galactomannan, (E) guar galactomannan, or (F) linear mannan. Panels A, B, and F were grown on a separate microplate from Panels C, D, and E, and are shown here together for ease of visualization. Growth analyses were conducted using an EPOCH2 microplate reader (Biotek) in biological triplicate for 48 h. Error bars depict standard deviation but are too small to be observed in many of the graphs. Complete growth statistics are available in Table .

    Article Snippet: C. japonicus strains were cultured in MOPS minimal medium from TekNova (cat. no. M2106), supplemented with 1.32 mM phosphate and 0.2% (w/v) glucose.

    Techniques: Standard Deviation

    Growth analyses of C. japonicus pJKN5 complement strains grown in MOPS defined media supplemented with 0.5% (w/v) of either (A) mannobiose, (B) mannotriose, (C) glucomannan, (D) carob galactomannan, (E) guar galactomannan, or (F) linear mannan. Notably, panels A, B, and F were grown on a separate microplate from panels C, D, and E and are shown together for ease of visualization. Growth analyses were conducted in an EPOCH2 microplate reader (Biotek) in biological triplicate for 48 h. Error bars depict standard deviation and complete growth statistics are available in Table .

    Journal: Molecular Microbiology

    Article Title: Late Stage Mannan Metabolism in Cellvibrio japonicus Requires the Combined Action of a Mannosyl‐Glucose Phosphorylase and a Mannobiose Epimerase

    doi: 10.1111/mmi.70043

    Figure Lengend Snippet: Growth analyses of C. japonicus pJKN5 complement strains grown in MOPS defined media supplemented with 0.5% (w/v) of either (A) mannobiose, (B) mannotriose, (C) glucomannan, (D) carob galactomannan, (E) guar galactomannan, or (F) linear mannan. Notably, panels A, B, and F were grown on a separate microplate from panels C, D, and E and are shown together for ease of visualization. Growth analyses were conducted in an EPOCH2 microplate reader (Biotek) in biological triplicate for 48 h. Error bars depict standard deviation and complete growth statistics are available in Table .

    Article Snippet: C. japonicus strains were cultured in MOPS minimal medium from TekNova (cat. no. M2106), supplemented with 1.32 mM phosphate and 0.2% (w/v) glucose.

    Techniques: Standard Deviation