acetatifactor muris Search Results


ab746797 porcincola intestinalis dsm 106895 mn537519 acetatifactor murist atcc baa 2170 hm989805  (ATCC)
90
ATCC ab746797 porcincola intestinalis dsm 106895 mn537519 acetatifactor murist atcc baa 2170 hm989805
Ab746797 Porcincola Intestinalis Dsm 106895 Mn537519 Acetatifactor Murist Atcc Baa 2170 Hm989805, supplied by ATCC, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/acetatifactor+muris/pmc07738495__41467_2020_19929_MOESM1_ESM-30-80-88?v=ATCC
Average 90 stars, based on 1 article reviews
ab746797 porcincola intestinalis dsm 106895 mn537519 acetatifactor murist atcc baa 2170 hm989805 - by Bioz Stars, 2026-07
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acetatifactor muris  (DSMZ)
94
DSMZ acetatifactor muris
Fecal microbiota in mice with glioma. A. Experimental design. B Alfa-diversity: biodiversity (inverse Simpson) and richness (number of bacterial species) among healthy (Healthy, gray, n = 22 biologically independent samples), sham-operated (sham, green, n = 7 biologically independent samples) and glioma mice (glioma, blue, n = 15 biologically independent samples). C. Beta-diversity following the Bray-Curtis dissimilarity distance algorithm, among healthy, sham and glioma mice. D. Experimental design. E Spearman correlation coefficient analysis between the relative abundance of all bacterial species found in glioma-bearing mice and tumor volumes (23 xy pairs) F. Spearman correlation coefficient graph between tumor volume and <t>Acetatifactor</t> muris abundance in glioma mice ( ρ = 0.619, p = 0.0016, n = 23 xy pairs). G. Analysis of the relative abundance of fecal Acetatifactor muris among healthy (gray, n = 30, 0.156 ± 0.057, * p = 0.012 vs glioma), sham-operated (green, n = 7, 0.207 ± 0.070, * p = 0.017 vs glioma by Brown-Forsythe ANOVA test) and glioma mice (blue, n = 23 1.450 ± 0.470). H. Spearman correlation coefficient graph between tumor volume and Muribaculum intestinale abundance in glioma mice ( ρ = -0.613, p = 0.0019, n = 23 xy pairs). I. Analysis of the relative abundance of fecal Muribaculum intestinale among healthy (gray, 26.75 ± 3.73, n = 30), sham-operated (green, n = 7, 29.40 ± 2.38) and glioma (blue, n = 23, 31.75 ± 3.17 ns by Brown-Forsythe and Welch ANOVA test).
Acetatifactor Muris, supplied by DSMZ, 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/acetatifactor+muris/pmc12867398-31-9-16?v=DSMZ
Average 94 stars, based on 1 article reviews
acetatifactor muris - by Bioz Stars, 2026-07
94/100 stars
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Image Search Results


Fecal microbiota in mice with glioma. A. Experimental design. B Alfa-diversity: biodiversity (inverse Simpson) and richness (number of bacterial species) among healthy (Healthy, gray, n = 22 biologically independent samples), sham-operated (sham, green, n = 7 biologically independent samples) and glioma mice (glioma, blue, n = 15 biologically independent samples). C. Beta-diversity following the Bray-Curtis dissimilarity distance algorithm, among healthy, sham and glioma mice. D. Experimental design. E Spearman correlation coefficient analysis between the relative abundance of all bacterial species found in glioma-bearing mice and tumor volumes (23 xy pairs) F. Spearman correlation coefficient graph between tumor volume and Acetatifactor muris abundance in glioma mice ( ρ = 0.619, p = 0.0016, n = 23 xy pairs). G. Analysis of the relative abundance of fecal Acetatifactor muris among healthy (gray, n = 30, 0.156 ± 0.057, * p = 0.012 vs glioma), sham-operated (green, n = 7, 0.207 ± 0.070, * p = 0.017 vs glioma by Brown-Forsythe ANOVA test) and glioma mice (blue, n = 23 1.450 ± 0.470). H. Spearman correlation coefficient graph between tumor volume and Muribaculum intestinale abundance in glioma mice ( ρ = -0.613, p = 0.0019, n = 23 xy pairs). I. Analysis of the relative abundance of fecal Muribaculum intestinale among healthy (gray, 26.75 ± 3.73, n = 30), sham-operated (green, n = 7, 29.40 ± 2.38) and glioma (blue, n = 23, 31.75 ± 3.17 ns by Brown-Forsythe and Welch ANOVA test).

Journal: Gut Microbes

Article Title: Muribaculum intestinale negatively impacts glioma growth in mice through the toll-like receptor 2

doi: 10.1080/19490976.2026.2623349

Figure Lengend Snippet: Fecal microbiota in mice with glioma. A. Experimental design. B Alfa-diversity: biodiversity (inverse Simpson) and richness (number of bacterial species) among healthy (Healthy, gray, n = 22 biologically independent samples), sham-operated (sham, green, n = 7 biologically independent samples) and glioma mice (glioma, blue, n = 15 biologically independent samples). C. Beta-diversity following the Bray-Curtis dissimilarity distance algorithm, among healthy, sham and glioma mice. D. Experimental design. E Spearman correlation coefficient analysis between the relative abundance of all bacterial species found in glioma-bearing mice and tumor volumes (23 xy pairs) F. Spearman correlation coefficient graph between tumor volume and Acetatifactor muris abundance in glioma mice ( ρ = 0.619, p = 0.0016, n = 23 xy pairs). G. Analysis of the relative abundance of fecal Acetatifactor muris among healthy (gray, n = 30, 0.156 ± 0.057, * p = 0.012 vs glioma), sham-operated (green, n = 7, 0.207 ± 0.070, * p = 0.017 vs glioma by Brown-Forsythe ANOVA test) and glioma mice (blue, n = 23 1.450 ± 0.470). H. Spearman correlation coefficient graph between tumor volume and Muribaculum intestinale abundance in glioma mice ( ρ = -0.613, p = 0.0019, n = 23 xy pairs). I. Analysis of the relative abundance of fecal Muribaculum intestinale among healthy (gray, 26.75 ± 3.73, n = 30), sham-operated (green, n = 7, 29.40 ± 2.38) and glioma (blue, n = 23, 31.75 ± 3.17 ns by Brown-Forsythe and Welch ANOVA test).

Article Snippet: Bacterial growing culture of Muribaculum intestinale (DSM 100739) and Acetatifactor muris (DSM 23669) were purchased from Leibniz Institute DSMZ and cultured in Wilkins-Chalgren anaerobe broth under anaerobic condition (hydrogen, 5%; carbon dioxide, 10%; nitrogen 85%) at 37 °C for 4 d. After static growth, bacterial cultures were centrifuged to separate cell pellets and supernatants (4,000 g for 10 min).

Techniques: