basal medium advanced dmem Search Results


90
Corning Life Sciences matrigel® growth factor reduced basement membrane matrix
Analysis of the effect of LPS preconditioning on the proregenerative ability <t>of</t> <t>rBM-MSCs.</t> (a–c) Photomontages showing the regenerated portions of the sciatic nerve that were inside the polyethylene tubes 4 weeks after transection. Axons were stained with TuJ1 antibodies (red). In the Vehicle group, only the <t>Matrigel®</t> solution was injected into the tube, while in the MSC and LPS-MSC groups, 5 × 10 5 rat bone marrow-derived mesenchymal stromal cells (rBM-MSCs) or lipopolysaccharide- (LPS-) preconditioned rBM-MSCs, respectively, were suspended in the Matrigel® solution and then injected into the tube immediately after sciatic nerve transection and tubulization. Scale bar: 200 μ m. (d–g) Quantitative analysis of nerve thickness, cell density, and number of TuJ1-positive axons (in the proximal and distal nerve segments) in each condition ( n = 5 rats per group; rBM-MSCs from only 1 animal were used in this experiment to reduce donor-related variability). Data are shown as individual values, median, and interquartile range. ∗ p < 0.05; Kruskal-Wallis test with Dunn's multiple comparisons test.
Matrigel® Growth Factor Reduced Basement Membrane Matrix, supplied by Corning Life Sciences, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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BioWhittaker Molecular Applications dmem
Analysis of the effect of LPS preconditioning on the proregenerative ability <t>of</t> <t>rBM-MSCs.</t> (a–c) Photomontages showing the regenerated portions of the sciatic nerve that were inside the polyethylene tubes 4 weeks after transection. Axons were stained with TuJ1 antibodies (red). In the Vehicle group, only the <t>Matrigel®</t> solution was injected into the tube, while in the MSC and LPS-MSC groups, 5 × 10 5 rat bone marrow-derived mesenchymal stromal cells (rBM-MSCs) or lipopolysaccharide- (LPS-) preconditioned rBM-MSCs, respectively, were suspended in the Matrigel® solution and then injected into the tube immediately after sciatic nerve transection and tubulization. Scale bar: 200 μ m. (d–g) Quantitative analysis of nerve thickness, cell density, and number of TuJ1-positive axons (in the proximal and distal nerve segments) in each condition ( n = 5 rats per group; rBM-MSCs from only 1 animal were used in this experiment to reduce donor-related variability). Data are shown as individual values, median, and interquartile range. ∗ p < 0.05; Kruskal-Wallis test with Dunn's multiple comparisons test.
Dmem, supplied by BioWhittaker Molecular Applications, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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EuroClone basal medium dmem/f12
Analysis of the effect of LPS preconditioning on the proregenerative ability <t>of</t> <t>rBM-MSCs.</t> (a–c) Photomontages showing the regenerated portions of the sciatic nerve that were inside the polyethylene tubes 4 weeks after transection. Axons were stained with TuJ1 antibodies (red). In the Vehicle group, only the <t>Matrigel®</t> solution was injected into the tube, while in the MSC and LPS-MSC groups, 5 × 10 5 rat bone marrow-derived mesenchymal stromal cells (rBM-MSCs) or lipopolysaccharide- (LPS-) preconditioned rBM-MSCs, respectively, were suspended in the Matrigel® solution and then injected into the tube immediately after sciatic nerve transection and tubulization. Scale bar: 200 μ m. (d–g) Quantitative analysis of nerve thickness, cell density, and number of TuJ1-positive axons (in the proximal and distal nerve segments) in each condition ( n = 5 rats per group; rBM-MSCs from only 1 animal were used in this experiment to reduce donor-related variability). Data are shown as individual values, median, and interquartile range. ∗ p < 0.05; Kruskal-Wallis test with Dunn's multiple comparisons test.
Basal Medium Dmem/F12, supplied by EuroClone, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Thermo Fisher stemprotm adipogenesis differentiation kit
Analysis of the effect of LPS preconditioning on the proregenerative ability <t>of</t> <t>rBM-MSCs.</t> (a–c) Photomontages showing the regenerated portions of the sciatic nerve that were inside the polyethylene tubes 4 weeks after transection. Axons were stained with TuJ1 antibodies (red). In the Vehicle group, only the <t>Matrigel®</t> solution was injected into the tube, while in the MSC and LPS-MSC groups, 5 × 10 5 rat bone marrow-derived mesenchymal stromal cells (rBM-MSCs) or lipopolysaccharide- (LPS-) preconditioned rBM-MSCs, respectively, were suspended in the Matrigel® solution and then injected into the tube immediately after sciatic nerve transection and tubulization. Scale bar: 200 μ m. (d–g) Quantitative analysis of nerve thickness, cell density, and number of TuJ1-positive axons (in the proximal and distal nerve segments) in each condition ( n = 5 rats per group; rBM-MSCs from only 1 animal were used in this experiment to reduce donor-related variability). Data are shown as individual values, median, and interquartile range. ∗ p < 0.05; Kruskal-Wallis test with Dunn's multiple comparisons test.
Stemprotm Adipogenesis Differentiation Kit, supplied by Thermo Fisher, 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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Thermo Fisher dmem basal culture medium high glucose
Analysis of the effect of LPS preconditioning on the proregenerative ability <t>of</t> <t>rBM-MSCs.</t> (a–c) Photomontages showing the regenerated portions of the sciatic nerve that were inside the polyethylene tubes 4 weeks after transection. Axons were stained with TuJ1 antibodies (red). In the Vehicle group, only the <t>Matrigel®</t> solution was injected into the tube, while in the MSC and LPS-MSC groups, 5 × 10 5 rat bone marrow-derived mesenchymal stromal cells (rBM-MSCs) or lipopolysaccharide- (LPS-) preconditioned rBM-MSCs, respectively, were suspended in the Matrigel® solution and then injected into the tube immediately after sciatic nerve transection and tubulization. Scale bar: 200 μ m. (d–g) Quantitative analysis of nerve thickness, cell density, and number of TuJ1-positive axons (in the proximal and distal nerve segments) in each condition ( n = 5 rats per group; rBM-MSCs from only 1 animal were used in this experiment to reduce donor-related variability). Data are shown as individual values, median, and interquartile range. ∗ p < 0.05; Kruskal-Wallis test with Dunn's multiple comparisons test.
Dmem Basal Culture Medium High Glucose, supplied by Thermo Fisher, 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 fbs mcf12a basal tn atcc dmem
Analysis of the effect of LPS preconditioning on the proregenerative ability <t>of</t> <t>rBM-MSCs.</t> (a–c) Photomontages showing the regenerated portions of the sciatic nerve that were inside the polyethylene tubes 4 weeks after transection. Axons were stained with TuJ1 antibodies (red). In the Vehicle group, only the <t>Matrigel®</t> solution was injected into the tube, while in the MSC and LPS-MSC groups, 5 × 10 5 rat bone marrow-derived mesenchymal stromal cells (rBM-MSCs) or lipopolysaccharide- (LPS-) preconditioned rBM-MSCs, respectively, were suspended in the Matrigel® solution and then injected into the tube immediately after sciatic nerve transection and tubulization. Scale bar: 200 μ m. (d–g) Quantitative analysis of nerve thickness, cell density, and number of TuJ1-positive axons (in the proximal and distal nerve segments) in each condition ( n = 5 rats per group; rBM-MSCs from only 1 animal were used in this experiment to reduce donor-related variability). Data are shown as individual values, median, and interquartile range. ∗ p < 0.05; Kruskal-Wallis test with Dunn's multiple comparisons test.
Fbs Mcf12a Basal Tn Atcc Dmem, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 96 stars, based on 1 article reviews
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DSMZ fbs hdq p1 basal tn dsmz dmem
Analysis of the effect of LPS preconditioning on the proregenerative ability <t>of</t> <t>rBM-MSCs.</t> (a–c) Photomontages showing the regenerated portions of the sciatic nerve that were inside the polyethylene tubes 4 weeks after transection. Axons were stained with TuJ1 antibodies (red). In the Vehicle group, only the <t>Matrigel®</t> solution was injected into the tube, while in the MSC and LPS-MSC groups, 5 × 10 5 rat bone marrow-derived mesenchymal stromal cells (rBM-MSCs) or lipopolysaccharide- (LPS-) preconditioned rBM-MSCs, respectively, were suspended in the Matrigel® solution and then injected into the tube immediately after sciatic nerve transection and tubulization. Scale bar: 200 μ m. (d–g) Quantitative analysis of nerve thickness, cell density, and number of TuJ1-positive axons (in the proximal and distal nerve segments) in each condition ( n = 5 rats per group; rBM-MSCs from only 1 animal were used in this experiment to reduce donor-related variability). Data are shown as individual values, median, and interquartile range. ∗ p < 0.05; Kruskal-Wallis test with Dunn's multiple comparisons test.
Fbs Hdq P1 Basal Tn Dsmz Dmem, supplied by DSMZ, 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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Average 93 stars, based on 1 article reviews
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Valiant Co Ltd dmem
Analysis of the effect of LPS preconditioning on the proregenerative ability <t>of</t> <t>rBM-MSCs.</t> (a–c) Photomontages showing the regenerated portions of the sciatic nerve that were inside the polyethylene tubes 4 weeks after transection. Axons were stained with TuJ1 antibodies (red). In the Vehicle group, only the <t>Matrigel®</t> solution was injected into the tube, while in the MSC and LPS-MSC groups, 5 × 10 5 rat bone marrow-derived mesenchymal stromal cells (rBM-MSCs) or lipopolysaccharide- (LPS-) preconditioned rBM-MSCs, respectively, were suspended in the Matrigel® solution and then injected into the tube immediately after sciatic nerve transection and tubulization. Scale bar: 200 μ m. (d–g) Quantitative analysis of nerve thickness, cell density, and number of TuJ1-positive axons (in the proximal and distal nerve segments) in each condition ( n = 5 rats per group; rBM-MSCs from only 1 animal were used in this experiment to reduce donor-related variability). Data are shown as individual values, median, and interquartile range. ∗ p < 0.05; Kruskal-Wallis test with Dunn's multiple comparisons test.
Dmem, supplied by Valiant Co Ltd, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
Corning Life Sciences dmem/f12 basal medium
Analysis of the effect of LPS preconditioning on the proregenerative ability <t>of</t> <t>rBM-MSCs.</t> (a–c) Photomontages showing the regenerated portions of the sciatic nerve that were inside the polyethylene tubes 4 weeks after transection. Axons were stained with TuJ1 antibodies (red). In the Vehicle group, only the <t>Matrigel®</t> solution was injected into the tube, while in the MSC and LPS-MSC groups, 5 × 10 5 rat bone marrow-derived mesenchymal stromal cells (rBM-MSCs) or lipopolysaccharide- (LPS-) preconditioned rBM-MSCs, respectively, were suspended in the Matrigel® solution and then injected into the tube immediately after sciatic nerve transection and tubulization. Scale bar: 200 μ m. (d–g) Quantitative analysis of nerve thickness, cell density, and number of TuJ1-positive axons (in the proximal and distal nerve segments) in each condition ( n = 5 rats per group; rBM-MSCs from only 1 animal were used in this experiment to reduce donor-related variability). Data are shown as individual values, median, and interquartile range. ∗ p < 0.05; Kruskal-Wallis test with Dunn's multiple comparisons test.
Dmem/F12 Basal Medium, supplied by Corning Life Sciences, 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/basal+medium+advanced+dmem/rpmi+1640/pmc11184968-126-18-21
Average 90 stars, based on 1 article reviews
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Danaher Inc neural basal medium
Analysis of the effect of LPS preconditioning on the proregenerative ability <t>of</t> <t>rBM-MSCs.</t> (a–c) Photomontages showing the regenerated portions of the sciatic nerve that were inside the polyethylene tubes 4 weeks after transection. Axons were stained with TuJ1 antibodies (red). In the Vehicle group, only the <t>Matrigel®</t> solution was injected into the tube, while in the MSC and LPS-MSC groups, 5 × 10 5 rat bone marrow-derived mesenchymal stromal cells (rBM-MSCs) or lipopolysaccharide- (LPS-) preconditioned rBM-MSCs, respectively, were suspended in the Matrigel® solution and then injected into the tube immediately after sciatic nerve transection and tubulization. Scale bar: 200 μ m. (d–g) Quantitative analysis of nerve thickness, cell density, and number of TuJ1-positive axons (in the proximal and distal nerve segments) in each condition ( n = 5 rats per group; rBM-MSCs from only 1 animal were used in this experiment to reduce donor-related variability). Data are shown as individual values, median, and interquartile range. ∗ p < 0.05; Kruskal-Wallis test with Dunn's multiple comparisons test.
Neural Basal Medium, supplied by Danaher Inc, 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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Becton Dickinson dmem/matrigel basement membrane matrix
Analysis of the effect of LPS preconditioning on the proregenerative ability <t>of</t> <t>rBM-MSCs.</t> (a–c) Photomontages showing the regenerated portions of the sciatic nerve that were inside the polyethylene tubes 4 weeks after transection. Axons were stained with TuJ1 antibodies (red). In the Vehicle group, only the <t>Matrigel®</t> solution was injected into the tube, while in the MSC and LPS-MSC groups, 5 × 10 5 rat bone marrow-derived mesenchymal stromal cells (rBM-MSCs) or lipopolysaccharide- (LPS-) preconditioned rBM-MSCs, respectively, were suspended in the Matrigel® solution and then injected into the tube immediately after sciatic nerve transection and tubulization. Scale bar: 200 μ m. (d–g) Quantitative analysis of nerve thickness, cell density, and number of TuJ1-positive axons (in the proximal and distal nerve segments) in each condition ( n = 5 rats per group; rBM-MSCs from only 1 animal were used in this experiment to reduce donor-related variability). Data are shown as individual values, median, and interquartile range. ∗ p < 0.05; Kruskal-Wallis test with Dunn's multiple comparisons test.
Dmem/Matrigel Basement Membrane Matrix, supplied by Becton Dickinson, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Beijing Solarbio Science medium
Analysis of the effect of LPS preconditioning on the proregenerative ability <t>of</t> <t>rBM-MSCs.</t> (a–c) Photomontages showing the regenerated portions of the sciatic nerve that were inside the polyethylene tubes 4 weeks after transection. Axons were stained with TuJ1 antibodies (red). In the Vehicle group, only the <t>Matrigel®</t> solution was injected into the tube, while in the MSC and LPS-MSC groups, 5 × 10 5 rat bone marrow-derived mesenchymal stromal cells (rBM-MSCs) or lipopolysaccharide- (LPS-) preconditioned rBM-MSCs, respectively, were suspended in the Matrigel® solution and then injected into the tube immediately after sciatic nerve transection and tubulization. Scale bar: 200 μ m. (d–g) Quantitative analysis of nerve thickness, cell density, and number of TuJ1-positive axons (in the proximal and distal nerve segments) in each condition ( n = 5 rats per group; rBM-MSCs from only 1 animal were used in this experiment to reduce donor-related variability). Data are shown as individual values, median, and interquartile range. ∗ p < 0.05; Kruskal-Wallis test with Dunn's multiple comparisons test.
Medium, supplied by Beijing Solarbio Science, 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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medium - by Bioz Stars, 2026-10
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Image Search Results


Analysis of the effect of LPS preconditioning on the proregenerative ability of rBM-MSCs. (a–c) Photomontages showing the regenerated portions of the sciatic nerve that were inside the polyethylene tubes 4 weeks after transection. Axons were stained with TuJ1 antibodies (red). In the Vehicle group, only the Matrigel® solution was injected into the tube, while in the MSC and LPS-MSC groups, 5 × 10 5 rat bone marrow-derived mesenchymal stromal cells (rBM-MSCs) or lipopolysaccharide- (LPS-) preconditioned rBM-MSCs, respectively, were suspended in the Matrigel® solution and then injected into the tube immediately after sciatic nerve transection and tubulization. Scale bar: 200 μ m. (d–g) Quantitative analysis of nerve thickness, cell density, and number of TuJ1-positive axons (in the proximal and distal nerve segments) in each condition ( n = 5 rats per group; rBM-MSCs from only 1 animal were used in this experiment to reduce donor-related variability). Data are shown as individual values, median, and interquartile range. ∗ p < 0.05; Kruskal-Wallis test with Dunn's multiple comparisons test.

Journal: Stem Cells International

Article Title: Preconditioning of Rat Bone Marrow-Derived Mesenchymal Stromal Cells with Toll-Like Receptor Agonists

doi: 10.1155/2019/7692973

Figure Lengend Snippet: Analysis of the effect of LPS preconditioning on the proregenerative ability of rBM-MSCs. (a–c) Photomontages showing the regenerated portions of the sciatic nerve that were inside the polyethylene tubes 4 weeks after transection. Axons were stained with TuJ1 antibodies (red). In the Vehicle group, only the Matrigel® solution was injected into the tube, while in the MSC and LPS-MSC groups, 5 × 10 5 rat bone marrow-derived mesenchymal stromal cells (rBM-MSCs) or lipopolysaccharide- (LPS-) preconditioned rBM-MSCs, respectively, were suspended in the Matrigel® solution and then injected into the tube immediately after sciatic nerve transection and tubulization. Scale bar: 200 μ m. (d–g) Quantitative analysis of nerve thickness, cell density, and number of TuJ1-positive axons (in the proximal and distal nerve segments) in each condition ( n = 5 rats per group; rBM-MSCs from only 1 animal were used in this experiment to reduce donor-related variability). Data are shown as individual values, median, and interquartile range. ∗ p < 0.05; Kruskal-Wallis test with Dunn's multiple comparisons test.

Article Snippet: 5 × 10 5 rBM-MSCs (or preconditioned rBM-MSCs), suspended in 15 μ L of a Matrigel® Growth Factor Reduced Basement Membrane Matrix (Corning) solution (1 : 3 in DMEM/F12 medium), were injected into the tube.

Techniques: Staining, Injection, Derivative Assay