3d culture medium Search Results


96
AMS Biotechnology cell culture system
Cell Culture System, supplied by AMS Biotechnology, 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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cell culture system - by Bioz Stars, 2026-03
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93
101Bio 3d cell culture gel
MKP-1 and MAPK expression in RT112 cells transfected with NC and MKP-1 siRNA. (A) Relative MKP-1 expression in the siNC and siMKP-1 groups was examined using reverse transcription-quantitative PCR. **P<0.01. (B) Representative microscopic images of siNC and siMKP-1 treated cells captured in both 2D and <t>3D</t> environments under a phase contrast microscope. (C) MKP-1 expression of the siNC and siMKP-1 groups, as determined via western blotting. GAPDH was used as the internal control. (D) Phosphorylated and total ERK1/2 protein expressions of the siNC and siMKP-1 group, as determined via western blotting. GAPDH was used as the internal control. (E) Phosphorylated and total p38 protein expressions of the siNC and siMKP-1 group, as determined via western blotting. GAPDH was used as the internal control. (F) Phosphorylated and total JNK protein expression levels of the siNC and siMKP-1 group, as determined via western blotting. GAPDH was used as the internal control. MKP-1, mitogen activated protein kinase phosphatase-1; NC, negative control; siMKP-1, MKP-1 small interfering RNA; siNC, small interfering negative control.
3d Cell Culture Gel, supplied by 101Bio, 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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3d cell culture gel - by Bioz Stars, 2026-03
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90
Vale Life Sciences happy cell asm 3d culture medium
MKP-1 and MAPK expression in RT112 cells transfected with NC and MKP-1 siRNA. (A) Relative MKP-1 expression in the siNC and siMKP-1 groups was examined using reverse transcription-quantitative PCR. **P<0.01. (B) Representative microscopic images of siNC and siMKP-1 treated cells captured in both 2D and <t>3D</t> environments under a phase contrast microscope. (C) MKP-1 expression of the siNC and siMKP-1 groups, as determined via western blotting. GAPDH was used as the internal control. (D) Phosphorylated and total ERK1/2 protein expressions of the siNC and siMKP-1 group, as determined via western blotting. GAPDH was used as the internal control. (E) Phosphorylated and total p38 protein expressions of the siNC and siMKP-1 group, as determined via western blotting. GAPDH was used as the internal control. (F) Phosphorylated and total JNK protein expression levels of the siNC and siMKP-1 group, as determined via western blotting. GAPDH was used as the internal control. MKP-1, mitogen activated protein kinase phosphatase-1; NC, negative control; siMKP-1, MKP-1 small interfering RNA; siNC, small interfering negative control.
Happy Cell Asm 3d Culture Medium, supplied by Vale 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/result/happy cell asm 3d culture medium/product/Vale Life Sciences
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happy cell asm 3d culture medium - by Bioz Stars, 2026-03
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90
COMSOL Inc 3d model of the designed planar miniature eit sensor with culture medium
MKP-1 and MAPK expression in RT112 cells transfected with NC and MKP-1 siRNA. (A) Relative MKP-1 expression in the siNC and siMKP-1 groups was examined using reverse transcription-quantitative PCR. **P<0.01. (B) Representative microscopic images of siNC and siMKP-1 treated cells captured in both 2D and <t>3D</t> environments under a phase contrast microscope. (C) MKP-1 expression of the siNC and siMKP-1 groups, as determined via western blotting. GAPDH was used as the internal control. (D) Phosphorylated and total ERK1/2 protein expressions of the siNC and siMKP-1 group, as determined via western blotting. GAPDH was used as the internal control. (E) Phosphorylated and total p38 protein expressions of the siNC and siMKP-1 group, as determined via western blotting. GAPDH was used as the internal control. (F) Phosphorylated and total JNK protein expression levels of the siNC and siMKP-1 group, as determined via western blotting. GAPDH was used as the internal control. MKP-1, mitogen activated protein kinase phosphatase-1; NC, negative control; siMKP-1, MKP-1 small interfering RNA; siNC, small interfering negative control.
3d Model Of The Designed Planar Miniature Eit Sensor With Culture Medium, supplied by COMSOL Inc, 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/result/3d model of the designed planar miniature eit sensor with culture medium/product/COMSOL Inc
Average 90 stars, based on 1 article reviews
3d model of the designed planar miniature eit sensor with culture medium - by Bioz Stars, 2026-03
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90
ScienCell 3d culture medium ecm
MKP-1 and MAPK expression in RT112 cells transfected with NC and MKP-1 siRNA. (A) Relative MKP-1 expression in the siNC and siMKP-1 groups was examined using reverse transcription-quantitative PCR. **P<0.01. (B) Representative microscopic images of siNC and siMKP-1 treated cells captured in both 2D and <t>3D</t> environments under a phase contrast microscope. (C) MKP-1 expression of the siNC and siMKP-1 groups, as determined via western blotting. GAPDH was used as the internal control. (D) Phosphorylated and total ERK1/2 protein expressions of the siNC and siMKP-1 group, as determined via western blotting. GAPDH was used as the internal control. (E) Phosphorylated and total p38 protein expressions of the siNC and siMKP-1 group, as determined via western blotting. GAPDH was used as the internal control. (F) Phosphorylated and total JNK protein expression levels of the siNC and siMKP-1 group, as determined via western blotting. GAPDH was used as the internal control. MKP-1, mitogen activated protein kinase phosphatase-1; NC, negative control; siMKP-1, MKP-1 small interfering RNA; siNC, small interfering negative control.
3d Culture Medium Ecm, supplied by ScienCell, 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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3d culture medium ecm - by Bioz Stars, 2026-03
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90
Nissan Chemical 3d sphere culture medium
<t>3D</t> <t>Sphere</t> Culture of Human Pluripotent Stem Cells (A) Complete inhibition of hPSC sphere sedimentation by low-acyl GG at 0.015%. KhES-1 spheres on day 4 were suspended in the culture medium with various concentrations of GG and observed after 16 hr. The scale bar represents 5 mm. (B) Fold increase in KhES-1 cell number in culture medium with or without GG in different culture vessels. The average fold increase from independent experiments indicates the cell number increase from days 0 to 5, and the error bars indicate the SD (n = 10 for tube-shaped bags and n = 4 for others). Significance calculations were performed using the Student’s t test. (C) A tube-shaped culturing bag made of a gas-permeable membrane (left) and polystyrene tubes (15 and 5 ml). (D) Morphologies of KhES-1 spheres on day 5 in the 3D sphere culture medium with 0.020% GG. The scale bar represents 200 μm. (E) Comparison of KhES-1 cell expansion rates in the 3D sphere culture using tube-shaped gas-permeable bags or culture plates. The graph shows exemplary expansion rate plotting. Average slopes and SD in the semilogarithmical plotting were obtained by calculating exponential trend lines from three independent experiments and indicated in each graph. See also <xref ref-type=Figure S6 and . " width="250" height="auto" />
3d Sphere Culture Medium, supplied by Nissan Chemical, 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/result/3d sphere culture medium/product/Nissan Chemical
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3d sphere culture medium - by Bioz Stars, 2026-03
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90
PRIMACYT Cell Culture Technology GmbH 3d-hmm medium
<t>3D</t> <t>Sphere</t> Culture of Human Pluripotent Stem Cells (A) Complete inhibition of hPSC sphere sedimentation by low-acyl GG at 0.015%. KhES-1 spheres on day 4 were suspended in the culture medium with various concentrations of GG and observed after 16 hr. The scale bar represents 5 mm. (B) Fold increase in KhES-1 cell number in culture medium with or without GG in different culture vessels. The average fold increase from independent experiments indicates the cell number increase from days 0 to 5, and the error bars indicate the SD (n = 10 for tube-shaped bags and n = 4 for others). Significance calculations were performed using the Student’s t test. (C) A tube-shaped culturing bag made of a gas-permeable membrane (left) and polystyrene tubes (15 and 5 ml). (D) Morphologies of KhES-1 spheres on day 5 in the 3D sphere culture medium with 0.020% GG. The scale bar represents 200 μm. (E) Comparison of KhES-1 cell expansion rates in the 3D sphere culture using tube-shaped gas-permeable bags or culture plates. The graph shows exemplary expansion rate plotting. Average slopes and SD in the semilogarithmical plotting were obtained by calculating exponential trend lines from three independent experiments and indicated in each graph. See also <xref ref-type=Figure S6 and . " width="250" height="auto" />
3d Hmm Medium, supplied by PRIMACYT Cell Culture Technology GmbH, 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/result/3d-hmm medium/product/PRIMACYT Cell Culture Technology GmbH
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3d-hmm medium - by Bioz Stars, 2026-03
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90
Corning Life Sciences tumor cell 3d culture mtec/plus medium
<t>3D</t> <t>Sphere</t> Culture of Human Pluripotent Stem Cells (A) Complete inhibition of hPSC sphere sedimentation by low-acyl GG at 0.015%. KhES-1 spheres on day 4 were suspended in the culture medium with various concentrations of GG and observed after 16 hr. The scale bar represents 5 mm. (B) Fold increase in KhES-1 cell number in culture medium with or without GG in different culture vessels. The average fold increase from independent experiments indicates the cell number increase from days 0 to 5, and the error bars indicate the SD (n = 10 for tube-shaped bags and n = 4 for others). Significance calculations were performed using the Student’s t test. (C) A tube-shaped culturing bag made of a gas-permeable membrane (left) and polystyrene tubes (15 and 5 ml). (D) Morphologies of KhES-1 spheres on day 5 in the 3D sphere culture medium with 0.020% GG. The scale bar represents 200 μm. (E) Comparison of KhES-1 cell expansion rates in the 3D sphere culture using tube-shaped gas-permeable bags or culture plates. The graph shows exemplary expansion rate plotting. Average slopes and SD in the semilogarithmical plotting were obtained by calculating exponential trend lines from three independent experiments and indicated in each graph. See also <xref ref-type=Figure S6 and . " width="250" height="auto" />
Tumor Cell 3d Culture Mtec/Plus 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/result/tumor cell 3d culture mtec/plus medium/product/Corning Life Sciences
Average 90 stars, based on 1 article reviews
tumor cell 3d culture mtec/plus medium - by Bioz Stars, 2026-03
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90
Biochrom heparmed, a williams medium e-based, 3d cell culture medium
<t>3D</t> <t>Sphere</t> Culture of Human Pluripotent Stem Cells (A) Complete inhibition of hPSC sphere sedimentation by low-acyl GG at 0.015%. KhES-1 spheres on day 4 were suspended in the culture medium with various concentrations of GG and observed after 16 hr. The scale bar represents 5 mm. (B) Fold increase in KhES-1 cell number in culture medium with or without GG in different culture vessels. The average fold increase from independent experiments indicates the cell number increase from days 0 to 5, and the error bars indicate the SD (n = 10 for tube-shaped bags and n = 4 for others). Significance calculations were performed using the Student’s t test. (C) A tube-shaped culturing bag made of a gas-permeable membrane (left) and polystyrene tubes (15 and 5 ml). (D) Morphologies of KhES-1 spheres on day 5 in the 3D sphere culture medium with 0.020% GG. The scale bar represents 200 μm. (E) Comparison of KhES-1 cell expansion rates in the 3D sphere culture using tube-shaped gas-permeable bags or culture plates. The graph shows exemplary expansion rate plotting. Average slopes and SD in the semilogarithmical plotting were obtained by calculating exponential trend lines from three independent experiments and indicated in each graph. See also <xref ref-type=Figure S6 and . " width="250" height="auto" />
Heparmed, A Williams Medium E Based, 3d Cell Culture Medium, supplied by Biochrom, 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/result/heparmed, a williams medium e-based, 3d cell culture medium/product/Biochrom
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heparmed, a williams medium e-based, 3d cell culture medium - by Bioz Stars, 2026-03
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90
BioWhittaker Molecular Applications 3-d cell culture base culture medium for the 3-d study (selected from the monolayer analysis)
<t>3D</t> <t>Sphere</t> Culture of Human Pluripotent Stem Cells (A) Complete inhibition of hPSC sphere sedimentation by low-acyl GG at 0.015%. KhES-1 spheres on day 4 were suspended in the culture medium with various concentrations of GG and observed after 16 hr. The scale bar represents 5 mm. (B) Fold increase in KhES-1 cell number in culture medium with or without GG in different culture vessels. The average fold increase from independent experiments indicates the cell number increase from days 0 to 5, and the error bars indicate the SD (n = 10 for tube-shaped bags and n = 4 for others). Significance calculations were performed using the Student’s t test. (C) A tube-shaped culturing bag made of a gas-permeable membrane (left) and polystyrene tubes (15 and 5 ml). (D) Morphologies of KhES-1 spheres on day 5 in the 3D sphere culture medium with 0.020% GG. The scale bar represents 200 μm. (E) Comparison of KhES-1 cell expansion rates in the 3D sphere culture using tube-shaped gas-permeable bags or culture plates. The graph shows exemplary expansion rate plotting. Average slopes and SD in the semilogarithmical plotting were obtained by calculating exponential trend lines from three independent experiments and indicated in each graph. See also <xref ref-type=Figure S6 and . " width="250" height="auto" />
3 D Cell Culture Base Culture Medium For The 3 D Study (Selected From The Monolayer Analysis), 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
https://www.bioz.com/result/3-d cell culture base culture medium for the 3-d study (selected from the monolayer analysis)/product/BioWhittaker Molecular Applications
Average 90 stars, based on 1 article reviews
3-d cell culture base culture medium for the 3-d study (selected from the monolayer analysis) - by Bioz Stars, 2026-03
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MKP-1 and MAPK expression in RT112 cells transfected with NC and MKP-1 siRNA. (A) Relative MKP-1 expression in the siNC and siMKP-1 groups was examined using reverse transcription-quantitative PCR. **P<0.01. (B) Representative microscopic images of siNC and siMKP-1 treated cells captured in both 2D and 3D environments under a phase contrast microscope. (C) MKP-1 expression of the siNC and siMKP-1 groups, as determined via western blotting. GAPDH was used as the internal control. (D) Phosphorylated and total ERK1/2 protein expressions of the siNC and siMKP-1 group, as determined via western blotting. GAPDH was used as the internal control. (E) Phosphorylated and total p38 protein expressions of the siNC and siMKP-1 group, as determined via western blotting. GAPDH was used as the internal control. (F) Phosphorylated and total JNK protein expression levels of the siNC and siMKP-1 group, as determined via western blotting. GAPDH was used as the internal control. MKP-1, mitogen activated protein kinase phosphatase-1; NC, negative control; siMKP-1, MKP-1 small interfering RNA; siNC, small interfering negative control.

Journal: Oncology Letters

Article Title: MKP-1 overexpression is associated with chemoresistance in bladder cancer via the MAPK pathway

doi: 10.3892/ol.2020.11741

Figure Lengend Snippet: MKP-1 and MAPK expression in RT112 cells transfected with NC and MKP-1 siRNA. (A) Relative MKP-1 expression in the siNC and siMKP-1 groups was examined using reverse transcription-quantitative PCR. **P<0.01. (B) Representative microscopic images of siNC and siMKP-1 treated cells captured in both 2D and 3D environments under a phase contrast microscope. (C) MKP-1 expression of the siNC and siMKP-1 groups, as determined via western blotting. GAPDH was used as the internal control. (D) Phosphorylated and total ERK1/2 protein expressions of the siNC and siMKP-1 group, as determined via western blotting. GAPDH was used as the internal control. (E) Phosphorylated and total p38 protein expressions of the siNC and siMKP-1 group, as determined via western blotting. GAPDH was used as the internal control. (F) Phosphorylated and total JNK protein expression levels of the siNC and siMKP-1 group, as determined via western blotting. GAPDH was used as the internal control. MKP-1, mitogen activated protein kinase phosphatase-1; NC, negative control; siMKP-1, MKP-1 small interfering RNA; siNC, small interfering negative control.

Article Snippet: 3D Cell Culture Gel (cat. no. P720M-10) was purchased from Col-Tgel Med ( http://www.101bio.com/P720_3D_cell_culture_gel.php ).

Techniques: Expressing, Transfection, Real-time Polymerase Chain Reaction, Microscopy, Western Blot, Negative Control, Small Interfering RNA

3D Sphere Culture of Human Pluripotent Stem Cells (A) Complete inhibition of hPSC sphere sedimentation by low-acyl GG at 0.015%. KhES-1 spheres on day 4 were suspended in the culture medium with various concentrations of GG and observed after 16 hr. The scale bar represents 5 mm. (B) Fold increase in KhES-1 cell number in culture medium with or without GG in different culture vessels. The average fold increase from independent experiments indicates the cell number increase from days 0 to 5, and the error bars indicate the SD (n = 10 for tube-shaped bags and n = 4 for others). Significance calculations were performed using the Student’s t test. (C) A tube-shaped culturing bag made of a gas-permeable membrane (left) and polystyrene tubes (15 and 5 ml). (D) Morphologies of KhES-1 spheres on day 5 in the 3D sphere culture medium with 0.020% GG. The scale bar represents 200 μm. (E) Comparison of KhES-1 cell expansion rates in the 3D sphere culture using tube-shaped gas-permeable bags or culture plates. The graph shows exemplary expansion rate plotting. Average slopes and SD in the semilogarithmical plotting were obtained by calculating exponential trend lines from three independent experiments and indicated in each graph. See also <xref ref-type=Figure S6 and . " width="100%" height="100%">

Journal: Stem Cell Reports

Article Title: A 3D Sphere Culture System Containing Functional Polymers for Large-Scale Human Pluripotent Stem Cell Production

doi: 10.1016/j.stemcr.2014.03.012

Figure Lengend Snippet: 3D Sphere Culture of Human Pluripotent Stem Cells (A) Complete inhibition of hPSC sphere sedimentation by low-acyl GG at 0.015%. KhES-1 spheres on day 4 were suspended in the culture medium with various concentrations of GG and observed after 16 hr. The scale bar represents 5 mm. (B) Fold increase in KhES-1 cell number in culture medium with or without GG in different culture vessels. The average fold increase from independent experiments indicates the cell number increase from days 0 to 5, and the error bars indicate the SD (n = 10 for tube-shaped bags and n = 4 for others). Significance calculations were performed using the Student’s t test. (C) A tube-shaped culturing bag made of a gas-permeable membrane (left) and polystyrene tubes (15 and 5 ml). (D) Morphologies of KhES-1 spheres on day 5 in the 3D sphere culture medium with 0.020% GG. The scale bar represents 200 μm. (E) Comparison of KhES-1 cell expansion rates in the 3D sphere culture using tube-shaped gas-permeable bags or culture plates. The graph shows exemplary expansion rate plotting. Average slopes and SD in the semilogarithmical plotting were obtained by calculating exponential trend lines from three independent experiments and indicated in each graph. See also Figure S6 and .

Article Snippet: The 3D sphere culture medium was prepared at Nissan Chemical Industries as follows.

Techniques: Inhibition, Sedimentation, Membrane, Comparison

Proof of Principle 3D hPSC Sphere Culture (A) A trial for larger-scale sphere culture by using 200 ml gas-permeable membrane bags. The scale bar represents 5 cm. (B) Comparison of cell yield calculated from the average cell number obtained in the 3D sphere or adherent culture using KhES-1 cell line. (C) Morphology of KhES-1 spheres cultured for 5 days in a 200 ml bag. The scale bar represents 200 μm.

Journal: Stem Cell Reports

Article Title: A 3D Sphere Culture System Containing Functional Polymers for Large-Scale Human Pluripotent Stem Cell Production

doi: 10.1016/j.stemcr.2014.03.012

Figure Lengend Snippet: Proof of Principle 3D hPSC Sphere Culture (A) A trial for larger-scale sphere culture by using 200 ml gas-permeable membrane bags. The scale bar represents 5 cm. (B) Comparison of cell yield calculated from the average cell number obtained in the 3D sphere or adherent culture using KhES-1 cell line. (C) Morphology of KhES-1 spheres cultured for 5 days in a 200 ml bag. The scale bar represents 200 μm.

Article Snippet: The 3D sphere culture medium was prepared at Nissan Chemical Industries as follows.

Techniques: Membrane, Comparison, Cell Culture