smc medium Search Results


96
Cell Applications Inc rat brain microvascular endothelial cell growth media
Figure 3 Three hours of hypoxia and 6 h of reperfusion lead to significant <t>endothelial</t> cell death in vitro in rat brain <t>microvascular</t> endothelial cells (RBMVEC; A). Non-specific gap junction blocker carbenoxolone, non-specific hemichannel blocker LaCl3, and connexin43 (Cx43) mimetic peptide protected endothelial cells against hypoxic injury, with the number of viable cells significantly higher than no treatment, while scrambled peptide did not have any protective effects. The number of viable cells was expressed as percentage of the control without hypoxia. Hypoxia and reperfusion also lead to significant propidium iodide dye uptake into primary rat brain microvascular endothelial cells indicating open hemichannels (B). Carbenoxolone, LaCl3 and connexin43 mimetic peptide significantly prevented dye uptake compared to no treatment, indicating hemichannel closure, while scrambled peptide did not have any effect. Stars denote statistical significance when compared to the control group or compared between groups in brackets; P 5 0.05.
Rat Brain Microvascular Endothelial Cell Growth Media, supplied by Cell Applications Inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/rat brain microvascular endothelial cell growth media/product/Cell Applications Inc
Average 96 stars, based on 1 article reviews
rat brain microvascular endothelial cell growth media - by Bioz Stars, 2026-03
96/100 stars
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90
Lonza smgmtm-2
Figure 3 Three hours of hypoxia and 6 h of reperfusion lead to significant <t>endothelial</t> cell death in vitro in rat brain <t>microvascular</t> endothelial cells (RBMVEC; A). Non-specific gap junction blocker carbenoxolone, non-specific hemichannel blocker LaCl3, and connexin43 (Cx43) mimetic peptide protected endothelial cells against hypoxic injury, with the number of viable cells significantly higher than no treatment, while scrambled peptide did not have any protective effects. The number of viable cells was expressed as percentage of the control without hypoxia. Hypoxia and reperfusion also lead to significant propidium iodide dye uptake into primary rat brain microvascular endothelial cells indicating open hemichannels (B). Carbenoxolone, LaCl3 and connexin43 mimetic peptide significantly prevented dye uptake compared to no treatment, indicating hemichannel closure, while scrambled peptide did not have any effect. Stars denote statistical significance when compared to the control group or compared between groups in brackets; P 5 0.05.
Smgmtm 2, supplied by Lonza, 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/smgmtm-2/product/Lonza
Average 90 stars, based on 1 article reviews
smgmtm-2 - by Bioz Stars, 2026-03
90/100 stars
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90
Cambrex smc basal medium
Figure 3 Three hours of hypoxia and 6 h of reperfusion lead to significant <t>endothelial</t> cell death in vitro in rat brain <t>microvascular</t> endothelial cells (RBMVEC; A). Non-specific gap junction blocker carbenoxolone, non-specific hemichannel blocker LaCl3, and connexin43 (Cx43) mimetic peptide protected endothelial cells against hypoxic injury, with the number of viable cells significantly higher than no treatment, while scrambled peptide did not have any protective effects. The number of viable cells was expressed as percentage of the control without hypoxia. Hypoxia and reperfusion also lead to significant propidium iodide dye uptake into primary rat brain microvascular endothelial cells indicating open hemichannels (B). Carbenoxolone, LaCl3 and connexin43 mimetic peptide significantly prevented dye uptake compared to no treatment, indicating hemichannel closure, while scrambled peptide did not have any effect. Stars denote statistical significance when compared to the control group or compared between groups in brackets; P 5 0.05.
Smc Basal Medium, supplied by Cambrex, 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/smc basal medium/product/Cambrex
Average 90 stars, based on 1 article reviews
smc basal medium - by Bioz Stars, 2026-03
90/100 stars
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90
ScienCell smc medium
Figure 3 Three hours of hypoxia and 6 h of reperfusion lead to significant <t>endothelial</t> cell death in vitro in rat brain <t>microvascular</t> endothelial cells (RBMVEC; A). Non-specific gap junction blocker carbenoxolone, non-specific hemichannel blocker LaCl3, and connexin43 (Cx43) mimetic peptide protected endothelial cells against hypoxic injury, with the number of viable cells significantly higher than no treatment, while scrambled peptide did not have any protective effects. The number of viable cells was expressed as percentage of the control without hypoxia. Hypoxia and reperfusion also lead to significant propidium iodide dye uptake into primary rat brain microvascular endothelial cells indicating open hemichannels (B). Carbenoxolone, LaCl3 and connexin43 mimetic peptide significantly prevented dye uptake compared to no treatment, indicating hemichannel closure, while scrambled peptide did not have any effect. Stars denote statistical significance when compared to the control group or compared between groups in brackets; P 5 0.05.
Smc Medium, 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
https://www.bioz.com/result/smc medium/product/ScienCell
Average 90 stars, based on 1 article reviews
smc medium - by Bioz Stars, 2026-03
90/100 stars
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90
PELOBIOTECH GmbH smc full medium pelobiotech pb-mh-200-2190
Figure 3 Three hours of hypoxia and 6 h of reperfusion lead to significant <t>endothelial</t> cell death in vitro in rat brain <t>microvascular</t> endothelial cells (RBMVEC; A). Non-specific gap junction blocker carbenoxolone, non-specific hemichannel blocker LaCl3, and connexin43 (Cx43) mimetic peptide protected endothelial cells against hypoxic injury, with the number of viable cells significantly higher than no treatment, while scrambled peptide did not have any protective effects. The number of viable cells was expressed as percentage of the control without hypoxia. Hypoxia and reperfusion also lead to significant propidium iodide dye uptake into primary rat brain microvascular endothelial cells indicating open hemichannels (B). Carbenoxolone, LaCl3 and connexin43 mimetic peptide significantly prevented dye uptake compared to no treatment, indicating hemichannel closure, while scrambled peptide did not have any effect. Stars denote statistical significance when compared to the control group or compared between groups in brackets; P 5 0.05.
Smc Full Medium Pelobiotech Pb Mh 200 2190, supplied by PELOBIOTECH 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/smc full medium pelobiotech pb-mh-200-2190/product/PELOBIOTECH GmbH
Average 90 stars, based on 1 article reviews
smc full medium pelobiotech pb-mh-200-2190 - by Bioz Stars, 2026-03
90/100 stars
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90
Bacto Laboratories smc medium
<t>Sporulation</t> and germination rates of C. difficile strains. (A) Sporulation. *P<0.05; **P<0.01. (B) Germination: Purified C. difficile spores were suspended in buffer supplemented with taurocholic acid and glycine to induce germination. Germination was monitored by plotting the ratio of the OD 600 at a given time to the OD 600 at time zero. Data are from three biological replicates and reported as mean ± SEM. ****p=0.0001(CD630E vs Xy06); ***p=0.0021 (Xy07 vs Xy06); ns: p=0.0714 (R20291 vs Xy06). (C) Spore colony-forming efficiency. Spore suspensions were serially diluted and plated on BHIS agar supplemented with 0.1%(w/v) taurocholic acid (TA). The spore colony-forming efficiency was defined as the percentage of total spores that gave rise to colonies on BHIS agar with 0.1% (w/v) TA, calculated by c.f.u. per ml colony count/c.f.u. per ml direct count by microscopy × 100%. Data are from three biological replicates and reported as mean ± SEM. * p=0.0276 (CD630E vs Xy06); ns: no significance (R20291, Xy07 vs Xy06). ns- not significant.
Smc Medium, supplied by Bacto Laboratories, 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/smc medium/product/Bacto Laboratories
Average 90 stars, based on 1 article reviews
smc medium - by Bioz Stars, 2026-03
90/100 stars
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90
ScienCell smc medium smcm
<t>Sporulation</t> and germination rates of C. difficile strains. (A) Sporulation. *P<0.05; **P<0.01. (B) Germination: Purified C. difficile spores were suspended in buffer supplemented with taurocholic acid and glycine to induce germination. Germination was monitored by plotting the ratio of the OD 600 at a given time to the OD 600 at time zero. Data are from three biological replicates and reported as mean ± SEM. ****p=0.0001(CD630E vs Xy06); ***p=0.0021 (Xy07 vs Xy06); ns: p=0.0714 (R20291 vs Xy06). (C) Spore colony-forming efficiency. Spore suspensions were serially diluted and plated on BHIS agar supplemented with 0.1%(w/v) taurocholic acid (TA). The spore colony-forming efficiency was defined as the percentage of total spores that gave rise to colonies on BHIS agar with 0.1% (w/v) TA, calculated by c.f.u. per ml colony count/c.f.u. per ml direct count by microscopy × 100%. Data are from three biological replicates and reported as mean ± SEM. * p=0.0276 (CD630E vs Xy06); ns: no significance (R20291, Xy07 vs Xy06). ns- not significant.
Smc Medium Smcm, 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
https://www.bioz.com/result/smc medium smcm/product/ScienCell
Average 90 stars, based on 1 article reviews
smc medium smcm - by Bioz Stars, 2026-03
90/100 stars
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90
ScienCell human smc medium
<t>Sporulation</t> and germination rates of C. difficile strains. (A) Sporulation. *P<0.05; **P<0.01. (B) Germination: Purified C. difficile spores were suspended in buffer supplemented with taurocholic acid and glycine to induce germination. Germination was monitored by plotting the ratio of the OD 600 at a given time to the OD 600 at time zero. Data are from three biological replicates and reported as mean ± SEM. ****p=0.0001(CD630E vs Xy06); ***p=0.0021 (Xy07 vs Xy06); ns: p=0.0714 (R20291 vs Xy06). (C) Spore colony-forming efficiency. Spore suspensions were serially diluted and plated on BHIS agar supplemented with 0.1%(w/v) taurocholic acid (TA). The spore colony-forming efficiency was defined as the percentage of total spores that gave rise to colonies on BHIS agar with 0.1% (w/v) TA, calculated by c.f.u. per ml colony count/c.f.u. per ml direct count by microscopy × 100%. Data are from three biological replicates and reported as mean ± SEM. * p=0.0276 (CD630E vs Xy06); ns: no significance (R20291, Xy07 vs Xy06). ns- not significant.
Human Smc Medium, 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
https://www.bioz.com/result/human smc medium/product/ScienCell
Average 90 stars, based on 1 article reviews
human smc medium - by Bioz Stars, 2026-03
90/100 stars
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90
PELOBIOTECH GmbH mesenchymal stem cell growth medium mscgmx
<t>Sporulation</t> and germination rates of C. difficile strains. (A) Sporulation. *P<0.05; **P<0.01. (B) Germination: Purified C. difficile spores were suspended in buffer supplemented with taurocholic acid and glycine to induce germination. Germination was monitored by plotting the ratio of the OD 600 at a given time to the OD 600 at time zero. Data are from three biological replicates and reported as mean ± SEM. ****p=0.0001(CD630E vs Xy06); ***p=0.0021 (Xy07 vs Xy06); ns: p=0.0714 (R20291 vs Xy06). (C) Spore colony-forming efficiency. Spore suspensions were serially diluted and plated on BHIS agar supplemented with 0.1%(w/v) taurocholic acid (TA). The spore colony-forming efficiency was defined as the percentage of total spores that gave rise to colonies on BHIS agar with 0.1% (w/v) TA, calculated by c.f.u. per ml colony count/c.f.u. per ml direct count by microscopy × 100%. Data are from three biological replicates and reported as mean ± SEM. * p=0.0276 (CD630E vs Xy06); ns: no significance (R20291, Xy07 vs Xy06). ns- not significant.
Mesenchymal Stem Cell Growth Medium Mscgmx, supplied by PELOBIOTECH 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/mesenchymal stem cell growth medium mscgmx/product/PELOBIOTECH GmbH
Average 90 stars, based on 1 article reviews
mesenchymal stem cell growth medium mscgmx - by Bioz Stars, 2026-03
90/100 stars
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90
Difco smc medium
<t>Sporulation</t> and germination rates of C. difficile strains. (A) Sporulation. *P<0.05; **P<0.01. (B) Germination: Purified C. difficile spores were suspended in buffer supplemented with taurocholic acid and glycine to induce germination. Germination was monitored by plotting the ratio of the OD 600 at a given time to the OD 600 at time zero. Data are from three biological replicates and reported as mean ± SEM. ****p=0.0001(CD630E vs Xy06); ***p=0.0021 (Xy07 vs Xy06); ns: p=0.0714 (R20291 vs Xy06). (C) Spore colony-forming efficiency. Spore suspensions were serially diluted and plated on BHIS agar supplemented with 0.1%(w/v) taurocholic acid (TA). The spore colony-forming efficiency was defined as the percentage of total spores that gave rise to colonies on BHIS agar with 0.1% (w/v) TA, calculated by c.f.u. per ml colony count/c.f.u. per ml direct count by microscopy × 100%. Data are from three biological replicates and reported as mean ± SEM. * p=0.0276 (CD630E vs Xy06); ns: no significance (R20291, Xy07 vs Xy06). ns- not significant.
Smc Medium, supplied by Difco, 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/smc medium/product/Difco
Average 90 stars, based on 1 article reviews
smc medium - by Bioz Stars, 2026-03
90/100 stars
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90
Lifeline Cell Technology smc media
<t>Sporulation</t> and germination rates of C. difficile strains. (A) Sporulation. *P<0.05; **P<0.01. (B) Germination: Purified C. difficile spores were suspended in buffer supplemented with taurocholic acid and glycine to induce germination. Germination was monitored by plotting the ratio of the OD 600 at a given time to the OD 600 at time zero. Data are from three biological replicates and reported as mean ± SEM. ****p=0.0001(CD630E vs Xy06); ***p=0.0021 (Xy07 vs Xy06); ns: p=0.0714 (R20291 vs Xy06). (C) Spore colony-forming efficiency. Spore suspensions were serially diluted and plated on BHIS agar supplemented with 0.1%(w/v) taurocholic acid (TA). The spore colony-forming efficiency was defined as the percentage of total spores that gave rise to colonies on BHIS agar with 0.1% (w/v) TA, calculated by c.f.u. per ml colony count/c.f.u. per ml direct count by microscopy × 100%. Data are from three biological replicates and reported as mean ± SEM. * p=0.0276 (CD630E vs Xy06); ns: no significance (R20291, Xy07 vs Xy06). ns- not significant.
Smc Media, supplied by Lifeline Cell Technology, 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/smc media/product/Lifeline Cell Technology
Average 90 stars, based on 1 article reviews
smc media - by Bioz Stars, 2026-03
90/100 stars
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90
Lonza smc basal medium with included serum and supplements
<t>Sporulation</t> and germination rates of C. difficile strains. (A) Sporulation. *P<0.05; **P<0.01. (B) Germination: Purified C. difficile spores were suspended in buffer supplemented with taurocholic acid and glycine to induce germination. Germination was monitored by plotting the ratio of the OD 600 at a given time to the OD 600 at time zero. Data are from three biological replicates and reported as mean ± SEM. ****p=0.0001(CD630E vs Xy06); ***p=0.0021 (Xy07 vs Xy06); ns: p=0.0714 (R20291 vs Xy06). (C) Spore colony-forming efficiency. Spore suspensions were serially diluted and plated on BHIS agar supplemented with 0.1%(w/v) taurocholic acid (TA). The spore colony-forming efficiency was defined as the percentage of total spores that gave rise to colonies on BHIS agar with 0.1% (w/v) TA, calculated by c.f.u. per ml colony count/c.f.u. per ml direct count by microscopy × 100%. Data are from three biological replicates and reported as mean ± SEM. * p=0.0276 (CD630E vs Xy06); ns: no significance (R20291, Xy07 vs Xy06). ns- not significant.
Smc Basal Medium With Included Serum And Supplements, supplied by Lonza, 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/smc basal medium with included serum and supplements/product/Lonza
Average 90 stars, based on 1 article reviews
smc basal medium with included serum and supplements - by Bioz Stars, 2026-03
90/100 stars
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Image Search Results


Figure 3 Three hours of hypoxia and 6 h of reperfusion lead to significant endothelial cell death in vitro in rat brain microvascular endothelial cells (RBMVEC; A). Non-specific gap junction blocker carbenoxolone, non-specific hemichannel blocker LaCl3, and connexin43 (Cx43) mimetic peptide protected endothelial cells against hypoxic injury, with the number of viable cells significantly higher than no treatment, while scrambled peptide did not have any protective effects. The number of viable cells was expressed as percentage of the control without hypoxia. Hypoxia and reperfusion also lead to significant propidium iodide dye uptake into primary rat brain microvascular endothelial cells indicating open hemichannels (B). Carbenoxolone, LaCl3 and connexin43 mimetic peptide significantly prevented dye uptake compared to no treatment, indicating hemichannel closure, while scrambled peptide did not have any effect. Stars denote statistical significance when compared to the control group or compared between groups in brackets; P 5 0.05.

Journal: Brain : a journal of neurology

Article Title: Connexin43 mimetic peptide reduces vascular leak and retinal ganglion cell death following retinal ischaemia.

doi: 10.1093/brain/awr338

Figure Lengend Snippet: Figure 3 Three hours of hypoxia and 6 h of reperfusion lead to significant endothelial cell death in vitro in rat brain microvascular endothelial cells (RBMVEC; A). Non-specific gap junction blocker carbenoxolone, non-specific hemichannel blocker LaCl3, and connexin43 (Cx43) mimetic peptide protected endothelial cells against hypoxic injury, with the number of viable cells significantly higher than no treatment, while scrambled peptide did not have any protective effects. The number of viable cells was expressed as percentage of the control without hypoxia. Hypoxia and reperfusion also lead to significant propidium iodide dye uptake into primary rat brain microvascular endothelial cells indicating open hemichannels (B). Carbenoxolone, LaCl3 and connexin43 mimetic peptide significantly prevented dye uptake compared to no treatment, indicating hemichannel closure, while scrambled peptide did not have any effect. Stars denote statistical significance when compared to the control group or compared between groups in brackets; P 5 0.05.

Article Snippet: Rat brain microvascular endothelial cells (R840K-05a, Cell Applications) were plated into 24-well plates (1 105 cells/well) in rat brain microvascular endothelial cell growth media (R819K-500, Cell Applications) and allowed to settle for 16 h. Medium was then removed and replaced with Dulbecco’s Modified Eagle’s Medium/F12 containing 0.5% foetal bovine serum and 1% glutamine.

Techniques: In Vitro, Control

Sporulation and germination rates of C. difficile strains. (A) Sporulation. *P<0.05; **P<0.01. (B) Germination: Purified C. difficile spores were suspended in buffer supplemented with taurocholic acid and glycine to induce germination. Germination was monitored by plotting the ratio of the OD 600 at a given time to the OD 600 at time zero. Data are from three biological replicates and reported as mean ± SEM. ****p=0.0001(CD630E vs Xy06); ***p=0.0021 (Xy07 vs Xy06); ns: p=0.0714 (R20291 vs Xy06). (C) Spore colony-forming efficiency. Spore suspensions were serially diluted and plated on BHIS agar supplemented with 0.1%(w/v) taurocholic acid (TA). The spore colony-forming efficiency was defined as the percentage of total spores that gave rise to colonies on BHIS agar with 0.1% (w/v) TA, calculated by c.f.u. per ml colony count/c.f.u. per ml direct count by microscopy × 100%. Data are from three biological replicates and reported as mean ± SEM. * p=0.0276 (CD630E vs Xy06); ns: no significance (R20291, Xy07 vs Xy06). ns- not significant.

Journal: Frontiers in Cellular and Infection Microbiology

Article Title: Genomic and phenotypic characterization of a Clostridioides difficile strain of the epidemic ST37 type from China

doi: 10.3389/fcimb.2024.1412408

Figure Lengend Snippet: Sporulation and germination rates of C. difficile strains. (A) Sporulation. *P<0.05; **P<0.01. (B) Germination: Purified C. difficile spores were suspended in buffer supplemented with taurocholic acid and glycine to induce germination. Germination was monitored by plotting the ratio of the OD 600 at a given time to the OD 600 at time zero. Data are from three biological replicates and reported as mean ± SEM. ****p=0.0001(CD630E vs Xy06); ***p=0.0021 (Xy07 vs Xy06); ns: p=0.0714 (R20291 vs Xy06). (C) Spore colony-forming efficiency. Spore suspensions were serially diluted and plated on BHIS agar supplemented with 0.1%(w/v) taurocholic acid (TA). The spore colony-forming efficiency was defined as the percentage of total spores that gave rise to colonies on BHIS agar with 0.1% (w/v) TA, calculated by c.f.u. per ml colony count/c.f.u. per ml direct count by microscopy × 100%. Data are from three biological replicates and reported as mean ± SEM. * p=0.0276 (CD630E vs Xy06); ns: no significance (R20291, Xy07 vs Xy06). ns- not significant.

Article Snippet: A mixture of 70:30 sporulation medium (70% SMC medium and 30% BHIS medium including 63 g Bacto peptone, 3.5 g protease peptone, 11.1 g BHI medium, 1.5 g yeast extract, 1.06 g Tris base, 0.7 g NH 4 SO4) was prepared.

Techniques: Purification, Microscopy