human umbilical vein vascular smooth muscle cell culture medium Search Results


90
Lonza human umbilical artery smooth muscle cells #cc-2579
Human Umbilical Artery Smooth Muscle Cells #Cc 2579, 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
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human umbilical artery smooth muscle cells #cc-2579 - by Bioz Stars, 2026-07
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Lonza human umbilical artery vsmcs
Human Umbilical Artery Vsmcs, 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
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Cell Applications Inc human umbilical artery smooth muscle cells
Human Umbilical Artery Smooth Muscle Cells, supplied by Cell Applications Inc, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/human+umbilical+vein+vascular+smooth+muscle+cell+culture+medium/pm21270819-45-0-9?v=Cell+Applications+Inc
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human umbilical artery smooth muscle cells - by Bioz Stars, 2026-07
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Lonza human umbilical vein endothelial cells (huvec
Human Umbilical Vein Endothelial Cells (Huvec, 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
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human umbilical vein endothelial cells (huvec - by Bioz Stars, 2026-07
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ScienCell human umbilical venous smooth muscle cells
Human Umbilical Venous Smooth Muscle Cells, 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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human umbilical venous smooth muscle cells - by Bioz Stars, 2026-07
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Cell Applications Inc human umbilical vein smooth muscle cells: huvsmc
Human Umbilical Vein Smooth Muscle Cells: Huvsmc, supplied by Cell Applications 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/product/human+umbilical+vein+vascular+smooth+muscle+cell+culture+medium/custom%402193-01%4010%2E1177%2F1358863x19866254?v=Cell+Applications+Inc
Average 90 stars, based on 1 article reviews
human umbilical vein smooth muscle cells: huvsmc - by Bioz Stars, 2026-07
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Lonza human umbilical cord vein smooth muscle cells
Human Umbilical Cord Vein Smooth Muscle Cells, 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
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Cell Applications Inc human umbilical vein cells
Human Umbilical Vein Cells, supplied by Cell Applications Inc, 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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human umbilical vein cells - by Bioz Stars, 2026-07
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ATCC human umbilical vein endothelial cell line
Immunohistochemistry staining of P-selectin in cremasteric endothelium after methylglyoxal (MG) treatment. MG at 25 or 50 mg/kg (dissolved in 200 μl saline) was injected intrascrotally for 5·5 hr, and the mouse cremaster muscles were collected and processed as described in the Materials and methods. The brown staining on the <t>endothelial</t> cells of cremasteric postcapillary venules reveals the expression of P-selectin. Saline and 500 ng tumour necrosis factor-α (TNF-α) were used as negative and positive controls, respectively (magnification: 400×).
Human Umbilical Vein Endothelial Cell Line, supplied by ATCC, 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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Lonza human umbilical artery vascular smooth muscle cells (vsmcs)
Microcontact printing used to provide spatial cues <t>for</t> <t>vascular</t> tissue self-organization. (A) Phase contrast images of <t>VSMCs</t> micropatterned into thin tissue lines of varying widths, indicated in each image, separated by 100 μm gaps. (scale bars =200 μm). (B) 3-D confocal image of 100 μm wide patterned VSMC tissue. (Green: f-actin, Blue: nuclei). Scale bar 100 μm. (C) Thickness map of tissue in B, using f-actin staining. (D) Tissue thickness as a function of pattern width and ECM (fibronectin (FN) and laminin (LN)) substrate (mean +/− SD).
Human Umbilical Artery Vascular Smooth Muscle Cells (Vsmcs), 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/product/human+umbilical+vein+vascular+smooth+muscle+cell+culture+medium/pmc08388149-254-0-11?v=Lonza
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human umbilical artery vascular smooth muscle cells (vsmcs) - by Bioz Stars, 2026-07
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ScienCell huasmc
Microcontact printing used to provide spatial cues <t>for</t> <t>vascular</t> tissue self-organization. (A) Phase contrast images of <t>VSMCs</t> micropatterned into thin tissue lines of varying widths, indicated in each image, separated by 100 μm gaps. (scale bars =200 μm). (B) 3-D confocal image of 100 μm wide patterned VSMC tissue. (Green: f-actin, Blue: nuclei). Scale bar 100 μm. (C) Thickness map of tissue in B, using f-actin staining. (D) Tissue thickness as a function of pattern width and ECM (fibronectin (FN) and laminin (LN)) substrate (mean +/− SD).
Huasmc, 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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Thermo Fisher primary human umbilical vein endothelial cells huvecs
Microcontact printing used to provide spatial cues <t>for</t> <t>vascular</t> tissue self-organization. (A) Phase contrast images of <t>VSMCs</t> micropatterned into thin tissue lines of varying widths, indicated in each image, separated by 100 μm gaps. (scale bars =200 μm). (B) 3-D confocal image of 100 μm wide patterned VSMC tissue. (Green: f-actin, Blue: nuclei). Scale bar 100 μm. (C) Thickness map of tissue in B, using f-actin staining. (D) Tissue thickness as a function of pattern width and ECM (fibronectin (FN) and laminin (LN)) substrate (mean +/− SD).
Primary Human Umbilical Vein Endothelial Cells Huvecs, 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
https://www.bioz.com/product/human+umbilical+vein+vascular+smooth+muscle+cell+culture+medium/pmc00209295-35-0-24?v=Thermo+Fisher
Average 99 stars, based on 1 article reviews
primary human umbilical vein endothelial cells huvecs - by Bioz Stars, 2026-07
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Image Search Results


Immunohistochemistry staining of P-selectin in cremasteric endothelium after methylglyoxal (MG) treatment. MG at 25 or 50 mg/kg (dissolved in 200 μl saline) was injected intrascrotally for 5·5 hr, and the mouse cremaster muscles were collected and processed as described in the Materials and methods. The brown staining on the endothelial cells of cremasteric postcapillary venules reveals the expression of P-selectin. Saline and 500 ng tumour necrosis factor-α (TNF-α) were used as negative and positive controls, respectively (magnification: 400×).

Journal: Immunology

Article Title: The role of endothelial cell adhesion molecules P-selectin, E-selectin and intercellular adhesion molecule-1 in leucocyte recruitment induced by exogenous methylglyoxal

doi: 10.1111/j.1365-2567.2012.03608.x

Figure Lengend Snippet: Immunohistochemistry staining of P-selectin in cremasteric endothelium after methylglyoxal (MG) treatment. MG at 25 or 50 mg/kg (dissolved in 200 μl saline) was injected intrascrotally for 5·5 hr, and the mouse cremaster muscles were collected and processed as described in the Materials and methods. The brown staining on the endothelial cells of cremasteric postcapillary venules reveals the expression of P-selectin. Saline and 500 ng tumour necrosis factor-α (TNF-α) were used as negative and positive controls, respectively (magnification: 400×).

Article Snippet: EA.hy926 cell, a hybrid human umbilical vein endothelial cell line, was obtained from the American Type Culture Collection (ATCC, Rockville, MD).

Techniques: Immunohistochemistry, Staining, Saline, Injection, Muscles, Expressing

Immunohistochemistry staining of E-selectin on cremasteric endothelium after methylglyoxal (MG) treatment. MG at 25 or 50 mg/kg (dissolved in 200 μl saline) was injected intrascrotally for 5·5 hr, and the mouse cremaster muscles were collected and processed as described in the Materials and methods. The brown staining on the endothelial cells of cremasteric postcapillary venules reveals the expression of E-selectin. Saline and 500 ng tumour necrosis factor-α (TNF-α) were used as negative and positive controls, respectively (magnification: 400×).

Journal: Immunology

Article Title: The role of endothelial cell adhesion molecules P-selectin, E-selectin and intercellular adhesion molecule-1 in leucocyte recruitment induced by exogenous methylglyoxal

doi: 10.1111/j.1365-2567.2012.03608.x

Figure Lengend Snippet: Immunohistochemistry staining of E-selectin on cremasteric endothelium after methylglyoxal (MG) treatment. MG at 25 or 50 mg/kg (dissolved in 200 μl saline) was injected intrascrotally for 5·5 hr, and the mouse cremaster muscles were collected and processed as described in the Materials and methods. The brown staining on the endothelial cells of cremasteric postcapillary venules reveals the expression of E-selectin. Saline and 500 ng tumour necrosis factor-α (TNF-α) were used as negative and positive controls, respectively (magnification: 400×).

Article Snippet: EA.hy926 cell, a hybrid human umbilical vein endothelial cell line, was obtained from the American Type Culture Collection (ATCC, Rockville, MD).

Techniques: Immunohistochemistry, Staining, Saline, Injection, Muscles, Expressing

Immunohistochemistry staining of intracellular adhesion molecule 1 (ICAM-1) on cremasteric endothelium after methylglyoxal (MG) treatment. MG at 25 or 50 mg/kg (dissolved in 200 μl saline) was injected intrascrotally for 5·5 hr, and the mouse cremaster muscles were collected and processed as described in the Materials and methods. The brown staining on the endothelial cells of cremasteric postcapillary venules reveals the expression of ICAM-1. Saline and 500 ng tumour necrosis factor-α (TNF-α) were used as negative and positive controls, respectively (magnification: 400×).

Journal: Immunology

Article Title: The role of endothelial cell adhesion molecules P-selectin, E-selectin and intercellular adhesion molecule-1 in leucocyte recruitment induced by exogenous methylglyoxal

doi: 10.1111/j.1365-2567.2012.03608.x

Figure Lengend Snippet: Immunohistochemistry staining of intracellular adhesion molecule 1 (ICAM-1) on cremasteric endothelium after methylglyoxal (MG) treatment. MG at 25 or 50 mg/kg (dissolved in 200 μl saline) was injected intrascrotally for 5·5 hr, and the mouse cremaster muscles were collected and processed as described in the Materials and methods. The brown staining on the endothelial cells of cremasteric postcapillary venules reveals the expression of ICAM-1. Saline and 500 ng tumour necrosis factor-α (TNF-α) were used as negative and positive controls, respectively (magnification: 400×).

Article Snippet: EA.hy926 cell, a hybrid human umbilical vein endothelial cell line, was obtained from the American Type Culture Collection (ATCC, Rockville, MD).

Techniques: Immunohistochemistry, Staining, Saline, Injection, Muscles, Expressing

Immunohistochemistry staining of vascular cell adhesion molecule 1 (VCAM-1) on cremasteric endothelium after methylglyoxal (MG) treatment. MG at 25 or 50 mg/kg (dissolved in 200 μl saline) was injected intrascrotally for 5·5 hr, and the mouse cremaster muscles were collected and processed as described in the Materials and methods. Saline and 500 ng tumour necrosis factor-α (TNF-α) were used as negative and positive controls, respectively. The brown staining on the endothelial cells of cremasteric postcapillary venules reveals the expression of VCAM-1 in the TNF-α-treated group. Both MG treatment groups show no apparent change of VCAM-1 expression after 5·5 hr MG treatment compared with saline control group (magnification: 400×).

Journal: Immunology

Article Title: The role of endothelial cell adhesion molecules P-selectin, E-selectin and intercellular adhesion molecule-1 in leucocyte recruitment induced by exogenous methylglyoxal

doi: 10.1111/j.1365-2567.2012.03608.x

Figure Lengend Snippet: Immunohistochemistry staining of vascular cell adhesion molecule 1 (VCAM-1) on cremasteric endothelium after methylglyoxal (MG) treatment. MG at 25 or 50 mg/kg (dissolved in 200 μl saline) was injected intrascrotally for 5·5 hr, and the mouse cremaster muscles were collected and processed as described in the Materials and methods. Saline and 500 ng tumour necrosis factor-α (TNF-α) were used as negative and positive controls, respectively. The brown staining on the endothelial cells of cremasteric postcapillary venules reveals the expression of VCAM-1 in the TNF-α-treated group. Both MG treatment groups show no apparent change of VCAM-1 expression after 5·5 hr MG treatment compared with saline control group (magnification: 400×).

Article Snippet: EA.hy926 cell, a hybrid human umbilical vein endothelial cell line, was obtained from the American Type Culture Collection (ATCC, Rockville, MD).

Techniques: Immunohistochemistry, Staining, Saline, Injection, Muscles, Expressing, Control

Methylglyoxal (MG)-induced expression of P-selectin, E-selectin and intracellular adhesion molecule 1 (ICAM-1) in cultured endothelial cells. EA.hy926 endothelial cells were cultured to 90% confluence and treated with PBS (negative control), 100 μm MG or 20 ng/ml tumour necrosis factor-α (TNF-α; positive control) for 4 hr. The expression of P-selectin, E-selectin and ICAM-1 in cell lysates was determined by Western blot.

Journal: Immunology

Article Title: The role of endothelial cell adhesion molecules P-selectin, E-selectin and intercellular adhesion molecule-1 in leucocyte recruitment induced by exogenous methylglyoxal

doi: 10.1111/j.1365-2567.2012.03608.x

Figure Lengend Snippet: Methylglyoxal (MG)-induced expression of P-selectin, E-selectin and intracellular adhesion molecule 1 (ICAM-1) in cultured endothelial cells. EA.hy926 endothelial cells were cultured to 90% confluence and treated with PBS (negative control), 100 μm MG or 20 ng/ml tumour necrosis factor-α (TNF-α; positive control) for 4 hr. The expression of P-selectin, E-selectin and ICAM-1 in cell lysates was determined by Western blot.

Article Snippet: EA.hy926 cell, a hybrid human umbilical vein endothelial cell line, was obtained from the American Type Culture Collection (ATCC, Rockville, MD).

Techniques: Expressing, Cell Culture, Negative Control, Positive Control, Western Blot

Effect of nuclear factor-κB (NF-κB) inhibition on methylglyoxal (MG) -induced endothelial adhesion molecule expression and leucocyte recruitment. BAY11-7082 at 20 mg/kg was injected to the mice 30 min before 25 mg/kg MG administration. The vehicle control group was injected with the same concentration of the solvent for BAY11-7082. After 4-hr MG injection, the mouse cremaster muscle was prepared for intravital microscopy. The muscle samples were then collected and processed for immunostaining after 1·5 hr intravital microscopy. The brown staining on the endothelial cells of cremasteric postcapillary venules reveals the expression levels of P-selectin, E-selectin and intracellular adhesion molecule 1 (ICAM-1; magnification: 400×) in the upper, middle and lower panels, respectively (a). The inhibitory effects of BAY11-7082 on MG-induced leucocyte rolling flux (b), rolling velocity (c), the number of adherent leucocytes (d) and the number of emigrated leucocytes (e) were determined. Values in (b) to (e) are means ± SEM (n = 3). *P < 0·05 compared with 25 mg/kg MG treatment group without BAY 11-7082.

Journal: Immunology

Article Title: The role of endothelial cell adhesion molecules P-selectin, E-selectin and intercellular adhesion molecule-1 in leucocyte recruitment induced by exogenous methylglyoxal

doi: 10.1111/j.1365-2567.2012.03608.x

Figure Lengend Snippet: Effect of nuclear factor-κB (NF-κB) inhibition on methylglyoxal (MG) -induced endothelial adhesion molecule expression and leucocyte recruitment. BAY11-7082 at 20 mg/kg was injected to the mice 30 min before 25 mg/kg MG administration. The vehicle control group was injected with the same concentration of the solvent for BAY11-7082. After 4-hr MG injection, the mouse cremaster muscle was prepared for intravital microscopy. The muscle samples were then collected and processed for immunostaining after 1·5 hr intravital microscopy. The brown staining on the endothelial cells of cremasteric postcapillary venules reveals the expression levels of P-selectin, E-selectin and intracellular adhesion molecule 1 (ICAM-1; magnification: 400×) in the upper, middle and lower panels, respectively (a). The inhibitory effects of BAY11-7082 on MG-induced leucocyte rolling flux (b), rolling velocity (c), the number of adherent leucocytes (d) and the number of emigrated leucocytes (e) were determined. Values in (b) to (e) are means ± SEM (n = 3). *P < 0·05 compared with 25 mg/kg MG treatment group without BAY 11-7082.

Article Snippet: EA.hy926 cell, a hybrid human umbilical vein endothelial cell line, was obtained from the American Type Culture Collection (ATCC, Rockville, MD).

Techniques: Inhibition, Expressing, Injection, Control, Concentration Assay, Solvent, Intravital Microscopy, Immunostaining, Staining

Microcontact printing used to provide spatial cues for vascular tissue self-organization. (A) Phase contrast images of VSMCs micropatterned into thin tissue lines of varying widths, indicated in each image, separated by 100 μm gaps. (scale bars =200 μm). (B) 3-D confocal image of 100 μm wide patterned VSMC tissue. (Green: f-actin, Blue: nuclei). Scale bar 100 μm. (C) Thickness map of tissue in B, using f-actin staining. (D) Tissue thickness as a function of pattern width and ECM (fibronectin (FN) and laminin (LN)) substrate (mean +/− SD).

Journal: Integrative biology : quantitative biosciences from nano to macro

Article Title: Vascular Smooth Muscle Contractility Depends on Cell Shape

doi: 10.1039/c1ib00061f

Figure Lengend Snippet: Microcontact printing used to provide spatial cues for vascular tissue self-organization. (A) Phase contrast images of VSMCs micropatterned into thin tissue lines of varying widths, indicated in each image, separated by 100 μm gaps. (scale bars =200 μm). (B) 3-D confocal image of 100 μm wide patterned VSMC tissue. (Green: f-actin, Blue: nuclei). Scale bar 100 μm. (C) Thickness map of tissue in B, using f-actin staining. (D) Tissue thickness as a function of pattern width and ECM (fibronectin (FN) and laminin (LN)) substrate (mean +/− SD).

Article Snippet: Human umbilical artery vascular smooth muscle cells (VSMCs) were purchased from Lonza (Walkersville, MD) at passage 3 and cultured in growth medium consisting of M199 culture medium (GIBCO, Invitrogen, Carlsbad, CA) supplemented with 10% fetal bovine serum (Invitrogen), 10 mM HEPES (GIBCO, Invitrogen, Carlsbad, CA), 3.5 g/L glucose, 2mg/L vitamin B-12, 50 U/ml penicillin and 50 U/mL streptomycin (GIBCO).

Techniques: Staining