human microvascular endothelial cell line 1 Search Results


microvascular endothelial cell line 1  (ATCC)
97
ATCC microvascular endothelial cell line 1
Microvascular Endothelial Cell Line 1, supplied by ATCC, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/microvascular endothelial cell line 1/product/ATCC
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microvascular endothelial cell line 1 - by Bioz Stars, 2026-02
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human microvascular endothelial cell line-1 (hmec-1)  (Procell Inc)
90
Procell Inc human microvascular endothelial cell line-1 (hmec-1)
Human Microvascular Endothelial Cell Line 1 (Hmec 1), supplied by Procell 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/human microvascular endothelial cell line-1 (hmec-1)/product/Procell Inc
Average 90 stars, based on 1 article reviews
human microvascular endothelial cell line-1 (hmec-1) - by Bioz Stars, 2026-02
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hmec-1  (iCell Bioscience Inc)
90
iCell Bioscience Inc hmec-1
Hmec 1, supplied by iCell Bioscience 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/hmec-1/product/iCell Bioscience Inc
Average 90 stars, based on 1 article reviews
hmec-1 - by Bioz Stars, 2026-02
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human microvascular endothelial cell line-1 (hmec-1)  (iCell Bioscience Inc)
90
iCell Bioscience Inc human microvascular endothelial cell line-1 (hmec-1)
Human Microvascular Endothelial Cell Line 1 (Hmec 1), supplied by iCell Bioscience 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/human microvascular endothelial cell line-1 (hmec-1)/product/iCell Bioscience Inc
Average 90 stars, based on 1 article reviews
human microvascular endothelial cell line-1 (hmec-1) - by Bioz Stars, 2026-02
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human microvascular endothelial cell line-1 (hmec-1) cells  (ScienCell)
90
ScienCell human microvascular endothelial cell line-1 (hmec-1) cells
The CM of Gli1-overexpressing NSCLC cells promoted angiogenesis in vitro and ex vivo. A Flowchart of evaluation the effect of Gli1-overexpressing A549 and NCI-H460 cells on <t>endothelial</t> cell and aorta rings. B-E The effect of CM from A549 Gli1 vector and NCI-H460 Gli1 vector cells on the migration, invasion and tube formation abilities of <t>HUVECs</t> and HMEC-1 cells. HUVECs and HMEC-1 cells were treated with CM for 48 h and subjected for wound healing ( B ), Transwell migration ( C ) and Tiranswell invasion ( D ), and tube formation assays ( E ). F Gli1-overexpressing NSCLC increased blood sprouting in aortic ring assay. G The CM of Gli1-overexpressing cells promoted the HBVP adhesion ability. H Schematic strategy of coculture tubule-like structure of endothelial cells and pericytes. I CM from Gli1-overexpressing cells enhanced the recruitment of HBVP to tubes formed by endothelial cell. All the data were showed as mean ± SD, n = 3. ** p < 0.01; *** p < 0.001 vs A549 NC vector or NCI-H460 NC vector cells
Human Microvascular Endothelial Cell Line 1 (Hmec 1) 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
https://www.bioz.com/result/human microvascular endothelial cell line-1 (hmec-1) cells/product/ScienCell
Average 90 stars, based on 1 article reviews
human microvascular endothelial cell line-1 (hmec-1) cells - by Bioz Stars, 2026-02
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human umbilical vein endothelial cells (huvec)  (iCell Bioscience Inc)
90
iCell Bioscience Inc human umbilical vein endothelial cells (huvec)
The CM of Gli1-overexpressing NSCLC cells promoted angiogenesis in vitro and ex vivo. A Flowchart of evaluation the effect of Gli1-overexpressing A549 and NCI-H460 cells on <t>endothelial</t> cell and aorta rings. B-E The effect of CM from A549 Gli1 vector and NCI-H460 Gli1 vector cells on the migration, invasion and tube formation abilities of <t>HUVECs</t> and HMEC-1 cells. HUVECs and HMEC-1 cells were treated with CM for 48 h and subjected for wound healing ( B ), Transwell migration ( C ) and Tiranswell invasion ( D ), and tube formation assays ( E ). F Gli1-overexpressing NSCLC increased blood sprouting in aortic ring assay. G The CM of Gli1-overexpressing cells promoted the HBVP adhesion ability. H Schematic strategy of coculture tubule-like structure of endothelial cells and pericytes. I CM from Gli1-overexpressing cells enhanced the recruitment of HBVP to tubes formed by endothelial cell. All the data were showed as mean ± SD, n = 3. ** p < 0.01; *** p < 0.001 vs A549 NC vector or NCI-H460 NC vector cells
Human Umbilical Vein Endothelial Cells (Huvec), supplied by iCell Bioscience Inc, 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, 2026-02
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endothelial cell growth medium  (Cambrex)
90
Cambrex endothelial cell growth medium
The CM of Gli1-overexpressing NSCLC cells promoted angiogenesis in vitro and ex vivo. A Flowchart of evaluation the effect of Gli1-overexpressing A549 and NCI-H460 cells on <t>endothelial</t> cell and aorta rings. B-E The effect of CM from A549 Gli1 vector and NCI-H460 Gli1 vector cells on the migration, invasion and tube formation abilities of <t>HUVECs</t> and HMEC-1 cells. HUVECs and HMEC-1 cells were treated with CM for 48 h and subjected for wound healing ( B ), Transwell migration ( C ) and Tiranswell invasion ( D ), and tube formation assays ( E ). F Gli1-overexpressing NSCLC increased blood sprouting in aortic ring assay. G The CM of Gli1-overexpressing cells promoted the HBVP adhesion ability. H Schematic strategy of coculture tubule-like structure of endothelial cells and pericytes. I CM from Gli1-overexpressing cells enhanced the recruitment of HBVP to tubes formed by endothelial cell. All the data were showed as mean ± SD, n = 3. ** p < 0.01; *** p < 0.001 vs A549 NC vector or NCI-H460 NC vector cells
Endothelial Cell Growth 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/endothelial cell growth medium/product/Cambrex
Average 90 stars, based on 1 article reviews
endothelial cell growth medium - by Bioz Stars, 2026-02
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vena8 endothelial+ biochips  (Cellix Limited)
90
Cellix Limited vena8 endothelial+ biochips
The CM of Gli1-overexpressing NSCLC cells promoted angiogenesis in vitro and ex vivo. A Flowchart of evaluation the effect of Gli1-overexpressing A549 and NCI-H460 cells on <t>endothelial</t> cell and aorta rings. B-E The effect of CM from A549 Gli1 vector and NCI-H460 Gli1 vector cells on the migration, invasion and tube formation abilities of <t>HUVECs</t> and HMEC-1 cells. HUVECs and HMEC-1 cells were treated with CM for 48 h and subjected for wound healing ( B ), Transwell migration ( C ) and Tiranswell invasion ( D ), and tube formation assays ( E ). F Gli1-overexpressing NSCLC increased blood sprouting in aortic ring assay. G The CM of Gli1-overexpressing cells promoted the HBVP adhesion ability. H Schematic strategy of coculture tubule-like structure of endothelial cells and pericytes. I CM from Gli1-overexpressing cells enhanced the recruitment of HBVP to tubes formed by endothelial cell. All the data were showed as mean ± SD, n = 3. ** p < 0.01; *** p < 0.001 vs A549 NC vector or NCI-H460 NC vector cells
Vena8 Endothelial+ Biochips, supplied by Cellix Limited, 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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Average 90 stars, based on 1 article reviews
vena8 endothelial+ biochips - by Bioz Stars, 2026-02
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huvec  (iCell Bioscience Inc)
90
iCell Bioscience Inc huvec
AA-NPs inhibited the EndMT process in <t>HUVECs</t> and HMEC-1 in vitro. After Ang II stimulation, the expression levels of collagen-I, fibronectin, CD31, α-SMA, and FSP-1 proteins in (A) HUVECs and (B) HMEC-1 treated with different concentrations of AA-NPs. (C) Morphological changes of HUVECs observed under a microscope before and after AA-NPs treatment. (D) Immunofluorescence staining of the mesenchymal marker α-SMA and vascular <t>endothelial</t> marker CD31 in HUVECs. All data are presented as the mean ± SD ( n = 3).
Huvec, supplied by iCell Bioscience 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/huvec/product/iCell Bioscience Inc
Average 90 stars, based on 1 article reviews
huvec - by Bioz Stars, 2026-02
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fetal bovine serum  (Thermo Fisher)
90
Thermo Fisher fetal bovine serum
AA-NPs inhibited the EndMT process in <t>HUVECs</t> and HMEC-1 in vitro. After Ang II stimulation, the expression levels of collagen-I, fibronectin, CD31, α-SMA, and FSP-1 proteins in (A) HUVECs and (B) HMEC-1 treated with different concentrations of AA-NPs. (C) Morphological changes of HUVECs observed under a microscope before and after AA-NPs treatment. (D) Immunofluorescence staining of the mesenchymal marker α-SMA and vascular <t>endothelial</t> marker CD31 in HUVECs. All data are presented as the mean ± SD ( n = 3).
Fetal Bovine Serum, supplied by Thermo Fisher, 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/fetal bovine serum/product/Thermo Fisher
Average 90 stars, based on 1 article reviews
fetal bovine serum - by Bioz Stars, 2026-02
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lsgs supplement  (Thermo Fisher)
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Thermo Fisher lsgs supplement
AA-NPs inhibited the EndMT process in <t>HUVECs</t> and HMEC-1 in vitro. After Ang II stimulation, the expression levels of collagen-I, fibronectin, CD31, α-SMA, and FSP-1 proteins in (A) HUVECs and (B) HMEC-1 treated with different concentrations of AA-NPs. (C) Morphological changes of HUVECs observed under a microscope before and after AA-NPs treatment. (D) Immunofluorescence staining of the mesenchymal marker α-SMA and vascular <t>endothelial</t> marker CD31 in HUVECs. All data are presented as the mean ± SD ( n = 3).
Lsgs Supplement, supplied by Thermo Fisher, 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/lsgs supplement/product/Thermo Fisher
Average 90 stars, based on 1 article reviews
lsgs supplement - by Bioz Stars, 2026-02
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dmem  (Thermo Fisher)
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Thermo Fisher dmem
AA-NPs inhibited the EndMT process in <t>HUVECs</t> and HMEC-1 in vitro. After Ang II stimulation, the expression levels of collagen-I, fibronectin, CD31, α-SMA, and FSP-1 proteins in (A) HUVECs and (B) HMEC-1 treated with different concentrations of AA-NPs. (C) Morphological changes of HUVECs observed under a microscope before and after AA-NPs treatment. (D) Immunofluorescence staining of the mesenchymal marker α-SMA and vascular <t>endothelial</t> marker CD31 in HUVECs. All data are presented as the mean ± SD ( n = 3).
Dmem, supplied by Thermo Fisher, 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/dmem/product/Thermo Fisher
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Image Search Results


The CM of Gli1-overexpressing NSCLC cells promoted angiogenesis in vitro and ex vivo. A Flowchart of evaluation the effect of Gli1-overexpressing A549 and NCI-H460 cells on endothelial cell and aorta rings. B-E The effect of CM from A549 Gli1 vector and NCI-H460 Gli1 vector cells on the migration, invasion and tube formation abilities of HUVECs and HMEC-1 cells. HUVECs and HMEC-1 cells were treated with CM for 48 h and subjected for wound healing ( B ), Transwell migration ( C ) and Tiranswell invasion ( D ), and tube formation assays ( E ). F Gli1-overexpressing NSCLC increased blood sprouting in aortic ring assay. G The CM of Gli1-overexpressing cells promoted the HBVP adhesion ability. H Schematic strategy of coculture tubule-like structure of endothelial cells and pericytes. I CM from Gli1-overexpressing cells enhanced the recruitment of HBVP to tubes formed by endothelial cell. All the data were showed as mean ± SD, n = 3. ** p < 0.01; *** p < 0.001 vs A549 NC vector or NCI-H460 NC vector cells

Journal: Journal of Experimental & Clinical Cancer Research : CR

Article Title: Gli1-mediated tumor cell-derived bFGF promotes tumor angiogenesis and pericyte coverage in non-small cell lung cancer

doi: 10.1186/s13046-024-03003-0

Figure Lengend Snippet: The CM of Gli1-overexpressing NSCLC cells promoted angiogenesis in vitro and ex vivo. A Flowchart of evaluation the effect of Gli1-overexpressing A549 and NCI-H460 cells on endothelial cell and aorta rings. B-E The effect of CM from A549 Gli1 vector and NCI-H460 Gli1 vector cells on the migration, invasion and tube formation abilities of HUVECs and HMEC-1 cells. HUVECs and HMEC-1 cells were treated with CM for 48 h and subjected for wound healing ( B ), Transwell migration ( C ) and Tiranswell invasion ( D ), and tube formation assays ( E ). F Gli1-overexpressing NSCLC increased blood sprouting in aortic ring assay. G The CM of Gli1-overexpressing cells promoted the HBVP adhesion ability. H Schematic strategy of coculture tubule-like structure of endothelial cells and pericytes. I CM from Gli1-overexpressing cells enhanced the recruitment of HBVP to tubes formed by endothelial cell. All the data were showed as mean ± SD, n = 3. ** p < 0.01; *** p < 0.001 vs A549 NC vector or NCI-H460 NC vector cells

Article Snippet: Human umbilical vein endothelial cells (HUVECs), human microvascular endothelial cell line-1 (HMEC-1) cells and human brain vascular pericytes (HBVPs) were provided by ScienCell Research Laboratories (Carlsbad, CA).

Techniques: In Vitro, Ex Vivo, Plasmid Preparation, Migration, Aortic Ring Assay

The CM from Gli1-knockdown NSCLC cells suppressed angiogenesis in vitro and ex vivo. A Schematic strategy of endothelial cells and aorta rings treated with CM from Gli1-knockdown NSCLC cells. B-E The CM from NCI-H1299 shGli1 cells or NCI-H1703 shGli1 cells suppressed the migration ( B and C ), invasion ( D ) and tube formation ( E ) abilities of HUVECs and HMEC-1 cell. F The CM from NCI-H1299 shGli1 cells or NCI-H1703 shGli1 cells reduced vessel sprouting in the rat aorta rings. G-I The CM from NCI-H1299 shGli1 cells and NCI-H1703 shGli1 cells inhibited HBVP adhesion ( G ) and recruitment to newly blood vessel (H and I). All the data were showed as mean ± SD, n = 3. ** p < 0.01; *** p < 0.001 vs NCI-H1299 sh NC or NCI-H1703 sh NC cells

Journal: Journal of Experimental & Clinical Cancer Research : CR

Article Title: Gli1-mediated tumor cell-derived bFGF promotes tumor angiogenesis and pericyte coverage in non-small cell lung cancer

doi: 10.1186/s13046-024-03003-0

Figure Lengend Snippet: The CM from Gli1-knockdown NSCLC cells suppressed angiogenesis in vitro and ex vivo. A Schematic strategy of endothelial cells and aorta rings treated with CM from Gli1-knockdown NSCLC cells. B-E The CM from NCI-H1299 shGli1 cells or NCI-H1703 shGli1 cells suppressed the migration ( B and C ), invasion ( D ) and tube formation ( E ) abilities of HUVECs and HMEC-1 cell. F The CM from NCI-H1299 shGli1 cells or NCI-H1703 shGli1 cells reduced vessel sprouting in the rat aorta rings. G-I The CM from NCI-H1299 shGli1 cells and NCI-H1703 shGli1 cells inhibited HBVP adhesion ( G ) and recruitment to newly blood vessel (H and I). All the data were showed as mean ± SD, n = 3. ** p < 0.01; *** p < 0.001 vs NCI-H1299 sh NC or NCI-H1703 sh NC cells

Article Snippet: Human umbilical vein endothelial cells (HUVECs), human microvascular endothelial cell line-1 (HMEC-1) cells and human brain vascular pericytes (HBVPs) were provided by ScienCell Research Laboratories (Carlsbad, CA).

Techniques: Knockdown, In Vitro, Ex Vivo, Migration

AA-NPs inhibited the EndMT process in HUVECs and HMEC-1 in vitro. After Ang II stimulation, the expression levels of collagen-I, fibronectin, CD31, α-SMA, and FSP-1 proteins in (A) HUVECs and (B) HMEC-1 treated with different concentrations of AA-NPs. (C) Morphological changes of HUVECs observed under a microscope before and after AA-NPs treatment. (D) Immunofluorescence staining of the mesenchymal marker α-SMA and vascular endothelial marker CD31 in HUVECs. All data are presented as the mean ± SD ( n = 3).

Journal: ACS Applied Materials & Interfaces

Article Title: Insights into the Mechanism of Supramolecular Self-Assembly in the Astragalus membranaceus – Angelica sinensis Codecoction

doi: 10.1021/acsami.3c09494

Figure Lengend Snippet: AA-NPs inhibited the EndMT process in HUVECs and HMEC-1 in vitro. After Ang II stimulation, the expression levels of collagen-I, fibronectin, CD31, α-SMA, and FSP-1 proteins in (A) HUVECs and (B) HMEC-1 treated with different concentrations of AA-NPs. (C) Morphological changes of HUVECs observed under a microscope before and after AA-NPs treatment. (D) Immunofluorescence staining of the mesenchymal marker α-SMA and vascular endothelial marker CD31 in HUVECs. All data are presented as the mean ± SD ( n = 3).

Article Snippet: Human umbilical vein endothelial cells (HUVEC) and human microvascular endothelial cell line-1 (HMEC-1) were purchased from iCell Bioscience Inc. (Shanghai, China) and cultured in DMEM (Gibco) containing 10% fetal bovine serum (Gibco) and 1% penicillin–streptomycin (Gibco).

Techniques: In Vitro, Expressing, Microscopy, Immunofluorescence, Staining, Marker