anti vegf antibody (Abcam)
Name:
Anti VEGFA antibody
Description:
Catalog Number:
ab46154
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1) Product Images from "Silencing of Transient Receptor Potential Channel 4 Alleviates oxLDL-induced Angiogenesis in Human Coronary Artery Endothelial Cells by Inhibition of VEGF and NF-κB"
Article Title: Silencing of Transient Receptor Potential Channel 4 Alleviates oxLDL-induced Angiogenesis in Human Coronary Artery Endothelial Cells by Inhibition of VEGF and NF-κB
Journal: Medical Science Monitor : International Medical Journal of Experimental and Clinical Research
doi: 10.12659/MSM.897634

Figure Legend Snippet: Silencing effect of TRPC4 on expression of VEGF and NF-κB p65. The expression levels of VEGF and NF-κB p65 were determined to examine the underlying molecular mechanism. TRPC4 – transient receptor potential channel 4; siRNA – small interfering RNA; NC – negative control; VEGF – vascular endothelial growth factor.
Techniques Used: Expressing, Small Interfering RNA, Negative Control
2) Product Images from "Role of VEGF-A in angiogenesis promoted by umbilical cord-derived mesenchymal stromal/stem cells: in vitro study"
Article Title: Role of VEGF-A in angiogenesis promoted by umbilical cord-derived mesenchymal stromal/stem cells: in vitro study
Journal: Stem Cell Research & Therapy
doi: 10.1186/s13287-016-0305-4

Figure Legend Snippet: Effects of UC-MSC-conditioned media on proliferation, directed migration, and motility of EA.hy926 cells. a Effects of UC-MSC-conditioned media on proliferation of EA.hy926 cells was determined by MTT assay. Cells were treated with UC-MSC-conditioned media or UC-MSC-conditioned media supplemented with anti-VEGF antibody for 1, 2, or 3 days. Control cells were treated with growth media for 3 days. Values are expressed as average ± SD of three replicates. * p
Techniques Used: Migration, MTT Assay

Figure Legend Snippet: Matrigel tube formation assay. a UC-MSCs, or EA.hy926 cells, or 1:1 mixed UC-MSC-EA.hy926 cells in the presence of growth media, or EA.hy926 cells in the presence of UC-MSC-conditioned media or UC-MSC-conditioned media supplemented with anti-VEGF antibody (total 35 × 10 3 cells per well) were cultured in 48-well plates coated with Matrigel. ( Right ) Representative images of morphological changes of networks. Scale bar 100 μm. ( Left ) Quantification of lengths of the tubes and numbers of branch points. Values are expressed as average ± SD. b PKH26-labeled UC-MSCs ( red ) became the basis of a mixed culture network, while PKH67-labeled EA.hy926 cells ( green ) were only associated with it. Scale bar 100 μm. c Cluster formation. ( Left ) Representative images of tight clusters formed in Matrigel by UC-MSCs, or EA.hy926 cells, or mixed UC-MSC-EA.hy926 cells 24 hours after seeding. Macrophotograph of the 48-well plate. ( Right ) Quantification of numbers of clusters. Values are expressed as average ± SD of three replicates. * p
Techniques Used: Tube Formation Assay, Cell Culture, Labeling

Figure Legend Snippet: Cell culture characterization. a Human UC-MSC immunophenotype, positive for CD73, CD90, and CD105 and negative for CD45, CD34, CD11b, CD19, and HLA-DR. b Multilineage differentiation of UC-MSCs. Differentiation into adipocytes was revealed by Sudan III staining for intracellular accumulated lipids. Differentiation into osteocytes was revealed by Alizarin Red S staining for calcium mineralization. Chondrogenic differentiation was revealed by Alcian blue staining for mucopolysaccharides. Scale bar 100 μm. c Positive staining of EA.hy926 cells for CD31 as endothelial marker. Scale bar 100 μm. d Concentration of soluble forms of VEGF-A (VEGF-A-121 and VEGF-A-165) in the EA.hy926-conditioned media and the UC-MSC-conditioned media. Values are expressed as average ± SD of three replicates. * p
Techniques Used: Cell Culture, Staining, Marker, Concentration Assay

Figure Legend Snippet: Endothelial differentiation of UC-MSCs. a Endothelial differentiation of UC-MSCs in monolayer. Three endothelial induction media were used for UC-MSC culture: EA.hy926-conditioned media mixed 1:1 with growth media; EA.hy926-conditioned media mixed 1:1 with growth media supplemented with VEGF-A-165 (50 ng/ml); and growth media supplemented with VEGF-A-165. Only EA.hy926-conditioned media supplemented with VEGF-A-165 led to the appearance of CD31 + cells in the culture. Cell nuclei were stained with DAPI. Scale bar 100 μm. b Endothelial differentiation of UC-MSCs in Matrigel. Cryosections of secondary sprouts promoted by PKH26-labeled UC-MSCs ( red ). Immunostaining of sections showed that, upon coculturing with EA.hy926 in Matrigel, the UC-MSCs started to express CD31 ( green ). Cell nuclei were stained with DAPI. Scale bar 100 μm. VEGF vascular endothelial growth factor (Color figure online)
Techniques Used: Staining, Labeling, Immunostaining
3) Product Images from "Role of VEGF-A in angiogenesis promoted by umbilical cord-derived mesenchymal stromal/stem cells: in vitro study"
Article Title: Role of VEGF-A in angiogenesis promoted by umbilical cord-derived mesenchymal stromal/stem cells: in vitro study
Journal: Stem Cell Research & Therapy
doi: 10.1186/s13287-016-0305-4

Figure Legend Snippet: Effects of UC-MSC-conditioned media on proliferation, directed migration, and motility of EA.hy926 cells. a Effects of UC-MSC-conditioned media on proliferation of EA.hy926 cells was determined by MTT assay. Cells were treated with UC-MSC-conditioned media or UC-MSC-conditioned media supplemented with anti-VEGF antibody for 1, 2, or 3 days. Control cells were treated with growth media for 3 days. Values are expressed as average ± SD of three replicates. * p
Techniques Used: Migration, MTT Assay

Figure Legend Snippet: Matrigel tube formation assay. a UC-MSCs, or EA.hy926 cells, or 1:1 mixed UC-MSC-EA.hy926 cells in the presence of growth media, or EA.hy926 cells in the presence of UC-MSC-conditioned media or UC-MSC-conditioned media supplemented with anti-VEGF antibody (total 35 × 10 3 cells per well) were cultured in 48-well plates coated with Matrigel. ( Right ) Representative images of morphological changes of networks. Scale bar 100 μm. ( Left ) Quantification of lengths of the tubes and numbers of branch points. Values are expressed as average ± SD. b PKH26-labeled UC-MSCs ( red ) became the basis of a mixed culture network, while PKH67-labeled EA.hy926 cells ( green ) were only associated with it. Scale bar 100 μm. c Cluster formation. ( Left ) Representative images of tight clusters formed in Matrigel by UC-MSCs, or EA.hy926 cells, or mixed UC-MSC-EA.hy926 cells 24 hours after seeding. Macrophotograph of the 48-well plate. ( Right ) Quantification of numbers of clusters. Values are expressed as average ± SD of three replicates. * p
Techniques Used: Tube Formation Assay, Cell Culture, Labeling

Figure Legend Snippet: Cell culture characterization. a Human UC-MSC immunophenotype, positive for CD73, CD90, and CD105 and negative for CD45, CD34, CD11b, CD19, and HLA-DR. b Multilineage differentiation of UC-MSCs. Differentiation into adipocytes was revealed by Sudan III staining for intracellular accumulated lipids. Differentiation into osteocytes was revealed by Alizarin Red S staining for calcium mineralization. Chondrogenic differentiation was revealed by Alcian blue staining for mucopolysaccharides. Scale bar 100 μm. c Positive staining of EA.hy926 cells for CD31 as endothelial marker. Scale bar 100 μm. d Concentration of soluble forms of VEGF-A (VEGF-A-121 and VEGF-A-165) in the EA.hy926-conditioned media and the UC-MSC-conditioned media. Values are expressed as average ± SD of three replicates. * p
Techniques Used: Cell Culture, Staining, Marker, Concentration Assay

Figure Legend Snippet: Endothelial differentiation of UC-MSCs. a Endothelial differentiation of UC-MSCs in monolayer. Three endothelial induction media were used for UC-MSC culture: EA.hy926-conditioned media mixed 1:1 with growth media; EA.hy926-conditioned media mixed 1:1 with growth media supplemented with VEGF-A-165 (50 ng/ml); and growth media supplemented with VEGF-A-165. Only EA.hy926-conditioned media supplemented with VEGF-A-165 led to the appearance of CD31 + cells in the culture. Cell nuclei were stained with DAPI. Scale bar 100 μm. b Endothelial differentiation of UC-MSCs in Matrigel. Cryosections of secondary sprouts promoted by PKH26-labeled UC-MSCs ( red ). Immunostaining of sections showed that, upon coculturing with EA.hy926 in Matrigel, the UC-MSCs started to express CD31 ( green ). Cell nuclei were stained with DAPI. Scale bar 100 μm. VEGF vascular endothelial growth factor (Color figure online)
Techniques Used: Staining, Labeling, Immunostaining
4) Product Images from "Role of VEGF-A in angiogenesis promoted by umbilical cord-derived mesenchymal stromal/stem cells: in vitro study"
Article Title: Role of VEGF-A in angiogenesis promoted by umbilical cord-derived mesenchymal stromal/stem cells: in vitro study
Journal: Stem Cell Research & Therapy
doi: 10.1186/s13287-016-0305-4

Figure Legend Snippet: Effects of UC-MSC-conditioned media on proliferation, directed migration, and motility of EA.hy926 cells. a Effects of UC-MSC-conditioned media on proliferation of EA.hy926 cells was determined by MTT assay. Cells were treated with UC-MSC-conditioned media or UC-MSC-conditioned media supplemented with anti-VEGF antibody for 1, 2, or 3 days. Control cells were treated with growth media for 3 days. Values are expressed as average ± SD of three replicates. * p
Techniques Used: Migration, MTT Assay

Figure Legend Snippet: Matrigel tube formation assay. a UC-MSCs, or EA.hy926 cells, or 1:1 mixed UC-MSC-EA.hy926 cells in the presence of growth media, or EA.hy926 cells in the presence of UC-MSC-conditioned media or UC-MSC-conditioned media supplemented with anti-VEGF antibody (total 35 × 10 3 cells per well) were cultured in 48-well plates coated with Matrigel. ( Right ) Representative images of morphological changes of networks. Scale bar 100 μm. ( Left ) Quantification of lengths of the tubes and numbers of branch points. Values are expressed as average ± SD. b PKH26-labeled UC-MSCs ( red ) became the basis of a mixed culture network, while PKH67-labeled EA.hy926 cells ( green ) were only associated with it. Scale bar 100 μm. c Cluster formation. ( Left ) Representative images of tight clusters formed in Matrigel by UC-MSCs, or EA.hy926 cells, or mixed UC-MSC-EA.hy926 cells 24 hours after seeding. Macrophotograph of the 48-well plate. ( Right ) Quantification of numbers of clusters. Values are expressed as average ± SD of three replicates. * p
Techniques Used: Tube Formation Assay, Cell Culture, Labeling

Figure Legend Snippet: Cell culture characterization. a Human UC-MSC immunophenotype, positive for CD73, CD90, and CD105 and negative for CD45, CD34, CD11b, CD19, and HLA-DR. b Multilineage differentiation of UC-MSCs. Differentiation into adipocytes was revealed by Sudan III staining for intracellular accumulated lipids. Differentiation into osteocytes was revealed by Alizarin Red S staining for calcium mineralization. Chondrogenic differentiation was revealed by Alcian blue staining for mucopolysaccharides. Scale bar 100 μm. c Positive staining of EA.hy926 cells for CD31 as endothelial marker. Scale bar 100 μm. d Concentration of soluble forms of VEGF-A (VEGF-A-121 and VEGF-A-165) in the EA.hy926-conditioned media and the UC-MSC-conditioned media. Values are expressed as average ± SD of three replicates. * p
Techniques Used: Cell Culture, Staining, Marker, Concentration Assay

Figure Legend Snippet: Endothelial differentiation of UC-MSCs. a Endothelial differentiation of UC-MSCs in monolayer. Three endothelial induction media were used for UC-MSC culture: EA.hy926-conditioned media mixed 1:1 with growth media; EA.hy926-conditioned media mixed 1:1 with growth media supplemented with VEGF-A-165 (50 ng/ml); and growth media supplemented with VEGF-A-165. Only EA.hy926-conditioned media supplemented with VEGF-A-165 led to the appearance of CD31 + cells in the culture. Cell nuclei were stained with DAPI. Scale bar 100 μm. b Endothelial differentiation of UC-MSCs in Matrigel. Cryosections of secondary sprouts promoted by PKH26-labeled UC-MSCs ( red ). Immunostaining of sections showed that, upon coculturing with EA.hy926 in Matrigel, the UC-MSCs started to express CD31 ( green ). Cell nuclei were stained with DAPI. Scale bar 100 μm. VEGF vascular endothelial growth factor (Color figure online)
Techniques Used: Staining, Labeling, Immunostaining
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