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human dermal blood endothelial cells  (PromoCell)


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    PromoCell human dermal blood endothelial cells
    Human Dermal Blood Endothelial Cells, supplied by PromoCell, used in various techniques. Bioz Stars score: 95/100, based on 80 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/human dermal blood endothelial cells/product/PromoCell
    Average 95 stars, based on 80 article reviews
    human dermal blood endothelial cells - by Bioz Stars, 2026-02
    95/100 stars

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    PromoCell primary human dermal blood endothelial cells hdbec
    Association of TF extracellular domain peptide constructs with cellular β1-integrin in <t>HDBEC.</t> HDBEC (5 × 10 4 ) were transfected to express TED, LED or UED constructs or control peptides. The interactions between the expressed peptides and β1-integrin were assessed by PLA using mouse anti-HA-tag (C29F4) and rabbit anti-β1-integrin antibodies. Positive controls were prepared using mouse anti-TF (HTF1) and rabbit anti-TF (FL295) antibodies, as well as mouse anti-TF (HTF1) and rabbit anti-β1-integrin antibodies. A negative control was prepared using the mouse anti-HA-tag antibody (C29F4) paired with a rabbit IgG isotype control antibody. ( A ) The cells were examined by fluorescence microscopy at ×40 magnification. ( B ) The number of red fluorescent interaction events and blue cell nuclei in each field of view was quantified using ImageJ.
    Primary Human Dermal Blood Endothelial Cells Hdbec, supplied by PromoCell, 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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    Association of TF extracellular domain peptide constructs with cellular β1-integrin in HDBEC. HDBEC (5 × 10 4 ) were transfected to express TED, LED or UED constructs or control peptides. The interactions between the expressed peptides and β1-integrin were assessed by PLA using mouse anti-HA-tag (C29F4) and rabbit anti-β1-integrin antibodies. Positive controls were prepared using mouse anti-TF (HTF1) and rabbit anti-TF (FL295) antibodies, as well as mouse anti-TF (HTF1) and rabbit anti-β1-integrin antibodies. A negative control was prepared using the mouse anti-HA-tag antibody (C29F4) paired with a rabbit IgG isotype control antibody. ( A ) The cells were examined by fluorescence microscopy at ×40 magnification. ( B ) The number of red fluorescent interaction events and blue cell nuclei in each field of view was quantified using ImageJ.

    Journal: Cancers

    Article Title: Identification of the Interacting Domains Between Tissue Factor and β1-Integrin and the Signalling Properties of the Two Fibronectin-like Domains of Tissue Factor

    doi: 10.3390/cancers17040644

    Figure Lengend Snippet: Association of TF extracellular domain peptide constructs with cellular β1-integrin in HDBEC. HDBEC (5 × 10 4 ) were transfected to express TED, LED or UED constructs or control peptides. The interactions between the expressed peptides and β1-integrin were assessed by PLA using mouse anti-HA-tag (C29F4) and rabbit anti-β1-integrin antibodies. Positive controls were prepared using mouse anti-TF (HTF1) and rabbit anti-TF (FL295) antibodies, as well as mouse anti-TF (HTF1) and rabbit anti-β1-integrin antibodies. A negative control was prepared using the mouse anti-HA-tag antibody (C29F4) paired with a rabbit IgG isotype control antibody. ( A ) The cells were examined by fluorescence microscopy at ×40 magnification. ( B ) The number of red fluorescent interaction events and blue cell nuclei in each field of view was quantified using ImageJ.

    Article Snippet: Primary human dermal blood endothelial cells (HDBEC) were obtained from PromoCell (Heidelberg, Germany) and cultured in MV media containing 5% ( v / v ) FCS and growth supplements (PromoCell).

    Techniques: Construct, Transfection, Control, Negative Control, Fluorescence, Microscopy

    Analysis of the availability of the EGF4-βTD domain following expression of TF peptides. ( A ) MDA-MB-231 cells (10 4 ) and ( B ) HDBEC (5 × 10 4 ) were transfected to express TED, LED, UED or control peptides. The cells were probed with an antibody against residues 579–799 of β1-integrin (EGF4 and βTD domains). The cells were then probed with HRP-conjugated anti-rabbit IgG antibody and developed using TMB-one solution HRP substrate. The amount of bound antibody was quantified by measuring the absorptions at 450 nm using a plate reader. Values were normalised to the number of cells in each well, as determined by crystal violet assay measurements.

    Journal: Cancers

    Article Title: Identification of the Interacting Domains Between Tissue Factor and β1-Integrin and the Signalling Properties of the Two Fibronectin-like Domains of Tissue Factor

    doi: 10.3390/cancers17040644

    Figure Lengend Snippet: Analysis of the availability of the EGF4-βTD domain following expression of TF peptides. ( A ) MDA-MB-231 cells (10 4 ) and ( B ) HDBEC (5 × 10 4 ) were transfected to express TED, LED, UED or control peptides. The cells were probed with an antibody against residues 579–799 of β1-integrin (EGF4 and βTD domains). The cells were then probed with HRP-conjugated anti-rabbit IgG antibody and developed using TMB-one solution HRP substrate. The amount of bound antibody was quantified by measuring the absorptions at 450 nm using a plate reader. Values were normalised to the number of cells in each well, as determined by crystal violet assay measurements.

    Article Snippet: Primary human dermal blood endothelial cells (HDBEC) were obtained from PromoCell (Heidelberg, Germany) and cultured in MV media containing 5% ( v / v ) FCS and growth supplements (PromoCell).

    Techniques: Expressing, Transfection, Control, Crystal Violet Assay

    The influence of TF extracellular domain peptide constructs on the conformation of cellular β1-integrin. ( A , B ) MDA-MB-231 cells (10 4 ) and ( C , D ) HDBEC (5 × 10 4 ) were transfected to express TED, LED, UED or control peptides. The cells were probed with antibodies that specifically recognised the ( A , C ) active/open (9EG7) or ( B , D ) inactive/closed (AIIB2) conformation of β1-integrin. The cells were then probed with HRP-conjugated anti-rat IgG or anti-rabbit IgG antibodies and developed using TMB-one solution HRP substrate. The amount of bound antibody was quantified by measuring the absorptions at 450 nm using a plate reader. Values were normalised to the number of cells in each well, as determined by crystal violet assay measurements.

    Journal: Cancers

    Article Title: Identification of the Interacting Domains Between Tissue Factor and β1-Integrin and the Signalling Properties of the Two Fibronectin-like Domains of Tissue Factor

    doi: 10.3390/cancers17040644

    Figure Lengend Snippet: The influence of TF extracellular domain peptide constructs on the conformation of cellular β1-integrin. ( A , B ) MDA-MB-231 cells (10 4 ) and ( C , D ) HDBEC (5 × 10 4 ) were transfected to express TED, LED, UED or control peptides. The cells were probed with antibodies that specifically recognised the ( A , C ) active/open (9EG7) or ( B , D ) inactive/closed (AIIB2) conformation of β1-integrin. The cells were then probed with HRP-conjugated anti-rat IgG or anti-rabbit IgG antibodies and developed using TMB-one solution HRP substrate. The amount of bound antibody was quantified by measuring the absorptions at 450 nm using a plate reader. Values were normalised to the number of cells in each well, as determined by crystal violet assay measurements.

    Article Snippet: Primary human dermal blood endothelial cells (HDBEC) were obtained from PromoCell (Heidelberg, Germany) and cultured in MV media containing 5% ( v / v ) FCS and growth supplements (PromoCell).

    Techniques: Construct, Transfection, Control, Crystal Violet Assay

    Comparison of the influence of protein constructs in TF + MDA-MB-231 and TF −  HDBEC.

    Journal: Cancers

    Article Title: Identification of the Interacting Domains Between Tissue Factor and β1-Integrin and the Signalling Properties of the Two Fibronectin-like Domains of Tissue Factor

    doi: 10.3390/cancers17040644

    Figure Lengend Snippet: Comparison of the influence of protein constructs in TF + MDA-MB-231 and TF − HDBEC.

    Article Snippet: Primary human dermal blood endothelial cells (HDBEC) were obtained from PromoCell (Heidelberg, Germany) and cultured in MV media containing 5% ( v / v ) FCS and growth supplements (PromoCell).

    Techniques: Comparison, Construct, Expressing

    The influence of TF extracellular domain peptide constructs on proliferative signalling in HDBEC. HDBEC (5 × 10 5 ) were transfected to express TED, LED, UED, EGF4-βTD or the control peptide. ( A ) Cells were lysed with Laemmli buffer, and Western blot analysis was carried out using antibodies against total ERK1/2, phosphorylated ERK1/2 and GAPDH. Images represent 2 separate experiments. ( B ) Band intensities were quantified using ImageJ and the ratio of pERK/tERK was calculated. ( C ) Cells were lysed, and the mRNA extracted and converted to cDNA using cell-2-cDNA kit. The expression of cyclin D1 and β-actin mRNA were measured using RT-PCR and the relative cyclin D1 expression levels calculated using the 2 −ΔΔCq method. ( D ) HDBEC (5 × 10 4 ) were transfected to express TED, LED, UED, EGF4-βTD or control peptide. The cells were incubated for 72 h and the number of cells were determined using the crystal violet assay.

    Journal: Cancers

    Article Title: Identification of the Interacting Domains Between Tissue Factor and β1-Integrin and the Signalling Properties of the Two Fibronectin-like Domains of Tissue Factor

    doi: 10.3390/cancers17040644

    Figure Lengend Snippet: The influence of TF extracellular domain peptide constructs on proliferative signalling in HDBEC. HDBEC (5 × 10 5 ) were transfected to express TED, LED, UED, EGF4-βTD or the control peptide. ( A ) Cells were lysed with Laemmli buffer, and Western blot analysis was carried out using antibodies against total ERK1/2, phosphorylated ERK1/2 and GAPDH. Images represent 2 separate experiments. ( B ) Band intensities were quantified using ImageJ and the ratio of pERK/tERK was calculated. ( C ) Cells were lysed, and the mRNA extracted and converted to cDNA using cell-2-cDNA kit. The expression of cyclin D1 and β-actin mRNA were measured using RT-PCR and the relative cyclin D1 expression levels calculated using the 2 −ΔΔCq method. ( D ) HDBEC (5 × 10 4 ) were transfected to express TED, LED, UED, EGF4-βTD or control peptide. The cells were incubated for 72 h and the number of cells were determined using the crystal violet assay.

    Article Snippet: Primary human dermal blood endothelial cells (HDBEC) were obtained from PromoCell (Heidelberg, Germany) and cultured in MV media containing 5% ( v / v ) FCS and growth supplements (PromoCell).

    Techniques: Construct, Transfection, Control, Western Blot, Expressing, Reverse Transcription Polymerase Chain Reaction, Incubation, Crystal Violet Assay