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pe conjugated monoclonal anti human integrin alpha 5 itga5 antibody  (Miltenyi Biotec)


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    Structured Review

    Miltenyi Biotec pe conjugated monoclonal anti human integrin alpha 5 itga5 antibody
    Pe Conjugated Monoclonal Anti Human Integrin Alpha 5 Itga5 Antibody, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 94/100, based on 10 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/integrin+alpha+5+cd49e/CD49e+Antibody%2C+anti-human%2C+REAfinity/pmc12966326-219-56-64
    Average 94 stars, based on 10 article reviews
    pe conjugated monoclonal anti human integrin alpha 5 itga5 antibody - by Bioz Stars, 2026-09
    94/100 stars

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    Related Articles

    Flow Cytometry:

    Article Title: Splenectomy reduces shear stress and inflammation in liver endothelial cells during regeneration after partial hepatectomy in mice.
    Article Snippet: .. Flow cytometry A 105 aliquote of LSECs isolated using magnetic sorting for the CD146 marker were incubated in 100 μl Rinsing Solution (Miltenyi Biotec, USA) with 5 μl primary antibodies to CD31 (PECAM-1) (PE-labeled, 130-111-540, clone REA784 | 390, Miltenyi Biotec, USA), integrin alpha-5 (CD49e) (PE-labeled, 130-122-072, AR TIC LE IN PR ES S clone REA1183 | 5H10-27, Miltenyi Biotec, USA), VCAM-1 (CD106) (PE-labeled, 130-116-323, clone REA971 | 429, Miltenyi Biotec, USA), VE-cadherin (CD144) (PE-labeled, 130-128-207, clone REA225 | BV13, Miltenyi Biotec, USA), Ki67 (FITC-labeled, 130- 117-691, clone REA183 | B56 Miltenyi Biotec, USA), CD146 (130- 102-230, clone ME-9F1, Miltenyi Biotec, USA), F4/80 (130-102- 422, REA126 | BM8, Miltenyi Biotec, USA ) at room temperature for 1 hour. .. The dynamics of CD3+ lymphocytes and NK1.1 cells in regenerating livers were analyzed similarly using 105 cells of the liver stromal fraction and primary antibodies to CD45 (PE-labeled, 130-102-596, clone 30F11, Miltenyi Biotec, USA), CD3 (APClabeled, MCA500APC, clone KT3, Bio-Rad USA), NK1.1 (VioBluelabeled, Biolegend, USA); the incubations proceeded for 1 hour.

    Article Title: Splenectomy reduces shear stress and inflammation in liver endothelial cells during regeneration after partial hepatectomy in mice
    Article Snippet: .. A 10 5 aliquote of LSECs isolated using magnetic sorting for the CD146 marker were incubated in 100 μl Rinsing Solution (Miltenyi Biotec, USA) with 5 μl primary antibodies to CD31 (PECAM-1) (PE-labeled, 130–111-540, clone REA784 | 390, Miltenyi Biotec, USA), integrin alpha-5 (CD49e) (PE-labeled, 130–122-072, clone REA1183 | 5H10-27, Miltenyi Biotec, USA), VCAM-1 (CD106) (PE-labeled, 130–116-323, clone REA971 | 429, Miltenyi Biotec, USA), VE-cadherin (CD144) (PE-labeled, 130–128-207, clone REA225 | BV13, Miltenyi Biotec, USA), Ki67 (FITC-labeled, 130–117-691, clone REA183 | B56 Miltenyi Biotec, USA), CD146 (130–102-230, clone ME-9F1, Miltenyi Biotec, USA), F4/80 (130–102-422, REA126 | BM8, Miltenyi Biotec, USA ) at room temperature for 1 h. The dynamics of CD3 + lymphocytes and NK1.1 cells in regenerating livers were analyzed similarly using 10 5 cells of the liver stromal fraction and primary antibodies to CD45 (PE-labeled, 130–102-596, clone 30F11, Miltenyi Biotec, USA), CD3 (APC-labeled, MCA500APC, clone KT3, Bio-Rad USA), NK1.1 (VioBlue-labeled, Biolegend, USA); the incubations proceeded for 1 h. Following the incubations, the cells were washed in PBS, resuspended in 0.5 ml PBS and analyzed in a MACSQuant 10 flow cytometer (Milteniy Biotech, Germany); the data were analyzed in FlowJo (LLC). ..

    Isolation:

    Article Title: Splenectomy reduces shear stress and inflammation in liver endothelial cells during regeneration after partial hepatectomy in mice.
    Article Snippet: .. Flow cytometry A 105 aliquote of LSECs isolated using magnetic sorting for the CD146 marker were incubated in 100 μl Rinsing Solution (Miltenyi Biotec, USA) with 5 μl primary antibodies to CD31 (PECAM-1) (PE-labeled, 130-111-540, clone REA784 | 390, Miltenyi Biotec, USA), integrin alpha-5 (CD49e) (PE-labeled, 130-122-072, AR TIC LE IN PR ES S clone REA1183 | 5H10-27, Miltenyi Biotec, USA), VCAM-1 (CD106) (PE-labeled, 130-116-323, clone REA971 | 429, Miltenyi Biotec, USA), VE-cadherin (CD144) (PE-labeled, 130-128-207, clone REA225 | BV13, Miltenyi Biotec, USA), Ki67 (FITC-labeled, 130- 117-691, clone REA183 | B56 Miltenyi Biotec, USA), CD146 (130- 102-230, clone ME-9F1, Miltenyi Biotec, USA), F4/80 (130-102- 422, REA126 | BM8, Miltenyi Biotec, USA ) at room temperature for 1 hour. .. The dynamics of CD3+ lymphocytes and NK1.1 cells in regenerating livers were analyzed similarly using 105 cells of the liver stromal fraction and primary antibodies to CD45 (PE-labeled, 130-102-596, clone 30F11, Miltenyi Biotec, USA), CD3 (APClabeled, MCA500APC, clone KT3, Bio-Rad USA), NK1.1 (VioBluelabeled, Biolegend, USA); the incubations proceeded for 1 hour.

    Article Title: Splenectomy reduces shear stress and inflammation in liver endothelial cells during regeneration after partial hepatectomy in mice
    Article Snippet: .. A 10 5 aliquote of LSECs isolated using magnetic sorting for the CD146 marker were incubated in 100 μl Rinsing Solution (Miltenyi Biotec, USA) with 5 μl primary antibodies to CD31 (PECAM-1) (PE-labeled, 130–111-540, clone REA784 | 390, Miltenyi Biotec, USA), integrin alpha-5 (CD49e) (PE-labeled, 130–122-072, clone REA1183 | 5H10-27, Miltenyi Biotec, USA), VCAM-1 (CD106) (PE-labeled, 130–116-323, clone REA971 | 429, Miltenyi Biotec, USA), VE-cadherin (CD144) (PE-labeled, 130–128-207, clone REA225 | BV13, Miltenyi Biotec, USA), Ki67 (FITC-labeled, 130–117-691, clone REA183 | B56 Miltenyi Biotec, USA), CD146 (130–102-230, clone ME-9F1, Miltenyi Biotec, USA), F4/80 (130–102-422, REA126 | BM8, Miltenyi Biotec, USA ) at room temperature for 1 h. The dynamics of CD3 + lymphocytes and NK1.1 cells in regenerating livers were analyzed similarly using 10 5 cells of the liver stromal fraction and primary antibodies to CD45 (PE-labeled, 130–102-596, clone 30F11, Miltenyi Biotec, USA), CD3 (APC-labeled, MCA500APC, clone KT3, Bio-Rad USA), NK1.1 (VioBlue-labeled, Biolegend, USA); the incubations proceeded for 1 h. Following the incubations, the cells were washed in PBS, resuspended in 0.5 ml PBS and analyzed in a MACSQuant 10 flow cytometer (Milteniy Biotech, Germany); the data were analyzed in FlowJo (LLC). ..

    Marker:

    Article Title: Splenectomy reduces shear stress and inflammation in liver endothelial cells during regeneration after partial hepatectomy in mice.
    Article Snippet: .. Flow cytometry A 105 aliquote of LSECs isolated using magnetic sorting for the CD146 marker were incubated in 100 μl Rinsing Solution (Miltenyi Biotec, USA) with 5 μl primary antibodies to CD31 (PECAM-1) (PE-labeled, 130-111-540, clone REA784 | 390, Miltenyi Biotec, USA), integrin alpha-5 (CD49e) (PE-labeled, 130-122-072, AR TIC LE IN PR ES S clone REA1183 | 5H10-27, Miltenyi Biotec, USA), VCAM-1 (CD106) (PE-labeled, 130-116-323, clone REA971 | 429, Miltenyi Biotec, USA), VE-cadherin (CD144) (PE-labeled, 130-128-207, clone REA225 | BV13, Miltenyi Biotec, USA), Ki67 (FITC-labeled, 130- 117-691, clone REA183 | B56 Miltenyi Biotec, USA), CD146 (130- 102-230, clone ME-9F1, Miltenyi Biotec, USA), F4/80 (130-102- 422, REA126 | BM8, Miltenyi Biotec, USA ) at room temperature for 1 hour. .. The dynamics of CD3+ lymphocytes and NK1.1 cells in regenerating livers were analyzed similarly using 105 cells of the liver stromal fraction and primary antibodies to CD45 (PE-labeled, 130-102-596, clone 30F11, Miltenyi Biotec, USA), CD3 (APClabeled, MCA500APC, clone KT3, Bio-Rad USA), NK1.1 (VioBluelabeled, Biolegend, USA); the incubations proceeded for 1 hour.

    Article Title: Splenectomy reduces shear stress and inflammation in liver endothelial cells during regeneration after partial hepatectomy in mice
    Article Snippet: .. A 10 5 aliquote of LSECs isolated using magnetic sorting for the CD146 marker were incubated in 100 μl Rinsing Solution (Miltenyi Biotec, USA) with 5 μl primary antibodies to CD31 (PECAM-1) (PE-labeled, 130–111-540, clone REA784 | 390, Miltenyi Biotec, USA), integrin alpha-5 (CD49e) (PE-labeled, 130–122-072, clone REA1183 | 5H10-27, Miltenyi Biotec, USA), VCAM-1 (CD106) (PE-labeled, 130–116-323, clone REA971 | 429, Miltenyi Biotec, USA), VE-cadherin (CD144) (PE-labeled, 130–128-207, clone REA225 | BV13, Miltenyi Biotec, USA), Ki67 (FITC-labeled, 130–117-691, clone REA183 | B56 Miltenyi Biotec, USA), CD146 (130–102-230, clone ME-9F1, Miltenyi Biotec, USA), F4/80 (130–102-422, REA126 | BM8, Miltenyi Biotec, USA ) at room temperature for 1 h. The dynamics of CD3 + lymphocytes and NK1.1 cells in regenerating livers were analyzed similarly using 10 5 cells of the liver stromal fraction and primary antibodies to CD45 (PE-labeled, 130–102-596, clone 30F11, Miltenyi Biotec, USA), CD3 (APC-labeled, MCA500APC, clone KT3, Bio-Rad USA), NK1.1 (VioBlue-labeled, Biolegend, USA); the incubations proceeded for 1 h. Following the incubations, the cells were washed in PBS, resuspended in 0.5 ml PBS and analyzed in a MACSQuant 10 flow cytometer (Milteniy Biotech, Germany); the data were analyzed in FlowJo (LLC). ..

    Incubation:

    Article Title: Splenectomy reduces shear stress and inflammation in liver endothelial cells during regeneration after partial hepatectomy in mice.
    Article Snippet: .. Flow cytometry A 105 aliquote of LSECs isolated using magnetic sorting for the CD146 marker were incubated in 100 μl Rinsing Solution (Miltenyi Biotec, USA) with 5 μl primary antibodies to CD31 (PECAM-1) (PE-labeled, 130-111-540, clone REA784 | 390, Miltenyi Biotec, USA), integrin alpha-5 (CD49e) (PE-labeled, 130-122-072, AR TIC LE IN PR ES S clone REA1183 | 5H10-27, Miltenyi Biotec, USA), VCAM-1 (CD106) (PE-labeled, 130-116-323, clone REA971 | 429, Miltenyi Biotec, USA), VE-cadherin (CD144) (PE-labeled, 130-128-207, clone REA225 | BV13, Miltenyi Biotec, USA), Ki67 (FITC-labeled, 130- 117-691, clone REA183 | B56 Miltenyi Biotec, USA), CD146 (130- 102-230, clone ME-9F1, Miltenyi Biotec, USA), F4/80 (130-102- 422, REA126 | BM8, Miltenyi Biotec, USA ) at room temperature for 1 hour. .. The dynamics of CD3+ lymphocytes and NK1.1 cells in regenerating livers were analyzed similarly using 105 cells of the liver stromal fraction and primary antibodies to CD45 (PE-labeled, 130-102-596, clone 30F11, Miltenyi Biotec, USA), CD3 (APClabeled, MCA500APC, clone KT3, Bio-Rad USA), NK1.1 (VioBluelabeled, Biolegend, USA); the incubations proceeded for 1 hour.

    Article Title: Splenectomy reduces shear stress and inflammation in liver endothelial cells during regeneration after partial hepatectomy in mice
    Article Snippet: .. A 10 5 aliquote of LSECs isolated using magnetic sorting for the CD146 marker were incubated in 100 μl Rinsing Solution (Miltenyi Biotec, USA) with 5 μl primary antibodies to CD31 (PECAM-1) (PE-labeled, 130–111-540, clone REA784 | 390, Miltenyi Biotec, USA), integrin alpha-5 (CD49e) (PE-labeled, 130–122-072, clone REA1183 | 5H10-27, Miltenyi Biotec, USA), VCAM-1 (CD106) (PE-labeled, 130–116-323, clone REA971 | 429, Miltenyi Biotec, USA), VE-cadherin (CD144) (PE-labeled, 130–128-207, clone REA225 | BV13, Miltenyi Biotec, USA), Ki67 (FITC-labeled, 130–117-691, clone REA183 | B56 Miltenyi Biotec, USA), CD146 (130–102-230, clone ME-9F1, Miltenyi Biotec, USA), F4/80 (130–102-422, REA126 | BM8, Miltenyi Biotec, USA ) at room temperature for 1 h. The dynamics of CD3 + lymphocytes and NK1.1 cells in regenerating livers were analyzed similarly using 10 5 cells of the liver stromal fraction and primary antibodies to CD45 (PE-labeled, 130–102-596, clone 30F11, Miltenyi Biotec, USA), CD3 (APC-labeled, MCA500APC, clone KT3, Bio-Rad USA), NK1.1 (VioBlue-labeled, Biolegend, USA); the incubations proceeded for 1 h. Following the incubations, the cells were washed in PBS, resuspended in 0.5 ml PBS and analyzed in a MACSQuant 10 flow cytometer (Milteniy Biotech, Germany); the data were analyzed in FlowJo (LLC). ..



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    Figure 1. Features of the aptamer and tested bladder cancer cell lines. A) The secondary structure of H02 full-length and Apt-Itg (nucleotides from 18 to 51, boxed); structures of the H02 full-length and Apt-Itg were predicted by using Mfold web server, and the calculated change in Gibbs free energy (ΔG) values are reported. B) AlphaFold 3 molecular docking result of <t>integrin</t> 𝛼5𝛽1-Apt-Itg binding complex; Apt-Itg, integrin 𝛼5 and integrin 𝛽1 predicted structures are shown in yellow, light blue and red, respectively. The predicted interaction of Apt-Itg with integrin 𝛼5, involving D154 and Y208 residues, is framed on the side. C) The expression of integrin 𝛼5𝛽1 by human and murine bladder cancer cell lines evaluated by western blot analysis of the 𝛼5 and 𝛽1 chain of the integrin. The expression of the housekeeping protein 𝛼-tubulin was used to estimate the relative fold of expression of integrin chains D). MB49-Luc; murine bladder cancer cell line.
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    Image Search Results


    Figure 1. Features of the aptamer and tested bladder cancer cell lines. A) The secondary structure of H02 full-length and Apt-Itg (nucleotides from 18 to 51, boxed); structures of the H02 full-length and Apt-Itg were predicted by using Mfold web server, and the calculated change in Gibbs free energy (ΔG) values are reported. B) AlphaFold 3 molecular docking result of integrin 𝛼5𝛽1-Apt-Itg binding complex; Apt-Itg, integrin 𝛼5 and integrin 𝛽1 predicted structures are shown in yellow, light blue and red, respectively. The predicted interaction of Apt-Itg with integrin 𝛼5, involving D154 and Y208 residues, is framed on the side. C) The expression of integrin 𝛼5𝛽1 by human and murine bladder cancer cell lines evaluated by western blot analysis of the 𝛼5 and 𝛽1 chain of the integrin. The expression of the housekeeping protein 𝛼-tubulin was used to estimate the relative fold of expression of integrin chains D). MB49-Luc; murine bladder cancer cell line.

    Journal: Advanced healthcare materials

    Article Title: Urine-Stable Aptamer-Conjugated Gold Nanorods for the Early Detection of High-Grade Bladder Cancer Residual Disease.

    doi: 10.1002/adhm.202403314

    Figure Lengend Snippet: Figure 1. Features of the aptamer and tested bladder cancer cell lines. A) The secondary structure of H02 full-length and Apt-Itg (nucleotides from 18 to 51, boxed); structures of the H02 full-length and Apt-Itg were predicted by using Mfold web server, and the calculated change in Gibbs free energy (ΔG) values are reported. B) AlphaFold 3 molecular docking result of integrin 𝛼5𝛽1-Apt-Itg binding complex; Apt-Itg, integrin 𝛼5 and integrin 𝛽1 predicted structures are shown in yellow, light blue and red, respectively. The predicted interaction of Apt-Itg with integrin 𝛼5, involving D154 and Y208 residues, is framed on the side. C) The expression of integrin 𝛼5𝛽1 by human and murine bladder cancer cell lines evaluated by western blot analysis of the 𝛼5 and 𝛽1 chain of the integrin. The expression of the housekeeping protein 𝛼-tubulin was used to estimate the relative fold of expression of integrin chains D). MB49-Luc; murine bladder cancer cell line.

    Article Snippet: For cell binding of anti-integrin α5 antibody (Ab-Itg), 2.0 × 105 T24 cells were detached from culture plates as described above and left untreated or incubated with Human Integrin alpha 5/CD49e Alexa Fluor488-conjugated Antibody (dilution 1:10, R&D system, Minneapolis, MN) in DPBS supplemented with 0.1% bovine serum albumin.

    Techniques: Binding Assay, Expressing, Western Blot

    Figure 4. Integrin 𝛼5 silencing results in reduced Apt-Itg binding. A) T24, RT112, and MB49-Luc cells were left untreated (NT) or transfected with the indicated Integrin 𝛼5 siRNAs or siRNA ctrl. At 24 h post-transfection, cells were harvested, and cell lysates prepared and immunoblotted with anti- integrin 𝛼5 or anti-integrin 𝛽1 antibody. Equal loading was confirmed by immunoblot with anti-𝛼-tubulin antibody. The histograms indicate the integrin chains/𝛼-tubulin ratio of the densitometric signals. Values are shown relative to siRNA ctrl, arbitrarily set to 1. B) Binding of 1 μm Alexa647-Apt-Itg to human and murine bladder cancer cells following 24 h-transfection with si-ITG𝛼5 (blue) and siRNA ctrl (red). C) Binding of Alexa488-Ab-Itg to T24 cells 24 h post-transfection. (B, C) The histogram indicates gMFI of aptamer- or antibody-treated cells normalized to the gMFI of siRNA ctrl untreated cells (black), arbitrarily set to 1. Bars depict mean ± SD of two independent experiments. *p < 0.005, **p < 0.001, and ***p < 0.0001.

    Journal: Advanced healthcare materials

    Article Title: Urine-Stable Aptamer-Conjugated Gold Nanorods for the Early Detection of High-Grade Bladder Cancer Residual Disease.

    doi: 10.1002/adhm.202403314

    Figure Lengend Snippet: Figure 4. Integrin 𝛼5 silencing results in reduced Apt-Itg binding. A) T24, RT112, and MB49-Luc cells were left untreated (NT) or transfected with the indicated Integrin 𝛼5 siRNAs or siRNA ctrl. At 24 h post-transfection, cells were harvested, and cell lysates prepared and immunoblotted with anti- integrin 𝛼5 or anti-integrin 𝛽1 antibody. Equal loading was confirmed by immunoblot with anti-𝛼-tubulin antibody. The histograms indicate the integrin chains/𝛼-tubulin ratio of the densitometric signals. Values are shown relative to siRNA ctrl, arbitrarily set to 1. B) Binding of 1 μm Alexa647-Apt-Itg to human and murine bladder cancer cells following 24 h-transfection with si-ITG𝛼5 (blue) and siRNA ctrl (red). C) Binding of Alexa488-Ab-Itg to T24 cells 24 h post-transfection. (B, C) The histogram indicates gMFI of aptamer- or antibody-treated cells normalized to the gMFI of siRNA ctrl untreated cells (black), arbitrarily set to 1. Bars depict mean ± SD of two independent experiments. *p < 0.005, **p < 0.001, and ***p < 0.0001.

    Article Snippet: For cell binding of anti-integrin α5 antibody (Ab-Itg), 2.0 × 105 T24 cells were detached from culture plates as described above and left untreated or incubated with Human Integrin alpha 5/CD49e Alexa Fluor488-conjugated Antibody (dilution 1:10, R&D system, Minneapolis, MN) in DPBS supplemented with 0.1% bovine serum albumin.

    Techniques: Binding Assay, Transfection, Western Blot