function blocking antibodies against β1 integrin Search Results


90
Merck KGaA a function-blocking anti-integrin β1 monoclonal antibody (20 mg/l)
Flow cytometry analysis of <t>integrin</t> surface expression. Cells were washed in blocking solution and stained with specific monoclonal antibodies as listed in materials and methods. Mouse IgG1-PE or mouse IgG2a-PE antibodies were used as isotype controls. Fluorescence was analyzed using a FACScan flow cytometer. The relative fluorescence unit values are given in percentage difference to the parental cell lines. Parental cell lines were set as 100%. One of three independent experiments is shown here. *P≤0.05 vs. controls.
A Function Blocking Anti Integrin β1 Monoclonal Antibody (20 Mg/L), supplied by Merck KGaA, 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/a function-blocking anti-integrin β1 monoclonal antibody (20 mg/l)/product/Merck KGaA
Average 90 stars, based on 1 article reviews
a function-blocking anti-integrin β1 monoclonal antibody (20 mg/l) - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier

90
Merck KGaA anti-integrin β1 clone p4c10 mab1987
Flow cytometry analysis of <t>integrin</t> surface expression. Cells were washed in blocking solution and stained with specific monoclonal antibodies as listed in materials and methods. Mouse IgG1-PE or mouse IgG2a-PE antibodies were used as isotype controls. Fluorescence was analyzed using a FACScan flow cytometer. The relative fluorescence unit values are given in percentage difference to the parental cell lines. Parental cell lines were set as 100%. One of three independent experiments is shown here. *P≤0.05 vs. controls.
Anti Integrin β1 Clone P4c10 Mab1987, supplied by Merck KGaA, 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/anti-integrin β1 clone p4c10 mab1987/product/Merck KGaA
Average 90 stars, based on 1 article reviews
anti-integrin β1 clone p4c10 mab1987 - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier

90
Becton Dickinson blocking antibodies against α1, α2, β1 integrins
Flow cytometry analysis of <t>integrin</t> surface expression. Cells were washed in blocking solution and stained with specific monoclonal antibodies as listed in materials and methods. Mouse IgG1-PE or mouse IgG2a-PE antibodies were used as isotype controls. Fluorescence was analyzed using a FACScan flow cytometer. The relative fluorescence unit values are given in percentage difference to the parental cell lines. Parental cell lines were set as 100%. One of three independent experiments is shown here. *P≤0.05 vs. controls.
Blocking Antibodies Against α1, α2, β1 Integrins, supplied by Becton Dickinson, 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/blocking antibodies against α1, α2, β1 integrins/product/Becton Dickinson
Average 90 stars, based on 1 article reviews
blocking antibodies against α1, α2, β1 integrins - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier

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Flow cytometry analysis of integrin surface expression. Cells were washed in blocking solution and stained with specific monoclonal antibodies as listed in materials and methods. Mouse IgG1-PE or mouse IgG2a-PE antibodies were used as isotype controls. Fluorescence was analyzed using a FACScan flow cytometer. The relative fluorescence unit values are given in percentage difference to the parental cell lines. Parental cell lines were set as 100%. One of three independent experiments is shown here. *P≤0.05 vs. controls.

Journal: Oncology Letters

Article Title: Blocking integrin β1 decreases adhesion in chemoresistant urothelial cancer cell lines

doi: 10.3892/ol.2017.6883

Figure Lengend Snippet: Flow cytometry analysis of integrin surface expression. Cells were washed in blocking solution and stained with specific monoclonal antibodies as listed in materials and methods. Mouse IgG1-PE or mouse IgG2a-PE antibodies were used as isotype controls. Fluorescence was analyzed using a FACScan flow cytometer. The relative fluorescence unit values are given in percentage difference to the parental cell lines. Parental cell lines were set as 100%. One of three independent experiments is shown here. *P≤0.05 vs. controls.

Article Snippet: Cells were preincubated for 60 min with a function-blocking anti-integrin β1 monoclonal antibody (20 mg/l) (MAB 2253Z; MerckMillipore, Darmstadt, Germany).

Techniques: Flow Cytometry, Expressing, Blocking Assay, Staining, Fluorescence

Expression of integrin β1 in non-malignant urothelium and urothelial cancer. (A) Normal urothelium showed a negative or a weak expression of intergrin β1 only in the basal cell layer. A higher integrin β1 expression was visible in samples of (B) non invasive low grade urothelial cancer, (C) non invasive high grade cancer, and (D) muscle invasive high grade cancer. Immunostaining of 4 representative tissue samples.

Journal: Oncology Letters

Article Title: Blocking integrin β1 decreases adhesion in chemoresistant urothelial cancer cell lines

doi: 10.3892/ol.2017.6883

Figure Lengend Snippet: Expression of integrin β1 in non-malignant urothelium and urothelial cancer. (A) Normal urothelium showed a negative or a weak expression of intergrin β1 only in the basal cell layer. A higher integrin β1 expression was visible in samples of (B) non invasive low grade urothelial cancer, (C) non invasive high grade cancer, and (D) muscle invasive high grade cancer. Immunostaining of 4 representative tissue samples.

Article Snippet: Cells were preincubated for 60 min with a function-blocking anti-integrin β1 monoclonal antibody (20 mg/l) (MAB 2253Z; MerckMillipore, Darmstadt, Germany).

Techniques: Expressing, Immunostaining

Influence on adhesion after blocking integrin β1. Bladder cancer cell lines were preincubated for 60 min with a monoclonal anti-integrin β1 blocking antibody (20 mg/l). Controls remained untreated. Cells were then subjected to the adhesion assay as indicated. Untreated parental cells were set as 100%. *P≤0.05 vs. controls.

Journal: Oncology Letters

Article Title: Blocking integrin β1 decreases adhesion in chemoresistant urothelial cancer cell lines

doi: 10.3892/ol.2017.6883

Figure Lengend Snippet: Influence on adhesion after blocking integrin β1. Bladder cancer cell lines were preincubated for 60 min with a monoclonal anti-integrin β1 blocking antibody (20 mg/l). Controls remained untreated. Cells were then subjected to the adhesion assay as indicated. Untreated parental cells were set as 100%. *P≤0.05 vs. controls.

Article Snippet: Cells were preincubated for 60 min with a function-blocking anti-integrin β1 monoclonal antibody (20 mg/l) (MAB 2253Z; MerckMillipore, Darmstadt, Germany).

Techniques: Blocking Assay, Cell Adhesion Assay

Influence on chemotaxis after blocking integrin β1. Bladder cancer cell lines were preincubated for 60 min with a monoclonal anti-integrin β1 blocking antibody (20 mg/l). Controls remained untreated. Cells were then subjected to the chemotaxis assay as indicated. Untreated parental cells were set as 100%. *P≤0.05 vs. controls.

Journal: Oncology Letters

Article Title: Blocking integrin β1 decreases adhesion in chemoresistant urothelial cancer cell lines

doi: 10.3892/ol.2017.6883

Figure Lengend Snippet: Influence on chemotaxis after blocking integrin β1. Bladder cancer cell lines were preincubated for 60 min with a monoclonal anti-integrin β1 blocking antibody (20 mg/l). Controls remained untreated. Cells were then subjected to the chemotaxis assay as indicated. Untreated parental cells were set as 100%. *P≤0.05 vs. controls.

Article Snippet: Cells were preincubated for 60 min with a function-blocking anti-integrin β1 monoclonal antibody (20 mg/l) (MAB 2253Z; MerckMillipore, Darmstadt, Germany).

Techniques: Chemotaxis Assay, Blocking Assay