dynamin ii Search Results


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Cell Signaling Technology Inc dynamin 2 2342 366
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Dynamin, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 85/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Becton Dickinson anti-dynamin-2
Dependence of CE on dynamin. (A) Localization of <t>dynamin-2</t> in uroepithelial tissue. The apical surface of an umbrella cell is indicated by arrows. (B) Effect of dynasore on CT during filling and voiding. Voiding was initiated at the arrow. The boxed region in the left panel is expanded in the right-hand panel. Control data are reproduced from Figure 1A. Values are mean±s.e.m. (n⩾5), and those values significantly different than control samples (P<0.5) are indicated with an asterisk. (C) Uptake of FITC-WGA and FITC-dextran in tissue treated with dynasore (250 μM). (D) Quantitation of FITC-WGA and FITC-dextran uptake in tissue treated with MβCD (10 mM), cyto-D (25 μg/ml), C3 toxin (1 μg/ml), dynasore (250 μM), or Y-27632 (25 μM). Values are mean±s.e.m. (n⩾10), and those values significantly different than control samples (P<0.05) are indicated with an asterisk. (E, F) Rat bladders were transduced in situ with adenovirus expressing GFP alone or GFP-labelled DN-dynaminK44A (DN-dynamin). The bladder was filled with Alexa647-WGA, stimulated to undergo voiding, excised, and then fixed and processed for immunofluorescence. (E) A transduced cell expressing DN-dynaminK44A (K44A) is indicated with an asterisk. (F) The uptake of Alex647-WGA was quantified in cells expressing GFP or DN-dynaminK44A (K44A) and normalized to uptake in adjacent cells that did not express exogenous protein. Data are mean±s.e.m. (n⩾70).
Anti Dynamin 2, 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/product/dynamin+ii/pmc02892371-419-15-21?v=Becton+Dickinson
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Schmid GmbH pcdna3.1/dyn2
Dependence of CE on dynamin. (A) Localization of <t>dynamin-2</t> in uroepithelial tissue. The apical surface of an umbrella cell is indicated by arrows. (B) Effect of dynasore on CT during filling and voiding. Voiding was initiated at the arrow. The boxed region in the left panel is expanded in the right-hand panel. Control data are reproduced from Figure 1A. Values are mean±s.e.m. (n⩾5), and those values significantly different than control samples (P<0.5) are indicated with an asterisk. (C) Uptake of FITC-WGA and FITC-dextran in tissue treated with dynasore (250 μM). (D) Quantitation of FITC-WGA and FITC-dextran uptake in tissue treated with MβCD (10 mM), cyto-D (25 μg/ml), C3 toxin (1 μg/ml), dynasore (250 μM), or Y-27632 (25 μM). Values are mean±s.e.m. (n⩾10), and those values significantly different than control samples (P<0.05) are indicated with an asterisk. (E, F) Rat bladders were transduced in situ with adenovirus expressing GFP alone or GFP-labelled DN-dynaminK44A (DN-dynamin). The bladder was filled with Alexa647-WGA, stimulated to undergo voiding, excised, and then fixed and processed for immunofluorescence. (E) A transduced cell expressing DN-dynaminK44A (K44A) is indicated with an asterisk. (F) The uptake of Alex647-WGA was quantified in cells expressing GFP or DN-dynaminK44A (K44A) and normalized to uptake in adjacent cells that did not express exogenous protein. Data are mean±s.e.m. (n⩾70).
Pcdna3.1/Dyn2, supplied by Schmid GmbH, 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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Schmid GmbH anti-dynamin ii antibodies
Dependence of CE on dynamin. (A) Localization of <t>dynamin-2</t> in uroepithelial tissue. The apical surface of an umbrella cell is indicated by arrows. (B) Effect of dynasore on CT during filling and voiding. Voiding was initiated at the arrow. The boxed region in the left panel is expanded in the right-hand panel. Control data are reproduced from Figure 1A. Values are mean±s.e.m. (n⩾5), and those values significantly different than control samples (P<0.5) are indicated with an asterisk. (C) Uptake of FITC-WGA and FITC-dextran in tissue treated with dynasore (250 μM). (D) Quantitation of FITC-WGA and FITC-dextran uptake in tissue treated with MβCD (10 mM), cyto-D (25 μg/ml), C3 toxin (1 μg/ml), dynasore (250 μM), or Y-27632 (25 μM). Values are mean±s.e.m. (n⩾10), and those values significantly different than control samples (P<0.05) are indicated with an asterisk. (E, F) Rat bladders were transduced in situ with adenovirus expressing GFP alone or GFP-labelled DN-dynaminK44A (DN-dynamin). The bladder was filled with Alexa647-WGA, stimulated to undergo voiding, excised, and then fixed and processed for immunofluorescence. (E) A transduced cell expressing DN-dynaminK44A (K44A) is indicated with an asterisk. (F) The uptake of Alex647-WGA was quantified in cells expressing GFP or DN-dynaminK44A (K44A) and normalized to uptake in adjacent cells that did not express exogenous protein. Data are mean±s.e.m. (n⩾70).
Anti Dynamin Ii Antibodies, supplied by Schmid GmbH, 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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Chiron Technologies Ltd dynamin ii peptides 607cdsqedvdswkasflra and 858ptiirpaepslld
Dependence of CE on dynamin. (A) Localization of <t>dynamin-2</t> in uroepithelial tissue. The apical surface of an umbrella cell is indicated by arrows. (B) Effect of dynasore on CT during filling and voiding. Voiding was initiated at the arrow. The boxed region in the left panel is expanded in the right-hand panel. Control data are reproduced from Figure 1A. Values are mean±s.e.m. (n⩾5), and those values significantly different than control samples (P<0.5) are indicated with an asterisk. (C) Uptake of FITC-WGA and FITC-dextran in tissue treated with dynasore (250 μM). (D) Quantitation of FITC-WGA and FITC-dextran uptake in tissue treated with MβCD (10 mM), cyto-D (25 μg/ml), C3 toxin (1 μg/ml), dynasore (250 μM), or Y-27632 (25 μM). Values are mean±s.e.m. (n⩾10), and those values significantly different than control samples (P<0.05) are indicated with an asterisk. (E, F) Rat bladders were transduced in situ with adenovirus expressing GFP alone or GFP-labelled DN-dynaminK44A (DN-dynamin). The bladder was filled with Alexa647-WGA, stimulated to undergo voiding, excised, and then fixed and processed for immunofluorescence. (E) A transduced cell expressing DN-dynaminK44A (K44A) is indicated with an asterisk. (F) The uptake of Alex647-WGA was quantified in cells expressing GFP or DN-dynaminK44A (K44A) and normalized to uptake in adjacent cells that did not express exogenous protein. Data are mean±s.e.m. (n⩾70).
Dynamin Ii Peptides 607cdsqedvdswkasflra And 858ptiirpaepslld, supplied by Chiron Technologies Ltd, 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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Image Search Results


Dependence of CE on dynamin. (A) Localization of dynamin-2 in uroepithelial tissue. The apical surface of an umbrella cell is indicated by arrows. (B) Effect of dynasore on CT during filling and voiding. Voiding was initiated at the arrow. The boxed region in the left panel is expanded in the right-hand panel. Control data are reproduced from Figure 1A. Values are mean±s.e.m. (n⩾5), and those values significantly different than control samples (P<0.5) are indicated with an asterisk. (C) Uptake of FITC-WGA and FITC-dextran in tissue treated with dynasore (250 μM). (D) Quantitation of FITC-WGA and FITC-dextran uptake in tissue treated with MβCD (10 mM), cyto-D (25 μg/ml), C3 toxin (1 μg/ml), dynasore (250 μM), or Y-27632 (25 μM). Values are mean±s.e.m. (n⩾10), and those values significantly different than control samples (P<0.05) are indicated with an asterisk. (E, F) Rat bladders were transduced in situ with adenovirus expressing GFP alone or GFP-labelled DN-dynaminK44A (DN-dynamin). The bladder was filled with Alexa647-WGA, stimulated to undergo voiding, excised, and then fixed and processed for immunofluorescence. (E) A transduced cell expressing DN-dynaminK44A (K44A) is indicated with an asterisk. (F) The uptake of Alex647-WGA was quantified in cells expressing GFP or DN-dynaminK44A (K44A) and normalized to uptake in adjacent cells that did not express exogenous protein. Data are mean±s.e.m. (n⩾70).

Journal: The EMBO Journal

Article Title: Compensatory endocytosis in bladder umbrella cells occurs through an integrin-regulated and RhoA- and dynamin-dependent pathway

doi: 10.1038/emboj.2010.91

Figure Lengend Snippet: Dependence of CE on dynamin. (A) Localization of dynamin-2 in uroepithelial tissue. The apical surface of an umbrella cell is indicated by arrows. (B) Effect of dynasore on CT during filling and voiding. Voiding was initiated at the arrow. The boxed region in the left panel is expanded in the right-hand panel. Control data are reproduced from Figure 1A. Values are mean±s.e.m. (n⩾5), and those values significantly different than control samples (P<0.5) are indicated with an asterisk. (C) Uptake of FITC-WGA and FITC-dextran in tissue treated with dynasore (250 μM). (D) Quantitation of FITC-WGA and FITC-dextran uptake in tissue treated with MβCD (10 mM), cyto-D (25 μg/ml), C3 toxin (1 μg/ml), dynasore (250 μM), or Y-27632 (25 μM). Values are mean±s.e.m. (n⩾10), and those values significantly different than control samples (P<0.05) are indicated with an asterisk. (E, F) Rat bladders were transduced in situ with adenovirus expressing GFP alone or GFP-labelled DN-dynaminK44A (DN-dynamin). The bladder was filled with Alexa647-WGA, stimulated to undergo voiding, excised, and then fixed and processed for immunofluorescence. (E) A transduced cell expressing DN-dynaminK44A (K44A) is indicated with an asterisk. (F) The uptake of Alex647-WGA was quantified in cells expressing GFP or DN-dynaminK44A (K44A) and normalized to uptake in adjacent cells that did not express exogenous protein. Data are mean±s.e.m. (n⩾70).

Article Snippet: Other antibodies used in these studies include mouse monoclonal antibodies specific for caveolin-1 and -2, dynamin-2, EEA1, and flotillin-1 (all from BD Biosciences; San Jose, CA), mouse monoclonal anti-giantin (provided by Dr Adam Linstedt, Carnegie Mellon University), and mouse monoclonal anti-AP2 α subunit antibody AP.6 and anti-clathrin heavy chain (provided by Dr Linton Traub, University of Pittsburgh).

Techniques: Quantitation Assay, In Situ, Expressing, Immunofluorescence