anti zo2 (Cell Signaling Technology Inc)
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Cell Signaling Technology Inc
anti zo2
Anti Zo2, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 94/100, based on 105 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/anti+zo2/ZO-2+Antibody/pm41634022-347-14-16
Average 94 stars, based on 105 article reviews
Anti Zo2, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 94/100, based on 105 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/anti+zo2/ZO-2+Antibody/pm41634022-347-14-16
Average 94 stars, based on 105 article reviews
anti zo2 - by Bioz Stars,
2026-10
94/100 stars
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Incubation:Article Title: In vivo dual RNA-Seq uncovers key effectors of epithelial barrier disruption by an extracellular pathogen Article Snippet: 10 μg of total proteins were loaded on a 12% SDS-PAGE (Mini-PROTEAN TGX Stain-Free precast gels, Biorad) and transferred onto nitrocellulose membrane. .. The membranes were blocked with PBS Tween20 0.1% containing 5% BSA for 1 h at RT and incubated overnight at 4 °C with the antibodies anti-ZO1 (13663; Cell Signaling), Article Title: In vivo dual RNA-Seq uncovers key effectors of epithelial barrier disruption by an extracellular pathogen. Article Snippet: At the indicated times, the cells were fixed with 4% paraformaldehyde for 15min at room temperature (RT) and subsequently incubated for 10min in 0.5% saponin (Sigma) in PBS and for 1 h in 1% BSA (Sigma) and 0.075% saponin in PBS. .. The cells were incubated overnight at 4 °C with the anti-ZO1 (13663; Cell Signaling), Article Title: In vivo dual RNA-Seq uncovers key effectors of epithelial barrier disruption by an extracellular pathogen Article Snippet: At the indicated times, the cells were fixed with 4% paraformaldehyde for 15 min at room temperature (RT) and subsequently incubated for 10 min in 0.5% saponin (Sigma) in PBS and for 1 h in 1% BSA (Sigma) and 0.075% saponin in PBS. .. The cells were incubated overnight at 4 °C with the anti-ZO1 (13663; Cell Signaling), Article Title: In Vivo Dual RNA-Seq uncovers key toxin-like effectors of epithelial barrier disruption and tissue colonization by an extracellular bacterial pathogen Article Snippet: At the indicated times, the cells were fixed with 4% paraformaldehyde for 15 min at room temperature (RT) and subsequently incubated for 10 min in 0.5% saponin (Sigma) in PBS and for 1 hr in 1% BSA (Sigma) and 0.075% saponin in PBS. .. The cells were incubated overnight at 4°C with the anti-ZO1 (13663; Cell Signaling), Article Title: In vivo dual RNA-Seq uncovers key effectors of epithelial barrier disruption by an extracellular pathogen. Article Snippet: 10 μg of total proteins were loaded on a 12% SDS-PAGE (Mini-PROTEAN TGX Stain-Free precast gels, Biorad) and transferred onto nitrocellulose membrane. .. The membranes were blocked with PBS Tween20 0.1% containing 5% BSA for 1 h at RT and incubated overnight at 4 °C with the antibodies anti-ZO1 (13663; Cell Signaling), Article Title: In Vivo Dual RNA-Seq uncovers key toxin-like effectors of epithelial barrier disruption and tissue colonization by an extracellular bacterial pathogen Article Snippet: .. The membranes were blocked with PBS Tween20 0.1% containing 5% BSA for 1 hr at RT and incubated overnight at 4°C with the antibodies anti-ZO1 (13663; Cell Signaling), other:Article Title: The Host Interactome of Spike Expands the Tropism of SARS-CoV-2 Article Snippet: The plasma membrane was stained with CF594 dye conjugated wheat germ agglutinin (Biotium), while ER was stained with the ER Cytopainter staining kit (AbCam) according to manufacturer recommendations. Transferring:Article Title: The Host Interactome of Spike Expands the Tropism of SARS-CoV-2 Article Snippet: Images were taken with a Zeiss LSM 780 confocal laser scanning microscope and analyzed using Fiji/ImageJ (v.2.1.0/1.53c). .. One volume of 2x SDS sample loading buffer was added to samples in TN buffer (1:1; v:v) and samples were heated to 50°C for 15 min. Proteins were separated on NuPAGE 4-12% Bis-Tris gels (Life technologies) before transferring proteins onto Nitrocellulose membranes and incubating with anti-BiP (C50B12, Cell Signaling Laboratories (CSL)), anti-ZO1 (D7D12, CSL), |