anti ha polyclonal antibody (Proteintech)
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Proteintech
anti ha polyclonal antibody
Anti Ha Polyclonal Antibody, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 1639 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/anti+ha+polyclonal+antibody/GFP+tag+Antibody/pm41910148-174-72-75
Average 96 stars, based on 1639 article reviews
Anti Ha Polyclonal Antibody, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 1639 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/anti+ha+polyclonal+antibody/GFP+tag+Antibody/pm41910148-174-72-75
Average 96 stars, based on 1639 article reviews
anti ha polyclonal antibody - by Bioz Stars,
2026-09
96/100 stars
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Fluorescence:Article Title: Glycosylated NS3/NS3A protein of bluetongue virus facilitates efficient viral egress via lipid raft anchoring. Article Snippet: .. Commercial antibodies used in this study included anti-FLAG (DYKDDDDK) monoclonal antibody (1:1,000 for immuno fluorescence assay [IFA], 1:10,000 for western blotting [WB]; 66008-4-Ig, Proteintech), Immunofluorescence:Article Title: Glycosylated NS3/NS3A protein of bluetongue virus facilitates efficient viral egress via lipid raft anchoring. Article Snippet: .. Commercial antibodies used in this study included anti-FLAG (DYKDDDDK) monoclonal antibody (1:1,000 for immuno fluorescence assay [IFA], 1:10,000 for western blotting [WB]; 66008-4-Ig, Proteintech), Article Title: Glycosylated NS3/NS3A protein of bluetongue virus facilitates efficient viral egress via lipid raft anchoring Article Snippet: .. Commercial antibodies used in this study included anti-FLAG (DYKDDDDK) monoclonal antibody (1:1,000 for immunofluorescence assay [IFA], 1:10,000 for western blotting [WB]; 66008-4-Ig, Proteintech), Western Blot:Article Title: Glycosylated NS3/NS3A protein of bluetongue virus facilitates efficient viral egress via lipid raft anchoring. Article Snippet: .. Commercial antibodies used in this study included anti-FLAG (DYKDDDDK) monoclonal antibody (1:1,000 for immuno fluorescence assay [IFA], 1:10,000 for western blotting [WB]; 66008-4-Ig, Proteintech), Article Title: Ubiquitously expressed transcript isoform 2 (UXT-V2) restricts HSV-2 replication by targeting glycoprotein B for degradation through ubiquitin-proteasome pathway Article Snippet: .. The commercial antibodies used in this study include: anti-Flag monoclonal antibody (1:5000 for immunoblotting, Sigma, St. Louis, MO; F3165), anti-His monoclonal antibody (1:2500 for immunoblotting, Sigma A7058), Article Title: Uropathogenic Escherichia coli invade luminal prostate cells via FimH-PPAP receptor binding. Article Snippet: Cells were collected at 48 h post transfection in lysis buffer containing 1% NP-40, 5% glycerol, 25 mM Tris, 150 mM NaCl, 1 mM EDTA and protease inhibitor cocktail (05892791001, Sigma-Aldrich). .. Cell lysis was completed by incubation on ice for 1 h, followed by centrifugation at 15,000 × g for 1 h. Pellets were discarded and PPAP expression was examined by western blot using Article Title: Uropathogenic Escherichia coli invade luminal prostate cells via FimH–PPAP receptor binding Article Snippet: Cells were collected at 48 h post transfection in lysis buffer containing 1% NP-40, 5% glycerol, 25 mM Tris, 150 mM NaCl, 1 mM EDTA and protease inhibitor cocktail (05892791001, Sigma-Aldrich). .. Cell lysis was completed by incubation on ice for 1 h, followed by centrifugation at 15,000 × g for 1 h. Pellets were discarded and PPAP expression was examined by western blot using Article Title: Glycosylated NS3/NS3A protein of bluetongue virus facilitates efficient viral egress via lipid raft anchoring Article Snippet: .. Commercial antibodies used in this study included anti-FLAG (DYKDDDDK) monoclonal antibody (1:1,000 for immunofluorescence assay [IFA], 1:10,000 for western blotting [WB]; 66008-4-Ig, Proteintech), Lysis:Article Title: Uropathogenic Escherichia coli invade luminal prostate cells via FimH-PPAP receptor binding. Article Snippet: Cells were collected at 48 h post transfection in lysis buffer containing 1% NP-40, 5% glycerol, 25 mM Tris, 150 mM NaCl, 1 mM EDTA and protease inhibitor cocktail (05892791001, Sigma-Aldrich). .. Cell lysis was completed by incubation on ice for 1 h, followed by centrifugation at 15,000 × g for 1 h. Pellets were discarded and PPAP expression was examined by western blot using Article Title: Uropathogenic Escherichia coli invade luminal prostate cells via FimH–PPAP receptor binding Article Snippet: Cells were collected at 48 h post transfection in lysis buffer containing 1% NP-40, 5% glycerol, 25 mM Tris, 150 mM NaCl, 1 mM EDTA and protease inhibitor cocktail (05892791001, Sigma-Aldrich). .. Cell lysis was completed by incubation on ice for 1 h, followed by centrifugation at 15,000 × g for 1 h. Pellets were discarded and PPAP expression was examined by western blot using Incubation:Article Title: Uropathogenic Escherichia coli invade luminal prostate cells via FimH-PPAP receptor binding. Article Snippet: Cells were collected at 48 h post transfection in lysis buffer containing 1% NP-40, 5% glycerol, 25 mM Tris, 150 mM NaCl, 1 mM EDTA and protease inhibitor cocktail (05892791001, Sigma-Aldrich). .. Cell lysis was completed by incubation on ice for 1 h, followed by centrifugation at 15,000 × g for 1 h. Pellets were discarded and PPAP expression was examined by western blot using Article Title: Uropathogenic Escherichia coli invade luminal prostate cells via FimH–PPAP receptor binding Article Snippet: Cells were collected at 48 h post transfection in lysis buffer containing 1% NP-40, 5% glycerol, 25 mM Tris, 150 mM NaCl, 1 mM EDTA and protease inhibitor cocktail (05892791001, Sigma-Aldrich). .. Cell lysis was completed by incubation on ice for 1 h, followed by centrifugation at 15,000 × g for 1 h. Pellets were discarded and PPAP expression was examined by western blot using Centrifugation:Article Title: Uropathogenic Escherichia coli invade luminal prostate cells via FimH-PPAP receptor binding. Article Snippet: Cells were collected at 48 h post transfection in lysis buffer containing 1% NP-40, 5% glycerol, 25 mM Tris, 150 mM NaCl, 1 mM EDTA and protease inhibitor cocktail (05892791001, Sigma-Aldrich). .. Cell lysis was completed by incubation on ice for 1 h, followed by centrifugation at 15,000 × g for 1 h. Pellets were discarded and PPAP expression was examined by western blot using Article Title: Uropathogenic Escherichia coli invade luminal prostate cells via FimH–PPAP receptor binding Article Snippet: Cells were collected at 48 h post transfection in lysis buffer containing 1% NP-40, 5% glycerol, 25 mM Tris, 150 mM NaCl, 1 mM EDTA and protease inhibitor cocktail (05892791001, Sigma-Aldrich). .. Cell lysis was completed by incubation on ice for 1 h, followed by centrifugation at 15,000 × g for 1 h. Pellets were discarded and PPAP expression was examined by western blot using Expressing:Article Title: Uropathogenic Escherichia coli invade luminal prostate cells via FimH-PPAP receptor binding. Article Snippet: Cells were collected at 48 h post transfection in lysis buffer containing 1% NP-40, 5% glycerol, 25 mM Tris, 150 mM NaCl, 1 mM EDTA and protease inhibitor cocktail (05892791001, Sigma-Aldrich). .. Cell lysis was completed by incubation on ice for 1 h, followed by centrifugation at 15,000 × g for 1 h. Pellets were discarded and PPAP expression was examined by western blot using Article Title: Uropathogenic Escherichia coli invade luminal prostate cells via FimH–PPAP receptor binding Article Snippet: Cells were collected at 48 h post transfection in lysis buffer containing 1% NP-40, 5% glycerol, 25 mM Tris, 150 mM NaCl, 1 mM EDTA and protease inhibitor cocktail (05892791001, Sigma-Aldrich). .. Cell lysis was completed by incubation on ice for 1 h, followed by centrifugation at 15,000 × g for 1 h. Pellets were discarded and PPAP expression was examined by western blot using |