192-well amine-functionalized slides (Arrayit Corporation)
90
Structured Review
Arrayit Corporation
192-well amine-functionalized slides
192 Well Amine Functionalized Slides, supplied by Arrayit Corporation, 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/192-well+amine-functionalized+slides/protein+a+g+modified+192+well+slides/us12072479-175-69-74
Average 90 stars, based on 1 article reviews
192 Well Amine Functionalized Slides, supplied by Arrayit Corporation, 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/192-well+amine-functionalized+slides/protein+a+g+modified+192+well+slides/us12072479-175-69-74
Average 90 stars, based on 1 article reviews
192-well amine-functionalized slides - by Bioz Stars,
2026-09
90/100 stars
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Binding Assay:Article Title: Dark-field microscope apparatus utilizing portable electronic communication device Article Snippet: Binding Affinity Assay Carboxyl-functionalized gold nanorods (“AuNRs”) (C12-25-650-TC-50, Nanopartz) were activated to covalently bond amine groups by mixing 40 μL of AuNR (4.22×1012/mL) with 20 μL of EDC/NHS-sulfo phosphate buffered saline (“PBS”) (2 mg/mL of 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride and 1 mg/mL of N-hydroxysulfosuccinimide (Sigma-Aldrich) for 10 minutes at 25° C. These amine-reactive AuNRs were then PBS-washed and 1 μL of indicated AuNR concentrations were applied to replicate wells on Article Title: Dark-field microscope apparatus utilizing portable electronic communication device Article Snippet: Binding Affinity Assay Carboxyl-functionalized gold nanorods (“AuNRs”) (C12-25-650-TC-50, Nanopartz) were activated to covalently bond amine groups by mixing 40 μL of AuNR (4.22×1012/mL) with 20 μL of EDC/NHS-sulfo phosphate buffered saline (“PBS”) (2 mg/mL of 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride and 1 mg/mL of N-hydroxysulfosuccinimide (Sigma-Aldrich) for 10 minutes at 25° C. These amine-reactive AuNRs were then PBS-washed and 1 μL of indicated AuNR concentrations were applied to replicate wells on Saline:Article Title: Dark-field microscope apparatus utilizing portable electronic communication device Article Snippet: Binding Affinity Assay Carboxyl-functionalized gold nanorods (“AuNRs”) (C12-25-650-TC-50, Nanopartz) were activated to covalently bond amine groups by mixing 40 μL of AuNR (4.22×1012/mL) with 20 μL of EDC/NHS-sulfo phosphate buffered saline (“PBS”) (2 mg/mL of 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride and 1 mg/mL of N-hydroxysulfosuccinimide (Sigma-Aldrich) for 10 minutes at 25° C. These amine-reactive AuNRs were then PBS-washed and 1 μL of indicated AuNR concentrations were applied to replicate wells on Article Title: Dark-field microscope apparatus utilizing portable electronic communication device Article Snippet: Binding Affinity Assay Carboxyl-functionalized gold nanorods (“AuNRs”) (C12-25-650-TC-50, Nanopartz) were activated to covalently bond amine groups by mixing 40 μL of AuNR (4.22×1012/mL) with 20 μL of EDC/NHS-sulfo phosphate buffered saline (“PBS”) (2 mg/mL of 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride and 1 mg/mL of N-hydroxysulfosuccinimide (Sigma-Aldrich) for 10 minutes at 25° C. These amine-reactive AuNRs were then PBS-washed and 1 μL of indicated AuNR concentrations were applied to replicate wells on Sonication:Article Title: Dark-field microscope apparatus utilizing portable electronic communication device Article Snippet: Binding Affinity Assay Carboxyl-functionalized gold nanorods (“AuNRs”) (C12-25-650-TC-50, Nanopartz) were activated to covalently bond amine groups by mixing 40 μL of AuNR (4.22×1012/mL) with 20 μL of EDC/NHS-sulfo phosphate buffered saline (“PBS”) (2 mg/mL of 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride and 1 mg/mL of N-hydroxysulfosuccinimide (Sigma-Aldrich) for 10 minutes at 25° C. These amine-reactive AuNRs were then PBS-washed and 1 μL of indicated AuNR concentrations were applied to replicate wells on Article Title: Dark-field microscope apparatus utilizing portable electronic communication device Article Snippet: Binding Affinity Assay Carboxyl-functionalized gold nanorods (“AuNRs”) (C12-25-650-TC-50, Nanopartz) were activated to covalently bond amine groups by mixing 40 μL of AuNR (4.22×1012/mL) with 20 μL of EDC/NHS-sulfo phosphate buffered saline (“PBS”) (2 mg/mL of 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride and 1 mg/mL of N-hydroxysulfosuccinimide (Sigma-Aldrich) for 10 minutes at 25° C. These amine-reactive AuNRs were then PBS-washed and 1 μL of indicated AuNR concentrations were applied to replicate wells on Hybridization:Article Title: Dark-field microscope apparatus utilizing portable electronic communication device Article Snippet: Binding Affinity Assay Carboxyl-functionalized gold nanorods (“AuNRs”) (C12-25-650-TC-50, Nanopartz) were activated to covalently bond amine groups by mixing 40 μL of AuNR (4.22×1012/mL) with 20 μL of EDC/NHS-sulfo phosphate buffered saline (“PBS”) (2 mg/mL of 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride and 1 mg/mL of N-hydroxysulfosuccinimide (Sigma-Aldrich) for 10 minutes at 25° C. These amine-reactive AuNRs were then PBS-washed and 1 μL of indicated AuNR concentrations were applied to replicate wells on Article Title: Dark-field microscope apparatus utilizing portable electronic communication device Article Snippet: Binding Affinity Assay Carboxyl-functionalized gold nanorods (“AuNRs”) (C12-25-650-TC-50, Nanopartz) were activated to covalently bond amine groups by mixing 40 μL of AuNR (4.22×1012/mL) with 20 μL of EDC/NHS-sulfo phosphate buffered saline (“PBS”) (2 mg/mL of 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride and 1 mg/mL of N-hydroxysulfosuccinimide (Sigma-Aldrich) for 10 minutes at 25° C. These amine-reactive AuNRs were then PBS-washed and 1 μL of indicated AuNR concentrations were applied to replicate wells on |