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Arrayit Corporation slides superaldehyde 2
Slides Superaldehyde 2, 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/superaldehyde/slides+superaldehyde+2/pm33973474-40-0-9
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Microarray:

Article Title: Specific detection of stable single nucleobase mismatch using SU-8 coated silicon nanowires platform.
Article Snippet: Author’s Accepted Manuscript Specific detection of stable single nucleobase mismatch using SU-8 coated silicon nanowires platform Melania Banu, Monica Simion, Marian C. Popescu, Pericle Varasteanu, Mihaela Kusko, Ileana C. Farcasanu PII: S0039-9140(18)30335-7 DOI: https://doi.org/10.1016/j.talanta.2018.03.095 Reference: TAL18529 To appear in: Talanta Received date: 4 December 2017 Revised date: 26 March 2018 Accepted date: 29 March 2018 Cite this article as: Melania Banu, Monica Simion, Marian C. Popescu, Pericle Varasteanu, Mihaela Kusko and Ileana C. Farcasanu, Specific detection of stable single nucleobase mismatch using SU-8 coated silicon nanowires platform, Talanta, https://doi.org/10.1016/j.talanta.2018.03.095 This is a PDF file of an unedited manuscript that has been accepted for publication.. As a service to our customers we are providing this early version of the manuscript.. The manuscript will undergo copyediting, typesetting, and review of the resulting galley proof before it is published in its final citable form.

Article Title: Spatial Bias in Antibody Microarrays May Be an Underappreciated Source of Variability.
Article Snippet: Antibodies against epidermal growth factor (EGF) and recombinant protein were purchased from R&D Systems (Minneapolis, MN, USA) (Table S1). .. Slides SuperAldehyde 2 (SM1) and SuperEpoxy 2 (SM3) from Arrayit (Sunnyvale, CA, USA), 2D-Aldehyde (SM2) from PolyAn (Berlin, Germany), epoxyfunctionalized Slide E (SM4) from Schott Nexterion (Louisville, KY, USA), and nitrocellulose-functionalized protein microarray (SM5) from Intuitive Bioscience (Middleton, WI, USA) were used. ..

Membrane:

Article Title: Rapid Detection and Trapping of Extracellular Vesicles by Electrokinetic Concentration for Liquid Biopsy on Chip
Article Snippet: .. To demonstrate this flexibility of interfacing witha variety of substrates, we also used superaldehyde glass substrate (Arrayit) as well as plain glass slide with 3D-printed microtraps to passively trap extracellular vesicles near the ion-selective membrane during ICP at 45 V/cm within 30 min. .. The traps (a semicircle of 2 μm in diameter was inscribed in a 2 μm × 4 μm rectangle at a height of ~4 μm.) were fabricated on a fused silica substrate using a two-photon polymerization lithography-based 3D printer (Nanoscribe GmbH, Stutensee, Germany).

other:

Article Title: Compounds for promoting liposomal and cellular adhesion and compositions and methods of use thereof
Article Snippet: Surface adhesion experiment was replicated with ArrayIt® Premium Superaldehyde and Streptavidin/Avidin substrate.

Article Title: On-Chip Fluorescence Switching System for Constructing a Rewritable Random Access Data Storage Device
Article Snippet: Aldehyde-modified glass slides (SuperAldehyde) were obtained from Arrayit Corporation (Sunnyvale, CA), and Glycine was purchased from Sigma-Aldrich (St. Louis, MO).

Article Title: Delivery of minimally dispersed liquid interfaces for sequential surface chemistry.
Article Snippet: We immobilized green fluorescent protein (GFP), (Abcam, Cambridge, UK) on an aldehyde-coated slide (SuperAldehyde 2, ArrayIt, Sunnyvale, CA), by depositing 1 μg μL−1 of GFP on the surface and incubating it overnight at 4 °C.

Article Title: Delivery of minimally dispersed liquid interfaces for sequential surface chemistry.
Article Snippet: Association kinetics measurement assay We prepared a test surface by incubating an aldehyde-coated slide (SuperAldehyde 2, ArrayIt, Sunnyvale, CA) with 100 μg mL−1 of rabbit IgG solution (Sigma-Aldrich, St. Louis, MO) at room temperature for 30 min. We rinsed the surface three times using PBS for 2 min, then blocked the surface using 1% BSA in PBS for 30 min, and rinsed the surface again with PBS.



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Captured extracellular vesicles on a <t>superaldehyde</t> glass based on surface binding after preconcentration at 45 V/cm for 30 min. ( a ) Electrokinetic preconcentration of extracellular vesicles in the microchannel, ( b ) The two white arrows and the black dotted square in the SEM image indicated areas of captured extracellular vesicles on a superaldehyde substrate after preconcentration. The SEM inset shows aggregated EVs with a size of <~200 nm.
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Captured extracellular vesicles on a <t>superaldehyde</t> glass based on surface binding after preconcentration at 45 V/cm for 30 min. ( a ) Electrokinetic preconcentration of extracellular vesicles in the microchannel, ( b ) The two white arrows and the black dotted square in the SEM image indicated areas of captured extracellular vesicles on a superaldehyde substrate after preconcentration. The SEM inset shows aggregated EVs with a size of <~200 nm.
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Captured extracellular vesicles on a <t>superaldehyde</t> glass based on surface binding after preconcentration at 45 V/cm for 30 min. ( a ) Electrokinetic preconcentration of extracellular vesicles in the microchannel, ( b ) The two white arrows and the black dotted square in the SEM image indicated areas of captured extracellular vesicles on a superaldehyde substrate after preconcentration. The SEM inset shows aggregated EVs with a size of <~200 nm.
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Captured extracellular vesicles on a <t>superaldehyde</t> glass based on surface binding after preconcentration at 45 V/cm for 30 min. ( a ) Electrokinetic preconcentration of extracellular vesicles in the microchannel, ( b ) The two white arrows and the black dotted square in the SEM image indicated areas of captured extracellular vesicles on a superaldehyde substrate after preconcentration. The SEM inset shows aggregated EVs with a size of <~200 nm.
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Image Search Results


Captured extracellular vesicles on a superaldehyde glass based on surface binding after preconcentration at 45 V/cm for 30 min. ( a ) Electrokinetic preconcentration of extracellular vesicles in the microchannel, ( b ) The two white arrows and the black dotted square in the SEM image indicated areas of captured extracellular vesicles on a superaldehyde substrate after preconcentration. The SEM inset shows aggregated EVs with a size of <~200 nm.

Journal: Micromachines

Article Title: Rapid Detection and Trapping of Extracellular Vesicles by Electrokinetic Concentration for Liquid Biopsy on Chip

doi: 10.3390/mi9060306

Figure Lengend Snippet: Captured extracellular vesicles on a superaldehyde glass based on surface binding after preconcentration at 45 V/cm for 30 min. ( a ) Electrokinetic preconcentration of extracellular vesicles in the microchannel, ( b ) The two white arrows and the black dotted square in the SEM image indicated areas of captured extracellular vesicles on a superaldehyde substrate after preconcentration. The SEM inset shows aggregated EVs with a size of <~200 nm.

Article Snippet: To demonstrate this flexibility of interfacing witha variety of substrates, we also used superaldehyde glass substrate (Arrayit) as well as plain glass slide with 3D-printed microtraps to passively trap extracellular vesicles near the ion-selective membrane during ICP at 45 V/cm within 30 min.

Techniques: Binding Assay