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TeleChem International superaldehyde substrates
Superaldehyde Substrates, supplied by TeleChem International, 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/superaldehyde+substrates/us10767227-370-10-16
Average 90 stars, based on 1 article reviews
superaldehyde substrates - by Bioz Stars, 2026-10
90/100 stars

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Related Articles

other:

Article Title: Protocol for small-scale RNA isolation and transcriptional profiling of developing Arabidopsis seeds.
Article Snippet: The cDNA microarrays were prepared from an Arabidopsis seed-specific cDNA library (5) by spotting 6000 DNA elements on aldehyde-coated glass substrates (SuperAldehyde; TeleChem International, Sunnyvale, CA, USA).

Article Title: Contrapuntal Networks of Gene Expression during Arabidopsis Seed Filling
Article Snippet: Amplification of cDNAs and printing of the microarrays on aldehyde-coated glass substrates (SuperAldehyde; TeleChem International, Sunnyvale, CA) were performed as described previously ( Girke et al., 2000 ).

Saline:

Article Title: Analysis of protein interaction and function with a 3-dimensional MALDI-MS protein array
Article Snippet: .. Protein arrays were then rinsed once with Trisbuffered saline (TBS; Pierce, Rockford, IL, USA) for 10 min, three consecutive washes with TBS plus 0.1% Tween® 20 (TBST) for 10 min each, and SuperblockTM solution in TBS (Pierce) for 1 h. Protein immobilization on SuperAldehyde (Telechem International, Sunnyvale, CA, USA) and HydroGel substrates were carried out according to the manufacturers’ recommendations. ..

Microarray:

Article Title: Photocleavage Based Affinity Purification and Printing of Cell-free Expressed Proteins: Application to Proteome Microarrays
Article Snippet: The streptavidin-alkaline phosphatase conjugate was from Bio-Rad Laboratories (Hercules, CA). .. Aldehyde and epoxy activated glass microarray substrates, SuperEpoxy and SuperAldehyde, were from TeleChem International, Inc. (ArrayItTM Division, Sunnyvale, CA). .. The Cy5-NHS mono-reactive ester labeling reagent was from GE Healthcare Bio-Sciences Corp. (Piscataway, NJ).



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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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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