innoscan 710 high resolution microarray scanner (Innopsys Inc)
86
Structured Review
Innopsys Inc
innoscan 710 high resolution microarray scanner
Innoscan 710 High Resolution Microarray Scanner, supplied by Innopsys Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/high+microarray+scanner/710al+innopsys+scanner/pmc13207355-405-10-15
Average 86 stars, based on 1 article reviews
Innoscan 710 High Resolution Microarray Scanner, supplied by Innopsys Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/high+microarray+scanner/710al+innopsys+scanner/pmc13207355-405-10-15
Average 86 stars, based on 1 article reviews
innoscan 710 high resolution microarray scanner - by Bioz Stars,
2026-11
86/100 stars
Images
Related Articles
Microarray:Article Title: Co-enrichment of proteins in extracellular vesicles. Article Snippet: The slides were incubated at room temperature on a shaker for 2 h. The detection antibodies were detected using either anti-species fluorescently-labelled secondary antibodies, fluorescently labelled streptavidin at a final concentration of 1 μg/mL diluted in 0.03% PBST with 3% BSA, or fluorescently labelled DNA oligos at a final concentration of 10 nM in PBS with 0.025% Tween- AR TI CL E IN P RE SS 20, 300 mM NaCl, 0.5 mg/mL sheared salmon sperm DNA (Thermo Fisher, USA) and 0.5% dextran sulfate (Sigma, USA).31 For intravesicular targets, an additional fixation (10 min with 4% paraformaldehyde), antigen retrieval (1 min with 90°C PBS), and quenching step (2 h with 0.03%PBST, 3% BSA and 0.3M glycine) were performed prior to detection antibody incubation.31 Finally, the slides were washed in a 0.03% PBST bath for 15 min (or 5 min for oligo- detected targets) on a shaker, dried using a centrifugal slide dryer before imaging. .. A Article Title: Conserved genetic and antigenic profiles of Pf12 and Pf41 in asymptomatic Plasmodium falciparum carriers in Tanzania. Article Snippet: .. Bound IgG antibodies were detected using Alexa Fluor 546-conjugated goat antihuman IgG (10 ng/μL; Invitrogen), and fluorescence signals were acquired using the Incubation:Article Title: Astrocytes transform the transcriptomic and epigenetic landscape of developing cortical neurons to promote activity via intrinsic excitability control Article Snippet: .. 120 antibodies were profiled using standard procedures, 1 hour incubation with primary followed by 30 min incubation with Dylight-800 anti-species secondary antibodies, with arrays imaged using an Article Title: A comprehensive pharmacological survey across heterogeneous patient-derived glioblastoma stem cell models Article Snippet: Clamps were removed and microarrays were washed three times for 5 min in PBS-T. Microarrays were then blocked for 10min with Super G Blocking Buffer at room temperature and again washed three times for 5 min in PBS-T. Three millilitres (3 mL) of IRDye 800CW Streptavidin (LI-COR Biosciences) was diluted 1:5000 in PBS-T supplemented with 5% BSA, 10% SuperG Blocking Buffer. .. Following blocking buffer (Superblock T20) for 10 min the detection of marker antibodies was performed in a two-step sequential assay (1) incubation of an array with primary analyte-specific antibody in blocking buffer for 60 min at room temperature and (2) removal of excess antibody by washing arrays with PBS-T, followed by a further incubation with blocking buffer and PBS-T washes, and incubation secondary antibody (Dylight-800-labeled anti-species antibodies diluted 1:2500 in Superblock T20) for 30 min. After further washing and slide drying, the arrays were imaged in the other:Article Title: A comprehensive pharmacological survey across heterogeneous patient-derived glioblastoma stem cell models Article Snippet: ladder (Invitrogen, #LC5925) followed by transfer to PVDF membrane (Bio-Rad, Trans -blot Turbo pack, #1704156) and blocking with 5% BSA/TBS-Tween (0.1% (v/v)). Fluorescence:Article Title: Conserved genetic and antigenic profiles of Pf12 and Pf41 in asymptomatic Plasmodium falciparum carriers in Tanzania. Article Snippet: .. Bound IgG antibodies were detected using Alexa Fluor 546-conjugated goat antihuman IgG (10 ng/μL; Invitrogen), and fluorescence signals were acquired using the Article Title: Sequencing-free On-chip detection of lung cancer by fluorescent enzymatic profiling of cfDNA methylation. Article Snippet: .. The slides were scanned using the Blocking Assay:Article Title: A comprehensive pharmacological survey across heterogeneous patient-derived glioblastoma stem cell models Article Snippet: Clamps were removed and microarrays were washed three times for 5 min in PBS-T. Microarrays were then blocked for 10min with Super G Blocking Buffer at room temperature and again washed three times for 5 min in PBS-T. Three millilitres (3 mL) of IRDye 800CW Streptavidin (LI-COR Biosciences) was diluted 1:5000 in PBS-T supplemented with 5% BSA, 10% SuperG Blocking Buffer. .. Following blocking buffer (Superblock T20) for 10 min the detection of marker antibodies was performed in a two-step sequential assay (1) incubation of an array with primary analyte-specific antibody in blocking buffer for 60 min at room temperature and (2) removal of excess antibody by washing arrays with PBS-T, followed by a further incubation with blocking buffer and PBS-T washes, and incubation secondary antibody (Dylight-800-labeled anti-species antibodies diluted 1:2500 in Superblock T20) for 30 min. After further washing and slide drying, the arrays were imaged in the Marker:Article Title: A comprehensive pharmacological survey across heterogeneous patient-derived glioblastoma stem cell models Article Snippet: Clamps were removed and microarrays were washed three times for 5 min in PBS-T. Microarrays were then blocked for 10min with Super G Blocking Buffer at room temperature and again washed three times for 5 min in PBS-T. Three millilitres (3 mL) of IRDye 800CW Streptavidin (LI-COR Biosciences) was diluted 1:5000 in PBS-T supplemented with 5% BSA, 10% SuperG Blocking Buffer. .. Following blocking buffer (Superblock T20) for 10 min the detection of marker antibodies was performed in a two-step sequential assay (1) incubation of an array with primary analyte-specific antibody in blocking buffer for 60 min at room temperature and (2) removal of excess antibody by washing arrays with PBS-T, followed by a further incubation with blocking buffer and PBS-T washes, and incubation secondary antibody (Dylight-800-labeled anti-species antibodies diluted 1:2500 in Superblock T20) for 30 min. After further washing and slide drying, the arrays were imaged in the Imaging:Article Title: Comparative analysis and correlation of cancer hotspot proteins and cell markers in tumor-normal adjacent breast and kidney samples using RPPA and LC-MS. Article Snippet: In addition, one slide per RPPA run was stained by FCF Fast Green (Sigma F7258) for total protein normalization of spots during the imaging process (see below). .. Slides were scanned as described below within a few hours after the last washing step and following a short drying protocol by spinning at 300 rpm for 5 min. (v) Slide/blot imaging and spot quantification: Slides were loaded (24 slides at a time, using an autoloader) in an Software:Article Title: Sequencing-free On-chip detection of lung cancer by fluorescent enzymatic profiling of cfDNA methylation. Article Snippet: .. The slides were scanned using the |
