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ISCAN Inc microarray scanner
Microarray Scanner, supplied by ISCAN Inc, 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/iscan+microarray+scanner/microarray+scanner/pmc05768753-130-43-46
Average 90 stars, based on 1 article reviews
microarray scanner - by Bioz Stars, 2026-09
90/100 stars

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Related Articles

Hybridization:

Article Title: Long-Term Maintenance of Human Pluripotent Stem Cells on cRGDfK-Presenting Synthetic Surfaces.
Article Snippet: .. 7Scientific RePORTS | (2018) 8:701 | DOI:10.1038/s41598-018-19209-0 could be attributed to a recently observed technical drift in the hybridisation chemistry of the Illumina HT 12V4 microarray platform, as well as an offset due to a new microarray scanner generation (iScan) that was used for these samples (Franz-Josef Müller, Zentrum für Integrative Psychiatrie Kiel, Germany, pers. comm.). ..

Article Title: Long-Term Maintenance of Human Pluripotent Stem Cells on cRGDfK-Presenting Synthetic Surfaces
Article Snippet: .. Minor variations between the PluritestTM data generated from this experiment and the reference data could be attributed to a recently observed technical drift in the hybridisation chemistry of the Illumina HT 12V4 microarray platform, as well as an offset due to a new microarray scanner generation (iScan) that was used for these samples (Franz-Josef Müller, Zentrum für Integrative Psychiatrie Kiel, Germany, pers . comm .). ..

Microarray:

Article Title: Long-Term Maintenance of Human Pluripotent Stem Cells on cRGDfK-Presenting Synthetic Surfaces.
Article Snippet: .. 7Scientific RePORTS | (2018) 8:701 | DOI:10.1038/s41598-018-19209-0 could be attributed to a recently observed technical drift in the hybridisation chemistry of the Illumina HT 12V4 microarray platform, as well as an offset due to a new microarray scanner generation (iScan) that was used for these samples (Franz-Josef Müller, Zentrum für Integrative Psychiatrie Kiel, Germany, pers. comm.). ..

Article Title: Genotype-Phenotype Analysis, Neuropsychological Assessment, and Growth Hormone Response in a Patient with 18p Deletion Syndrome.
Article Snippet: 18p deletion syndrome is a rare chromosomal disease caused by deletion of the short arm of chromosome 18.. By using cytogenetic and SNP array analysis, we identified a girl with 18p deletion syndrome exhibiting craniofacial anomalies, intellectual disability, and short stature.. G-banding analysis of metaphase cells revealed an abnormal karyotype 46,XX,del(18)(p10).

Article Title: Long-Term Maintenance of Human Pluripotent Stem Cells on cRGDfK-Presenting Synthetic Surfaces
Article Snippet: .. Minor variations between the PluritestTM data generated from this experiment and the reference data could be attributed to a recently observed technical drift in the hybridisation chemistry of the Illumina HT 12V4 microarray platform, as well as an offset due to a new microarray scanner generation (iScan) that was used for these samples (Franz-Josef Müller, Zentrum für Integrative Psychiatrie Kiel, Germany, pers . comm .). ..

Generated:

Article Title: Long-Term Maintenance of Human Pluripotent Stem Cells on cRGDfK-Presenting Synthetic Surfaces
Article Snippet: .. Minor variations between the PluritestTM data generated from this experiment and the reference data could be attributed to a recently observed technical drift in the hybridisation chemistry of the Illumina HT 12V4 microarray platform, as well as an offset due to a new microarray scanner generation (iScan) that was used for these samples (Franz-Josef Müller, Zentrum für Integrative Psychiatrie Kiel, Germany, pers . comm .). ..



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Pedigree and genetic analysis for family 1. (A) Genetic pedigree of family 1; black circle II.1 indicates the affected child (P1). (B) SeqPilot ® CNV analysis: reduced copy number for the RUNX1 exons for the index patient (green columns) compared to the patients analyzed in the same enrichment (blue), indicating a heterozygous RUNX1 -gene deletion. (C) Chromosomal <t>microarray</t> analysis: 1.56 Mb deletion (21q22.11q22.12 shown as a red bar) including RUNX1 .
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Image Search Results


Pedigree and genetic analysis for family 1. (A) Genetic pedigree of family 1; black circle II.1 indicates the affected child (P1). (B) SeqPilot ® CNV analysis: reduced copy number for the RUNX1 exons for the index patient (green columns) compared to the patients analyzed in the same enrichment (blue), indicating a heterozygous RUNX1 -gene deletion. (C) Chromosomal microarray analysis: 1.56 Mb deletion (21q22.11q22.12 shown as a red bar) including RUNX1 .

Journal: Frontiers in Medicine

Article Title: RUNX1-FPDMM in families with mild thrombocytopenia and platelet function anomalies: a case series

doi: 10.3389/fmed.2025.1657054

Figure Lengend Snippet: Pedigree and genetic analysis for family 1. (A) Genetic pedigree of family 1; black circle II.1 indicates the affected child (P1). (B) SeqPilot ® CNV analysis: reduced copy number for the RUNX1 exons for the index patient (green columns) compared to the patients analyzed in the same enrichment (blue), indicating a heterozygous RUNX1 -gene deletion. (C) Chromosomal microarray analysis: 1.56 Mb deletion (21q22.11q22.12 shown as a red bar) including RUNX1 .

Article Snippet: Scanning and image acquisition were performed using an Illumina iScan microarray scanner.

Techniques: Microarray