19k human oligoarrays (Compugen Inc)
90
Structured Review
Compugen Inc
19k human oligoarrays
19k Human Oligoarrays, supplied by Compugen 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/19k+human+oligoarrays/human+19+000+oligonucleotide+library/pmc02561934-163-49-48
Average 90 stars, based on 1 article reviews
19k Human Oligoarrays, supplied by Compugen 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/19k+human+oligoarrays/human+19+000+oligonucleotide+library/pmc02561934-163-49-48
Average 90 stars, based on 1 article reviews
19k human oligoarrays - by Bioz Stars,
2026-09
90/100 stars
Images
Related Articles
SDS Page:Article Title: Mutation of C20orf7 Disrupts Complex I Assembly and Causes Lethal Neonatal Mitochondrial Disease Article Snippet: Uncorrected clones were genotyped with microsatellite markers and Affymetrix 50K XbaI SNP chips, which confirmed that at least two clones had deleted all or part of the candidate region (not shown). .. However, these data did not provide significant narrowing of the candidate region. fig ft0 fig mode=article f1 caption a4 SDS-PAGE Western Blotting of MMCT Clones To begin searching for a candidate gene in this interval that may underlie the observed complex I deficiency, we performed gene-expression analysis with Western Blot:Article Title: Mutation of C20orf7 Disrupts Complex I Assembly and Causes Lethal Neonatal Mitochondrial Disease Article Snippet: Uncorrected clones were genotyped with microsatellite markers and Affymetrix 50K XbaI SNP chips, which confirmed that at least two clones had deleted all or part of the candidate region (not shown). .. However, these data did not provide significant narrowing of the candidate region. fig ft0 fig mode=article f1 caption a4 SDS-PAGE Western Blotting of MMCT Clones To begin searching for a candidate gene in this interval that may underlie the observed complex I deficiency, we performed gene-expression analysis with Clone Assay:Article Title: Mutation of C20orf7 Disrupts Complex I Assembly and Causes Lethal Neonatal Mitochondrial Disease Article Snippet: Uncorrected clones were genotyped with microsatellite markers and Affymetrix 50K XbaI SNP chips, which confirmed that at least two clones had deleted all or part of the candidate region (not shown). .. However, these data did not provide significant narrowing of the candidate region. fig ft0 fig mode=article f1 caption a4 SDS-PAGE Western Blotting of MMCT Clones To begin searching for a candidate gene in this interval that may underlie the observed complex I deficiency, we performed gene-expression analysis with |