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human genome cgh microarray kit 244k  (Agilent technologies)


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    Agilent technologies human genome cgh microarray kit 244k
    Human Genome Cgh Microarray Kit 244k, supplied by Agilent technologies, 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/human+genome+cgh+microarray+kit+244k/pmc03790698-69-14-20
    Average 90 stars, based on 1 article reviews
    human genome cgh microarray kit 244k - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    Microarray:

    Article Title: FGFR2 loss sensitizes MYCN‐amplified neuroblastoma CHP134 cells to CHK1 inhibitor–induced apoptosis
    Article Snippet: .. High‐resolution aCGH was performed using the Agilent Human Genome CGH Microarray Kit 244K (Agilent Technologies) according to the manufacturer's protocol (Agilent Oligonucleotide Array‐Based CGH for Genomic DNA Analysis, version 3.1 August 2009). .. Data was extracted from scanned microarray images using the Feature Extraction Software v11.0.1.1 (Agilent Technologies).

    Article Title: Meiotic pairing error in an infertile male bearing reciprocal deletion of chromosome 13.
    Article Snippet: .. Oligonucleotide Array Comparative Genomic Hybridization Analysis—To characterize the breakpoints of the chromosome involved, or the gene copy number deletion caused by the rearrangement, a genomic-wide high-density oligonucleotide array comparative genomic hybridization (oaCGH) analysis was performed using the Human Genome CGH Microarray kit 244K (Agilent Technologies Inc, Santa Clara, California). ..

    Article Title: Complex de novo chromosomal rearrangement at 15q11-q13 involving an intrachromosomal triplication in a patient with a severe neuropsychological phenotype: clinical report and review of the literature.
    Article Snippet: Complex De Novo Chromosomal Rearrangement at 15q11–q13 Involving an Intrachromosomal Triplication in a Patient With a Severe Neuropsychological Phenotype: Clinical Report and Review of the Literature Chiara Castronovo,* Milena Crippa, Ilaria Bestetti, Daniela Rusconi, Silvia Russo, Lidia Larizza, Roberto Sangermani, Maria Teresa Bonati, and Palma Finelli Laboratory of Medical Cytogenetics and Molecular Genetics, IRCCS Istituto Auxologico Italiano, Milano, Italy Department of Medical Biotechnology and Translational Medicine, University of Milan, Milano, Italy Medical Genetics, Department of Health Sciences, University of Milan, Milano, Italy Clinic of Neuropediatrics, San Carlo Borromeo Hospital, Milano, Italy Clinic of Clinical Genetics, San Luca Hospital, IRCCS Istituto Auxologico Italiano, Milano, Italy

    Article Title: A homozygous mutation of C12orf65 causes spastic paraplegia with optic atrophy and neuropathy (SPG55).
    Article Snippet: Division of Neurology, Department of Internal Medicine, Jichi Medical University, Tochigi, Japan Department of Neurology, Interdisciplinary Graduate School of Medicine and Engineering, University of Yamanashi, Yamanashi, Japan Department of Neurology, Graduate School of Medicine, University of Tokyo, Tokyo, Japan Department of Mental Retardation and Birth Defect Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry, Tokyo, Japan

    Article Title: Molecular characterization of a mosaic NIPBL deletion in a Cornelia de Lange patient with severe phenotype.
    Article Snippet: Cornelia de Lange syndrome (CdLS, OMIM #122470, #300590, #610759, #614701, #300882) is a rare neurodevelopmental syndrome characterized by growth retardation, intellectual disability, dysmorphic facial features, multisystem malformations, and limb reduction defects.. Wide variability of phenotypes is common among CdLS patients.. Mutations in genes encoding either regulators (NIPBL, HDAC8) or subunits (SMC1A, SMC3, RAD21) of the cohesin complex, are altogether found in approximately 65% of CdLS patients.

    Article Title: Meiotic pairing error in an infertile male bearing reciprocal deletion of chromosome 13.
    Article Snippet: .. Materials and Methods Oligonucleotide Array Comparative Genomic Hybridization Analysis—To characterize the breakpoints of the chromosome involved, or the gene copy number deletion caused by the rearrangement, a genomic-wide high-density oligonucleotide array comparative genomic hybridization (oaCGH) analysis was performed using the Human Genome CGH Microarray kit 244K (Agilent Technologies Inc, Santa Clara, California). ..

    Article Title: GSTT1 Copy Number Gain and ZNF Overexpression Are Predictors of Poor Response to Imatinib in Gastrointestinal Stromal Tumors
    Article Snippet: .. Array comparative genomic hybridization (aCGH) was performed on the 32 cases using the Agilent Human Genome CGH Microarray Kit 244K (Agilent Technologies, Santa Clara, CA, USA). .. We followed the procedures for DNA digestion, labeling, and hybridization described in Agilent’s protocol version 4.0.

    Article Title: Small mosaic deletion encompassing the snoRNAs and SNURF-SNRPN results in an atypical Prader-Willi syndrome phenotype.
    Article Snippet: Small Mosaic Deletion Encompassing the snoRNAs and SNURF-SNRPN Results in an Atypical Prader– Willi Syndrome Phenotype Britt-Marie Anderlid,* Johanna Lundin, Helena Malmgren, Mikael Lehtihet, and Ann Nordgren Department of Molecular Medicine and Surgery, Clinal Genetic Unit, Centre of Molecular Medicine, Karolinska Institutet, Stockholm, Sweden Department of Clinical Genetics, Karolinska University Hospital, Stockholm, Sweden Department of Medicine/Huddinge, Karolinska Institutet and Centre for Andrology and Sexual Medicine, Karolinska University Hospital, Stockholm, Sweden

    Hybridization:

    Article Title: Meiotic pairing error in an infertile male bearing reciprocal deletion of chromosome 13.
    Article Snippet: .. Oligonucleotide Array Comparative Genomic Hybridization Analysis—To characterize the breakpoints of the chromosome involved, or the gene copy number deletion caused by the rearrangement, a genomic-wide high-density oligonucleotide array comparative genomic hybridization (oaCGH) analysis was performed using the Human Genome CGH Microarray kit 244K (Agilent Technologies Inc, Santa Clara, California). ..

    Article Title: Meiotic pairing error in an infertile male bearing reciprocal deletion of chromosome 13.
    Article Snippet: .. Materials and Methods Oligonucleotide Array Comparative Genomic Hybridization Analysis—To characterize the breakpoints of the chromosome involved, or the gene copy number deletion caused by the rearrangement, a genomic-wide high-density oligonucleotide array comparative genomic hybridization (oaCGH) analysis was performed using the Human Genome CGH Microarray kit 244K (Agilent Technologies Inc, Santa Clara, California). ..

    Article Title: GSTT1 Copy Number Gain and ZNF Overexpression Are Predictors of Poor Response to Imatinib in Gastrointestinal Stromal Tumors
    Article Snippet: .. Array comparative genomic hybridization (aCGH) was performed on the 32 cases using the Agilent Human Genome CGH Microarray Kit 244K (Agilent Technologies, Santa Clara, CA, USA). .. We followed the procedures for DNA digestion, labeling, and hybridization described in Agilent’s protocol version 4.0.



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