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whole human genome 4 * 44 k microarrays (g4112f) applying for gene expression profiling  (Agilent technologies)


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    Agilent technologies whole human genome 4 * 44 k microarrays (g4112f) applying for gene expression profiling
    Whole Human Genome 4 * 44 K Microarrays (G4112f) Applying For Gene Expression Profiling, 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/microarray+profiling+of+human+gene+expression/pm36077272-320-7-32
    Average 90 stars, based on 1 article reviews
    whole human genome 4 * 44 k microarrays (g4112f) applying for gene expression profiling - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    Expressing:

    Article Title: In silico prediction and validation of potential therapeutic genes in pancreatic β-cells associated with type 2 diabetes.
    Article Snippet: Gene expression profiling of GSE20966, using the Agilent‐014850 Whole Human Genome Microarray 4x44 K G4112F platform (Agilent Technologies, Inc.), deposited by Marselli et al (21) was downloaded from the GEO database (http://www.ncbi.nlm. nih.gov/geo/).

    Microarray:

    Article Title: In silico prediction and validation of potential therapeutic genes in pancreatic β-cells associated with type 2 diabetes.
    Article Snippet: Gene expression profiling of GSE20966, using the Agilent‐014850 Whole Human Genome Microarray 4x44 K G4112F platform (Agilent Technologies, Inc.), deposited by Marselli et al (21) was downloaded from the GEO database (http://www.ncbi.nlm. nih.gov/geo/).



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    Validation of genes identified using microarray. MCF7 and TAMR cells were transfected with silencer negative control siRNA, ATF2 siRNA1 and ATF2 siRNA2. qRT-PCR was carried out using Taqman primers for the genes indicated. Data analysis for each cell line was carried out relative to the siControl ( n = 3) and asterisks indicate the genes that were significantly changed after ATF2 knockdown (* p < 0.05, ** p < 0.005)

    Journal: Breast Cancer Research : BCR

    Article Title: Activating transcription factor-2 (ATF2) is a key determinant of resistance to endocrine treatment in an in vitro model of breast cancer

    doi: 10.1186/s13058-020-01359-7

    Figure Lengend Snippet: Validation of genes identified using microarray. MCF7 and TAMR cells were transfected with silencer negative control siRNA, ATF2 siRNA1 and ATF2 siRNA2. qRT-PCR was carried out using Taqman primers for the genes indicated. Data analysis for each cell line was carried out relative to the siControl ( n = 3) and asterisks indicate the genes that were significantly changed after ATF2 knockdown (* p < 0.05, ** p < 0.005)

    Article Snippet: We also performed a microarray gene expression profiling (Illumina Human HT12_v4) to explore alterations in gene expression between MCF7 and TAMRs after ATF2 silencing and confirmed gene expression changes by quantitative RT-PCR.

    Techniques: Biomarker Discovery, Microarray, Transfection, Negative Control, Quantitative RT-PCR, Knockdown