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microarray codelink bioarray  (Bioarray Inc)

 
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    Bioarray Inc microarray codelink bioarray
    Microarray Codelink Bioarray, supplied by Bioarray 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/codelink+bioarray/codelink+bioarray/pmc08461075-30-27-30
    Average 90 stars, based on 1 article reviews
    microarray codelink bioarray - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    Incubation:

    Article Title: Does estrogen deficiency cause lacrimal gland inflammation and aqueous-deficient dry eye in mice?
    Article Snippet: Samples were then dried, and cRNA was generated with a CodeLink Expression Assay Reagent Kit (Amersham), recovered with an RNeasy kit (Qiagen) and quantified with an UV spectrophotometer. .. Fragmented and biotin-labeled cRNA was incubated and shaken at 300 rpm on a CodeLink Bioarray at 37°C for 18 hours. .. After this time period, the Bioarray was washed, exposed to streptavidin-Alexa 647, and scanned by utilizing ScanArray Express software and a ScanArray Express HT scanner (Packard BioScience, Meriden, CT) with the laser set at 635 nm, laser power at 100%, and photomultiplier tube voltage at 60%.

    Article Title: Therapeutic modulation of ocular surface lubrication
    Article Snippet: After sample drying, cRNA was made with a CodeLink Expression Assay Reagent Kit (Amersham), recovered with an RNeasy kit (Qiagen) and quantified with an UV spectrophotometer. .. Fragmented, biotin-labeled cRNA was then incubated and agitated (300 rpm shaker) on a CodeLink Bioarray at 37° C. for 18 hours. .. The Bioarray was washed, exposed to streptavidin-Alexa 647, and scanned by using ScanArray Express software and a ScanArray Express HT scanner (Packard BioScience, Meriden, Conn.) with the laser set at 635 nm, laser power at 100%, and photomultiplier tube voltage at 60%.

    Comparison:

    Article Title: Biomarkers for assessing idiopathic pulmonary fibrosis
    Article Snippet: .. Wu W, Dave N, Tseng G C, Richards T, Xing E P, Kaminski N. Comparison of normalization methods for CodeLink Bioarray data. ..

    Article Title: BAL Cell Gene Expression in Severe Asthma Reveals Mechanisms of Severe Disease and Influences of Medications
    Article Snippet: Wu W, Dave N, Tseng GC, Richards T, Xing EP, Kaminski N. Comparison of normalization methods for CodeLink Bioarray data. .. Wu W, Dave N, Tseng GC, Richards T, Xing EP, Kaminski N. Comparison of normalization methods for CodeLink Bioarray data. ..

    Article Title: Comprehensive and Reproducible Untargeted Lipidomic Workflow Using LC-QTOF Validated for Human Plasma Analysis.
    Article Snippet: .. Wu, W.; Dave, N.; Tseng, G. C.; Richards, T.; Xing, E. P.; Kaminski, N. Comparison of normalization methods for CodeLink Bioarray data. ..

    Software:

    Article Title: KIR+ CD8+ T Lymphocytes in Cancer Immunosurveillance and Patient Survival: Gene Expression Profiling
    Article Snippet: Microrrays were read with a GenePix 4000B laser scanner (Axon Instruments, Union City, CA, USA), and then quantified, and normalized using CodeLink Software 5.0 (Applied Microarrays). .. Normalized data from the CodeLink software package were analyzed and only the genes that passed the CodeLink Bioarray quality controls were selected. ..

    Muscles:

    Article Title: Differences in histone modifications between slow- and fast-twitch muscle of adult rats and following overload, denervation, or valproic acid administration.
    Article Snippet: We used a commercial service for microarray analysis, which included CodeLink Bioarray (Applied Microarrays, Tempe, AZ) and SurePrint G3 Rat GE 8 60K Microarray (Agilent Technologies, Santa Clara, CA). .. Comparisons between plantaris and soleus muscles were double-checked using two different arrays, and the RNA sample obtained from the overload experiment was determined by CodeLink Bioarray only. .. Full data of gene expression using Agilent Microarray are available on the Gene Expression Omnibus (GEO) database managed by the National Center J Appl Physiol • doi:10.1152/japplphysiol.00289.2015 • www.jappl.org for Biological Information (identification number GSE62028).



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    Transcriptional profiling of KIR2D− and KIR2D+ CD8+ T cells. ( A ) Differential gene expression profile <t>(CodeLink</t> Genome Array) of KIR− (column 1), KIR2DL1/S1+ (column 2), and KIR2DL2/L3/S2+ (column 3) CD8+ T cell subsets. The figure shows the top 40 most significantly modulated genes (designed with http://www.ehbio.com/ImageGP/ ). ( B ) Total number of up- and down-regulated genes in each KIR2D+ CD8+ T cell subset (analysis performed with jvenn software). ( C ) Microarray results were confirmed with real time quantitative RT-PCR (qPCR) analysis. Expression ratio (upper plot) and relative fold changes (lower plot) are shown for microarray and qPCR assays, respectively. Differential gene expression was considered significant with p < 0.05 in three independent cells preparations. Mean fold-changes in gene transcript expression levels between KIR2D− and KIR2D+ were evaluated with 2 ΔΔCt . ( D ) Shows the normalized intensity of important molecules in the cytotoxic T cell biology and interleukin or interleukin receptors.
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    Transcriptional profiling of KIR2D− and KIR2D+ CD8+ T cells. ( A ) Differential gene expression profile <t>(CodeLink</t> Genome Array) of KIR− (column 1), KIR2DL1/S1+ (column 2), and KIR2DL2/L3/S2+ (column 3) CD8+ T cell subsets. The figure shows the top 40 most significantly modulated genes (designed with http://www.ehbio.com/ImageGP/ ). ( B ) Total number of up- and down-regulated genes in each KIR2D+ CD8+ T cell subset (analysis performed with jvenn software). ( C ) Microarray results were confirmed with real time quantitative RT-PCR (qPCR) analysis. Expression ratio (upper plot) and relative fold changes (lower plot) are shown for microarray and qPCR assays, respectively. Differential gene expression was considered significant with p < 0.05 in three independent cells preparations. Mean fold-changes in gene transcript expression levels between KIR2D− and KIR2D+ were evaluated with 2 ΔΔCt . ( D ) Shows the normalized intensity of important molecules in the cytotoxic T cell biology and interleukin or interleukin receptors.
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    Image Search Results


    Transcriptional profiling of KIR2D− and KIR2D+ CD8+ T cells. ( A ) Differential gene expression profile (CodeLink Genome Array) of KIR− (column 1), KIR2DL1/S1+ (column 2), and KIR2DL2/L3/S2+ (column 3) CD8+ T cell subsets. The figure shows the top 40 most significantly modulated genes (designed with http://www.ehbio.com/ImageGP/ ). ( B ) Total number of up- and down-regulated genes in each KIR2D+ CD8+ T cell subset (analysis performed with jvenn software). ( C ) Microarray results were confirmed with real time quantitative RT-PCR (qPCR) analysis. Expression ratio (upper plot) and relative fold changes (lower plot) are shown for microarray and qPCR assays, respectively. Differential gene expression was considered significant with p < 0.05 in three independent cells preparations. Mean fold-changes in gene transcript expression levels between KIR2D− and KIR2D+ were evaluated with 2 ΔΔCt . ( D ) Shows the normalized intensity of important molecules in the cytotoxic T cell biology and interleukin or interleukin receptors.

    Journal: Cancers

    Article Title: KIR+ CD8+ T Lymphocytes in Cancer Immunosurveillance and Patient Survival: Gene Expression Profiling

    doi: 10.3390/cancers12102991

    Figure Lengend Snippet: Transcriptional profiling of KIR2D− and KIR2D+ CD8+ T cells. ( A ) Differential gene expression profile (CodeLink Genome Array) of KIR− (column 1), KIR2DL1/S1+ (column 2), and KIR2DL2/L3/S2+ (column 3) CD8+ T cell subsets. The figure shows the top 40 most significantly modulated genes (designed with http://www.ehbio.com/ImageGP/ ). ( B ) Total number of up- and down-regulated genes in each KIR2D+ CD8+ T cell subset (analysis performed with jvenn software). ( C ) Microarray results were confirmed with real time quantitative RT-PCR (qPCR) analysis. Expression ratio (upper plot) and relative fold changes (lower plot) are shown for microarray and qPCR assays, respectively. Differential gene expression was considered significant with p < 0.05 in three independent cells preparations. Mean fold-changes in gene transcript expression levels between KIR2D− and KIR2D+ were evaluated with 2 ΔΔCt . ( D ) Shows the normalized intensity of important molecules in the cytotoxic T cell biology and interleukin or interleukin receptors.

    Article Snippet: Normalized data from the CodeLink software package were analyzed and only the genes that passed the CodeLink Bioarray quality controls were selected.

    Techniques: Gene Expression, Software, Microarray, Quantitative RT-PCR, Expressing