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    Agilent technologies mouse mirna microarrays agilent technologies
    Temporal correlation between the expression of global miRNAs and renal function indexes. (A) Temporal <t>miRNA</t> expression change within 48 h after renal IRI. miRNA abundance is defined as raw <t>microarray</t> signal output normalized to the blank value 0.1; ∗ p
    Mouse Mirna Microarrays Agilent Technologies, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 85/100, based on 57 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Agilent technologies sureprint g3 mouse gene expression microarray 8x60k ver 2 0 agilent technologies cat
    Temporal correlation between the expression of global miRNAs and renal function indexes. (A) Temporal <t>miRNA</t> expression change within 48 h after renal IRI. miRNA abundance is defined as raw <t>microarray</t> signal output normalized to the blank value 0.1; ∗ p
    Sureprint G3 Mouse Gene Expression Microarray 8x60k Ver 2 0 Agilent Technologies Cat, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 93/100, based on 34 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Agilent technologies mouse microarrays
    Assessment of the specificity of the ChIP protocol. A) Arx immunoprecipitation from N2a cells transfected with an Arx-expressing vector or a vector alone and using the Arx C-14 antibody from Santa Cruz. Detection using the anti-Arx-HD antibody revealed a major band at approximately 80 kD, which corresponds to the size of Arx protein. TE: total extracts, IP: immunoprecipitation, Ig: immunoglobulins. B) Enrichment of Ebf3 , Lmo1 and Shox2 promoter regions was assessed by qPCR using either Arx or PolII-immunoprecipitates or using no antibody and was compared to the total input. Gapdh was used as a positive control with DNA Pol II. Here, we show an example of the results obtained in a ChIP experiment with Arx C-14 antibody from Santa Cruz. The enrichment of Ebf3 , Lmo1 and Shox2 was checked similarly for each replicate experiment before DNA was applied to the <t>microarrays.</t>
    Mouse Microarrays, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 88/100, based on 40 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Agilent technologies mouse agilent
    Assessment of the specificity of the ChIP protocol. A) Arx immunoprecipitation from N2a cells transfected with an Arx-expressing vector or a vector alone and using the Arx C-14 antibody from Santa Cruz. Detection using the anti-Arx-HD antibody revealed a major band at approximately 80 kD, which corresponds to the size of Arx protein. TE: total extracts, IP: immunoprecipitation, Ig: immunoglobulins. B) Enrichment of Ebf3 , Lmo1 and Shox2 promoter regions was assessed by qPCR using either Arx or PolII-immunoprecipitates or using no antibody and was compared to the total input. Gapdh was used as a positive control with DNA Pol II. Here, we show an example of the results obtained in a ChIP experiment with Arx C-14 antibody from Santa Cruz. The enrichment of Ebf3 , Lmo1 and Shox2 was checked similarly for each replicate experiment before DNA was applied to the <t>microarrays.</t>
    Mouse Agilent, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 86/100, based on 30 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Agilent technologies 22k mouse microarrays
    Assessment of the specificity of the ChIP protocol. A) Arx immunoprecipitation from N2a cells transfected with an Arx-expressing vector or a vector alone and using the Arx C-14 antibody from Santa Cruz. Detection using the anti-Arx-HD antibody revealed a major band at approximately 80 kD, which corresponds to the size of Arx protein. TE: total extracts, IP: immunoprecipitation, Ig: immunoglobulins. B) Enrichment of Ebf3 , Lmo1 and Shox2 promoter regions was assessed by qPCR using either Arx or PolII-immunoprecipitates or using no antibody and was compared to the total input. Gapdh was used as a positive control with DNA Pol II. Here, we show an example of the results obtained in a ChIP experiment with Arx C-14 antibody from Santa Cruz. The enrichment of Ebf3 , Lmo1 and Shox2 was checked similarly for each replicate experiment before DNA was applied to the <t>microarrays.</t>
    22k Mouse Microarrays, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 85/100, based on 5 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Agilent technologies mouse oligo microarrays
    Gene sets from <t>microarray</t> experiment Single cell suspension of HT168M1 human melanoma cell line was semiorthotopically implanted into newborn SCID mice. The RNA expression pattern of this, metastatic version of the primary tumor was investigated via Agilent Mouse <t>Oligo</t> Microarray Platform. The stromal expression changes were compared to healthy, age matched controls and the nineteen genes showing the largest expressional changes were selected for further validation.
    Mouse Oligo Microarrays, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 88/100, based on 72 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Agilent technologies mouse promoter array
    Gene sets from <t>microarray</t> experiment Single cell suspension of HT168M1 human melanoma cell line was semiorthotopically implanted into newborn SCID mice. The RNA expression pattern of this, metastatic version of the primary tumor was investigated via Agilent Mouse <t>Oligo</t> Microarray Platform. The stromal expression changes were compared to healthy, age matched controls and the nineteen genes showing the largest expressional changes were selected for further validation.
    Mouse Promoter Array, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 88/100, based on 18 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Agilent technologies mouse microrna microarray
    Gene sets from <t>microarray</t> experiment Single cell suspension of HT168M1 human melanoma cell line was semiorthotopically implanted into newborn SCID mice. The RNA expression pattern of this, metastatic version of the primary tumor was investigated via Agilent Mouse <t>Oligo</t> Microarray Platform. The stromal expression changes were compared to healthy, age matched controls and the nineteen genes showing the largest expressional changes were selected for further validation.
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    Agilent technologies mouse 44k oligoarray
    Gene sets from <t>microarray</t> experiment Single cell suspension of HT168M1 human melanoma cell line was semiorthotopically implanted into newborn SCID mice. The RNA expression pattern of this, metastatic version of the primary tumor was investigated via Agilent Mouse <t>Oligo</t> Microarray Platform. The stromal expression changes were compared to healthy, age matched controls and the nineteen genes showing the largest expressional changes were selected for further validation.
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    Agilent technologies mouse microarray slide
    Gene sets from <t>microarray</t> experiment Single cell suspension of HT168M1 human melanoma cell line was semiorthotopically implanted into newborn SCID mice. The RNA expression pattern of this, metastatic version of the primary tumor was investigated via Agilent Mouse <t>Oligo</t> Microarray Platform. The stromal expression changes were compared to healthy, age matched controls and the nineteen genes showing the largest expressional changes were selected for further validation.
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    Agilent technologies a mouse microarray platform
    Gene sets from <t>microarray</t> experiment Single cell suspension of HT168M1 human melanoma cell line was semiorthotopically implanted into newborn SCID mice. The RNA expression pattern of this, metastatic version of the primary tumor was investigated via Agilent Mouse <t>Oligo</t> Microarray Platform. The stromal expression changes were compared to healthy, age matched controls and the nineteen genes showing the largest expressional changes were selected for further validation.
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    Agilent technologies agilentʼs mouse microarrays
    Gene sets from <t>microarray</t> experiment Single cell suspension of HT168M1 human melanoma cell line was semiorthotopically implanted into newborn SCID mice. The RNA expression pattern of this, metastatic version of the primary tumor was investigated via Agilent Mouse <t>Oligo</t> Microarray Platform. The stromal expression changes were compared to healthy, age matched controls and the nineteen genes showing the largest expressional changes were selected for further validation.
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    Agilent technologies mouse cgi array
    Gene sets from <t>microarray</t> experiment Single cell suspension of HT168M1 human melanoma cell line was semiorthotopically implanted into newborn SCID mice. The RNA expression pattern of this, metastatic version of the primary tumor was investigated via Agilent Mouse <t>Oligo</t> Microarray Platform. The stromal expression changes were compared to healthy, age matched controls and the nineteen genes showing the largest expressional changes were selected for further validation.
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    Agilent technologies mouse genomic probes
    Gene sets from <t>microarray</t> experiment Single cell suspension of HT168M1 human melanoma cell line was semiorthotopically implanted into newborn SCID mice. The RNA expression pattern of this, metastatic version of the primary tumor was investigated via Agilent Mouse <t>Oligo</t> Microarray Platform. The stromal expression changes were compared to healthy, age matched controls and the nineteen genes showing the largest expressional changes were selected for further validation.
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    Agilent technologies mouse oligo microarray 44k
    Scanned image of cDNA <t>microarray</t> chips. After labeling of cRNA, samples from the control-, DNCB-, DNCB + AB-, and DNCB + horse oil-treated mice were hybridized onto mouse <t>oligo</t> microarray slides, which were then scanned and analyzed. DNCB, 2, 4-dinitrochlorobenzene; AB, Atobarrier lotion.
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    Agilent technologies 1m mouse promoter microarrays
    Scanned image of cDNA <t>microarray</t> chips. After labeling of cRNA, samples from the control-, DNCB-, DNCB + AB-, and DNCB + horse oil-treated mice were hybridized onto mouse <t>oligo</t> microarray slides, which were then scanned and analyzed. DNCB, 2, 4-dinitrochlorobenzene; AB, Atobarrier lotion.
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    Agilent technologies mouse genome array
    Scanned image of cDNA <t>microarray</t> chips. After labeling of cRNA, samples from the control-, DNCB-, DNCB + AB-, and DNCB + horse oil-treated mice were hybridized onto mouse <t>oligo</t> microarray slides, which were then scanned and analyzed. DNCB, 2, 4-dinitrochlorobenzene; AB, Atobarrier lotion.
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    Image Search Results


    Temporal correlation between the expression of global miRNAs and renal function indexes. (A) Temporal miRNA expression change within 48 h after renal IRI. miRNA abundance is defined as raw microarray signal output normalized to the blank value 0.1; ∗ p

    Journal: PeerJ

    Article Title: Global miRNA expression is temporally correlated with acute kidney injury in mice

    doi: 10.7717/peerj.1729

    Figure Lengend Snippet: Temporal correlation between the expression of global miRNAs and renal function indexes. (A) Temporal miRNA expression change within 48 h after renal IRI. miRNA abundance is defined as raw microarray signal output normalized to the blank value 0.1; ∗ p

    Article Snippet: Global miRNA expression was detected in the tissue samples using the Agilent mouse miRNA microarray (Release 19.0, 8 × 60K).

    Techniques: Expressing, Microarray

    Assessment of the specificity of the ChIP protocol. A) Arx immunoprecipitation from N2a cells transfected with an Arx-expressing vector or a vector alone and using the Arx C-14 antibody from Santa Cruz. Detection using the anti-Arx-HD antibody revealed a major band at approximately 80 kD, which corresponds to the size of Arx protein. TE: total extracts, IP: immunoprecipitation, Ig: immunoglobulins. B) Enrichment of Ebf3 , Lmo1 and Shox2 promoter regions was assessed by qPCR using either Arx or PolII-immunoprecipitates or using no antibody and was compared to the total input. Gapdh was used as a positive control with DNA Pol II. Here, we show an example of the results obtained in a ChIP experiment with Arx C-14 antibody from Santa Cruz. The enrichment of Ebf3 , Lmo1 and Shox2 was checked similarly for each replicate experiment before DNA was applied to the microarrays.

    Journal: PLoS ONE

    Article Title: High-Throughput Analysis of Promoter Occupancy Reveals New Targets for Arx, a Gene Mutated in Mental Retardation and Interneuronopathies

    doi: 10.1371/journal.pone.0025181

    Figure Lengend Snippet: Assessment of the specificity of the ChIP protocol. A) Arx immunoprecipitation from N2a cells transfected with an Arx-expressing vector or a vector alone and using the Arx C-14 antibody from Santa Cruz. Detection using the anti-Arx-HD antibody revealed a major band at approximately 80 kD, which corresponds to the size of Arx protein. TE: total extracts, IP: immunoprecipitation, Ig: immunoglobulins. B) Enrichment of Ebf3 , Lmo1 and Shox2 promoter regions was assessed by qPCR using either Arx or PolII-immunoprecipitates or using no antibody and was compared to the total input. Gapdh was used as a positive control with DNA Pol II. Here, we show an example of the results obtained in a ChIP experiment with Arx C-14 antibody from Santa Cruz. The enrichment of Ebf3 , Lmo1 and Shox2 was checked similarly for each replicate experiment before DNA was applied to the microarrays.

    Article Snippet: Identification of an Arx-binding motif in ChIP-positive sequences obtained from Arx-transfected N2a cells The mouse promoter microarrays from Agilent Technologies (G4490A) consist of two arrays with approximately 244 000 60-mer oligonucleotide probes spaced every 100–300 bp across regions of interest.

    Techniques: Chromatin Immunoprecipitation, Immunoprecipitation, Transfection, Expressing, Plasmid Preparation, Real-time Polymerase Chain Reaction, Positive Control

    Gene sets from microarray experiment Single cell suspension of HT168M1 human melanoma cell line was semiorthotopically implanted into newborn SCID mice. The RNA expression pattern of this, metastatic version of the primary tumor was investigated via Agilent Mouse Oligo Microarray Platform. The stromal expression changes were compared to healthy, age matched controls and the nineteen genes showing the largest expressional changes were selected for further validation.

    Journal: Oncotarget

    Article Title: The importance of microenvironment: the role of CCL8 in metastasis formation of melanoma

    doi:

    Figure Lengend Snippet: Gene sets from microarray experiment Single cell suspension of HT168M1 human melanoma cell line was semiorthotopically implanted into newborn SCID mice. The RNA expression pattern of this, metastatic version of the primary tumor was investigated via Agilent Mouse Oligo Microarray Platform. The stromal expression changes were compared to healthy, age matched controls and the nineteen genes showing the largest expressional changes were selected for further validation.

    Article Snippet: Agilent mouse oligo microarray analysis The Agilent Mouse Oligo Microarray is comprised of 22,575 (60-mer) oligonucleotide probes representing 20,000 mouse genes and transcripts in the mouse genome.

    Techniques: Microarray, Mouse Assay, RNA Expression, Expressing

    Scanned image of cDNA microarray chips. After labeling of cRNA, samples from the control-, DNCB-, DNCB + AB-, and DNCB + horse oil-treated mice were hybridized onto mouse oligo microarray slides, which were then scanned and analyzed. DNCB, 2, 4-dinitrochlorobenzene; AB, Atobarrier lotion.

    Journal: Journal of Veterinary Science

    Article Title: Restoration of the inflammatory gene expression by horse oil in DNCB-treated mice skin

    doi: 10.4142/jvs.2020.21.e15

    Figure Lengend Snippet: Scanned image of cDNA microarray chips. After labeling of cRNA, samples from the control-, DNCB-, DNCB + AB-, and DNCB + horse oil-treated mice were hybridized onto mouse oligo microarray slides, which were then scanned and analyzed. DNCB, 2, 4-dinitrochlorobenzene; AB, Atobarrier lotion.

    Article Snippet: The fragmented cRNA was resuspended with 2× hybridization buffer and directly pipetted onto assembled Mouse Oligo Microarray 44K (Agilent Technology).

    Techniques: Microarray, Labeling, Mouse Assay