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whole mouse genome 4 × 44k oligo microarrays  (Agilent technologies)


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    Agilent technologies whole mouse genome 4 × 44k oligo microarrays
    Whole Mouse Genome 4 × 44k Oligo Microarrays, 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/whole+mouse+genome+oligo+4_44k+microarray/pmc03672050-149-25-24
    Average 90 stars, based on 1 article reviews
    whole mouse genome 4 × 44k oligo microarrays - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    Microarray:

    Article Title: Transcriptomics and proteomics analyses of the PACAP38 influenced ischemic brain in permanent middle cerebral artery occlusion model mice
    Article Snippet: The gels were stained (8 μL of 10 mg/mL ethidium bromide in 200 mL 1X TAE buffer) for approximately 7 minutes and the stained bands were visualized with the ChemiDoc XRS+ imaging system (Bio-Rad, 6000 Alfred Nobel Drive, Hercules, CA 94547, USA). .. A mouse 4 × 44K whole genome oligo DNA microarray chip (G4122F, Agilent Technologies, Palo Alto, CA, USA) was used for global gene expression analysis using the ipsilateral (ischemic) hemisphere. .. Briefly, total RNA (900 ng; 300 ng for each replicate pooled) was labeled with either Cy3 or Cy5 dye using an Agilent Low RNA Input Fluorescent Linear Amplification Kit (Agilent).

    Article Title: Microarray Analysis of Gene Expression Changes in Neuroplastin 65-Knockout Mice: Implications for Abnormal Cognition and Emotional Disorders.
    Article Snippet: One microgram of total RNA was amplified and labeled with a One-Color Quick Amp Labeling Kit (5190-0442, Agilent Technologies, Santa Clara, CA). .. The fluorescencelabeled cRNA was hybridized onto the Whole Mouse Genome Oligo Microarray (4 9 44K, Agilent Technologies, Santa Clara, CA) using the Agilent Gene Expression Hybridization Kit (5188-5242, Agilent Technologies, Santa Clara, CA). .. Chips were washed and scanned by a microarray scanner (G2565BA, Agilent Technologies, Santa Clara, CA).

    Article Title: B cell hyperactivation in an Ackr4-deficient mouse strain is not caused by lack of ACKR4 expression.
    Article Snippet: 1Institute of Immunology, Hannover Medical School, Carl-Neuberg-Straße, Hannover, Germany 2Cluster of Excellence RESIST (EXC 2155), HannoverMedical School, Carl-Neuberg-Straße, Hannover, Germany Correspondence Prof.Dr.. ReinholdFörster,HannoverMedical School, Carl-Neuberg-Straße1, 30625 Hannover,Germany.. E-mail: foerster.reinhold@mh-hannover.de Abstract The majority of genetically modified C57BL/6 mice contain congenic passenger DNA around the targeted gene locus as they were generated from 129-derived embryonic stem cells (ESCs) with subsequent backcrossing to the C57BL/6 genetic background.When studying the role of atypical chemokine receptor 4 (ACKR4) in the immune system, we realized that the two available Ackr4deficientmouse strains (Ackr4−/− andAckr4GFP/GFP) show profoundly different phenotypes: Compared to wild-type and Ackr4GFP/GFP mice, Ackr4−/− mice show a strong accumulation of plasma blasts in mesenteric lymph node and spleen as well as increased B cell proliferation after in vitro activation.

    Gene Expression:

    Article Title: Transcriptomics and proteomics analyses of the PACAP38 influenced ischemic brain in permanent middle cerebral artery occlusion model mice
    Article Snippet: The gels were stained (8 μL of 10 mg/mL ethidium bromide in 200 mL 1X TAE buffer) for approximately 7 minutes and the stained bands were visualized with the ChemiDoc XRS+ imaging system (Bio-Rad, 6000 Alfred Nobel Drive, Hercules, CA 94547, USA). .. A mouse 4 × 44K whole genome oligo DNA microarray chip (G4122F, Agilent Technologies, Palo Alto, CA, USA) was used for global gene expression analysis using the ipsilateral (ischemic) hemisphere. .. Briefly, total RNA (900 ng; 300 ng for each replicate pooled) was labeled with either Cy3 or Cy5 dye using an Agilent Low RNA Input Fluorescent Linear Amplification Kit (Agilent).

    Article Title: Microarray Analysis of Gene Expression Changes in Neuroplastin 65-Knockout Mice: Implications for Abnormal Cognition and Emotional Disorders.
    Article Snippet: One microgram of total RNA was amplified and labeled with a One-Color Quick Amp Labeling Kit (5190-0442, Agilent Technologies, Santa Clara, CA). .. The fluorescencelabeled cRNA was hybridized onto the Whole Mouse Genome Oligo Microarray (4 9 44K, Agilent Technologies, Santa Clara, CA) using the Agilent Gene Expression Hybridization Kit (5188-5242, Agilent Technologies, Santa Clara, CA). .. Chips were washed and scanned by a microarray scanner (G2565BA, Agilent Technologies, Santa Clara, CA).

    Hybridization:

    Article Title: Microarray Analysis of Gene Expression Changes in Neuroplastin 65-Knockout Mice: Implications for Abnormal Cognition and Emotional Disorders.
    Article Snippet: One microgram of total RNA was amplified and labeled with a One-Color Quick Amp Labeling Kit (5190-0442, Agilent Technologies, Santa Clara, CA). .. The fluorescencelabeled cRNA was hybridized onto the Whole Mouse Genome Oligo Microarray (4 9 44K, Agilent Technologies, Santa Clara, CA) using the Agilent Gene Expression Hybridization Kit (5188-5242, Agilent Technologies, Santa Clara, CA). .. Chips were washed and scanned by a microarray scanner (G2565BA, Agilent Technologies, Santa Clara, CA).

    other:

    Article Title: The role of transcriptional factor D-site-binding protein in circadian CCL2 gene expression in anti-Thy1 nephritis
    Article Snippet: The whole-mouse genome Oligo Microarray 4 × 44k V2 gene kit (Agilent, Santa Clara, CA, USA) was used to detect mRNA expression profiles, according to the manufacturer’s instructions.

    Article Title: D-site binding protein regulates cell proliferation through mediating cell cycle progression in rat mesangial cells.
    Article Snippet: Over proliferation of glomerular mesangial cells (MCs) disturbs mesangial homeostasis and leads to renal damage in mesangioproliferative glomerulonephritis.. It is documented that transcriptional factors may be involved in the proliferation of MCs.. This study aims to identify the key transcriptional factor that prevents the MCs from over proliferation and to clarify its regulatory mechanism.

    Article Title: Identification of Gene Expression Changes from Colitis to CRC in the Mouse CAC Model
    Article Snippet: The mouse expression profiles were scanned using an Agilent Whole Mouse Genome Oligo Microarray (4×44K) platform for the states of AD, D, and K, and each state was assessed with 3 biological replicates.

    Article Title: Prenatal Alcohol Exposure Impairs the Placenta–Cortex Transcriptomic Signature, Leading to Dysregulation of Angiogenic Pathways
    Article Snippet: One-color comparative hybridization was performed using Whole Mouse Genome Oligo 4_44K Microarray (G2519F-014868, Agilent Technologies, Les Ulis, France) to compare gene expression profiling. cRNAs were synthesized from 100 ng total RNA, labeled using a Quick Amp Labeling Kit (Agilent Technologies), and hybridized on microarrays at 65 °C for 17 h. Raw hybridization data, evaluated on every probe 5 μm-sized array, using a DNA microarray scanner G2565CA (Agilent Technologies), were extracted with Feature Extraction Software 10.5.1.1 (Agilent Technologies), then transferred to Genespring ® (GX 12.6 software, Agilent Technologies) for data processing (normalization) and data mining ( B).

    Labeling:

    Article Title: GATA 2 hypomorphism induces chronic myelomonocytic leukemia in mice
    Article Snippet: .. For microarray analyses, RNA quality was verified with an Agilent‐2100 Bioanalyzer; RNA was labeled with Cy3 using a Low Input Quick Amp Labeling Kit and hybridized to a Whole Mouse Genome Oligo Microarray (4 × 44K; Agilent Technologies, Santa Clara, CA, USA) according to the manufacturer's instructions. .. Microarray slide scanning was undertaken with an Agilent DNA microarray scanner.

    Expressing:

    Article Title: B cell hyperactivation in an Ackr4-deficient mouse strain is not caused by lack of ACKR4 expression.
    Article Snippet: 1Institute of Immunology, Hannover Medical School, Carl-Neuberg-Straße, Hannover, Germany 2Cluster of Excellence RESIST (EXC 2155), HannoverMedical School, Carl-Neuberg-Straße, Hannover, Germany Correspondence Prof.Dr.. ReinholdFörster,HannoverMedical School, Carl-Neuberg-Straße1, 30625 Hannover,Germany.. E-mail: foerster.reinhold@mh-hannover.de Abstract The majority of genetically modified C57BL/6 mice contain congenic passenger DNA around the targeted gene locus as they were generated from 129-derived embryonic stem cells (ESCs) with subsequent backcrossing to the C57BL/6 genetic background.When studying the role of atypical chemokine receptor 4 (ACKR4) in the immune system, we realized that the two available Ackr4deficientmouse strains (Ackr4−/− andAckr4GFP/GFP) show profoundly different phenotypes: Compared to wild-type and Ackr4GFP/GFP mice, Ackr4−/− mice show a strong accumulation of plasma blasts in mesenteric lymph node and spleen as well as increased B cell proliferation after in vitro activation.



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    Agilent technologies whole mouse genome oligo microarray (cat. no. g4122f; 4×44k;
    GO analysis of gene expression arrays. (A) Gene expression profile analysis of undifferented BM-MSCs, 3D hepatocyte-like cells and primary mice hepatocyte by cDNA <t>microarray.</t> (B) Gene Ontology analysis of downregulation and (C) Gene Ontology analysis of upregulation. GO enrichment analysis demonstrated that signaling pathways associated with liver function were the most significantly upregulated, and cell cycle-associated signaling pathways were the most significantly downregulated in 3D hepatocyte-like cells, relative to mouse BM-MSCs. GO, gene ontology; BM-MSCs, bone marrow-derived mesenchymal stem cells.
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    Agilent technologies whole mouse genome (4 × 44k) oligo microarrays
    GO analysis of gene expression arrays. (A) Gene expression profile analysis of undifferented BM-MSCs, 3D hepatocyte-like cells and primary mice hepatocyte by cDNA <t>microarray.</t> (B) Gene Ontology analysis of downregulation and (C) Gene Ontology analysis of upregulation. GO enrichment analysis demonstrated that signaling pathways associated with liver function were the most significantly upregulated, and cell cycle-associated signaling pathways were the most significantly downregulated in 3D hepatocyte-like cells, relative to mouse BM-MSCs. GO, gene ontology; BM-MSCs, bone marrow-derived mesenchymal stem cells.
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    Image Search Results


    GO analysis of gene expression arrays. (A) Gene expression profile analysis of undifferented BM-MSCs, 3D hepatocyte-like cells and primary mice hepatocyte by cDNA microarray. (B) Gene Ontology analysis of downregulation and (C) Gene Ontology analysis of upregulation. GO enrichment analysis demonstrated that signaling pathways associated with liver function were the most significantly upregulated, and cell cycle-associated signaling pathways were the most significantly downregulated in 3D hepatocyte-like cells, relative to mouse BM-MSCs. GO, gene ontology; BM-MSCs, bone marrow-derived mesenchymal stem cells.

    Journal: Molecular Medicine Reports

    Article Title: Hepatic differentiation of mouse bone marrow-derived mesenchymal stem cells using a novel 3D culture system

    doi: 10.3892/mmr.2017.7818

    Figure Lengend Snippet: GO analysis of gene expression arrays. (A) Gene expression profile analysis of undifferented BM-MSCs, 3D hepatocyte-like cells and primary mice hepatocyte by cDNA microarray. (B) Gene Ontology analysis of downregulation and (C) Gene Ontology analysis of upregulation. GO enrichment analysis demonstrated that signaling pathways associated with liver function were the most significantly upregulated, and cell cycle-associated signaling pathways were the most significantly downregulated in 3D hepatocyte-like cells, relative to mouse BM-MSCs. GO, gene ontology; BM-MSCs, bone marrow-derived mesenchymal stem cells.

    Article Snippet: Sample labeling and array hybridization were performed with Whole Mouse Genome Oligo Microarray (cat. no. G4122F; 4×44K; Agilent Technologies, Inc., Santa Clara, CA, USA).

    Techniques: Expressing, Microarray, Derivative Assay