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microarray data analysis tool software package  (Filgen Inc)

 
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    Structured Review

    Filgen Inc microarray data analysis tool software package
    A, Electrophoresis of whole serum (WS) or fractionated serum IgG derived from a systemic lupus erythematosus (SLE) patient (L) and a normal subject (N). Molecular weight marker (M) is shown at the right. B, Scatterplot of entire gene set considered by <t>microarray</t> analysis to be expressed in podocytes (P < 0.05). The position of each dot on the scatterplot corresponds to the normalized average signal intensity (log scale) of a single gene. The normalized average signal intensity after exposure to SLE IgG and normal IgG is shown on the x and y axes, respectively. Broken red lines represent normal IgG:SLE IgG ratios of 2.0 (top; 2-fold greater expression in normal IgG) and 0.5 (bottom; 2-fold greater expression in SLE IgG). Black broken line is the mean.
    Microarray Data Analysis Tool Software Package, supplied by Filgen 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/microarray+data+analysis+tool+software+package/microarray+data+analysis+tool/pmc06103450-168-7-13
    Average 90 stars, based on 1 article reviews
    microarray data analysis tool software package - by Bioz Stars, 2026-09
    90/100 stars

    Images

    1) Product Images from "Lupus Nephritis IgG Induction of Calcium/Calmodulin-Dependent Protein Kinase IV Expression in Podocytes and Alteration of Their Function"

    Article Title: Lupus Nephritis IgG Induction of Calcium/Calmodulin-Dependent Protein Kinase IV Expression in Podocytes and Alteration of Their Function

    Journal: Arthritis & rheumatology (Hoboken, N.J.)

    doi: 10.1002/art.39499

    A, Electrophoresis of whole serum (WS) or fractionated serum IgG derived from a systemic lupus erythematosus (SLE) patient (L) and a normal subject (N). Molecular weight marker (M) is shown at the right. B, Scatterplot of entire gene set considered by microarray analysis to be expressed in podocytes (P < 0.05). The position of each dot on the scatterplot corresponds to the normalized average signal intensity (log scale) of a single gene. The normalized average signal intensity after exposure to SLE IgG and normal IgG is shown on the x and y axes, respectively. Broken red lines represent normal IgG:SLE IgG ratios of 2.0 (top; 2-fold greater expression in normal IgG) and 0.5 (bottom; 2-fold greater expression in SLE IgG). Black broken line is the mean.
    Figure Legend Snippet: A, Electrophoresis of whole serum (WS) or fractionated serum IgG derived from a systemic lupus erythematosus (SLE) patient (L) and a normal subject (N). Molecular weight marker (M) is shown at the right. B, Scatterplot of entire gene set considered by microarray analysis to be expressed in podocytes (P < 0.05). The position of each dot on the scatterplot corresponds to the normalized average signal intensity (log scale) of a single gene. The normalized average signal intensity after exposure to SLE IgG and normal IgG is shown on the x and y axes, respectively. Broken red lines represent normal IgG:SLE IgG ratios of 2.0 (top; 2-fold greater expression in normal IgG) and 0.5 (bottom; 2-fold greater expression in SLE IgG). Black broken line is the mean.

    Techniques Used: Electrophoresis, Derivative Assay, Molecular Weight, Marker, Microarray, Expressing

    Related Articles

    Microarray:

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    Article Title: Increased fatty acid synthesis and disturbed lipid metabolism in Neuro2a cells after repeated cocaine exposure: A preliminary study.
    Article Snippet: Chronic use of cocaine prompts neurodegeneration and neuroinflammation.. Lipids play pivotal roles in neuronal function and pathology.. Although evidence correlates cocaine use with the alteration of lipid metabolism in blood and brain, the precise mechanism remains to be elucidated.

    Article Title: Sustained splenic contraction after daily cocaine administration in rats
    Article Snippet: The purified total RNA was examined for integrity on a BioAnalyzer (Agilent Technologies), and hybridized to Clariom TM S array (Thermo Fisher Scientific). .. The results were deposited in the GEO database ( https://www.ncbi.nlm.nih.gov/geo/ , accession number GSE167238) and analyzed using the Microarray Data Analysis Tool (Filgen Inc, Nagoya, Japan) and the DAVID functional annotation tool ( https://david.ncifcrf.gov/summary.jsp ). ..

    Article Title: microRNA-203 inhibits migration and invasion of canine tonsillar squamous cell carcinoma cells by targeting SLUG
    Article Snippet: .. The data were analyzed using the Microarray Data Analysis tool (Filgen, Inc., Aichi, Japan), and miRNAs showing >2-fold differential expression are indicated in a heatmap. ..

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    Software:

    Article Title: Increased fatty acid synthesis and disturbed lipid metabolism in Neuro2a cells after repeated cocaine exposure: A preliminary study.
    Article Snippet: Chronic use of cocaine prompts neurodegeneration and neuroinflammation.. Lipids play pivotal roles in neuronal function and pathology.. Although evidence correlates cocaine use with the alteration of lipid metabolism in blood and brain, the precise mechanism remains to be elucidated.

    Functional Assay:

    Article Title: Sustained splenic contraction after daily cocaine administration in rats
    Article Snippet: The purified total RNA was examined for integrity on a BioAnalyzer (Agilent Technologies), and hybridized to Clariom TM S array (Thermo Fisher Scientific). .. The results were deposited in the GEO database ( https://www.ncbi.nlm.nih.gov/geo/ , accession number GSE167238) and analyzed using the Microarray Data Analysis Tool (Filgen Inc, Nagoya, Japan) and the DAVID functional annotation tool ( https://david.ncifcrf.gov/summary.jsp ). ..

    Quantitative Proteomics:

    Article Title: microRNA-203 inhibits migration and invasion of canine tonsillar squamous cell carcinoma cells by targeting SLUG
    Article Snippet: .. The data were analyzed using the Microarray Data Analysis tool (Filgen, Inc., Aichi, Japan), and miRNAs showing >2-fold differential expression are indicated in a heatmap. ..

    other:

    Article Title: Augmented effect of fibroblast growth factor 18 in bone morphogenetic protein 2-induced calvarial bone healing by activation of CCL2/CCR2 axis on M2 macrophage polarization
    Article Snippet: Data were analyzed by the Expression ConsoleTM Software (Thermo Fisher Scientific Inc., USA) and the target gene list was sorted by the Microarray Dara Analysis Tool (Filgen Inc., Japan) and Microsoft Excel (Microsoft Corporation, USA).



    Similar Products

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    Filgen Inc microarray data analysis tool software package
    A, Electrophoresis of whole serum (WS) or fractionated serum IgG derived from a systemic lupus erythematosus (SLE) patient (L) and a normal subject (N). Molecular weight marker (M) is shown at the right. B, Scatterplot of entire gene set considered by <t>microarray</t> analysis to be expressed in podocytes (P < 0.05). The position of each dot on the scatterplot corresponds to the normalized average signal intensity (log scale) of a single gene. The normalized average signal intensity after exposure to SLE IgG and normal IgG is shown on the x and y axes, respectively. Broken red lines represent normal IgG:SLE IgG ratios of 2.0 (top; 2-fold greater expression in normal IgG) and 0.5 (bottom; 2-fold greater expression in SLE IgG). Black broken line is the mean.
    Microarray Data Analysis Tool Software Package, supplied by Filgen 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/microarray+data+analysis+tool+software+package/microarray+data+analysis+tool/pmc06103450-168-7-13
    Average 90 stars, based on 1 article reviews
    microarray data analysis tool software package - by Bioz Stars, 2026-09
    90/100 stars
      Buy from Supplier

    Image Search Results


    A, Electrophoresis of whole serum (WS) or fractionated serum IgG derived from a systemic lupus erythematosus (SLE) patient (L) and a normal subject (N). Molecular weight marker (M) is shown at the right. B, Scatterplot of entire gene set considered by microarray analysis to be expressed in podocytes (P < 0.05). The position of each dot on the scatterplot corresponds to the normalized average signal intensity (log scale) of a single gene. The normalized average signal intensity after exposure to SLE IgG and normal IgG is shown on the x and y axes, respectively. Broken red lines represent normal IgG:SLE IgG ratios of 2.0 (top; 2-fold greater expression in normal IgG) and 0.5 (bottom; 2-fold greater expression in SLE IgG). Black broken line is the mean.

    Journal: Arthritis & rheumatology (Hoboken, N.J.)

    Article Title: Lupus Nephritis IgG Induction of Calcium/Calmodulin-Dependent Protein Kinase IV Expression in Podocytes and Alteration of Their Function

    doi: 10.1002/art.39499

    Figure Lengend Snippet: A, Electrophoresis of whole serum (WS) or fractionated serum IgG derived from a systemic lupus erythematosus (SLE) patient (L) and a normal subject (N). Molecular weight marker (M) is shown at the right. B, Scatterplot of entire gene set considered by microarray analysis to be expressed in podocytes (P < 0.05). The position of each dot on the scatterplot corresponds to the normalized average signal intensity (log scale) of a single gene. The normalized average signal intensity after exposure to SLE IgG and normal IgG is shown on the x and y axes, respectively. Broken red lines represent normal IgG:SLE IgG ratios of 2.0 (top; 2-fold greater expression in normal IgG) and 0.5 (bottom; 2-fold greater expression in SLE IgG). Black broken line is the mean.

    Article Snippet: Scan data images were analyzed using the Microarray Data Analysis Tool software package (Filgen), a comprehensive program that also produced the gene ontology and Z score reports.

    Techniques: Electrophoresis, Derivative Assay, Molecular Weight, Marker, Microarray, Expressing