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image analysis software nonlinear dynamics progenesis samespots version 2.3  (Nonlinear Dynamics)

 
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    Nonlinear Dynamics image analysis software nonlinear dynamics progenesis samespots version 2.3
    Image Analysis Software Nonlinear Dynamics Progenesis Samespots Version 2.3, supplied by Nonlinear Dynamics, 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/nonlinear+dynamics+image+analysis+software/computer+software+progenesis+samespots+version+2+0/pm28089893-192-23-26
    Average 90 stars, based on 1 article reviews
    image analysis software nonlinear dynamics progenesis samespots version 2.3 - by Bioz Stars, 2026-10
    90/100 stars

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    Software:

    Article Title: Time-dependent changes in protein expression in rainbow trout muscle following hypoxia.
    Article Snippet: Article history: Received 13 October 2011 Accepted 2 February 2012 Available online 21 February 2012 Adaptation to hypoxia is a complex process, and individual proteins will be upor downregulated in order to address the main challenges at any given time.. To investigate the dynamicsof the adaptation, rainbow trout (Oncorhynchusmykiss) was exposed to 30%of normal oxygen tension for 1, 2, 5 and 24 h respectively, after which muscle samples were taken.. The successful investigation of numerous proteins in a single study was achieved by selectively separating the sarcoplasmic proteins using 2-DE.

    Article Title: Proteomic characterization of the interactions between fish serum proteins and waterborne bacteria reveals the suppression of anti-oxidative defense as a serum-mediated antimicrobial mechanism.
    Article Snippet: Accepted Manuscript Proteomic characterization of the interactions between fish serum proteins and waterborne bacteria reveals the suppression of anti-oxidative defense as a serummediated antimicrobial mechanism Miao Dong, Yimin Liang, Rajkumar Ramalingam, Sze Wing Tang, Wei Shen, Rui Ye, Singaram Gopalakrishnan, Doris Wai Ting Au, Yun Wah Lam PII: S1050-4648(17)30023-2 DOI: 10.1016/j.fsi.2017.01.013 Reference: YFSIM 4390 To appear in: Fish and Shellfish Immunology Received Date: 29 July 2016 Revised Date: 6 January 2017 Accepted Date: 7 January 2017 Please cite this article as: Dong M, Liang Y, Ramalingam R, Tang SW, Shen W, Ye R, Gopalakrishnan S, Ting Au DW, Lam YW, Proteomic characterization of the interactions between fish serum proteins and waterborne bacteria reveals the suppression of anti-oxidative defense as a serum-mediated antimicrobial mechanism, Fish and Shellfish Immunology (2017), doi: 10.1016/j.fsi.2017.01.013.. This is a PDF file of an unedited manuscript that has been accepted for publication.. As a service to our customers we are providing this early version of the manuscript.

    other:

    Article Title: Differential proteome-metabolome profiling of YCA1-knock-out and wild type cells reveals novel metabolic pathways and cellular processes dependent on the yeast metacaspase.
    Article Snippet: The yeast Saccharomyces cerevisiae expresses one member of the metacaspase Cys protease family, encoded by the YCA1 gene.. Combination of proteomics and metabolomics data showed that YCA1 deletion down-regulated glycolysis, the TCA cycle and alcoholic fermentation as compared with WT cells.. Dyca1 cells also showed a down-regulation of the pentose phosphate pathway and accumulation of pyruvate, correlated with higher levels of certain amino acids found in these cells.

    Article Title: Investigation of adipocyte proteome during the differentiation of brown preadipocytes.
    Article Snippet: Investigation of adipocyte proteome during the differentiation of brown preadipocytes Abu Hena Mostafa Kamal, Won Kon Kim, Kun Cho, Anna Park, Jeong-Ki Min, Baek Soo Han, Sung Goo Park, Sang Chul Lee⁎, Kwang-Hee Bae⁎⁎ Research Center for Integrated Cellulomics, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon 305-806, Republic of Korea Division of Mass Spectrometry Research, Korea Basic Science Institute (KBSI), Ochang, Chungbuk 863-883, Republic of Korea Medical Proteomics Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon 305-806, Republic of Korea

    Article Title: Proteome and metabolome profiling of wild-type and YCA1-knock-out yeast cells during acetic acid-induced programmed cell death.
    Article Snippet: Caspase proteases are responsible for the regulated disassembly of the cell into apoptotic bodies during mammalian apoptosis.. Structural homologs of the caspase family (called metacaspases) are involved in programmed cell death in single-cell eukaryotes, yet the molecular mechanisms that contribute to death are currently undefined.. Recent evidence revealed that a programmed cell death process is induced by acid acetic (AA-PCD) in Saccharomyces cerevisiae both in presence and in absence of metacaspase encoding gene YCA1.

    Staining:

    Article Title: Proteomic characterization of the interactions between fish serum proteins and waterborne bacteria reveals the suppression of anti-oxidative defense as a serum-mediated antimicrobial mechanism.
    Article Snippet: Accepted Manuscript Proteomic characterization of the interactions between fish serum proteins and waterborne bacteria reveals the suppression of anti-oxidative defense as a serummediated antimicrobial mechanism Miao Dong, Yimin Liang, Rajkumar Ramalingam, Sze Wing Tang, Wei Shen, Rui Ye, Singaram Gopalakrishnan, Doris Wai Ting Au, Yun Wah Lam PII: S1050-4648(17)30023-2 DOI: 10.1016/j.fsi.2017.01.013 Reference: YFSIM 4390 To appear in: Fish and Shellfish Immunology Received Date: 29 July 2016 Revised Date: 6 January 2017 Accepted Date: 7 January 2017 Please cite this article as: Dong M, Liang Y, Ramalingam R, Tang SW, Shen W, Ye R, Gopalakrishnan S, Ting Au DW, Lam YW, Proteomic characterization of the interactions between fish serum proteins and waterborne bacteria reveals the suppression of anti-oxidative defense as a serum-mediated antimicrobial mechanism, Fish and Shellfish Immunology (2017), doi: 10.1016/j.fsi.2017.01.013.. This is a PDF file of an unedited manuscript that has been accepted for publication.. As a service to our customers we are providing this early version of the manuscript.

    Two-Dimensional Gel Electrophoresis:

    Article Title: Proteomic characterization of the interactions between fish serum proteins and waterborne bacteria reveals the suppression of anti-oxidative defense as a serum-mediated antimicrobial mechanism.
    Article Snippet: Accepted Manuscript Proteomic characterization of the interactions between fish serum proteins and waterborne bacteria reveals the suppression of anti-oxidative defense as a serummediated antimicrobial mechanism Miao Dong, Yimin Liang, Rajkumar Ramalingam, Sze Wing Tang, Wei Shen, Rui Ye, Singaram Gopalakrishnan, Doris Wai Ting Au, Yun Wah Lam PII: S1050-4648(17)30023-2 DOI: 10.1016/j.fsi.2017.01.013 Reference: YFSIM 4390 To appear in: Fish and Shellfish Immunology Received Date: 29 July 2016 Revised Date: 6 January 2017 Accepted Date: 7 January 2017 Please cite this article as: Dong M, Liang Y, Ramalingam R, Tang SW, Shen W, Ye R, Gopalakrishnan S, Ting Au DW, Lam YW, Proteomic characterization of the interactions between fish serum proteins and waterborne bacteria reveals the suppression of anti-oxidative defense as a serum-mediated antimicrobial mechanism, Fish and Shellfish Immunology (2017), doi: 10.1016/j.fsi.2017.01.013.. This is a PDF file of an unedited manuscript that has been accepted for publication.. As a service to our customers we are providing this early version of the manuscript.

    Binding Assay:

    Article Title: Proteomic characterization of the interactions between fish serum proteins and waterborne bacteria reveals the suppression of anti-oxidative defense as a serum-mediated antimicrobial mechanism.
    Article Snippet: Accepted Manuscript Proteomic characterization of the interactions between fish serum proteins and waterborne bacteria reveals the suppression of anti-oxidative defense as a serummediated antimicrobial mechanism Miao Dong, Yimin Liang, Rajkumar Ramalingam, Sze Wing Tang, Wei Shen, Rui Ye, Singaram Gopalakrishnan, Doris Wai Ting Au, Yun Wah Lam PII: S1050-4648(17)30023-2 DOI: 10.1016/j.fsi.2017.01.013 Reference: YFSIM 4390 To appear in: Fish and Shellfish Immunology Received Date: 29 July 2016 Revised Date: 6 January 2017 Accepted Date: 7 January 2017 Please cite this article as: Dong M, Liang Y, Ramalingam R, Tang SW, Shen W, Ye R, Gopalakrishnan S, Ting Au DW, Lam YW, Proteomic characterization of the interactions between fish serum proteins and waterborne bacteria reveals the suppression of anti-oxidative defense as a serum-mediated antimicrobial mechanism, Fish and Shellfish Immunology (2017), doi: 10.1016/j.fsi.2017.01.013.. This is a PDF file of an unedited manuscript that has been accepted for publication.. As a service to our customers we are providing this early version of the manuscript.

    Bacteria:

    Article Title: Proteomic characterization of the interactions between fish serum proteins and waterborne bacteria reveals the suppression of anti-oxidative defense as a serum-mediated antimicrobial mechanism.
    Article Snippet: Accepted Manuscript Proteomic characterization of the interactions between fish serum proteins and waterborne bacteria reveals the suppression of anti-oxidative defense as a serummediated antimicrobial mechanism Miao Dong, Yimin Liang, Rajkumar Ramalingam, Sze Wing Tang, Wei Shen, Rui Ye, Singaram Gopalakrishnan, Doris Wai Ting Au, Yun Wah Lam PII: S1050-4648(17)30023-2 DOI: 10.1016/j.fsi.2017.01.013 Reference: YFSIM 4390 To appear in: Fish and Shellfish Immunology Received Date: 29 July 2016 Revised Date: 6 January 2017 Accepted Date: 7 January 2017 Please cite this article as: Dong M, Liang Y, Ramalingam R, Tang SW, Shen W, Ye R, Gopalakrishnan S, Ting Au DW, Lam YW, Proteomic characterization of the interactions between fish serum proteins and waterborne bacteria reveals the suppression of anti-oxidative defense as a serum-mediated antimicrobial mechanism, Fish and Shellfish Immunology (2017), doi: 10.1016/j.fsi.2017.01.013.. This is a PDF file of an unedited manuscript that has been accepted for publication.. As a service to our customers we are providing this early version of the manuscript.

    Labeling:

    Article Title: Proteomic characterization of the interactions between fish serum proteins and waterborne bacteria reveals the suppression of anti-oxidative defense as a serum-mediated antimicrobial mechanism.
    Article Snippet: Accepted Manuscript Proteomic characterization of the interactions between fish serum proteins and waterborne bacteria reveals the suppression of anti-oxidative defense as a serummediated antimicrobial mechanism Miao Dong, Yimin Liang, Rajkumar Ramalingam, Sze Wing Tang, Wei Shen, Rui Ye, Singaram Gopalakrishnan, Doris Wai Ting Au, Yun Wah Lam PII: S1050-4648(17)30023-2 DOI: 10.1016/j.fsi.2017.01.013 Reference: YFSIM 4390 To appear in: Fish and Shellfish Immunology Received Date: 29 July 2016 Revised Date: 6 January 2017 Accepted Date: 7 January 2017 Please cite this article as: Dong M, Liang Y, Ramalingam R, Tang SW, Shen W, Ye R, Gopalakrishnan S, Ting Au DW, Lam YW, Proteomic characterization of the interactions between fish serum proteins and waterborne bacteria reveals the suppression of anti-oxidative defense as a serum-mediated antimicrobial mechanism, Fish and Shellfish Immunology (2017), doi: 10.1016/j.fsi.2017.01.013.. This is a PDF file of an unedited manuscript that has been accepted for publication.. As a service to our customers we are providing this early version of the manuscript.



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    Nonlinear Dynamics total lab nonlinear dynamics image analysis software
    Heterozygous (+/−) FVB/N K14-T7PKCε mice were crossed for four generations to wildtype (−/−) outcrossed SKH-1 hairless mice for transmission of the transgene and hairlessness. a: Phenotype of female SKH-1K14-T7PKCε transgenic mice. Shown are the photographs of adult SKH-1 hairless PKCε transgenic mouse and its wildtype littermate at 11 weeks of age. b: Skin histology. The dorsal skin from a wildtype and PKCε SKH-1 hairless transgenic mouse was fixed in 10% neutral buffered formalin and embedded in paraffin, and sections (4μm) were stained with hematoxylin and eosin. c: Immunohistochemical staining for PKCε expression, scale bars = 50 μm. d: Epidermal PKC isoform expression profiles in PKCε SKH-1 hairless transgenic mice and their wildtype littermates; results representative of three replicates. e: The quantification of proteins (normalized to β-actin) was done by densitometry <t>analysis</t> using Total <t>Lab</t> <t>Nonlinear</t> <t>Dynamics</t> <t>Image</t> Analysis <t>Software</t> (Nonlinear, USA).
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    Image Search Results


    Heterozygous (+/−) FVB/N K14-T7PKCε mice were crossed for four generations to wildtype (−/−) outcrossed SKH-1 hairless mice for transmission of the transgene and hairlessness. a: Phenotype of female SKH-1K14-T7PKCε transgenic mice. Shown are the photographs of adult SKH-1 hairless PKCε transgenic mouse and its wildtype littermate at 11 weeks of age. b: Skin histology. The dorsal skin from a wildtype and PKCε SKH-1 hairless transgenic mouse was fixed in 10% neutral buffered formalin and embedded in paraffin, and sections (4μm) were stained with hematoxylin and eosin. c: Immunohistochemical staining for PKCε expression, scale bars = 50 μm. d: Epidermal PKC isoform expression profiles in PKCε SKH-1 hairless transgenic mice and their wildtype littermates; results representative of three replicates. e: The quantification of proteins (normalized to β-actin) was done by densitometry analysis using Total Lab Nonlinear Dynamics Image Analysis Software (Nonlinear, USA).

    Journal:

    Article Title: PKCε overexpression, irrespective of genetic background, sensitizes skin to ultraviolet radiation-induced development of squamous cell carcinomas

    doi: 10.1038/jid.2009.212

    Figure Lengend Snippet: Heterozygous (+/−) FVB/N K14-T7PKCε mice were crossed for four generations to wildtype (−/−) outcrossed SKH-1 hairless mice for transmission of the transgene and hairlessness. a: Phenotype of female SKH-1K14-T7PKCε transgenic mice. Shown are the photographs of adult SKH-1 hairless PKCε transgenic mouse and its wildtype littermate at 11 weeks of age. b: Skin histology. The dorsal skin from a wildtype and PKCε SKH-1 hairless transgenic mouse was fixed in 10% neutral buffered formalin and embedded in paraffin, and sections (4μm) were stained with hematoxylin and eosin. c: Immunohistochemical staining for PKCε expression, scale bars = 50 μm. d: Epidermal PKC isoform expression profiles in PKCε SKH-1 hairless transgenic mice and their wildtype littermates; results representative of three replicates. e: The quantification of proteins (normalized to β-actin) was done by densitometry analysis using Total Lab Nonlinear Dynamics Image Analysis Software (Nonlinear, USA).

    Article Snippet: The dorsal skin from a wildtype and PKCε SKH-1 hairless transgenic mouse was fixed in 10% neutral buffered formalin and embedded in paraffin, and sections (4μm) were stained with hematoxylin and eosin. c : Immunohistochemical staining for PKCε expression, scale bars = 50 μm. d : Epidermal PKC isoform expression profiles in PKCε SKH-1 hairless transgenic mice and their wildtype littermates; results representative of three replicates. e: The quantification of proteins (normalized to β-actin) was done by densitometry analysis using Total Lab Nonlinear Dynamics Image Analysis Software (Nonlinear, USA).

    Techniques: Transmission Assay, Transgenic Assay, Staining, Immunohistochemical staining, Expressing, Software

    Female PKCε transgenic SKH-1 hairless mice (TG) and their wildtype littermates (WT) (3 mice per group) were exposed to a single UVR dose (1kJ/m2). The mice were sacrificed at 1, 3, and 6 hrs post UVR exposure. The mouse epidermis was scraped off and total lysate was prepared. Total epidermal lysate from three mice was pooled for the western blot analysis. a and b: The epidermal lysate (25μg protein) was subjected to SDS-PAGE followed by immunoblot analysis using indicated antibodies. Equal loading was confirmed by stripping and reprobing the blots with β-actin antibody. c and d: The quantification of proteins (normalized to β-actin) was done by densitometry analysis using Total Lab Nonlinear Dynamics Image Analysis Software (Nonlinear, USA).

    Journal:

    Article Title: PKCε overexpression, irrespective of genetic background, sensitizes skin to ultraviolet radiation-induced development of squamous cell carcinomas

    doi: 10.1038/jid.2009.212

    Figure Lengend Snippet: Female PKCε transgenic SKH-1 hairless mice (TG) and their wildtype littermates (WT) (3 mice per group) were exposed to a single UVR dose (1kJ/m2). The mice were sacrificed at 1, 3, and 6 hrs post UVR exposure. The mouse epidermis was scraped off and total lysate was prepared. Total epidermal lysate from three mice was pooled for the western blot analysis. a and b: The epidermal lysate (25μg protein) was subjected to SDS-PAGE followed by immunoblot analysis using indicated antibodies. Equal loading was confirmed by stripping and reprobing the blots with β-actin antibody. c and d: The quantification of proteins (normalized to β-actin) was done by densitometry analysis using Total Lab Nonlinear Dynamics Image Analysis Software (Nonlinear, USA).

    Article Snippet: The dorsal skin from a wildtype and PKCε SKH-1 hairless transgenic mouse was fixed in 10% neutral buffered formalin and embedded in paraffin, and sections (4μm) were stained with hematoxylin and eosin. c : Immunohistochemical staining for PKCε expression, scale bars = 50 μm. d : Epidermal PKC isoform expression profiles in PKCε SKH-1 hairless transgenic mice and their wildtype littermates; results representative of three replicates. e: The quantification of proteins (normalized to β-actin) was done by densitometry analysis using Total Lab Nonlinear Dynamics Image Analysis Software (Nonlinear, USA).

    Techniques: Transgenic Assay, Western Blot, SDS Page, Stripping Membranes, Software