ºÝºÝߣshows by User: susanwn / http://www.slideshare.net/images/logo.gif ºÝºÝߣshows by User: susanwn / Fri, 09 Jun 2017 08:12:47 GMT ºÝºÝߣShare feed for ºÝºÝߣshows by User: susanwn The complete guide to protein identification /slideshow/the-complete-guide-to-protein-identification/76791390 thecompleteguidetoproteinidentification-170609081247
As a significant part of proteomics research, protein identification is widely used to identify a protein or characterize a protein. But how can one identify a protein successfully? A very direct answer is to find the sequence of amino acids of the protein, but as we all know, the process is time-consuming and annoying due to the necessary procedures,including the usage of several restriction enzymes and running gels and finding masses… and so on. After all those steps, one has to think about if the protein of interest has been identified already.]]>

As a significant part of proteomics research, protein identification is widely used to identify a protein or characterize a protein. But how can one identify a protein successfully? A very direct answer is to find the sequence of amino acids of the protein, but as we all know, the process is time-consuming and annoying due to the necessary procedures,including the usage of several restriction enzymes and running gels and finding masses… and so on. After all those steps, one has to think about if the protein of interest has been identified already.]]>
Fri, 09 Jun 2017 08:12:47 GMT /slideshow/the-complete-guide-to-protein-identification/76791390 susanwn@slideshare.net(susanwn) The complete guide to protein identification susanwn As a significant part of proteomics research, protein identification is widely used to identify a protein or characterize a protein. But how can one identify a protein successfully? A very direct answer is to find the sequence of amino acids of the protein, but as we all know, the process is time-consuming and annoying due to the necessary procedures,including the usage of several restriction enzymes and running gels and finding masses… and so on. After all those steps, one has to think about if the protein of interest has been identified already. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/thecompleteguidetoproteinidentification-170609081247-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> As a significant part of proteomics research, protein identification is widely used to identify a protein or characterize a protein. But how can one identify a protein successfully? A very direct answer is to find the sequence of amino acids of the protein, but as we all know, the process is time-consuming and annoying due to the necessary procedures,including the usage of several restriction enzymes and running gels and finding masses… and so on. After all those steps, one has to think about if the protein of interest has been identified already.
The complete guide to protein identification from Susan Rey
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Peptide mass fingerprinting analysis /slideshow/peptide-mass-fingerprinting-analysis/66293921 peptidemassfingerprintinganalysis-160922093613
Creative Proteomics provides Peptide Mass Fingerprinting (PMF) analysis and ions searching against database for rapid identification of proteins.]]>

Creative Proteomics provides Peptide Mass Fingerprinting (PMF) analysis and ions searching against database for rapid identification of proteins.]]>
Thu, 22 Sep 2016 09:36:12 GMT /slideshow/peptide-mass-fingerprinting-analysis/66293921 susanwn@slideshare.net(susanwn) Peptide mass fingerprinting analysis susanwn Creative Proteomics provides Peptide Mass Fingerprinting (PMF) analysis and ions searching against database for rapid identification of proteins. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/peptidemassfingerprintinganalysis-160922093613-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> Creative Proteomics provides Peptide Mass Fingerprinting (PMF) analysis and ions searching against database for rapid identification of proteins.
Peptide mass fingerprinting analysis from Susan Rey
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Post translational modification glycosylation (2) /slideshow/post-translational-modification-glycosylation-2/64461026 posttranslationalmodificationglycosylation2-160728054409
For many proteins and peptides, disulfide bridges are prerequisite for their proper biological function. ]]>

For many proteins and peptides, disulfide bridges are prerequisite for their proper biological function. ]]>
Thu, 28 Jul 2016 05:44:09 GMT /slideshow/post-translational-modification-glycosylation-2/64461026 susanwn@slideshare.net(susanwn) Post translational modification glycosylation (2) susanwn For many proteins and peptides, disulfide bridges are prerequisite for their proper biological function. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/posttranslationalmodificationglycosylation2-160728054409-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> For many proteins and peptides, disulfide bridges are prerequisite for their proper biological function.
Post translational modification glycosylation (2) from Susan Rey
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Applications of protein array in diagnostics and genomic and proteomic /slideshow/applications-of-protein-array-in-diagnostics-and-genomic-and-proteomic-56228160/56228160 applicationsofproteinarrayindiagnosticsandgenomicandproteomic-151217054931
icroarray technology can simultaneously analyze thousands of parameters in a single experiment. Micro-point of capture molecules are fixed into ranks on a solid support and exposed to samples containing corresponding binding molecules. Complex formation in each micro-point can be detected by the readout system, which is based on fluorescence, chemiluminescence, mass spectrometry, radioactive or electrochemistry. Miniaturization and parallelization binding assays, whose analysis power can be also enlarged by microarray gene expression analysis, is sensitive. These systems can be used to detect the degree of hybridization and immobilized DNA microarray probes will be exposed to complementary target. Currently, the development of protein array has demonstrated its applications in enzyme-substrate, DNA- protein and different types of protein - protein interactions. In this post, we will discuss the capture-molecule-ligand analysis, analyze its theoretical advantages and disadvantage and its influence in diagnostics, genomic and proteomics.]]>

icroarray technology can simultaneously analyze thousands of parameters in a single experiment. Micro-point of capture molecules are fixed into ranks on a solid support and exposed to samples containing corresponding binding molecules. Complex formation in each micro-point can be detected by the readout system, which is based on fluorescence, chemiluminescence, mass spectrometry, radioactive or electrochemistry. Miniaturization and parallelization binding assays, whose analysis power can be also enlarged by microarray gene expression analysis, is sensitive. These systems can be used to detect the degree of hybridization and immobilized DNA microarray probes will be exposed to complementary target. Currently, the development of protein array has demonstrated its applications in enzyme-substrate, DNA- protein and different types of protein - protein interactions. In this post, we will discuss the capture-molecule-ligand analysis, analyze its theoretical advantages and disadvantage and its influence in diagnostics, genomic and proteomics.]]>
Thu, 17 Dec 2015 05:49:31 GMT /slideshow/applications-of-protein-array-in-diagnostics-and-genomic-and-proteomic-56228160/56228160 susanwn@slideshare.net(susanwn) Applications of protein array in diagnostics and genomic and proteomic susanwn icroarray technology can simultaneously analyze thousands of parameters in a single experiment. Micro-point of capture molecules are fixed into ranks on a solid support and exposed to samples containing corresponding binding molecules. Complex formation in each micro-point can be detected by the readout system, which is based on fluorescence, chemiluminescence, mass spectrometry, radioactive or electrochemistry. Miniaturization and parallelization binding assays, whose analysis power can be also enlarged by microarray gene expression analysis, is sensitive. These systems can be used to detect the degree of hybridization and immobilized DNA microarray probes will be exposed to complementary target. Currently, the development of protein array has demonstrated its applications in enzyme-substrate, DNA- protein and different types of protein - protein interactions. In this post, we will discuss the capture-molecule-ligand analysis, analyze its theoretical advantages and disadvantage and its influence in diagnostics, genomic and proteomics. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/applicationsofproteinarrayindiagnosticsandgenomicandproteomic-151217054931-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> icroarray technology can simultaneously analyze thousands of parameters in a single experiment. Micro-point of capture molecules are fixed into ranks on a solid support and exposed to samples containing corresponding binding molecules. Complex formation in each micro-point can be detected by the readout system, which is based on fluorescence, chemiluminescence, mass spectrometry, radioactive or electrochemistry. Miniaturization and parallelization binding assays, whose analysis power can be also enlarged by microarray gene expression analysis, is sensitive. These systems can be used to detect the degree of hybridization and immobilized DNA microarray probes will be exposed to complementary target. Currently, the development of protein array has demonstrated its applications in enzyme-substrate, DNA- protein and different types of protein - protein interactions. In this post, we will discuss the capture-molecule-ligand analysis, analyze its theoretical advantages and disadvantage and its influence in diagnostics, genomic and proteomics.
Applications of protein array in diagnostics and genomic and proteomic from Susan Rey
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Applications of protein array in diagnostics and genomic and proteomic /slideshow/applications-of-protein-array-in-diagnostics-and-genomic-and-proteomic-55594506/55594506 applicationsofproteinarrayindiagnosticsandgenomicandproteomic-151128022723-lva1-app6891
Microarray technology can simultaneously analyze thousands of parameters in a single experiment. Micro-point of capture molecules are fixed into ranks on a solid support and exposed to samples containing corresponding binding molecules. Complex formation in each micro-point can be detected by the readout system, which is based on fluorescence, chemiluminescence, mass spectrometry, radioactive or electrochemistry. Miniaturization and parallelization binding assays, whose analysis power can be also enlarged by microarray gene expression analysis, is sensitive. These systems can be used to detect the degree of hybridization and immobilized DNA microarray probes will be exposed to complementary target. Currently, the development of protein array has demonstrated its applications in enzyme-substrate, DNA- protein and different types of protein - protein interactions. In this post, we will discuss the capture-molecule-ligand analysis, analyze its theoretical advantages and disadvantage and its influence in diagnostics, genomic and proteomics.]]>

Microarray technology can simultaneously analyze thousands of parameters in a single experiment. Micro-point of capture molecules are fixed into ranks on a solid support and exposed to samples containing corresponding binding molecules. Complex formation in each micro-point can be detected by the readout system, which is based on fluorescence, chemiluminescence, mass spectrometry, radioactive or electrochemistry. Miniaturization and parallelization binding assays, whose analysis power can be also enlarged by microarray gene expression analysis, is sensitive. These systems can be used to detect the degree of hybridization and immobilized DNA microarray probes will be exposed to complementary target. Currently, the development of protein array has demonstrated its applications in enzyme-substrate, DNA- protein and different types of protein - protein interactions. In this post, we will discuss the capture-molecule-ligand analysis, analyze its theoretical advantages and disadvantage and its influence in diagnostics, genomic and proteomics.]]>
Sat, 28 Nov 2015 02:27:23 GMT /slideshow/applications-of-protein-array-in-diagnostics-and-genomic-and-proteomic-55594506/55594506 susanwn@slideshare.net(susanwn) Applications of protein array in diagnostics and genomic and proteomic susanwn Microarray technology can simultaneously analyze thousands of parameters in a single experiment. Micro-point of capture molecules are fixed into ranks on a solid support and exposed to samples containing corresponding binding molecules. Complex formation in each micro-point can be detected by the readout system, which is based on fluorescence, chemiluminescence, mass spectrometry, radioactive or electrochemistry. Miniaturization and parallelization binding assays, whose analysis power can be also enlarged by microarray gene expression analysis, is sensitive. These systems can be used to detect the degree of hybridization and immobilized DNA microarray probes will be exposed to complementary target. Currently, the development of protein array has demonstrated its applications in enzyme-substrate, DNA- protein and different types of protein - protein interactions. In this post, we will discuss the capture-molecule-ligand analysis, analyze its theoretical advantages and disadvantage and its influence in diagnostics, genomic and proteomics. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/applicationsofproteinarrayindiagnosticsandgenomicandproteomic-151128022723-lva1-app6891-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> Microarray technology can simultaneously analyze thousands of parameters in a single experiment. Micro-point of capture molecules are fixed into ranks on a solid support and exposed to samples containing corresponding binding molecules. Complex formation in each micro-point can be detected by the readout system, which is based on fluorescence, chemiluminescence, mass spectrometry, radioactive or electrochemistry. Miniaturization and parallelization binding assays, whose analysis power can be also enlarged by microarray gene expression analysis, is sensitive. These systems can be used to detect the degree of hybridization and immobilized DNA microarray probes will be exposed to complementary target. Currently, the development of protein array has demonstrated its applications in enzyme-substrate, DNA- protein and different types of protein - protein interactions. In this post, we will discuss the capture-molecule-ligand analysis, analyze its theoretical advantages and disadvantage and its influence in diagnostics, genomic and proteomics.
Applications of protein array in diagnostics and genomic and proteomic from Susan Rey
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The 7th International Conference on Ubiquitination and Ubiquitin Protein /slideshow/the-7th-international-conference-on-ubiquitination-and-ubiquitin-protein/53856648 the7thinternationalmeetinginubiquizitionand-151013031929-lva1-app6891
On 10th to 13th May, 2014, the 7th international conference on ubiquitination and ubiquitin protein was held in Shanghai Jiaotong University. This conference was jointly organized by the university of Texas MD Anderson Cancer Center and Shanghai Jiaotong University. Many famous scientists came together to discuss this significant emerging field on the clinical application.]]>

On 10th to 13th May, 2014, the 7th international conference on ubiquitination and ubiquitin protein was held in Shanghai Jiaotong University. This conference was jointly organized by the university of Texas MD Anderson Cancer Center and Shanghai Jiaotong University. Many famous scientists came together to discuss this significant emerging field on the clinical application.]]>
Tue, 13 Oct 2015 03:19:29 GMT /slideshow/the-7th-international-conference-on-ubiquitination-and-ubiquitin-protein/53856648 susanwn@slideshare.net(susanwn) The 7th International Conference on Ubiquitination and Ubiquitin Protein susanwn On 10th to 13th May, 2014, the 7th international conference on ubiquitination and ubiquitin protein was held in Shanghai Jiaotong University. This conference was jointly organized by the university of Texas MD Anderson Cancer Center and Shanghai Jiaotong University. Many famous scientists came together to discuss this significant emerging field on the clinical application. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/the7thinternationalmeetinginubiquizitionand-151013031929-lva1-app6891-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> On 10th to 13th May, 2014, the 7th international conference on ubiquitination and ubiquitin protein was held in Shanghai Jiaotong University. This conference was jointly organized by the university of Texas MD Anderson Cancer Center and Shanghai Jiaotong University. Many famous scientists came together to discuss this significant emerging field on the clinical application.
The 7th International Conference on Ubiquitination and Ubiquitin Protein from Susan Rey
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