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generation iii cho hcp kit  (Cygnus Technologies)

 
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    Cygnus Technologies generation iii cho hcp kit
    The robustness of the SWATH <t>CHO</t> global spectral library in quantification of CHO proteome. ( a ) The correlation between the ∆RT and the predicted retention times in <t>three</t> LC-MS instrumental setups. The red colored “×” represented the 11 iRT reference peptides. ( b ) The violin plot showed the distribution of observed and predicted retention times in three instrumental setups. ( c ) The bar charts showed the numbers of confidently quantified proteins (left) and peptides (right) after 20%, 10% and 5% CV cutoff. ( d ) The CV distribution of all the identified proteins (left) and peptides (right) in three LC-MS instrumental setups. The median CV values in each condition were highlighted. ( e ) Venn diagram analysis of confidently quantified protein ID (at 20% CV cutoff and 1% peptide FDR) between three CHO cell lines. The total protein IDs of respective cell lines were indicated in brackets. ( f ) The violin plot showed the distribution of the protein CV values across three CHO cell lines with the median CV values highlighted in white color. NF6600: nanoflow LC coupled to TripleTOF 6600; CF5600: capillary flow LC coupled to TripleTOF 5600 + ; MF6600: microflow LC coupled to TripleTOF 6600.
    Generation Iii Cho Hcp Kit, supplied by Cygnus 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/result/generation iii cho hcp kit/product/Cygnus Technologies
    Average 90 stars, based on 1 article reviews
    generation iii cho hcp kit - by Bioz Stars, 2026-05
    90/100 stars

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    1) Product Images from "A comprehensive CHO SWATH-MS spectral library for robust quantitative profiling of 10,000 proteins"

    Article Title: A comprehensive CHO SWATH-MS spectral library for robust quantitative profiling of 10,000 proteins

    Journal: Scientific Data

    doi: 10.1038/s41597-020-00594-z

    The robustness of the SWATH CHO global spectral library in quantification of CHO proteome. ( a ) The correlation between the ∆RT and the predicted retention times in three LC-MS instrumental setups. The red colored “×” represented the 11 iRT reference peptides. ( b ) The violin plot showed the distribution of observed and predicted retention times in three instrumental setups. ( c ) The bar charts showed the numbers of confidently quantified proteins (left) and peptides (right) after 20%, 10% and 5% CV cutoff. ( d ) The CV distribution of all the identified proteins (left) and peptides (right) in three LC-MS instrumental setups. The median CV values in each condition were highlighted. ( e ) Venn diagram analysis of confidently quantified protein ID (at 20% CV cutoff and 1% peptide FDR) between three CHO cell lines. The total protein IDs of respective cell lines were indicated in brackets. ( f ) The violin plot showed the distribution of the protein CV values across three CHO cell lines with the median CV values highlighted in white color. NF6600: nanoflow LC coupled to TripleTOF 6600; CF5600: capillary flow LC coupled to TripleTOF 5600 + ; MF6600: microflow LC coupled to TripleTOF 6600.
    Figure Legend Snippet: The robustness of the SWATH CHO global spectral library in quantification of CHO proteome. ( a ) The correlation between the ∆RT and the predicted retention times in three LC-MS instrumental setups. The red colored “×” represented the 11 iRT reference peptides. ( b ) The violin plot showed the distribution of observed and predicted retention times in three instrumental setups. ( c ) The bar charts showed the numbers of confidently quantified proteins (left) and peptides (right) after 20%, 10% and 5% CV cutoff. ( d ) The CV distribution of all the identified proteins (left) and peptides (right) in three LC-MS instrumental setups. The median CV values in each condition were highlighted. ( e ) Venn diagram analysis of confidently quantified protein ID (at 20% CV cutoff and 1% peptide FDR) between three CHO cell lines. The total protein IDs of respective cell lines were indicated in brackets. ( f ) The violin plot showed the distribution of the protein CV values across three CHO cell lines with the median CV values highlighted in white color. NF6600: nanoflow LC coupled to TripleTOF 6600; CF5600: capillary flow LC coupled to TripleTOF 5600 + ; MF6600: microflow LC coupled to TripleTOF 6600.

    Techniques Used: Data-independent acquisition, Liquid Chromatography with Mass Spectroscopy



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    The robustness of the SWATH <t>CHO</t> global spectral library in quantification of CHO proteome. ( a ) The correlation between the ∆RT and the predicted retention times in <t>three</t> LC-MS instrumental setups. The red colored “×” represented the 11 iRT reference peptides. ( b ) The violin plot showed the distribution of observed and predicted retention times in three instrumental setups. ( c ) The bar charts showed the numbers of confidently quantified proteins (left) and peptides (right) after 20%, 10% and 5% CV cutoff. ( d ) The CV distribution of all the identified proteins (left) and peptides (right) in three LC-MS instrumental setups. The median CV values in each condition were highlighted. ( e ) Venn diagram analysis of confidently quantified protein ID (at 20% CV cutoff and 1% peptide FDR) between three CHO cell lines. The total protein IDs of respective cell lines were indicated in brackets. ( f ) The violin plot showed the distribution of the protein CV values across three CHO cell lines with the median CV values highlighted in white color. NF6600: nanoflow LC coupled to TripleTOF 6600; CF5600: capillary flow LC coupled to TripleTOF 5600 + ; MF6600: microflow LC coupled to TripleTOF 6600.
    Generation Iii Cho Hcp Kit, supplied by Cygnus Technologies, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    The robustness of the SWATH <t>CHO</t> global spectral library in quantification of CHO proteome. ( a ) The correlation between the ∆RT and the predicted retention times in <t>three</t> LC-MS instrumental setups. The red colored “×” represented the 11 iRT reference peptides. ( b ) The violin plot showed the distribution of observed and predicted retention times in three instrumental setups. ( c ) The bar charts showed the numbers of confidently quantified proteins (left) and peptides (right) after 20%, 10% and 5% CV cutoff. ( d ) The CV distribution of all the identified proteins (left) and peptides (right) in three LC-MS instrumental setups. The median CV values in each condition were highlighted. ( e ) Venn diagram analysis of confidently quantified protein ID (at 20% CV cutoff and 1% peptide FDR) between three CHO cell lines. The total protein IDs of respective cell lines were indicated in brackets. ( f ) The violin plot showed the distribution of the protein CV values across three CHO cell lines with the median CV values highlighted in white color. NF6600: nanoflow LC coupled to TripleTOF 6600; CF5600: capillary flow LC coupled to TripleTOF 5600 + ; MF6600: microflow LC coupled to TripleTOF 6600.
    Hcp Elisa Kit Generation Iii Cho Hcp Kit, supplied by Cygnus Technologies, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    The robustness of the SWATH CHO global spectral library in quantification of CHO proteome. ( a ) The correlation between the ∆RT and the predicted retention times in three LC-MS instrumental setups. The red colored “×” represented the 11 iRT reference peptides. ( b ) The violin plot showed the distribution of observed and predicted retention times in three instrumental setups. ( c ) The bar charts showed the numbers of confidently quantified proteins (left) and peptides (right) after 20%, 10% and 5% CV cutoff. ( d ) The CV distribution of all the identified proteins (left) and peptides (right) in three LC-MS instrumental setups. The median CV values in each condition were highlighted. ( e ) Venn diagram analysis of confidently quantified protein ID (at 20% CV cutoff and 1% peptide FDR) between three CHO cell lines. The total protein IDs of respective cell lines were indicated in brackets. ( f ) The violin plot showed the distribution of the protein CV values across three CHO cell lines with the median CV values highlighted in white color. NF6600: nanoflow LC coupled to TripleTOF 6600; CF5600: capillary flow LC coupled to TripleTOF 5600 + ; MF6600: microflow LC coupled to TripleTOF 6600.

    Journal: Scientific Data

    Article Title: A comprehensive CHO SWATH-MS spectral library for robust quantitative profiling of 10,000 proteins

    doi: 10.1038/s41597-020-00594-z

    Figure Lengend Snippet: The robustness of the SWATH CHO global spectral library in quantification of CHO proteome. ( a ) The correlation between the ∆RT and the predicted retention times in three LC-MS instrumental setups. The red colored “×” represented the 11 iRT reference peptides. ( b ) The violin plot showed the distribution of observed and predicted retention times in three instrumental setups. ( c ) The bar charts showed the numbers of confidently quantified proteins (left) and peptides (right) after 20%, 10% and 5% CV cutoff. ( d ) The CV distribution of all the identified proteins (left) and peptides (right) in three LC-MS instrumental setups. The median CV values in each condition were highlighted. ( e ) Venn diagram analysis of confidently quantified protein ID (at 20% CV cutoff and 1% peptide FDR) between three CHO cell lines. The total protein IDs of respective cell lines were indicated in brackets. ( f ) The violin plot showed the distribution of the protein CV values across three CHO cell lines with the median CV values highlighted in white color. NF6600: nanoflow LC coupled to TripleTOF 6600; CF5600: capillary flow LC coupled to TripleTOF 5600 + ; MF6600: microflow LC coupled to TripleTOF 6600.

    Article Snippet: HCP content in DSP samples was determined by ELISA using a Generation III CHO HCP kit (Cygnus Technologies, Southport, NC) according to the manufacturer’s instructions.

    Techniques: Data-independent acquisition, Liquid Chromatography with Mass Spectroscopy