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BIOTAGE automatic peptide synthesizer syro i
Automatic Peptide Synthesizer Syro I, supplied by BIOTAGE, 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/syro-i/syro+i+peptide+synthesizer/pmc09996831__bi2c00656_si_001-124-10-14
Average 90 stars, based on 1 article reviews
automatic peptide synthesizer syro i - by Bioz Stars, 2026-10
90/100 stars

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Related Articles

Purification:

Article Title: Manipulating Active Structure and Function of Cationic Antimicrobial Peptide CM15 with the Polysulfonated Drug Suramin: A Step Closer to in Vivo Complexity
Article Snippet: Szigy rt ,[a] Kata Horv ti,[b] Szilvia Bősze,[b] Judit Henczk ,[c] Bernadett P lyi,[c] Csaba N meth,[a] Zolt n Varga,[a] Ferenc Zsila,[a] and Tam s Beke-Somfai*[a] cbic_201800801_sm_miscellaneous_information.pdf Supporting Information Experimental Section Peptide synthesis and purification: CM15 was produced on solid phase (Fmoc-Rink Amide MBHA, capacity = 0.67 mmol/g) resin in an automated peptide synthesizer (Syro-I, Biotage) using standard Fmoc/tBu strategy with DIC/HOBt coupling reagents, as previously described.

Article Title: Optimizing lipopeptide bioactivity: The impact of non-ionic surfactant dressing
Article Snippet: Peptide L1 was synthesized on Fmoc-Rink Amide MBHA resin (capacity = 0.67 mmol/g) in an automated peptide synthesizer (Syro-I, Biotage, Uppsala, Sweden) using standard Fmoc/tBu strategy with DIC/HOBt coupling reagents.

Article Title: Enhanced cellular uptake of a new, in silico identified antitubercular candidate by peptide conjugation.
Article Snippet: Mycobacterium tuberculosis is a successful pathogen, and it can survive in infected macrophages in dormant phase for years and decades.. The therapy of tuberculosis takes at least six months, and the slow-growing bacterium is resistant to many antibiotics.. The development of novel antimicrobials to counter the emergence of bacteria resistant to current therapies is urgently needed.

Article Title: Optimizing lipopeptide bioactivity: The impact of non-ionic surfactant dressing
Article Snippet: Peptide L1 was synthesized on Fmoc-Rink Amide MBHA resin (capacity = 0.67 mmol/g) in an automated peptide synthesizer (Syro-I; Biotage, Uppsala, Sweden) using standard Fmoc/ t Bu strategy with DIC/HOBt coupling reagents.

Article Title: A Convenient Synthetic Method to Improve Immunogenicity of Mycobacterium tuberculosis Related T-Cell Epitope Peptides
Article Snippet: Peptides were produced on solid phase (Fmoc-Rink Amide MBHA resin, capacity = 0.67 mmol/g) in an automated peptide synthesizer (Syro-I, Biotage, Uppsala, Sweden) using a standard Fmoc/tBu strategy with DIC/HOBt coupling reagents.

Article Title: Drug Conjugation Induced Modulation of Structural and Membrane Interaction Features of Cationic Cell-Permeable Peptides
Article Snippet: Peptides were produced on solid phase (Fmoc-Rink Amide MBHA resin, capacity = 0.67 mmol/g), in an automated peptide synthesizer (Syro-I, Biotage, Uppsala, Sweden), using standard Fmoc/tBu strategy with DIC/HOBt coupling reagents.

Produced:

Article Title: Manipulating Active Structure and Function of Cationic Antimicrobial Peptide CM15 with the Polysulfonated Drug Suramin: A Step Closer to in Vivo Complexity
Article Snippet: Szigy rt ,[a] Kata Horv ti,[b] Szilvia Bősze,[b] Judit Henczk ,[c] Bernadett P lyi,[c] Csaba N meth,[a] Zolt n Varga,[a] Ferenc Zsila,[a] and Tam s Beke-Somfai*[a] cbic_201800801_sm_miscellaneous_information.pdf Supporting Information Experimental Section Peptide synthesis and purification: CM15 was produced on solid phase (Fmoc-Rink Amide MBHA, capacity = 0.67 mmol/g) resin in an automated peptide synthesizer (Syro-I, Biotage) using standard Fmoc/tBu strategy with DIC/HOBt coupling reagents, as previously described.

Article Title: Optimizing lipopeptide bioactivity: The impact of non-ionic surfactant dressing
Article Snippet: Peptide L1 was synthesized on Fmoc-Rink Amide MBHA resin (capacity = 0.67 mmol/g) in an automated peptide synthesizer (Syro-I, Biotage, Uppsala, Sweden) using standard Fmoc/tBu strategy with DIC/HOBt coupling reagents.

Article Title: Enhanced cellular uptake of a new, in silico identified antitubercular candidate by peptide conjugation.
Article Snippet: Mycobacterium tuberculosis is a successful pathogen, and it can survive in infected macrophages in dormant phase for years and decades.. The therapy of tuberculosis takes at least six months, and the slow-growing bacterium is resistant to many antibiotics.. The development of novel antimicrobials to counter the emergence of bacteria resistant to current therapies is urgently needed.

Article Title: Optimizing lipopeptide bioactivity: The impact of non-ionic surfactant dressing
Article Snippet: Peptide L1 was synthesized on Fmoc-Rink Amide MBHA resin (capacity = 0.67 mmol/g) in an automated peptide synthesizer (Syro-I; Biotage, Uppsala, Sweden) using standard Fmoc/ t Bu strategy with DIC/HOBt coupling reagents.

Article Title: A Convenient Synthetic Method to Improve Immunogenicity of Mycobacterium tuberculosis Related T-Cell Epitope Peptides
Article Snippet: Peptides were produced on solid phase (Fmoc-Rink Amide MBHA resin, capacity = 0.67 mmol/g) in an automated peptide synthesizer (Syro-I, Biotage, Uppsala, Sweden) using a standard Fmoc/tBu strategy with DIC/HOBt coupling reagents.

Article Title: Drug Conjugation Induced Modulation of Structural and Membrane Interaction Features of Cationic Cell-Permeable Peptides
Article Snippet: Peptides were produced on solid phase (Fmoc-Rink Amide MBHA resin, capacity = 0.67 mmol/g), in an automated peptide synthesizer (Syro-I, Biotage, Uppsala, Sweden), using standard Fmoc/tBu strategy with DIC/HOBt coupling reagents.

Sequencing:

Article Title: Manipulating Active Structure and Function of Cationic Antimicrobial Peptide CM15 with the Polysulfonated Drug Suramin: A Step Closer to in Vivo Complexity
Article Snippet: Szigy rt ,[a] Kata Horv ti,[b] Szilvia Bősze,[b] Judit Henczk ,[c] Bernadett P lyi,[c] Csaba N meth,[a] Zolt n Varga,[a] Ferenc Zsila,[a] and Tam s Beke-Somfai*[a] cbic_201800801_sm_miscellaneous_information.pdf Supporting Information Experimental Section Peptide synthesis and purification: CM15 was produced on solid phase (Fmoc-Rink Amide MBHA, capacity = 0.67 mmol/g) resin in an automated peptide synthesizer (Syro-I, Biotage) using standard Fmoc/tBu strategy with DIC/HOBt coupling reagents, as previously described.

Article Title: Optimizing lipopeptide bioactivity: The impact of non-ionic surfactant dressing
Article Snippet: Peptide L1 was synthesized on Fmoc-Rink Amide MBHA resin (capacity = 0.67 mmol/g) in an automated peptide synthesizer (Syro-I, Biotage, Uppsala, Sweden) using standard Fmoc/tBu strategy with DIC/HOBt coupling reagents.

Article Title: Enhanced cellular uptake of a new, in silico identified antitubercular candidate by peptide conjugation.
Article Snippet: Mycobacterium tuberculosis is a successful pathogen, and it can survive in infected macrophages in dormant phase for years and decades.. The therapy of tuberculosis takes at least six months, and the slow-growing bacterium is resistant to many antibiotics.. The development of novel antimicrobials to counter the emergence of bacteria resistant to current therapies is urgently needed.

Article Title: Optimizing lipopeptide bioactivity: The impact of non-ionic surfactant dressing
Article Snippet: Peptide L1 was synthesized on Fmoc-Rink Amide MBHA resin (capacity = 0.67 mmol/g) in an automated peptide synthesizer (Syro-I; Biotage, Uppsala, Sweden) using standard Fmoc/ t Bu strategy with DIC/HOBt coupling reagents.

Article Title: A Convenient Synthetic Method to Improve Immunogenicity of Mycobacterium tuberculosis Related T-Cell Epitope Peptides
Article Snippet: Peptides were produced on solid phase (Fmoc-Rink Amide MBHA resin, capacity = 0.67 mmol/g) in an automated peptide synthesizer (Syro-I, Biotage, Uppsala, Sweden) using a standard Fmoc/tBu strategy with DIC/HOBt coupling reagents.

Article Title: Drug Conjugation Induced Modulation of Structural and Membrane Interaction Features of Cationic Cell-Permeable Peptides
Article Snippet: Peptides were produced on solid phase (Fmoc-Rink Amide MBHA resin, capacity = 0.67 mmol/g), in an automated peptide synthesizer (Syro-I, Biotage, Uppsala, Sweden), using standard Fmoc/tBu strategy with DIC/HOBt coupling reagents.



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