rink-amide Search Results


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  • 99
    Gyros Protein Technologies rink amide mbha resin
    Rink Amide Mbha Resin, supplied by Gyros Protein Technologies, used in various techniques. Bioz Stars score: 99/100, based on 28 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rink amide mbha resin/product/Gyros Protein Technologies
    Average 99 stars, based on 28 article reviews
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    99
    Millipore rink amide
    Rink Amide, supplied by Millipore, used in various techniques. Bioz Stars score: 99/100, based on 159 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rink amide/product/Millipore
    Average 99 stars, based on 159 article reviews
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    93
    BIOTAGE rink amide chemmatrix
    ( a ) Schematic representation of a PNA monomer unit. ( b ) Schematic representation of the cycle of microwave-assisted PNA synthesis on solid support. Fmoc/Bhoc are orthologous protecting groups for primary and nucleobase amino groups, respectively. The applied microwave pulse is indicated by a filled star symbol. The empty star represents an applied microwave pulse when the growing chain consists of natural amino acids only, or no microwave if the synthesized chain contains at least one PNA monomer. Activator: PyBOP; base: DIPEA for amino acids or DIPEA/Lutidine for PNA; final cleavage/deprotection: TFA/TIS/H 2 O 95:2.5:2.5. ( c ) Typical MALDI-TOF mass spectra of crude 23-mer PNA (sequence a ) synthesized by standard automated non-microwave method on a PAL-PEG-PS solid support (left panel) or by microwave-assisted synthesis on a PAL-PEG-PS support (sequence a , centre panel) or on a <t>ChemMatrix</t> solid support (sequence b , right panel).
    Rink Amide Chemmatrix, supplied by BIOTAGE, used in various techniques. Bioz Stars score: 93/100, based on 22 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Average 93 stars, based on 22 article reviews
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    99
    Millipore rink amide aminomethyl polystyrene resin
    ( a ) Schematic representation of a PNA monomer unit. ( b ) Schematic representation of the cycle of microwave-assisted PNA synthesis on solid support. Fmoc/Bhoc are orthologous protecting groups for primary and nucleobase amino groups, respectively. The applied microwave pulse is indicated by a filled star symbol. The empty star represents an applied microwave pulse when the growing chain consists of natural amino acids only, or no microwave if the synthesized chain contains at least one PNA monomer. Activator: PyBOP; base: DIPEA for amino acids or DIPEA/Lutidine for PNA; final cleavage/deprotection: TFA/TIS/H 2 O 95:2.5:2.5. ( c ) Typical MALDI-TOF mass spectra of crude 23-mer PNA (sequence a ) synthesized by standard automated non-microwave method on a PAL-PEG-PS solid support (left panel) or by microwave-assisted synthesis on a PAL-PEG-PS support (sequence a , centre panel) or on a <t>ChemMatrix</t> solid support (sequence b , right panel).
    Rink Amide Aminomethyl Polystyrene Resin, supplied by Millipore, used in various techniques. Bioz Stars score: 99/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    93
    BIOTAGE h rink amide
    ( a ) Schematic representation of a PNA monomer unit. ( b ) Schematic representation of the cycle of microwave-assisted PNA synthesis on solid support. Fmoc/Bhoc are orthologous protecting groups for primary and nucleobase amino groups, respectively. The applied microwave pulse is indicated by a filled star symbol. The empty star represents an applied microwave pulse when the growing chain consists of natural amino acids only, or no microwave if the synthesized chain contains at least one PNA monomer. Activator: PyBOP; base: DIPEA for amino acids or DIPEA/Lutidine for PNA; final cleavage/deprotection: TFA/TIS/H 2 O 95:2.5:2.5. ( c ) Typical MALDI-TOF mass spectra of crude 23-mer PNA (sequence a ) synthesized by standard automated non-microwave method on a PAL-PEG-PS solid support (left panel) or by microwave-assisted synthesis on a PAL-PEG-PS support (sequence a , centre panel) or on a <t>ChemMatrix</t> solid support (sequence b , right panel).
    H Rink Amide, supplied by BIOTAGE, used in various techniques. Bioz Stars score: 93/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    87
    Mimotopes rink amide lanterns
    ( a ) Schematic representation of a PNA monomer unit. ( b ) Schematic representation of the cycle of microwave-assisted PNA synthesis on solid support. Fmoc/Bhoc are orthologous protecting groups for primary and nucleobase amino groups, respectively. The applied microwave pulse is indicated by a filled star symbol. The empty star represents an applied microwave pulse when the growing chain consists of natural amino acids only, or no microwave if the synthesized chain contains at least one PNA monomer. Activator: PyBOP; base: DIPEA for amino acids or DIPEA/Lutidine for PNA; final cleavage/deprotection: TFA/TIS/H 2 O 95:2.5:2.5. ( c ) Typical MALDI-TOF mass spectra of crude 23-mer PNA (sequence a ) synthesized by standard automated non-microwave method on a PAL-PEG-PS solid support (left panel) or by microwave-assisted synthesis on a PAL-PEG-PS support (sequence a , centre panel) or on a <t>ChemMatrix</t> solid support (sequence b , right panel).
    Rink Amide Lanterns, supplied by Mimotopes, used in various techniques. Bioz Stars score: 87/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    93
    GL Biochem rink amide linker
    ( a ) Schematic representation of a PNA monomer unit. ( b ) Schematic representation of the cycle of microwave-assisted PNA synthesis on solid support. Fmoc/Bhoc are orthologous protecting groups for primary and nucleobase amino groups, respectively. The applied microwave pulse is indicated by a filled star symbol. The empty star represents an applied microwave pulse when the growing chain consists of natural amino acids only, or no microwave if the synthesized chain contains at least one PNA monomer. Activator: PyBOP; base: DIPEA for amino acids or DIPEA/Lutidine for PNA; final cleavage/deprotection: TFA/TIS/H 2 O 95:2.5:2.5. ( c ) Typical MALDI-TOF mass spectra of crude 23-mer PNA (sequence a ) synthesized by standard automated non-microwave method on a PAL-PEG-PS solid support (left panel) or by microwave-assisted synthesis on a PAL-PEG-PS support (sequence a , centre panel) or on a <t>ChemMatrix</t> solid support (sequence b , right panel).
    Rink Amide Linker, supplied by GL Biochem, used in various techniques. Bioz Stars score: 93/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    99
    Millipore materials rink amide 4 methylbenzhydrylamine resin
    ( a ) Schematic representation of a PNA monomer unit. ( b ) Schematic representation of the cycle of microwave-assisted PNA synthesis on solid support. Fmoc/Bhoc are orthologous protecting groups for primary and nucleobase amino groups, respectively. The applied microwave pulse is indicated by a filled star symbol. The empty star represents an applied microwave pulse when the growing chain consists of natural amino acids only, or no microwave if the synthesized chain contains at least one PNA monomer. Activator: PyBOP; base: DIPEA for amino acids or DIPEA/Lutidine for PNA; final cleavage/deprotection: TFA/TIS/H 2 O 95:2.5:2.5. ( c ) Typical MALDI-TOF mass spectra of crude 23-mer PNA (sequence a ) synthesized by standard automated non-microwave method on a PAL-PEG-PS solid support (left panel) or by microwave-assisted synthesis on a PAL-PEG-PS support (sequence a , centre panel) or on a <t>ChemMatrix</t> solid support (sequence b , right panel).
    Materials Rink Amide 4 Methylbenzhydrylamine Resin, supplied by Millipore, used in various techniques. Bioz Stars score: 99/100, based on 13 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Average 99 stars, based on 13 article reviews
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    92
    Iris Biotech rink amide linker
    ( a ) Schematic representation of a PNA monomer unit. ( b ) Schematic representation of the cycle of microwave-assisted PNA synthesis on solid support. Fmoc/Bhoc are orthologous protecting groups for primary and nucleobase amino groups, respectively. The applied microwave pulse is indicated by a filled star symbol. The empty star represents an applied microwave pulse when the growing chain consists of natural amino acids only, or no microwave if the synthesized chain contains at least one PNA monomer. Activator: PyBOP; base: DIPEA for amino acids or DIPEA/Lutidine for PNA; final cleavage/deprotection: TFA/TIS/H 2 O 95:2.5:2.5. ( c ) Typical MALDI-TOF mass spectra of crude 23-mer PNA (sequence a ) synthesized by standard automated non-microwave method on a PAL-PEG-PS solid support (left panel) or by microwave-assisted synthesis on a PAL-PEG-PS support (sequence a , centre panel) or on a <t>ChemMatrix</t> solid support (sequence b , right panel).
    Rink Amide Linker, supplied by Iris Biotech, used in various techniques. Bioz Stars score: 92/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    92
    Millipore fmoc rink amide mbha resin
    ( a ) Schematic representation of a PNA monomer unit. ( b ) Schematic representation of the cycle of microwave-assisted PNA synthesis on solid support. Fmoc/Bhoc are orthologous protecting groups for primary and nucleobase amino groups, respectively. The applied microwave pulse is indicated by a filled star symbol. The empty star represents an applied microwave pulse when the growing chain consists of natural amino acids only, or no microwave if the synthesized chain contains at least one PNA monomer. Activator: PyBOP; base: DIPEA for amino acids or DIPEA/Lutidine for PNA; final cleavage/deprotection: TFA/TIS/H 2 O 95:2.5:2.5. ( c ) Typical MALDI-TOF mass spectra of crude 23-mer PNA (sequence a ) synthesized by standard automated non-microwave method on a PAL-PEG-PS solid support (left panel) or by microwave-assisted synthesis on a PAL-PEG-PS support (sequence a , centre panel) or on a <t>ChemMatrix</t> solid support (sequence b , right panel).
    Fmoc Rink Amide Mbha Resin, supplied by Millipore, used in various techniques. Bioz Stars score: 92/100, based on 29 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    89
    CS Bio rink amide resin
    ( a ) Schematic representation of a PNA monomer unit. ( b ) Schematic representation of the cycle of microwave-assisted PNA synthesis on solid support. Fmoc/Bhoc are orthologous protecting groups for primary and nucleobase amino groups, respectively. The applied microwave pulse is indicated by a filled star symbol. The empty star represents an applied microwave pulse when the growing chain consists of natural amino acids only, or no microwave if the synthesized chain contains at least one PNA monomer. Activator: PyBOP; base: DIPEA for amino acids or DIPEA/Lutidine for PNA; final cleavage/deprotection: TFA/TIS/H 2 O 95:2.5:2.5. ( c ) Typical MALDI-TOF mass spectra of crude 23-mer PNA (sequence a ) synthesized by standard automated non-microwave method on a PAL-PEG-PS solid support (left panel) or by microwave-assisted synthesis on a PAL-PEG-PS support (sequence a , centre panel) or on a <t>ChemMatrix</t> solid support (sequence b , right panel).
    Rink Amide Resin, supplied by CS Bio, used in various techniques. Bioz Stars score: 89/100, based on 20 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    95
    Iris Biotech rink amide resin
    ( a ) Schematic representation of a PNA monomer unit. ( b ) Schematic representation of the cycle of microwave-assisted PNA synthesis on solid support. Fmoc/Bhoc are orthologous protecting groups for primary and nucleobase amino groups, respectively. The applied microwave pulse is indicated by a filled star symbol. The empty star represents an applied microwave pulse when the growing chain consists of natural amino acids only, or no microwave if the synthesized chain contains at least one PNA monomer. Activator: PyBOP; base: DIPEA for amino acids or DIPEA/Lutidine for PNA; final cleavage/deprotection: TFA/TIS/H 2 O 95:2.5:2.5. ( c ) Typical MALDI-TOF mass spectra of crude 23-mer PNA (sequence a ) synthesized by standard automated non-microwave method on a PAL-PEG-PS solid support (left panel) or by microwave-assisted synthesis on a PAL-PEG-PS support (sequence a , centre panel) or on a <t>ChemMatrix</t> solid support (sequence b , right panel).
    Rink Amide Resin, supplied by Iris Biotech, used in various techniques. Bioz Stars score: 95/100, based on 19 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    94
    Merck KGaA rink amide resin
    ( a ) Schematic representation of a PNA monomer unit. ( b ) Schematic representation of the cycle of microwave-assisted PNA synthesis on solid support. Fmoc/Bhoc are orthologous protecting groups for primary and nucleobase amino groups, respectively. The applied microwave pulse is indicated by a filled star symbol. The empty star represents an applied microwave pulse when the growing chain consists of natural amino acids only, or no microwave if the synthesized chain contains at least one PNA monomer. Activator: PyBOP; base: DIPEA for amino acids or DIPEA/Lutidine for PNA; final cleavage/deprotection: TFA/TIS/H 2 O 95:2.5:2.5. ( c ) Typical MALDI-TOF mass spectra of crude 23-mer PNA (sequence a ) synthesized by standard automated non-microwave method on a PAL-PEG-PS solid support (left panel) or by microwave-assisted synthesis on a PAL-PEG-PS support (sequence a , centre panel) or on a <t>ChemMatrix</t> solid support (sequence b , right panel).
    Rink Amide Resin, supplied by Merck KGaA, used in various techniques. Bioz Stars score: 94/100, based on 37 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    85
    Millipore fmoc rink amide linker
    ( a ) Schematic representation of a PNA monomer unit. ( b ) Schematic representation of the cycle of microwave-assisted PNA synthesis on solid support. Fmoc/Bhoc are orthologous protecting groups for primary and nucleobase amino groups, respectively. The applied microwave pulse is indicated by a filled star symbol. The empty star represents an applied microwave pulse when the growing chain consists of natural amino acids only, or no microwave if the synthesized chain contains at least one PNA monomer. Activator: PyBOP; base: DIPEA for amino acids or DIPEA/Lutidine for PNA; final cleavage/deprotection: TFA/TIS/H 2 O 95:2.5:2.5. ( c ) Typical MALDI-TOF mass spectra of crude 23-mer PNA (sequence a ) synthesized by standard automated non-microwave method on a PAL-PEG-PS solid support (left panel) or by microwave-assisted synthesis on a PAL-PEG-PS support (sequence a , centre panel) or on a <t>ChemMatrix</t> solid support (sequence b , right panel).
    Fmoc Rink Amide Linker, supplied by Millipore, used in various techniques. Bioz Stars score: 85/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    94
    BIOTAGE rink amide resin
    ( a ) Schematic representation of a PNA monomer unit. ( b ) Schematic representation of the cycle of microwave-assisted PNA synthesis on solid support. Fmoc/Bhoc are orthologous protecting groups for primary and nucleobase amino groups, respectively. The applied microwave pulse is indicated by a filled star symbol. The empty star represents an applied microwave pulse when the growing chain consists of natural amino acids only, or no microwave if the synthesized chain contains at least one PNA monomer. Activator: PyBOP; base: DIPEA for amino acids or DIPEA/Lutidine for PNA; final cleavage/deprotection: TFA/TIS/H 2 O 95:2.5:2.5. ( c ) Typical MALDI-TOF mass spectra of crude 23-mer PNA (sequence a ) synthesized by standard automated non-microwave method on a PAL-PEG-PS solid support (left panel) or by microwave-assisted synthesis on a PAL-PEG-PS support (sequence a , centre panel) or on a <t>ChemMatrix</t> solid support (sequence b , right panel).
    Rink Amide Resin, supplied by BIOTAGE, used in various techniques. Bioz Stars score: 94/100, based on 47 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rink amide resin/product/BIOTAGE
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    93
    Thermo Fisher rink amide resin
    ( a ) Schematic representation of a PNA monomer unit. ( b ) Schematic representation of the cycle of microwave-assisted PNA synthesis on solid support. Fmoc/Bhoc are orthologous protecting groups for primary and nucleobase amino groups, respectively. The applied microwave pulse is indicated by a filled star symbol. The empty star represents an applied microwave pulse when the growing chain consists of natural amino acids only, or no microwave if the synthesized chain contains at least one PNA monomer. Activator: PyBOP; base: DIPEA for amino acids or DIPEA/Lutidine for PNA; final cleavage/deprotection: TFA/TIS/H 2 O 95:2.5:2.5. ( c ) Typical MALDI-TOF mass spectra of crude 23-mer PNA (sequence a ) synthesized by standard automated non-microwave method on a PAL-PEG-PS solid support (left panel) or by microwave-assisted synthesis on a PAL-PEG-PS support (sequence a , centre panel) or on a <t>ChemMatrix</t> solid support (sequence b , right panel).
    Rink Amide Resin, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 93/100, based on 43 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    86
    Chem Impex International rink amide
    ( a ) Schematic representation of a PNA monomer unit. ( b ) Schematic representation of the cycle of microwave-assisted PNA synthesis on solid support. Fmoc/Bhoc are orthologous protecting groups for primary and nucleobase amino groups, respectively. The applied microwave pulse is indicated by a filled star symbol. The empty star represents an applied microwave pulse when the growing chain consists of natural amino acids only, or no microwave if the synthesized chain contains at least one PNA monomer. Activator: PyBOP; base: DIPEA for amino acids or DIPEA/Lutidine for PNA; final cleavage/deprotection: TFA/TIS/H 2 O 95:2.5:2.5. ( c ) Typical MALDI-TOF mass spectra of crude 23-mer PNA (sequence a ) synthesized by standard automated non-microwave method on a PAL-PEG-PS solid support (left panel) or by microwave-assisted synthesis on a PAL-PEG-PS support (sequence a , centre panel) or on a <t>ChemMatrix</t> solid support (sequence b , right panel).
    Rink Amide, supplied by Chem Impex International, used in various techniques. Bioz Stars score: 86/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    94
    AnaSpec rink amide resin
    ( a ) Schematic representation of a PNA monomer unit. ( b ) Schematic representation of the cycle of microwave-assisted PNA synthesis on solid support. Fmoc/Bhoc are orthologous protecting groups for primary and nucleobase amino groups, respectively. The applied microwave pulse is indicated by a filled star symbol. The empty star represents an applied microwave pulse when the growing chain consists of natural amino acids only, or no microwave if the synthesized chain contains at least one PNA monomer. Activator: PyBOP; base: DIPEA for amino acids or DIPEA/Lutidine for PNA; final cleavage/deprotection: TFA/TIS/H 2 O 95:2.5:2.5. ( c ) Typical MALDI-TOF mass spectra of crude 23-mer PNA (sequence a ) synthesized by standard automated non-microwave method on a PAL-PEG-PS solid support (left panel) or by microwave-assisted synthesis on a PAL-PEG-PS support (sequence a , centre panel) or on a <t>ChemMatrix</t> solid support (sequence b , right panel).
    Rink Amide Resin, supplied by AnaSpec, used in various techniques. Bioz Stars score: 94/100, based on 24 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    93
    Pcas Biomatrix rink amide chemmatix resin
    ( a ) Schematic representation of a PNA monomer unit. ( b ) Schematic representation of the cycle of microwave-assisted PNA synthesis on solid support. Fmoc/Bhoc are orthologous protecting groups for primary and nucleobase amino groups, respectively. The applied microwave pulse is indicated by a filled star symbol. The empty star represents an applied microwave pulse when the growing chain consists of natural amino acids only, or no microwave if the synthesized chain contains at least one PNA monomer. Activator: PyBOP; base: DIPEA for amino acids or DIPEA/Lutidine for PNA; final cleavage/deprotection: TFA/TIS/H 2 O 95:2.5:2.5. ( c ) Typical MALDI-TOF mass spectra of crude 23-mer PNA (sequence a ) synthesized by standard automated non-microwave method on a PAL-PEG-PS solid support (left panel) or by microwave-assisted synthesis on a PAL-PEG-PS support (sequence a , centre panel) or on a <t>ChemMatrix</t> solid support (sequence b , right panel).
    Rink Amide Chemmatix Resin, supplied by Pcas Biomatrix, used in various techniques. Bioz Stars score: 93/100, based on 6 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    86
    Peptides International rink amide clear resin
    ( a ) Schematic representation of a PNA monomer unit. ( b ) Schematic representation of the cycle of microwave-assisted PNA synthesis on solid support. Fmoc/Bhoc are orthologous protecting groups for primary and nucleobase amino groups, respectively. The applied microwave pulse is indicated by a filled star symbol. The empty star represents an applied microwave pulse when the growing chain consists of natural amino acids only, or no microwave if the synthesized chain contains at least one PNA monomer. Activator: PyBOP; base: DIPEA for amino acids or DIPEA/Lutidine for PNA; final cleavage/deprotection: TFA/TIS/H 2 O 95:2.5:2.5. ( c ) Typical MALDI-TOF mass spectra of crude 23-mer PNA (sequence a ) synthesized by standard automated non-microwave method on a PAL-PEG-PS solid support (left panel) or by microwave-assisted synthesis on a PAL-PEG-PS support (sequence a , centre panel) or on a <t>ChemMatrix</t> solid support (sequence b , right panel).
    Rink Amide Clear Resin, supplied by Peptides International, used in various techniques. Bioz Stars score: 86/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    92
    Bachem rink amide
    ( a ) Schematic representation of a PNA monomer unit. ( b ) Schematic representation of the cycle of microwave-assisted PNA synthesis on solid support. Fmoc/Bhoc are orthologous protecting groups for primary and nucleobase amino groups, respectively. The applied microwave pulse is indicated by a filled star symbol. The empty star represents an applied microwave pulse when the growing chain consists of natural amino acids only, or no microwave if the synthesized chain contains at least one PNA monomer. Activator: PyBOP; base: DIPEA for amino acids or DIPEA/Lutidine for PNA; final cleavage/deprotection: TFA/TIS/H 2 O 95:2.5:2.5. ( c ) Typical MALDI-TOF mass spectra of crude 23-mer PNA (sequence a ) synthesized by standard automated non-microwave method on a PAL-PEG-PS solid support (left panel) or by microwave-assisted synthesis on a PAL-PEG-PS support (sequence a , centre panel) or on a <t>ChemMatrix</t> solid support (sequence b , right panel).
    Rink Amide, supplied by Bachem, used in various techniques. Bioz Stars score: 92/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    92
    GL Biochem rink amide
    ( a ) Schematic representation of a PNA monomer unit. ( b ) Schematic representation of the cycle of microwave-assisted PNA synthesis on solid support. Fmoc/Bhoc are orthologous protecting groups for primary and nucleobase amino groups, respectively. The applied microwave pulse is indicated by a filled star symbol. The empty star represents an applied microwave pulse when the growing chain consists of natural amino acids only, or no microwave if the synthesized chain contains at least one PNA monomer. Activator: PyBOP; base: DIPEA for amino acids or DIPEA/Lutidine for PNA; final cleavage/deprotection: TFA/TIS/H 2 O 95:2.5:2.5. ( c ) Typical MALDI-TOF mass spectra of crude 23-mer PNA (sequence a ) synthesized by standard automated non-microwave method on a PAL-PEG-PS solid support (left panel) or by microwave-assisted synthesis on a PAL-PEG-PS support (sequence a , centre panel) or on a <t>ChemMatrix</t> solid support (sequence b , right panel).
    Rink Amide, supplied by GL Biochem, used in various techniques. Bioz Stars score: 92/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Average 92 stars, based on 3 article reviews
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    Iris Biotech rink amide
    ( a ) Schematic representation of a PNA monomer unit. ( b ) Schematic representation of the cycle of microwave-assisted PNA synthesis on solid support. Fmoc/Bhoc are orthologous protecting groups for primary and nucleobase amino groups, respectively. The applied microwave pulse is indicated by a filled star symbol. The empty star represents an applied microwave pulse when the growing chain consists of natural amino acids only, or no microwave if the synthesized chain contains at least one PNA monomer. Activator: PyBOP; base: DIPEA for amino acids or DIPEA/Lutidine for PNA; final cleavage/deprotection: TFA/TIS/H 2 O 95:2.5:2.5. ( c ) Typical MALDI-TOF mass spectra of crude 23-mer PNA (sequence a ) synthesized by standard automated non-microwave method on a PAL-PEG-PS solid support (left panel) or by microwave-assisted synthesis on a PAL-PEG-PS support (sequence a , centre panel) or on a <t>ChemMatrix</t> solid support (sequence b , right panel).
    Rink Amide, supplied by Iris Biotech, used in various techniques. Bioz Stars score: 90/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    AnaSpec rink amide
    ( a ) Schematic representation of a PNA monomer unit. ( b ) Schematic representation of the cycle of microwave-assisted PNA synthesis on solid support. Fmoc/Bhoc are orthologous protecting groups for primary and nucleobase amino groups, respectively. The applied microwave pulse is indicated by a filled star symbol. The empty star represents an applied microwave pulse when the growing chain consists of natural amino acids only, or no microwave if the synthesized chain contains at least one PNA monomer. Activator: PyBOP; base: DIPEA for amino acids or DIPEA/Lutidine for PNA; final cleavage/deprotection: TFA/TIS/H 2 O 95:2.5:2.5. ( c ) Typical MALDI-TOF mass spectra of crude 23-mer PNA (sequence a ) synthesized by standard automated non-microwave method on a PAL-PEG-PS solid support (left panel) or by microwave-assisted synthesis on a PAL-PEG-PS support (sequence a , centre panel) or on a <t>ChemMatrix</t> solid support (sequence b , right panel).
    Rink Amide, supplied by AnaSpec, 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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    CEM Corporation rink amide
    ( a ) Schematic representation of a PNA monomer unit. ( b ) Schematic representation of the cycle of microwave-assisted PNA synthesis on solid support. Fmoc/Bhoc are orthologous protecting groups for primary and nucleobase amino groups, respectively. The applied microwave pulse is indicated by a filled star symbol. The empty star represents an applied microwave pulse when the growing chain consists of natural amino acids only, or no microwave if the synthesized chain contains at least one PNA monomer. Activator: PyBOP; base: DIPEA for amino acids or DIPEA/Lutidine for PNA; final cleavage/deprotection: TFA/TIS/H 2 O 95:2.5:2.5. ( c ) Typical MALDI-TOF mass spectra of crude 23-mer PNA (sequence a ) synthesized by standard automated non-microwave method on a PAL-PEG-PS solid support (left panel) or by microwave-assisted synthesis on a PAL-PEG-PS support (sequence a , centre panel) or on a <t>ChemMatrix</t> solid support (sequence b , right panel).
    Rink Amide, supplied by CEM Corporation, used in various techniques. Bioz Stars score: 92/100, based on 5 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Iris Biotech fmoc rink amide mbha
    ( a ) Schematic representation of a PNA monomer unit. ( b ) Schematic representation of the cycle of microwave-assisted PNA synthesis on solid support. Fmoc/Bhoc are orthologous protecting groups for primary and nucleobase amino groups, respectively. The applied microwave pulse is indicated by a filled star symbol. The empty star represents an applied microwave pulse when the growing chain consists of natural amino acids only, or no microwave if the synthesized chain contains at least one PNA monomer. Activator: PyBOP; base: DIPEA for amino acids or DIPEA/Lutidine for PNA; final cleavage/deprotection: TFA/TIS/H 2 O 95:2.5:2.5. ( c ) Typical MALDI-TOF mass spectra of crude 23-mer PNA (sequence a ) synthesized by standard automated non-microwave method on a PAL-PEG-PS solid support (left panel) or by microwave-assisted synthesis on a PAL-PEG-PS support (sequence a , centre panel) or on a <t>ChemMatrix</t> solid support (sequence b , right panel).
    Fmoc Rink Amide Mbha, supplied by Iris Biotech, used in various techniques. Bioz Stars score: 94/100, based on 6 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Chem Impex International rink amide mbha resins
    ( a ) Schematic representation of a PNA monomer unit. ( b ) Schematic representation of the cycle of microwave-assisted PNA synthesis on solid support. Fmoc/Bhoc are orthologous protecting groups for primary and nucleobase amino groups, respectively. The applied microwave pulse is indicated by a filled star symbol. The empty star represents an applied microwave pulse when the growing chain consists of natural amino acids only, or no microwave if the synthesized chain contains at least one PNA monomer. Activator: PyBOP; base: DIPEA for amino acids or DIPEA/Lutidine for PNA; final cleavage/deprotection: TFA/TIS/H 2 O 95:2.5:2.5. ( c ) Typical MALDI-TOF mass spectra of crude 23-mer PNA (sequence a ) synthesized by standard automated non-microwave method on a PAL-PEG-PS solid support (left panel) or by microwave-assisted synthesis on a PAL-PEG-PS support (sequence a , centre panel) or on a <t>ChemMatrix</t> solid support (sequence b , right panel).
    Rink Amide Mbha Resins, supplied by Chem Impex International, used in various techniques. Bioz Stars score: 85/100, based on 12 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Merck KGaA rink amide
    ( a ) Schematic representation of a PNA monomer unit. ( b ) Schematic representation of the cycle of microwave-assisted PNA synthesis on solid support. Fmoc/Bhoc are orthologous protecting groups for primary and nucleobase amino groups, respectively. The applied microwave pulse is indicated by a filled star symbol. The empty star represents an applied microwave pulse when the growing chain consists of natural amino acids only, or no microwave if the synthesized chain contains at least one PNA monomer. Activator: PyBOP; base: DIPEA for amino acids or DIPEA/Lutidine for PNA; final cleavage/deprotection: TFA/TIS/H 2 O 95:2.5:2.5. ( c ) Typical MALDI-TOF mass spectra of crude 23-mer PNA (sequence a ) synthesized by standard automated non-microwave method on a PAL-PEG-PS solid support (left panel) or by microwave-assisted synthesis on a PAL-PEG-PS support (sequence a , centre panel) or on a <t>ChemMatrix</t> solid support (sequence b , right panel).
    Rink Amide, supplied by Merck KGaA, used in various techniques. Bioz Stars score: 85/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Gyros Protein Technologies rink amide mbha resin ll
    ( a ) Schematic representation of a PNA monomer unit. ( b ) Schematic representation of the cycle of microwave-assisted PNA synthesis on solid support. Fmoc/Bhoc are orthologous protecting groups for primary and nucleobase amino groups, respectively. The applied microwave pulse is indicated by a filled star symbol. The empty star represents an applied microwave pulse when the growing chain consists of natural amino acids only, or no microwave if the synthesized chain contains at least one PNA monomer. Activator: PyBOP; base: DIPEA for amino acids or DIPEA/Lutidine for PNA; final cleavage/deprotection: TFA/TIS/H 2 O 95:2.5:2.5. ( c ) Typical MALDI-TOF mass spectra of crude 23-mer PNA (sequence a ) synthesized by standard automated non-microwave method on a PAL-PEG-PS solid support (left panel) or by microwave-assisted synthesis on a PAL-PEG-PS support (sequence a , centre panel) or on a <t>ChemMatrix</t> solid support (sequence b , right panel).
    Rink Amide Mbha Resin Ll, supplied by Gyros Protein Technologies, used in various techniques. Bioz Stars score: 93/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Pcas Biomatrix h rink amide chemmatrix resin
    Shows the ESI-MS diagrams of the c-myc PNA. The left picture describes the <t>H-Rink-Amide-ChemMatrix®</t> Resin deprotected with pyrrolidine and the right picture depicts the diagram of the reaction product synthesized with the TentaGel® R RAM high swell Rapp Polymer under identical deprotection conditions.
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    Image Search Results


    ( a ) Schematic representation of a PNA monomer unit. ( b ) Schematic representation of the cycle of microwave-assisted PNA synthesis on solid support. Fmoc/Bhoc are orthologous protecting groups for primary and nucleobase amino groups, respectively. The applied microwave pulse is indicated by a filled star symbol. The empty star represents an applied microwave pulse when the growing chain consists of natural amino acids only, or no microwave if the synthesized chain contains at least one PNA monomer. Activator: PyBOP; base: DIPEA for amino acids or DIPEA/Lutidine for PNA; final cleavage/deprotection: TFA/TIS/H 2 O 95:2.5:2.5. ( c ) Typical MALDI-TOF mass spectra of crude 23-mer PNA (sequence a ) synthesized by standard automated non-microwave method on a PAL-PEG-PS solid support (left panel) or by microwave-assisted synthesis on a PAL-PEG-PS support (sequence a , centre panel) or on a ChemMatrix solid support (sequence b , right panel).

    Journal: Nucleic Acids Research

    Article Title: Efficient inhibition of miR-155 function in vivo by peptide nucleic acids

    doi: 10.1093/nar/gkq160

    Figure Lengend Snippet: ( a ) Schematic representation of a PNA monomer unit. ( b ) Schematic representation of the cycle of microwave-assisted PNA synthesis on solid support. Fmoc/Bhoc are orthologous protecting groups for primary and nucleobase amino groups, respectively. The applied microwave pulse is indicated by a filled star symbol. The empty star represents an applied microwave pulse when the growing chain consists of natural amino acids only, or no microwave if the synthesized chain contains at least one PNA monomer. Activator: PyBOP; base: DIPEA for amino acids or DIPEA/Lutidine for PNA; final cleavage/deprotection: TFA/TIS/H 2 O 95:2.5:2.5. ( c ) Typical MALDI-TOF mass spectra of crude 23-mer PNA (sequence a ) synthesized by standard automated non-microwave method on a PAL-PEG-PS solid support (left panel) or by microwave-assisted synthesis on a PAL-PEG-PS support (sequence a , centre panel) or on a ChemMatrix solid support (sequence b , right panel).

    Article Snippet: PNA oligomers containing a C-terminal amide were synthesized with Rink-Amide ChemMatrix (Matrix Innovation) solid support, and PyBOP (benzotriazol-1-yltris-pyrrolidinophosphonium hexafluorophosphate) as coupling agent.

    Techniques: Synthesized, Sequencing

    Shows the ESI-MS diagrams of the c-myc PNA. The left picture describes the H-Rink-Amide-ChemMatrix® Resin deprotected with pyrrolidine and the right picture depicts the diagram of the reaction product synthesized with the TentaGel® R RAM high swell Rapp Polymer under identical deprotection conditions.

    Journal: International Journal of Medical Sciences

    Article Title: SPPS Resins Impact the PNA-Syntheses' Improvement

    doi: 10.7150/ijms.5374

    Figure Lengend Snippet: Shows the ESI-MS diagrams of the c-myc PNA. The left picture describes the H-Rink-Amide-ChemMatrix® Resin deprotected with pyrrolidine and the right picture depicts the diagram of the reaction product synthesized with the TentaGel® R RAM high swell Rapp Polymer under identical deprotection conditions.

    Article Snippet: The syntheses were performed in a 5 μmol scale on a H-Rink-Amide-ChemMatrix® resin (PCAS BioMatrix, Saint-Jean-sur-Richelieu, Canada) loading 0.52 mmol/g and on a TentaGel® R RAM high swell resin (RAPP Polymers, Tuebingen, Germany) loading 0.62 mmol/g.

    Techniques: Mass Spectrometry, Synthesized

    Visualizes the deprotection in every coupling step (left bars) and shows a better performance of pyrrolidine (right diagrams in the parts A and B). This is compared to piperidine in the final step. Each measurement was collected after a base treatment of 2.5 minutes. The upper part ( A ) shows the TentaGel® R RAM high swell Rapp Polymers and the lower part illustrates the H-Rink-Amide-ChemMatrix® Resin bars ( B ). The products after the deprotection by piperidine are shown in the left column whereas the right column of the figure represents the bars of the pyrrolidine deprotected molecules. The height of the bars represents the amount of the Fmoc-group removed. The apparatus follows a cut off line 5% in front of the first bar. As soon as the second bar is lower then the adjusted value the program continoues, if not, a further deprotection is carried out.

    Journal: International Journal of Medical Sciences

    Article Title: SPPS Resins Impact the PNA-Syntheses' Improvement

    doi: 10.7150/ijms.5374

    Figure Lengend Snippet: Visualizes the deprotection in every coupling step (left bars) and shows a better performance of pyrrolidine (right diagrams in the parts A and B). This is compared to piperidine in the final step. Each measurement was collected after a base treatment of 2.5 minutes. The upper part ( A ) shows the TentaGel® R RAM high swell Rapp Polymers and the lower part illustrates the H-Rink-Amide-ChemMatrix® Resin bars ( B ). The products after the deprotection by piperidine are shown in the left column whereas the right column of the figure represents the bars of the pyrrolidine deprotected molecules. The height of the bars represents the amount of the Fmoc-group removed. The apparatus follows a cut off line 5% in front of the first bar. As soon as the second bar is lower then the adjusted value the program continoues, if not, a further deprotection is carried out.

    Article Snippet: The syntheses were performed in a 5 μmol scale on a H-Rink-Amide-ChemMatrix® resin (PCAS BioMatrix, Saint-Jean-sur-Richelieu, Canada) loading 0.52 mmol/g and on a TentaGel® R RAM high swell resin (RAPP Polymers, Tuebingen, Germany) loading 0.62 mmol/g.

    Techniques:

    Also shows the graphs of the HPLC chromatogram of the c-myc PNA synthesized on the peptide synthesizer 433A equipped with the special deprotection module with fixed deprotection time. Here the left side reveals the H-Rink-Amide-ChemMatrix® Resin [loading 0.52 mmol/g] deprotected with piperidine and the right picture exhibit the diagram of the pyrrolidine experiment. (detection A Ch2 /280 nm). The yields are 5.5 mg (26.4%) deprotected with piperidine and, with pyrrolidine 7.8 mg (37.5%). The product peaks are shown at 11.693 in the left and at 11.565 in the right diagram. The left picture displays more peaks than the right picture.

    Journal: International Journal of Medical Sciences

    Article Title: SPPS Resins Impact the PNA-Syntheses' Improvement

    doi: 10.7150/ijms.5374

    Figure Lengend Snippet: Also shows the graphs of the HPLC chromatogram of the c-myc PNA synthesized on the peptide synthesizer 433A equipped with the special deprotection module with fixed deprotection time. Here the left side reveals the H-Rink-Amide-ChemMatrix® Resin [loading 0.52 mmol/g] deprotected with piperidine and the right picture exhibit the diagram of the pyrrolidine experiment. (detection A Ch2 /280 nm). The yields are 5.5 mg (26.4%) deprotected with piperidine and, with pyrrolidine 7.8 mg (37.5%). The product peaks are shown at 11.693 in the left and at 11.565 in the right diagram. The left picture displays more peaks than the right picture.

    Article Snippet: The syntheses were performed in a 5 μmol scale on a H-Rink-Amide-ChemMatrix® resin (PCAS BioMatrix, Saint-Jean-sur-Richelieu, Canada) loading 0.52 mmol/g and on a TentaGel® R RAM high swell resin (RAPP Polymers, Tuebingen, Germany) loading 0.62 mmol/g.

    Techniques: High Performance Liquid Chromatography, Synthesized