| Item Name |
Product Image |
Price |
Sterically protected ligand (isobutyl - side chains), results in an Extra Stable bonded phase at low pH where most peptide separations are performed. The 160 Angstrom pore size was specially chosen for the molecular weight range of peptides. The... |
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... more info
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Sterically protected ligand (isobutyl - side chains), results in an Extra Stable bonded phase at low pH where most peptide separations are performed. The 160 Angstrom pore size was specially chosen for the molecular weight range of peptides. The... |
|
... more info
|
Sterically protected ligand (isobutyl - side chains), results in an Extra Stable bonded phase at low pH where most peptide separations are performed. The 160 Angstrom pore size was specially chosen for the molecular weight range of peptides. The... |
|
... more info
|
Sterically protected ligand (isobutyl - side chains), results in an Extra Stable bonded phase at low pH where most peptide separations are performed. The 160 Angstrom pore size was specially chosen for the molecular weight range of peptides. The... |
|
... more info
|
Sterically protected ligand (isobutyl - side chains), results in an Extra Stable bonded phase at low pH where most peptide separations are performed. The 160 Angstrom pore size was specially chosen for the molecular weight range of peptides. The... |
|
... more info
|
Highly retentive and selective for protonated basic analytes and molecules containing aromatic moities. End-capped pentafluorophenyl with a propyl spacer. |
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... more info
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Highly retentive and selective for protonated basic analytes and molecules containing aromatic moities. End-capped pentafluorophenyl with a propyl spacer. |
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... more info
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Highly retentive and selective for protonated basic analytes and molecules containing aromatic moities. End-capped pentafluorophenyl with a propyl spacer. |
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... more info
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Highly retentive and selective for protonated basic analytes and molecules containing aromatic moities. End-capped pentafluorophenyl with a propyl spacer. |
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... more info
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Highly retentive and selective for protonated basic analytes and molecules containing aromatic moities. End-capped pentafluorophenyl with a propyl spacer. |
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... more info
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Alternative selectivity to alkyl bonded phases, recommended for aromatic groups. Compatible with highly aqueous mobile phases to facilitate the retention and separation of polar compounds. Base-deactivated for good peak shapes when separating basic... |
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... more info
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Alternative selectivity to alkyl bonded phases, recommended for aromatic groups. Compatible with highly aqueous mobile phases to facilitate the retention and separation of polar compounds. Base-deactivated for good peak shapes when separating basic... |
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... more info
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Alternative selectivity to alkyl bonded phases, recommended for aromatic groups. Compatible with highly aqueous mobile phases to facilitate the retention and separation of polar compounds. Base-deactivated for good peak shapes when separating basic... |
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... more info
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Alternative selectivity to alkyl bonded phases, recommended for aromatic groups. Compatible with highly aqueous mobile phases to facilitate the retention and separation of polar compounds. Base-deactivated for good peak shapes when separating basic... |
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... more info
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Alternative selectivity to alkyl bonded phases, recommended for aromatic groups. Compatible with highly aqueous mobile phases to facilitate the retention and separation of polar compounds. Base-deactivated for good peak shapes when separating basic... |
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... more info
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Alternative selectivity to alkyl bonded phases, recommended for aromatic groups. Compatible with highly aqueous mobile phases to facilitate the retention and separation of polar compounds. Base-deactivated for good peak shapes when separating basic... |
|
... more info
|
Alternative selectivity to alkyl bonded phases, recommended for aromatic groups. Compatible with highly aqueous mobile phases to facilitate the retention and separation of polar compounds. Base-deactivated for good peak shapes when separating basic... |
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... more info
|
Alternative selectivity to alkyl bonded phases, recommended for aromatic groups. Compatible with highly aqueous mobile phases to facilitate the retention and separation of polar compounds. Base-deactivated for good peak shapes when separating basic... |
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... more info
|
Alternative selectivity to alkyl bonded phases, recommended for aromatic groups. Compatible with highly aqueous mobile phases to facilitate the retention and separation of polar compounds. Base-deactivated for good peak shapes when separating basic... |
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... more info
|
Alternative selectivity to alkyl bonded phases, recommended for aromatic groups. Compatible with highly aqueous mobile phases to facilitate the retention and separation of polar compounds. Base-deactivated for good peak shapes when separating basic... |
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... more info
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