GC Radioactivity Detectors

Standard building block for introduction of phenylglcine residues by Fmoc SPPS. Associated Protocols and Technical Articles Cleavage and Deprotection Protocols for Fmoc SPPS Linkage Replaces: 04-12-1117 Analysis Note Color (visual): white to slight

Standard building block for introduction of phenylglcine residues by Fmoc SPPS. Associated Protocols and Technical Articles Cleavage and Deprotection Protocols for Fmoc SPPS Linkage Replaces: 04-12-1117 Analysis Note Color (visual): white to slight

A derivative for the introduction of symmetric dimethyl-arginine during Fmoc SPPS. Coupling can be carried out using any standard activation method.

A derivative for the introduction of symmetric dimethyl-arginine during Fmoc SPPS. Coupling can be carried out using any standard activation method.

Building block for the introduction of selenocysteine during Fmoc SPPS [1,2,3] . Selenocysteine derivatives can undergo enantiomerization during coupling and can form dehydroalanine and &#946-piperidinylalanine containing side products during

An excellent building block for the preparation of phosphothreonine-containing peptides [1,2] by Fmoc SPPS. This derivative can be introduced using standard activation methods, such as PyBOP &#174 and TBTU.

Useful derivative for the synthesis of phosphothreonine peptides by the Fmoc SPPS global phosphorylation methodology. Associated Protocols and Technical Articles Cleavage and Deprotection Protocols for Fmoc SPPS Literature references [1] P.

Standard building block for introduction of Tic amino-acid residues by Fmoc SPPS Associated Protocols and Technical Articles Cleavage and Deprotection Protocols for Fmoc SPPS Literature references [1] M. Vincent, et al.

Standard building block for introduction of Tic amino-acid residues by Fmoc SPPS Associated Protocols and Technical Articles Cleavage and Deprotection Protocols for Fmoc SPPS Literature references [1] M. Vincent, et al.

Pre-loaded resin for synthesis of peptide acids containing a C-terminal tryptophan amino-acid residue by Fmoc SPPS. The N -in-Boc group helps minimize reattachment of peptides during TFA-mediated cleavage.

Standard building block for introduction of O-methyl-tyrosine amino-acid residues by Fmoc SPPS Associated Protocols and Technical Articles Cleavage and Deprotection Protocols for Fmoc SPPS Linkage Replaces: 04-12-1118 Analysis Note Color (visual):

Fmoc-Tyr(PO(NMe 2 ) 2 )-OH is a useful derivative for the synthesis of phosphotyrosine-containing peptides by Fmoc SPPS [1] . As the side-chain phosphate group is fully protected, this derivative is compatible with all coupling methods.