Welcome to Iris Biotech
For better service please confirm your country and language we detected.
Währung
EUR
Amino Acids
-
Diazirine Amino Acids: Photocrosslinking Applications
Two selected publications were summarized in this article in order to highlight the impressive utility of amino acids incorporating the diazirine photophore.
Weiterlesen
-
Fmoc-L-Lys(Nvoc)-OH
o-Nitroveratryloxycarbonyl (Nvoc) is a photocleavable side chain protecting group for lysine that can be removed by irradiation with UV light (350 nm).
Weiterlesen
-
H-L-Lys(Suc)-OH*HCl
Succinylation of proteins on the epsilon-amino group of lysine residues is a posttranslational modification that is still poorly understood.
Weiterlesen
-
Hydrolysis-Stable Mimics of Phosphorylated Amino Acids (Ser, Thr and Tyr)
Phosphorylation of serine, threonine and tyrosine is counted among the most important posttranslational modifications that occur in organisms.
Weiterlesen
-
Diazirine Amino Acids for Photo Cross-Linkage in Living Cells
Iris Biotech introduces a comprehensive set of photo-crosslinking amino acids bearing the diazirine moiety.
Weiterlesen
-
beta,beta-Dimethyl Amino Acids
The use of bioactive peptides has increased over the recent years as they attracted attention for their use as therapeutic agents.
Weiterlesen
-
Fmoc-L-Cys(Propargyl)-OH
This alkyne-functionalized cysteine building block can be incorporated into peptides via the Fmoc strategy.
Weiterlesen
-
Standard Fmoc Amino Acid Building Blocks
Amino acids of high quality are crucial for the synthesis of peptides with a high purity.
Weiterlesen
-
Application of the Trt and Fmoc groups for the protection of polyfunctional α-amino acids
Abstract: Ditrityl amino acids Trt-Lys(Trt)-OH (Trt = CPh3), Trt-Orn(Trt)-OH, Trt-Ser(Trt)-OH, and Trt-Hse(Trt)-OH were prepared and used in the synthesis of trityl-protected peptides, e.g., Trt-Ser(Trt)-Phe-NH2.
Weiterlesen -
Triamino Acids
Fmoc-L-Dap(2-Boc-aminoethyl)-OH is the first in a series of new triamino acid building blocks. This azalysine is useful for introducing positive charges into a peptide, or for creating branched structures.
Weiterlesen
