Standard Fluorescence Label
BIOSYNTAN offers fluorescently labeled peptides with following standard dyes:
Fluorescein & Rhodamine Label
Fluorescein-isothiocyanat (FITC) shows certain instability,...
Fatty Acids & Carboxylic Acids
The modification of peptides with carboxylic or fatty acids increases solubility in unpolar solvents and affinity to cell membranes. Additionally, such peptides can be...
Side Chain Cyclization
In this type of cyclization a stable amide bond is formed between a side chain carboxyl group of aspartic acid or glutamic acid and an amino group of lysine. Homologues of...
Peptides for Ligation
Specifically modified amino acids in peptides open up a wide range of ligation reactions. Orthogonal and biocompatible reactions render various methods of modification and...
Labeled Peptides
Labeling of peptides is often required to address biochemical and analytical questions. BIOSYNTAN offers peptide synthesis with different labels matching various research...
D-Amino Acids
Opposite stereochemistry in the α-position of essential amino acids produces interesting new features. Firstly, D-amino acids increase the stability of peptides against...
Biotinylation
The extraordinary strong interaction of biotin and avidin/streptavidin is used for plenty of different applications in biochemistry. Biotin derivatization of peptides generates a very...
Click Chemistry
Introduced in 2001 by M. Meldal, the Cu-catalyzed azide alkyne cycloaddition (CuAAC) gained enormous potential in peptide chemistry. An azide reacts with an alkyne moiety in order to...
Native Chemical Ligation
Introduced in 1994 by S. B. Kent, Native Chemical Ligation (NCL) is the most popular of the ligation reactions, particularly for the chemical synthesis of longer peptides or...