This document presents a set of requirements for Traffic Engineering over Multiprotocol Label Switching (MPLS). It identifies the functional capabilities required to implement policies that facilitate efficient and reliable network operations in an MPLS domain. These capabilities can be used to optimize the utilization of network resources and to enhance traffic oriented performance characteristics.
Various 5'O-N-protected deoxynucleoside-3'-O-beta-cyanoethyl-N,N-dialkylamino-/N- morpholinophosphoramidites were prepared from beta-cyanoethyl monochlorophosphoramidites of N,N-dimethylamine, N,N-diisopropylamine and N-morpholine. These active deoxynucleoside phosphates have successfully been used for oligodeoxynucleotide synthesis on controlled pore glass as polymer support and are very suitable for automated DNA-synthesis due to their stability in solution. The intermediate dichloro-beta- cyanoethoxyphosphine can easily be prepared free from any PC1(3) contamination. The active monomers obtained from beta-cyanoethyl monochloro N,N- diisopropylaminophosphoramidites are favoured. Cleavage of the oligonucleotide chain from the polymer support, N-deacylation and deprotection of beta-cyanoethyl group from the phosphate triester moiety can be performed in one step with concentrated aqueous ammonia. Mixed oligodeoxynucleotides are characterized by the sequencing method of Maxam and Gilbert.
An acetic anhydride pyridine mixture acetylates hydroxyl groups in tissue sections. The acetyl groups can be removed from tissue sections by weak alkali.
Sections acetylated by acetic anhydride pyridine no longer produce aldehydes after oxidation by periodic acid. Acetylated sections subjected to weak alkali regain the ability to produce aldehydes after oxidation by periodic acid. Acetylation of tissue sections and the removal of acetyl groups by weak alkali can be used as histochemical confirmation of the carbohydrate nature of materials coloring with Schiff's reagent after periodic acid.
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