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Nitrilotriacetic acid (NTA) is the aminopolycarboxylic acid with the formula N(CH 2 CO 2 H) 3. It is a colourless solid. It is a colourless solid. Its conjugate base nitrilotriacetate is used as a chelating agent for Ca 2+ , Co 2+ , Cu 2+ , and Fe 3+ .
This chronological list of biophysically notable protein and nucleic acid structures is loosely based on a review in the Biophysical Journal. [1] The list includes all the first dozen distinct structures, those that broke new ground in subject or method, and those that became model systems for work in future biophysical areas of research.
diethylenetriamineacetic acid DTMA [1] NH 2 C 2 H 4 NHC 2 H 4 NHCH 2 COOH linear NNNO 1– Co iso-diethylenetriamineacetic acid i-DTMA [1] (NH 2 C 2 H 4) 2 NCH 2 COOH tripodal N N 2NO 1– Co Jäger's N2O2 ligand linear acacen ONNO N 2 O 2: Ni Naphthalocyanine: C 48 H 26 N 8: ring NNNN 714.79 Nitrilotriacetic acid: NTA N(CH 2 CO 2 H) 3 ...
Further substitution gives nitrilotriacetic acid, NTA, which is a tetradentate ligand. [3] These compounds can be described as aminopolycarboxylates. Related ligands can be derived from other amino acids other than glycine, notably aspartic acid. Binding of a metal complex by the iminodiacetate anion
Examples of methods for adding polyhistidine tags. (A) The polyhistidine tag is added by inserting the DNA encoding a protein of interest in a vector that has the tag ready to fuse at the C-terminus. (B) The polyhistidine tag is added using primers containing the tag coding sequence as an overhang on the forward primer. After PCR amplification ...
.alpha.,.alpha.',.alpha.''-Trimethylaminetricarboxylic acid 2,2',2''-Nitrilotriacetic acid Acetic acid, nitrilotri- (8CI) alpha,alpha',alpha''-Trimethylaminetricarboxylic acid alpha,alpha',alpha''-trimethylaminetricarboxylic acid aminotriacetic acid Aminotriacetic acid Chel 300 chel 300 Complexon I Complexone I(R) Glycine, N,N-bis(carboxymethyl)- (9CI) hampshire nta acid Hampshire NTA acid ...
N-acyl amides are a general class of endogenous fatty acid compounds characterized by a fatty acyl group linked to a primary amine metabolite by an amide bond. Broadly speaking, N-acyl amides fall into several categories: amino acid conjugates (e.g., N-arachidonoyl-glycine), neurotransmitter conjugates (e.g., N-arachidonoyl-serotonin), ethanolamine conjugates (e.g., anandamide), and taurine ...
A representation of the structure of myoglobin, showing alpha helices, represented by ribbons.This protein was the first to have its structure solved by X-ray crystallography by Max Perutz and Sir John Cowdery Kendrew in 1958, for which they received a Nobel Prize in Chemistry