D ornithine

Manufactured by Merck Group

Sourced in United Kingdom

D-ornithine is a non-essential amino acid that can be used in laboratory settings for various research purposes. It serves as a precursor for the synthesis of other biochemical compounds. The core function of D-ornithine is to provide a building block for the study of metabolic pathways and the development of analytical techniques.

Automatically generated - may contain errors

Lab products found in correlation

Adocbl, by Merck Group (2 mentions) Glucose oxidase from aspergillus niger, by Merck Group (1 mentions) S 2 2 5 5 tetramethyl 2 5 dihydro 1h pyrrol 3 yl methyl methanesulfonothioate mtsl, by LGC (1 mentions) Inorganic salts, by Thermo Fisher Scientific (1 mentions) Putrescine, by Merck Group (1 mentions) D arginine, by Merck Group (1 mentions)

Spelling variants of this product

Poly-d-ornithine (7 citations) Poly d‐l‐ornithine (PLO; (2 citations)

3 protocols using d ornithine

Enzymatic Cofactor Synthesis Protocol

Check if the same lab product or an alternative is used in the 5 most similar protocols

AdoCbl, PLP, d-ornithine, d,l-2,4-diaminobutyric acid (DAB) and glucose oxidase (from Aspergillus niger) were obtained from Sigma-Aldrich (Dorset, UK).

Menon B.R., Menon N., Fisher K., Rigby S.E., Leys D, & Scrutton N.S. (2015). Glutamate 338 is an electrostatic facilitator of C–Co bond breakage in a dynamic/electrostatic model of catalysis by ornithine aminomutase. The Febs Journal, 282(7), 1242-1255.

+ Open protocol

+ Expand

Characterization of Cofactor Binding

Check if the same lab product or an alternative is used in the 5 most similar protocols

AdoCbl, PLP, d-ornithine, dl-2,4-diaminobutyric acid (DABA), dl-2,3-diaminopropanioc acid (DAPA), trypsin, and glucose oxidase (from Aspergillus niger) were obtained from Sigma. S-(2,2,5,5-Tetramethyl-2,5-dihydro-1H-pyrrol-3-yl)methyl methanesulfonothioate (MTSL) was from Toronto Research Chemicals Inc. Rosetta(DE3)pLysS and other competent cells were purchased from EMD Biosciences.

Menon B.R., Fisher K., Rigby S.E., Scrutton N.S, & Leys D. (2014). A Conformational Sampling Model for Radical Catalysis in Pyridoxal Phosphate- and Cobalamin-dependent Enzymes. The Journal of Biological Chemistry, 289(49), 34161-34174.

+ Open protocol

+ Expand

Amino Acid Synthesis and Purification

Check if the same lab product or an alternative is used in the 5 most similar protocols

d-lysine and d-ornithine were products of Alfa Aesar. d-arginine and putrescine were obtained from Sigma-Aldrich. Buffers, inorganic salts, and solvents were obtained from Fisher Scientific.

Meiners S., Xu A, & Schindler M. (1991). Gap junction protein homologue from Arabidopsis thaliana: evidence for connexins in plants.. Proceedings of the National Academy of Sciences of the United States of America, 88(10), 4119-4122.

+ Open protocol

+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Revolutionizing how scientists
search and build protocols!