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Description
Molecular Formula: C5H11NO2S
Molecular Weight: 149.2
CAS Number: 63-68-3
pKA: 2.28, 9.21
Melting Point: 280 - 282 °C
Rotation: +23.40 (50 mg/ml, 6 M HCl, 20 °C)
Methionine is one of the common sulfur-containing amino acids. The biosynthesis of methionine
initially occurs by the condensation of homoserine and succinyl-CoA via the action of homoserine acyltransferase. Subsequently, cystathionine g-synthase displaces the succinate group with cysteine to give cystathionine. Cystathionine a-lyase then hydrolyzes cystathionine to produce homocysteine. Transfer of a methyl group from N5-methyltetrahydrofolate to the homocysteine forms methionine.
Methionine is a common methyl-group donor to various substrates, such as creatine, epinephrine, ergosterol, and choline. Methionine is a relatively hydrophobic amino acid residue, and as such is frequently buried in protein three-dimensional structure, making modification of methionine residues difficult.
A review of the oxidation of methionine as it relates to oxidation of b-amyloid peptides has been
published.
Precautions and Disclaimer
For Laboratory Use Only. Not for drug, household or other uses.
Preparation Instructions
This product is soluble in 1 M HCl (50 mg/ml), yielding a clear, colorless solution. This product is
also soluble in water (50 mg/ml), with heat as needed.
Storage/Stability
Stock solutions are stable for approximately five years at 2 - 8 °C
Documents
Disclaimer: For laboratory research use only.
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