L5501
L-Lysine
≥98% (TLC), suitable for ligand binding assays
Synonym(s):
(S)-2,6-Diaminocaproic acid
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Product Name
L-Lysine, ≥98% (TLC)
Quality Level
Assay
≥98% (TLC)
form
powder
technique(s)
ligand binding assay: suitable
color
white to off-white
mp
215 °C (dec.) (lit.)
solubility
H2O: soluble
SMILES string
NCCCC[C@H](N)C(O)=O
InChI
1S/C6H14N2O2/c7-4-2-1-3-5(8)6(9)10/h5H,1-4,7-8H2,(H,9,10)/t5-/m0/s1
InChI key
KDXKERNSBIXSRK-YFKPBYRVSA-N
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General description
L-lysine contains basic side chain and is hydrophilic in nature. The N-butyl amino group in the side chain is found to be protonated at physiological pH. Upon degradation, L-lysine gives ketone bodies. Transamination of lysine with α-ketoglutarate produces acetoacetyl CoA. L-lysine serves as a precursor for secondary metabolites, such as β-lactam antibiotics. It also serves as a precursor for the biosynthesis of α-aminoadipic acid.
Application
L-Lysine is an essential proteinogenic α amino acid used in a wide range of applications. It has been used:
- as a supplement in cell culture media
- as a substrate for enzymes such as L-lysine oxidase (EC 1.4.3.14)
- as a component of poly-lysine polymers
- as a substrate for oxidation and glycation mechanism studies
- in the preparation of cobaltous lysine
Storage Class Code
11 - Combustible Solids
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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The Journal of comparative neurology, 281(1), 143-158 (1989-03-01)
The retinal topography of the adult coral trout Plectropoma leopardus (Serranidae, Perciformes) is examined in Nissl-stained material and confirmed by means of retrograde labelling with cobalt-lysine from the optic nerve. Concentric isodensity contours surround a temporoventral area centralis of over
Textbook of Biochemistry: With Clinical Correlations (5th ed.), 97-97 (2002)
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society, 30(12), 1235-1242 (1982-12-01)
The introduction of heavy metals directly into living neuronal tissue has received little attention as a method for defining connections in the vertebrate nervous system. Procedures are described for the use of cobaltous-lysine to trace visual pathways with light microscopy.
Molecular & cellular proteomics : MCP, 11(3), M111-M111 (2011-09-23)
Measuring the properties of endogenous cell proteins, such as expression level, subcellular localization, and turnover rates, on a whole proteome level remains a major challenge in the postgenome era. Quantitative methods for measuring mRNA expression do not reliably predict corresponding
Biochemistry (3rd Edition), 19-20 (1988)
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