L9037
L-Lysine monohydrate
98.5-101.5% dry basis, suitable for cell culture, BioReagent, non-animal source
동의어(들):
L-Lysine hydrate (1:1), Lysine monohydrate
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크기 선택
제품정보 (DICE 배송 시 비용 별도)
실험식(Hill 표기법):
C6H14N2O2 · H2O
CAS 번호:
Molecular Weight:
164.20
NACRES:
NA.26
PubChem Substance ID:
UNSPSC Code:
12352209
EC Number:
200-294-2
MDL number:
Beilstein/REAXYS Number:
4349963
제품 이름
L-Lysine monohydrate, BioReagent, suitable for cell culture, from non-animal source
InChI
1S/C6H14N2O2.H2O/c7-4-2-1-3-5(8)6(9)10;/h5H,1-4,7-8H2,(H,9,10);1H2/t5-;/m0./s1
SMILES string
[H]O[H].NCCCC[C@H](N)C(O)=O
InChI key
HZRUTVAFDWTKGD-JEDNCBNOSA-N
biological source
non-animal source
product line
BioReagent
assay
98.5-101.5% dry basis
form
crystalline powder
technique(s)
cell culture | mammalian: suitable
impurities
endotoxin, tested
color
white
mp
215 °C
solubility
H2O: soluble
Quality Level
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General description
L-Lysine is an amino acid with a basic side chain and is amphipathic in nature. It has a protonated alkyl amino group and is fully protonated at physiological pH. L-lysine mainly participates in electrostatic interactions in proteins.
Application
L-Lysine monohydrate has been used in:
- SILAC (stable isotope labeling by amino acids in cell culture) method
- the complete synthetic (C) medium for positive selection screening of yeast cells
- the growth medium for cells
Biochem/physiol Actions
L-Lysine is an essential proteinogenic α amino acid used in a wide range of applications including as a non-animal sourced supplement in cell culture media, a substrate of enzymes such as L-lysine oxidase (EC 1.4.3.14), a component of poly-lysine polymers, and a substrate for oxidation and glycation mechanism studies.
저장 등급
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Shao-En Ong et al.
Nature protocols, 1(6), 2650-2660 (2007-04-05)
Stable isotope labeling by amino acids in cell culture (SILAC) is a simple, robust, yet powerful approach in mass spectrometry (MS)-based quantitative proteomics. SILAC labels cellular proteomes through normal metabolic processes, incorporating non-radioactive, stable isotope-containing amino acids in newly synthesized
Daniel Kalb et al.
Chembiochem : a European journal of chemical biology, 16(10), 1426-1430 (2015-05-13)
L-α-Aminoadipic acid reductases catalyze the ATP- and NADPH-dependent reduction of L-α-aminoadipic acid to the corresponding 6-semialdehyde during fungal L-lysine biosynthesis. These reductases resemble peptide synthetases with regard to their multidomain composition but feature a unique domain of elusive function--now referred
Harvey RA, et al.
Biochemistry (Lippincott's illustrated reviews) (2011)
W L McKeehan et al.
Proceedings of the National Academy of Sciences of the United States of America, 73(6), 2023-2027 (1976-06-01)
The trace element selenium is essential for clonal growth of diploid fibroblasts from human fetal lung (WI-38) in media containing small amounts of serum protein. Maximum growth stimulation is obtained when 30 nM neutralized selenious acid is added to a
Garrett RH and Grisham CM
Biochemistry (2016)
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