추천 제품
Quality Level
분석
≥98.5% (NT)
mp
207-209 °C (dec.) (lit.)
SMILES string
NCCCCCC(O)=O
InChI
1S/C6H13NO2/c7-5-3-1-2-4-6(8)9/h1-5,7H2,(H,8,9)
InChI key
SLXKOJJOQWFEFD-UHFFFAOYSA-N
유전자 정보
human ... PLAT(5327) , PLG(5340)
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일반 설명
6-Aminohexanoic acid, or 6-aminocaproic acid, acts as an inhibitor of serine proteases. It shares structural similarities with the natural amino acid lysine but lacks an α-amino group.
애플리케이션
6-Aminohexanoic acid has been used as a component of the growth medium for tenogenic differentiation of mesenchymal stem cells. It has also been used in the preparation of modified graphene quantum dots.
생화학적/생리학적 작용
Lysine analog. Promotes rapid dissociation of plasmin, thereby inhibiting the activation of plasminogen and subsequent fibrinolysis. Reported to inhibit plasminogen binding to activated platelets. An early report indicated that it inhibits the activation of the first component of the complement system. Binds and inactivates Carboxypeptidase B.
기타 정보
Improves solubilization of membrane proteins in electrophoresis
Storage Class Code
11 - Combustible Solids
WGK
WGK 2
Flash Point (°F)
404.6 - 408.2 °F
Flash Point (°C)
207 - 209 °C
개인 보호 장비
dust mask type N95 (US), Eyeshields, Gloves
이미 열람한 고객
Purification strategies for membrane proteins
Journal of Separation Science, 2, 1-8 (2003)
Plant physiology, 141(2), 546-556 (2006-04-11)
Most extant cyanobacteria contain C16 fatty acids in the sn-2 positions of glycerolipids, which are regulated by lysophosphatidic acid acyltransferase (LPAAT; EC 2.3.1.51). Synechocystis sp. PCC6803 contains sll1848, sll1752, and slr2060 as putative acyltransferase genes. sll1848 was recently reported to
The Importance of 6-Aminohexanoic Acid as a Hydrophobic, Flexible Structural Element
International Journal of Molecular Sciences, 22(22), 12122-12122 (2021)
Post-synthetic modification of graphene quantum dots bestows enhanced biosensing and antibiofilm ability: efficiency face
Royal Society of Chemistry Advances, 12(20), 12310-12320 (2022)
Analytical biochemistry, 199(2), 223-231 (1991-12-01)
A discontinuous electrophoretic system for the isolation of membrane proteins from acrylamide gels has been developed using equipment for sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE). Coomassie dyes were introduced to induce a charge shift on the proteins and aminocaproic acid
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