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L2752

Sigma-Aldrich

Leu-Leu

>98% (TLC), suitable for ligand binding assays

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About This Item

Empirische Formel (Hill-System):
C12H24N2O3
CAS-Nummer:
3303-31-9
Molekulargewicht:
244.33
EG-Nummer:
221-976-6
MDL-Nummer:
MFCD00065185
UNSPSC-Code:
12352202
PubChem Substanz-ID:
24896323
NACRES:
NA.26

product name

Leu-Leu,

Assay

>98% (TLC)

Qualitätsniveau

200

Form

powder

Methode(n)

ligand binding assay: suitable

Farbe

white to off-white

Lagertemp.

−20°C

SMILES String

CC(C)C[C@H](N)C(=O)N[C@@H](CC(C)C)C(O)=O

InChI

1S/C12H24N2O3/c1-7(2)5-9(13)11(15)14-10(12(16)17)6-8(3)4/h7-10H,5-6,13H2,1-4H3,(H,14,15)(H,16,17)/t9-,10-/m0/s1

InChIKey

LCPYQJIKPJDLLB-UWVGGRQHSA-N

Verwandte Kategorien

Amino Acid Sequence

Leu-Leu

Biochem./physiol. Wirkung

Leucylleucine (Leu-Leu) may be used to study the functionality of dileucine motifs such as the motif responsible for internalization and targeting of vesicular acetylcholine transporter and clathrin adaptors AP-1 and AP-2.

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)

Analysenzertifikate (COA)

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Journal of neuroinflammation, 15(1), 161-161 (2018-05-29)
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A van Boven et al.
Biochimie, 70(4), 535-542 (1988-04-01)
Different strains of Lactococcus lactis ssp. cremoris hydrolyze peptides at different rates while the cell-free extracts of these strains all show the same or much higher rates of hydrolysis. These observations indicate that the uptake of peptides is the rate-limiting
Lingling Zhang et al.
Oncogene, 39(49), 7196-7208 (2020-10-11)
Metastasis is responsible for the death of most breast cancer patients. Robo1 has been implicated as a tumor suppressor for various cancers including breast cancer. However, it is not well understood how Robo1 expression is regulated during tumorigenesis. In this
S Martinez-Arca et al.
Journal of cell science, 113 ( Pt 10), 1705-1715 (2000-04-19)
The mechanisms by which the insulin-sensitive glucose transporter, GLUT4, is targeted and retained in a storage compartment near to the Golgi complex are poorly understood. Here we report that removal of the carboxyl-terminal acidic Pro(505)AspGluAsnAsp(509) sequence prevents the storage of
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