L2752

Leu-Leu

Name: Leu-Leu
Brand: SIGMA

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

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この商品について

実験式（ヒル表記法）:

C₁₂H₂₄N₂O₃

CAS番号:

3303-31-9

分子量:

244.33

NACRES:

NA.26

PubChem Substance ID:

24896323

UNSPSC Code:

12352202

EC Number:

221-976-6

MDL number:

MFCD00065185

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製品名

Leu-Leu,

InChI key

LCPYQJIKPJDLLB-UWVGGRQHSA-N

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

SMILES string

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

assay

>98% (TLC)

form

powder

technique(s)

ligand binding assay: suitable

color

white to off-white

storage temp.

−20°C

Quality Level

200

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当該品目	C1141	L8753	H2504
Sigma-Aldrich L2752 Leu-Leu	Sigma-Aldrich C1141 Z-Phe-Leu	Sigma-Aldrich L8753 Leu-Pro hydrochloride	Sigma-Aldrich H2504 His-Leu
form powder	form powder	form powder	form solid
assay >98% (TLC)	assay ≥98% (TLC)	assay ≥98%	assay ≥98% (TLC)
technique(s) ligand binding assay: suitable	technique(s) ligand binding assay: suitable	technique(s) ligand binding assay: suitable	technique(s) ligand binding assay: suitable
storage temp. −20°C	storage temp. −20°C	storage temp. −20°C	storage temp. −20°C
Quality Level 200	Quality Level 200	Quality Level 200	Quality Level 200
color white to off-white	color white	color white	color white to off-white

Biochem/physiol Actions

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.

保管分類

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

適用法令

試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。

L2752-1G: + L2752-250MG: + L2752-BULK: + L2752-5G: + L2752-VAR: + L2752-100MG:

jan

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Physiological Concentration of H2O2 Supports Dopamine Neuronal Survival via Activation of Nrf2 Signaling in Glial Cells.

Guoqing Wang et al.

Cellular and molecular neurobiology, 41(1), 163-171 (2020-04-23)

Traditionally, hydrogen peroxide (H2O2) was formed from cellular oxidative metabolism and often viewed as toxic waste. In fact, H2O2 was a benefit messenger for neuron-glia signaling and synaptic transmission. Thus, H2O2 was a double-edged sword and neuroprotection vs. neurotoxicity produced

Dual modulation on glial cells by tetrahydroxystilbene glucoside protects against dopamine neuronal loss.

Yanzhen Zhou et al.

Journal of neuroinflammation, 15(1), 161-161 (2018-05-29)

Microglia-mediated neuroinflammation is recognized to mainly contribute to the pathogenesis of Parkinson's disease (PD). Tetrahydroxystilbene glucoside (TSG) has been proved to be beneficial for health with a great number of pharmacological properties. We examined the effects of TSG against dopamine

Utilization of dipeptides by Lactococcus lactis ssp. cremoris.

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

PRRG4 promotes breast cancer metastasis through the recruitment of NEDD4 and downregulation of Robo1.

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

Intracellular targeting and retention of the glucose transporter GLUT4 by the perinuclear storage compartment involves distinct carboxyl-tail motifs.

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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