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810251P

Avanti

NBD-6 Cholesterol

Avanti Polar Lipids 810251P, powder

Synonym(s):
5-cholesten-3β-ol 6-[(7-nitro-2-1,3-benzoxadiazol-4-yl)amino]caproate
Empirical Formula (Hill Notation):
C39H58N4O5
CAS Number:
Molecular Weight:
662.90
NACRES:
NA.25

Assay

>99% (TLC)

form

powder

packaging

pkg of 1 × 1 mg (810251P-1mg)

manufacturer/tradename

Avanti Polar Lipids 810251P

shipped in

dry ice

storage temp.

−20°C

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810250C810252P810250P
NBD-6 Cholesterol Avanti Polar Lipids 810251P, powder

Avanti

810251P

NBD-6 Cholesterol

25-NBD Cholesterol Avanti Polar Lipids 810250C

Avanti

810250C

25-NBD Cholesterol

NBD-12 Cholesterol Avanti Polar Lipids 810252P, powder

Avanti

810252P

NBD-12 Cholesterol

25-NBD Cholesterol Avanti Polar Lipids

Avanti

810250P

25-NBD Cholesterol

form

powder

form

liquid

form

powder

form

powder

packaging

pkg of 1 × 1 mg (810251P-1mg)

packaging

pkg of 1 × 1 mL (810250C-10mg), pkg of 1 × 1 mL (810250C-1mg), pkg of 1 × 1 mL (810250C-5mg)

packaging

pkg of 1 × 1 mg (810252P-1mg)

packaging

pkg of 1 × 1 mg (810250P-1mg), pkg of 1 × 10 mg (810250P-10mg), pkg of 1 × 5 mg (810250P-5mg)

manufacturer/tradename

Avanti Polar Lipids 810251P

manufacturer/tradename

Avanti Polar Lipids 810250C

manufacturer/tradename

Avanti Polar Lipids 810252P

manufacturer/tradename

Avanti Polar Lipids

shipped in

dry ice

shipped in

dry ice

shipped in

dry ice

shipped in

dry ice

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

General description

NBD-6 Cholesterol is a fluorescent analog of the lipoprotein compound cholesterol, with NBD (2-(4-nitro-2,1,3-benzoxadiazol-7-yl) aminoethyl) being the fluorescent group.

Application

NBD-6 Cholesterol has been used for NBD-cholesterol binding assay, to study the binding of fluorescent NBD cholesterol in the binding pocket concerning ASTER domains.

Biochem/physiol Actions

Cholesterol is produced from acetyl-CoA by a complex multistep mevalonate pathway. In mammals, liver is the main site of de novo cholesterol synthesis contributing to almost 80% of total cholesterol synthesis. Cholesterol and its metabolites, along with its precursors, play important roles in cellular membrane physiology. They also have roles in reproductive biology, dietary nutrient absorption, stress responses, salt and water balance and calcium metabolism.

Packaging

5 mL Amber Glass Screw Cap Vial (810251P-1mg)

Storage Class Code

11 - Combustible Solids


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Molecular Nutrition And Food Research, 277-290 (2016)
Fluorescent and Luminescent Probes for Biological Activity (1999)
Cholesterol in health and disease.
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The Journal of clinical investigation, 110(5), 583-590 (2002-09-05)
Pedro M R Cruz et al.
Frontiers in pharmacology, 4, 119-119 (2013-10-05)
While the unique metabolic activities of malignant tissues as potential targets for cancer therapeutics has been the subject of several recent reviews, the role of cholesterol metabolism in this context is yet to be fully explored. Cholesterol is an essential
Jaspreet Sandhu et al.
Cell, 175(2), 514-529 (2018-09-18)
The mechanisms underlying sterol transport in mammalian cells are poorly understood. In particular, how cholesterol internalized from HDL is made available to the cell for storage or modification is unknown. Here, we describe three ER-resident proteins (Aster-A, -B, -C) that

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