C4951
Cholesterol-Water Soluble
powder, BioReagent, suitable for cell culture
Synonyme(s) :
Cholesterol–methyl-β-cyclodextrin
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A propos de cet article
NACRES:
NA.75
UNSPSC Code:
12352211
Service technique
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Laissez-nous vous aiderbiological source
ovine wool
Quality Level
product line
BioReagent
form
powder
technique(s)
cell culture | mammalian: suitable
solubility
H2O: 300 mg/mL
shipped in
ambient
storage temp.
−20°C
Application
Cholesterol-Water Soluble has been used:
- in free cholesterol (FC) overloading of rat smooth muscle cells (SMCs)
- in cytotoxicity assay
- for the incubation of CD4+ T cells with Helicobacter pylori
- to study the membrane cholesterol level in SH-SY5Y human neuroblastoma cells
- to study the effects of cholesterol on cell viability and 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) reduction in primary cultured rat hippocampal neurons
- as a supplement for growth of bacterial culture
- to examine the interaction of S protein with angiotensin-converting enzyme 2 (ACE2)
- to investigate the effects of cholesterol on potassium currents in the inner hair cells of guinea pigs
- for reversible inhibition of proteinase K
Packaging
Package size based on cholesterol
Preparation Note
Preparea solution at 300mg/mL in water. Let thesolution sit undisturbed for one hour after diluting to obtain completesolubilization of product.
Other Notes
Contains approx. 40 mg of cholesterol per gram; balance methyl-β-cyclodextrin.
Classe de stockage
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Cholesterol influences potassium currents in inner hair cells isolated from guinea pig cochlea
Kimitsuki T
Auris, Nasus, Larynx, 44(1), 46-51 (2017)
Barbora Melkes et al.
Naunyn-Schmiedeberg's archives of pharmacology, 389(12), 1289-1300 (2016-09-08)
There are some indications that biased μ-opioid ligands may diversely affect μ-opioid receptor (MOR) properties. Here, we used confocal fluorescence recovery after photobleaching (FRAP) to study the regulation by different MOR agonists of receptor movement within the plasma membrane of
ATR-101, a selective and potent inhibitor of Acyl-CoA acyltransferase 1, induces apoptosis in H295R adrenocortical cells and in the adrenal cortex of dogs
LaPensee CR, et al.
Endocrinology, 157(5), 1775-1788 (2016)