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Merck
CN

P5297

Palmitoyl coenzyme A–Agarose

saline suspension

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UNSPSC Code:
41106500
NACRES:
NA.56
MDL number:
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form

saline suspension

extent of labeling

1-3 mg per mL

matrix

Cross-linked 4% beaded agarose

matrix activation

cyanogen bromide

matrix attachment

amino

matrix spacer

7 atoms

storage temp.

2-8°C

Application

Palmitoyl coenzyme A-agarose is used in protein chromatography and affinity chromatography. Palmitoyl coenzyme A-agarose has been used to identify the human mitochondrial linoleoyl-coenzyme A monolysocardiolipin acyltransferase (MLCL AT-1).

Physical form

Suspension in 0.5 M NaCl containing preservative

存储类别

12 - Non Combustible Liquids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


历史批次信息供参考:

分析证书(COA)

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Torben Helledie et al.
Molecular and cellular biochemistry, 239(1-2), 157-164 (2002-12-14)
Peroxisome proliferator-activated receptors (PPARs) are nuclear hormone receptors that are activated by a number of fatty acids and fatty acid derivatives. By contrast, we have recently shown that acyl-CoA esters display PPAR antagonistic properties in vitro. We have also shown
X Wang et al.
FEBS letters, 370(1-2), 15-18 (1995-08-14)
Membrane-bound fatty acyl-CoA reductase from the green alga Botryococcus braunii has been solubilized from the microsomal preparation by 0.1% octyl beta-glucoside and purified to near homogeneity by Blue A agarose and palmitoyl-CoA agarose affinity column chromatography. The molecular mass of
M Elholm et al.
The Journal of biological chemistry, 276(24), 21410-21416 (2001-03-30)
The peroxisome proliferator-activated receptor alpha (PPARalpha) is a ligand-activated transcription factor and a key regulator of lipid homeostasis. Numerous fatty acids and eicosanoids serve as ligands and activators for PPARalpha. Here we demonstrate that S-hexadecyl-CoA, a nonhydrolyzable palmitoyl-CoA analog, antagonizes
Daisuke Miyazawa et al.
Biochimica et biophysica acta, 1631(1), 17-25 (2003-02-08)
We have shown previously that the phospholipase A (PLA) activity specific for phosphatidic acid (PA) in porcine platelet membranes is of the A(1) type (PA-PLA(1)) [J. Biol. Chem. 259 (1984) 5083]. In the present study, the PA-PLA(1) was solubilized in
William J Driscoll et al.
The Journal of biological chemistry, 282(31), 22353-22363 (2007-05-15)
Oleamide (cis-9-octadecenamide) is the prototype member of an emerging class of lipid signaling molecules collectively known as the primary fatty acid amides. Current evidence suggests that oleamide participates in the biochemical mechanisms underlying the drive to sleep, thermoregulation, and antinociception.

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