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Merck
CN

P5297

Palmitoyl coenzyme A–Agarose

saline suspension

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About This Item

UNSPSC Code:
41106500
NACRES:
NA.56
MDL number:
Technical Service
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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


Storage Class

12 - Non Combustible Liquids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable



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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.
Tong Guo et al.
The Journal of cell biology, 177(2), 289-303 (2007-04-18)
We define the dynamics of spatial and temporal reorganization of the team of proteins and lipids serving peroxisome division. The peroxisome becomes competent for division only after it acquires the complete set of matrix proteins involved in lipid metabolism. Overloading
F Domergue et al.
Lipids, 35(5), 487-494 (2000-07-25)
Oleoyl-CoA elongase catalyzes four successive reactions: condensation of malonyl-CoA to oleoyl-CoA, reduction, dehydration, and another reduction. Evidence supporting this mechanism and the multienzymatic nature of the elongation complex are reported. A particulate membrane fraction from rapeseed is able to elongate



Global Trade Item Number

SKUGTIN
P5297-10ML04061837773624
P5297-5ML04061834378815
P5297-1ML04061834378723