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1353054-45-1

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1353054-45-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1353054-45-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,3,0,5 and 4 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1353054-45:
(9*1)+(8*3)+(7*5)+(6*3)+(5*0)+(4*5)+(3*4)+(2*4)+(1*5)=131
131 % 10 = 1
So 1353054-45-1 is a valid CAS Registry Number.

1353054-45-1Downstream Products

1353054-45-1Relevant articles and documents

Benzophenone-containing fatty acids and their related photosensitive fluorescent new probes: Design, physico-chemical properties and preliminary functional investigations

Hilbold, Beno?t,Perrault, Marie,Ehret, Christophe,Niu, Song-Lin,Frisch, Beno?t,Pécheur, Eve-Isabelle,Bourel-Bonnet, Line

, p. 7464 - 7473 (2012/01/06)

Hydrophobic photoaffinity labeling is a powerful strategy to identify hydrophobic segments within molecules, in particular membrane proteins. Here we report the design and synthesis of a novel family of fluorescent and photosensitive lipid tools, which have a common amino acid scaffold functionalized by three groups: (i) a first fatty acid chain grafted with a photoactivatable benzophenone moiety (Fatty Acid BenzoPhenone, FABP), (ii) a second fatty acid chain to ensure anchoring into a half-bilayer or hydrophobic environment, and (iii) a fluorescent carboxytetramethylrhodamine headgroup (CTMR) to detect the photolabeled compound. We present data of the synthesis and characterization of three lipid tools whose benzophenone ring is situated at various distances from the central scaffold. We could therefore establish structure/properties relationships dependent upon the depth of insertion of benzophenone into the membrane. Our lipid tools were extensively characterized both physico- and bio-chemically, and we assessed their functionality in vitro using bacterioRhodopsin (bR). We thus provide the scientific community with novel and reliable tools for the identification and study of hydrophobic regions in proteins.

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