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A0796

Sigma-Aldrich

p-Aminomethylbenzenesulfonamide–Agarose

saline suspension

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About This Item

Numéro MDL:
Code UNSPSC :
23151817

Forme

saline suspension

Ampleur du marquage

≥6 mg per mL

Matrice

crosslinked 4% beaded agarose

Activation de la matrice

cyanogen bromide

Fixation de matrice

amino

Espaceur de matrice

1 atom

Température de stockage

2-8°C

Application

p-Aminomethylbenzenesulfonamide is an agarose in saline suspension that can be used in affinity chromatography, protein chromatography and specialty resins. p-Aminomethylbenzenesulfonamide has been used in studies assessing inhibition of mitochondrial carbonic anhydrase and ureagenesis.

Forme physique

Suspension in 0.5 M NaCl containing preservative.

Pictogrammes

Exclamation mark

Mention d'avertissement

Warning

Mentions de danger

Conseils de prudence

Classification des risques

Skin Sens. 1

Code de la classe de stockage

13 - Non Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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Consulter la Bibliothèque de documents

B Ulmasov et al.
Proceedings of the National Academy of Sciences of the United States of America, 97(26), 14212-14217 (2000-12-20)
Carbonic anhydrase XII (CA XII) is a transmembrane glycoprotein with an active extracellular CA domain that is overexpressed on cell surfaces of certain cancers. Its expression has been linked to tumor invasiveness. To characterize its catalytic properties, we purified recombinant
S J Dodgson et al.
Journal of applied physiology (Bethesda, Md. : 1985), 60(2), 646-652 (1986-02-01)
The amount of urea produced in 60 min, [urea]t = 60, from intact guinea pig hepatocytes incubated in NH4Cl, oleate, lactate, NaHCO3, and ornithine at 37 degrees C at pH 7.1 is decreased by ethoxzolamide (EZ): Ki,EZ [urea]t = 60
D K Srivastava et al.
Journal of the American Chemical Society, 129(17), 5528-5537 (2007-04-05)
Despite the similarity in the active site pockets of carbonic anhydrase (CA) isozymes I and II, the binding affinities of benzenesulfonamide inhibitors are invariably higher with CA II as compared to CA I. To explore the structural basis of this
B E Alber et al.
Proceedings of the National Academy of Sciences of the United States of America, 91(15), 6909-6913 (1994-07-19)
Carbonic anhydrase (CA) from acetate-grown Methanosarcina thermophila was purified > 10,000-fold (22% recovery) to apparent homogeneity with a specific activity of 4872 units/mg. The estimated native molecular mass of the enzyme is 84 kDa based on gel filtration chromatography. SDS/PAGE
S J Dodgson
Journal of applied physiology (Bethesda, Md. : 1985), 63(5), 2134-2141 (1987-11-01)
The amount of urea synthesized in intact guinea pig hepatocytes in 60 min ([urea]t=60), was determined at 37 degrees C in Krebs-Henseleit buffer plus (in mM) 10 NH4Cl, 5 lactate, and 10 ornithine in 5% CO2-95% O2. The concentrations of

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