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b-Glucuronidase, Snail (Helix pomatia)

b-Glucuronidase, Snail (Helix pomatia)

Cat no: G3060-04

Supplier: United States Biological
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b-Glucuronidase has been found in tissue extracts of mammals and other vertebrates, digestive juices of snails, molluscs, locusts, bacteria and plants. The enzyme catalyzes the hydrolysis of b-glucuronides and also the transfer of glucuronly radicals to acceptor alcohols. b-Glucuronidase is a structural protein of the endoplasmic reticulum,. Its occurence in the lysozomes is due to changes in the endoplasmic reticulum. b-Glucuronidase catalyzes the following reaction: b-Glucuronidase b-D-Glucuronide + H2O ---> Alcohol + D-Glucuronate Aryl Sulfatase Activity: As reported Activity: ~2000/mg Protein Extinction Coefficient: 4.08 Unit Definition: 1 unit is equal to the amount of enzyme which liberates 1ug of phenolphthalein from phenolphthalein glucuronide per hour at 37 degrees C, pH 5. Specificity: The enzyme hydrolyzes a large variety of conjugated glucuronides but not alpha-or beta-glucosides. Inhibitors: Strongly, reversibly inhibited by various organic peroxides Application: Suitable for use in urine steroid determinations. Storage and Stability: Lyophilized powder may be stored at -20 degrees C. Stable for 6 months at -20 degrees C. Reconstitute with sterile 2% sodium chloride. Prepare fresh per assay.
Catalogue number: G3060-04
Size: 1MU
Form: Supplied as a lyophilized powder. Reconstitute with sterile 2% sodium chloride to 5mg/ml.
Alternative names: EC=3.2.1.31; Beta-D-Glucuronide; glucuronosohydrolase
References: 1. O.H. Lowry et al. J. Biol. Chem. (1951), 193, 265. 2. Fishman, W.H. and Bernfield, P. (1955) Methods of Enzymology, 1, 262-269 3. Combie, J., Blake, J.W., Nugent, T.E., and Tobin, T. (1982) Clin. Chem., 28, 83-86. 4. Fishman, W.H. (1974) Method of Enzymatic Analysis (Bergmeyer, H.U.) 2nd ed., II, 929-932.

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