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Key Documents

1.04114

Sigma-Aldrich

ß-Glucuronidase/aryl sulfatase

(from Helix pomatia) stabilized aqueous solution for biochemistry EC 3.2.1.31 + EC 3.1.6.1

Synonym(s):

Aryl sulfatase

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About This Item

UNSPSC Code:
12352204

biological source

Helix pomatia

Quality Level

100

form

liquid

density

1.1 g/cm3 at 20 °C

storage temp.

2-8°C

Application

β-Glucuronidase/arylsulfatase has been used:
  • to study the existence of gluco- or sulphoconjugated analytes in pig plasma samples
  • to hydrolyze corticosteroid conjugates
  • as a component of the sodium-acetate buffer for hydrolysis of Parus major fecal extracts

Biochem/physiol Actions

β-Glucuronidase is involved in the physiological activity and toxicity of several xenobiotics and drugs. It catalyzes the elimination of glucuronic acid from β-D-glucuronides.

Analysis Note

β-Glucuronidase (4-Nitrophenyl-β-D-glucuronide; pH 3.8; 38.0 °C): about 30 U/ml
Arylsulfatase (4-Nitrophenylsulfate potassiumsalt; pH 6.2; 38.0 °C): about 60 U/ml

Pictograms

Health hazard
GHS08

Signal Word

Danger

Hazard Statements

H317 - H334

Hazard Classifications

Resp. Sens. 1 - Skin Sens. 1

Storage Class Code

12 - Non Combustible Liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

EU REACH Annex XVII (Restriction List)

CAS No.

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Punsaldulam Dashnyam et al.
Scientific reports, 8(1), 16372-16372 (2018-11-08)
Gut bacterial β-D-glucuronidases (GUSs) catalyze the removal of glucuronic acid from liver-produced β-D-glucuronides. These reactions can have deleterious consequences when they reverse xenobiotic metabolism. The human gut contains hundreds of GUSs of variable sequences and structures. To understand how any
Determination of androstenone levels in porcine plasma by LC-MS/MS
Chen G, et al.
Food Chemistry, 122(4), 1278-1282 (2010)
Jens Hinge Andersen et al.
Analytica chimica acta, 617(1-2), 216-224 (2008-05-20)
A solid phase extraction (SPE) method for extraction and clean up of 9 synthetic corticosteroids was optimized for quantification by reversed-phase high-performance liquid chromatography/negative electrospray ionisation mass spectrometry. Clean up was accomplished using a mixed mode polymeric strong anion exchange
Tapio Eeva et al.
Ecotoxicology (London, England), 23(5), 914-928 (2014-04-05)
We manipulated dietary lead (Pb) levels of nestlings in wild populations of the great tit (Parus major L) to find out if environmentally relevant Pb levels would affect some physiological biomarkers (haematocrit [HT], fecal corticosterone metabolites [CORT], heat shock proteins

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