详细说明
- Purity>90%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining.
- Endotoxin Level<1.0 EU per 1 μg of the protein by the LAL method.
- ActivityMeasured by its ability to hydrolyze UDP-Glucose. The specific activity is >15 pmol/min/μg, as measured under the described conditions. See Activity Assay Protocol on .
- SourceE. coli-derived
msyB
(Thr2-Arg124)
Accession # P25738GSENLYFQGH C. difficile TcdA
(Met1-Leu542, Arg184Asn)
Accession # P16154HHHHHH N-terminus C-terminus - N-terminal Sequence
AnalysisThr2 (msyB) - Predicted Molecular Mass79 kDa
- SDS-PAGE78 kDa, reducing conditions
8619-GT | | |
Formulation Supplied as a 0.2 μm filtered solution in Tris, NaCl and Glycerol. | ||
Shipping The product is shipped with polar packs. Upon receipt, store it immediately at the temperature recommended below. | ||
Stability & Storage: Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
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- Glycosyltransferase Activity Kit (Catalog # )
- Assay Buffer: 25 mM Tris, 150 mM NaCl, 10 mM MnCl2, 5 mM CaCl2, 150 mM K2SO4, pH 7.0
- Recombinant C. difficile Toxin A/TcdA (rC.d.TcdA) (Catalog # 8619-GT)
- UDP-Glucose (Calbiochem, Catalog # 670120), 10 mM stock in 25% Ethanol
- 96-well Clear Plate (Catalog # )
- Plate Reader (Model: SpectraMax Plus by Molecular Devices) or equivalent
- Dilute 1 mM Phosphate Standard provided by the Glycosyltransferase Kit by adding 40 µL of the 1 mM Phosphate Standard to 360 µL of Assay Buffer for a 100 µM stock.
- Prepare the standard curve by performing seven one-half serial dilutions of the 100 µM Phosphate stock using Assay Buffer. The standard curve has a range of 0.039 to 2.5 nmol per well.
- Prepare reaction mixture containing 0.8 mM UDP-Glucose and 8 µg/mL Coupling Phosphatase 1 in Assay Buffer.
- Dilute rC.d.TcdA to 40 ng/µL in Assay Buffer.
- Load 50 µL of each dilution of the standard curve into a plate. Include a curve blank containing 50 μL of Assay Buffer.
- Load 25 µL of 40 ng/µL rC.d.TcdA into empty wells of the same plate as the curve. Include a Control containing 25 μL of Assay Buffer.
- Add 25 µL of the reaction mixture to all wells, excluding the standard curve.
- Seal plate and incubate at room temperature for 40 minutes.
- Add 30 µL of the Malachite Green Reagent A to all wells. Mix briefly.
- Add 100 µL of deionized water to all wells. Mix briefly.
- Add 30 µL of the Malachite Green Reagent B to all wells. Mix and incubate sealed plate for 20 minutes at room temperature.
- Read plate at 620 nm (absorbance) in endpoint mode.
- Calculate specific activity:
Specific Activity (pmol/min/µg) = | Phosphate released* (nmol) x (1000 pmol/nmol) |
Incubation time (min) x amount of enzyme (µg) |
*Derived from the phosphate standard curve using linear or 4-parameter fitting and adjusted for Control
Per Reaction:- rC.d.TcdA: 1 µg
- Coupling Phosphatase 1: 0.2 µg
- UDP-Glucose: 0.4 mM
5-fold greater than that of TcdA.
- References:
- Wilkins, T.D. and Lyerly, D.M. (2003) J. Clin. Microbiol 41:53.
- Kyne, L. et al. (2002) Clin. Infect. Dis. 34:346.
- Voth, D.E. and Ballard, J.D. (2005) Clin. Microbiol. Rev. 18:247.
- Chaves-Olarte, E. et al. (1996) J. Biol. Chem. 271:6925.
- Just I, et al. (1995) J. Biol. Chem. 270:13932.
- Hammond, G.A. and Johnson, J.L. (1995) Microb. Pathog. 19:203.
- Ciesla, W.P. Jr. and Bobak, D.A. (1998) J. Biol. Chem. 273:16021.
- Entrez Gene IDs:8470358 (C. difficile)
- Alternate Names:TcdA; ToxA; Toxin A