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616377

Sigma-Aldrich

Toxin B, Clostridium difficile

A high molecular weight glucosyltransferase that inhibits small GTPases, such as Rho, Rac, and Cdc42, by glucosylation of a threonine residue.

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Synonym(s):
Cytotoxin
UNSPSC Code:
12352200

Quality Level

form

lyophilized

manufacturer/tradename

Calbiochem®

availability

not available in, Canada

storage condition

do not freeze

solubility

sterile distilled water: soluble

storage temp.

2-8°C

General description

A high molecular weight glucosyltransferase that inhibits small GTPases, such as Rho, Rac, and Cdc42 by glucosylation of a threonine residue. This results in the shutdown of signal transduction cascades, leading to depolymerization of the cytoskeleton, gene transcription of a number of stress-activated protein kinases (SAPKs), and a decrease in the synthesis of phosphatidylinositol 4,5-bisphosphate. May also block serotonin release, and stimulate the production of phospholipases C and D. Due to its ability to affect depolymerization of the cytoskeleton, toxin B has been shown to inhibit biphasic muscle contraction. Unlike Exoenzyme C3 (Cat. No. 341208), this toxin does not require assistance to permeabilize cells.
A high molecular weight glucosyltransferase that inhibits small GTPases, such as Rho, Rac, and Cdc42, by glucosylation of a threonine residue.
A high molecular weight glucosyltransferase that inhibits small GTPases, such as Rho, Rac, and Cdc42, by glucosylation of a threonine residue. This results in the shutdown of signal transduction cascades, leading to depolymerization of the cytoskeleton, gene transcription of a number of stress-activated protein kinases (SAPKs), and a decrease in the synthesis of phosphatidylinositiol 4,5-bisphosphate. May also block serotonin release, and stimulate the production of phospholipases C and D. Due to its ability to affect depolymerization of the cytoskeleton, toxin B has been shown to inhibit biphasic muscle contraction. Unlike Exoenzyme C3 (Cat. No. 341208), this toxin does not require assistance to permeabilize cells.

Biochem/physiol Actions

Cytotoxic as determined in a cell rounding assay using human foreskin cells.
Primary Target
Small GTPases, such as Rho, Rac, and Cdc42
Product does not compete with ATP.

Warning

Toxicity: Irritant (B)

Physical form

Lyophilized from 50 mM Tris, 50 mM NaCl, 0.1% trehalose, pH 7.5.

Reconstitution

Following reconstitution, refrigerate (4°C). Stock solutions are stable for up to 2 weeks at 4°C. Toxin B activity will decrease after 2 weeks at 4°C following reconstitution.
Please see vial label for lot-specific reconstitution volume.

Analysis Note

major band at >200 kDa

Other Notes

Mackay, D.J. and Hall, A. 1998. J. Biol. Chem. 273, 20685.
Prepens, U., et al. 1996. J. Biol. Chem. 271, 7324.
Schmidt, M., et al. 1996. Eur. J. Biochem. 240, 707.
Wilkins, T.D. and Lyerly, D.M. 1996. Trends Microbiol. 4, 49.

Legal Information

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

Pictograms

Skull and crossbones

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Acute Tox. 3 Dermal

WGK

WGK 3

Regulatory Information

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