227039
Cholera Toxin, B Subunit, Vibrio cholerae, Type Inaba 569B - Calbiochem
Subunit of cholera toxin responsible for binding to GM1 ganglioside receptors in membranes.
质量水平
表单
solid
制造商/商品名称
Calbiochem®
储存条件
do not freeze
溶解性
sterile distilled water: soluble
运输
ambient
储存温度
2-8°C
一般描述
Cholera toxin is an oligomeric protein consisting of a single A subunit (M.W. 28,000) containing two polypeptide chains, A1 and A2 , and a B subunit (M.W. 55,000) containing five polypeptide chains. Cholera toxin is the pathogenic agent responsible for the symptoms of cholera. Cholera toxin is also a potent activator of adenylate cyclase that binds the ADP-ribosylation factor and modulates its activity. The A subunit catalyzes the ADP-ribosylation of GS that leads to the persistent activation of adenylate cyclase. The consequent increase in intracellular cAMP levels stimulates Cl- secretion and leads to severe dehydration. The B subunit binds specifically to GM1 ganglioside receptors, which are expressed ubiquitously in mammalian cells, and assists in the transport of the A subunit through the membrane. When used alone, the B subunit will block the action of toxin on intact cells. Purified B subunit is produced by a modification of the methods published by Lai, C.Y., et al.
Subunit of cholera toxin responsible for binding to GM1 ganglioside receptors in membranes. When used along, will block the action of toxin on intact cells.
生化/生理作用
Cell permeable: no
Cholera Toxin, B Subunit is tested for its effectiveness in binding antitoxin using the antitoxin combining power assay described by Craig, J.P., et al.
Primary Target
GM1 ganglioside receptors
GM1 ganglioside receptors
Reversible: no
包装
yes
外形
Lyophilized from 200 mM NaCl, 50 mM Tris-HCl, 3 mM NaN₃, 1 mM EDTA, pH 7.5.
制备说明
Following reconstitution, refrigerate (4°C). Stock solutions are stable for up to 6 months at 4°C. DO NOT FREEZE reconstituted solutions.
其他说明
Due to the nature of the Hazardous Materials in this shipment, additional shipping charges may be applied to your order. Certain sizes may be exempt from the additional hazardous materials shipping charges. Please contact your local sales office for more information regarding these charges.
McCloskey, M.A. and Zhang, L. 2000. J. Cell. Biol.148, 137.
Mulhein, S.A., et al. 1989. J. Membr. Biol. 109, 21.
Tsai, S.-C., et al. 1988. J. Biol. Chem.263, 1768.
Van Heynigen, S. 1982. Biosci. Rep.2, 135.
Mekalanos, J.J., et al. 1978. Infect. Immun.20, 552.
Gill, D.M. 1976. Biochemistry15, 1242.
Lai, C.Y., et al. 1976. J. Infect. Dis.139, 674.
Rappaport, R.S., et al. 1974. Infect. Immun.9, 294.
Craig, J.P. 1971. In Kadies, S., et al. (Eds.). Microbial Toxins. New York. Academic Press, 2A, 189.
Mulhein, S.A., et al. 1989. J. Membr. Biol. 109, 21.
Tsai, S.-C., et al. 1988. J. Biol. Chem.263, 1768.
Van Heynigen, S. 1982. Biosci. Rep.2, 135.
Mekalanos, J.J., et al. 1978. Infect. Immun.20, 552.
Gill, D.M. 1976. Biochemistry15, 1242.
Lai, C.Y., et al. 1976. J. Infect. Dis.139, 674.
Rappaport, R.S., et al. 1974. Infect. Immun.9, 294.
Craig, J.P. 1971. In Kadies, S., et al. (Eds.). Microbial Toxins. New York. Academic Press, 2A, 189.
法律信息
Not available for sale outside of the United States.
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
免责声明
Toxicity: Highly Toxic (H)
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