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一般說明
Cholera Toxin (CT) is secreted by Vibrio cholerae. CT upregulates cell surface molecules, such as co-stimulatory molecules and chemokine receptors in antigen presenting cells(APCs), murine and human dendritic cells (DCs). It enhances the secretion of interleukin 1 (IL-1) from macrophages and stimulates their APC function. CT also functions as an immunomodulator.
應用
Cholera Toxin A Subunit from Vibrio cholerae has been used as a specific probe for trimeric G proteins in membrane motility assays.
生化／生理作用
Catalyzes ADP-ribosylation of the α-subunit of G proteins, reducing GTPase activity and activating the α-subunit; also catalyzes ADP-ribosylation of cell membrane adenylyl cyclase
外觀
Lyophilized powder containing Tris buffer salts, sodium chloride, sodium azide and sodium EDTA
重構
When reconstituted with 1 mL of water, the solution will contain 0.05 M Tris buffer salts, pH 7.5, 0.2 M NaCl, 0.003 M NaN3, and 0.001 M sodium EDTA. Store reconstituted solutions in the refrigerator.
訊號詞
Warning
危險聲明
危險分類
Acute Tox. 4 Inhalation - Aquatic Chronic 3
儲存類別代碼
11 - Combustible Solids
水污染物質分類（WGK）
WGK 3
閃點（°F）
Not applicable
閃點（°C）
Not applicable
In Vitro Reconstitution of Microtubule Plus End-directed, GTPgammaS-sensitive Motility of Golgi Membranes
Fullerton AT, et al.
Molecular Biology of the Cell, 9(10), 2699-2714 (1998)
Actions of cholera toxin and the prevention and treatment of cholera
Holmgren J.
Nature, 292(5822), 413-413 (1981)
Cholera toxin: a paradigm of a multifunctional protein
Bharati K and Ganguly NK
The Indian Journal of Medical Research, 133(2), 179-179 (2011)
Irina N Marinova et al.
STAR protocols, 2(3), 100668-100668 (2021-09-07)
Glycosylation is one of the most common protein modifications in living organisms and has important regulatory roles in animal tissue development and homeostasis. Here, we present a protocol for generation of 3D organotypic skin models using CRISPR-Cas9 genetically engineered human
Jiwei Liu et al.
EMBO reports, 21(2), e48597-e48597 (2019-12-14)
Histone lysine demethylase 1 (LSD1), the first identified histone demethylase, is overexpressed in multiple tumor types, including breast cancer. However, the mechanisms that cause LSD1 dysregulation in breast cancer remain largely unclear. Here, we report that protein arginine methyltransferase 4
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