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Apical sodium bile acid transporter asbt inhibitor

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The apical sodium-bile acid transporter (ASBT) inhibitor is a laboratory product that functions to inhibit the ASBT, a transporter responsible for the reabsorption of bile acids in the terminal ileum.

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Lab products found in correlation

Histamine eia kit, by Cayman Chemical (2 mentions) Mouse and human primers, by Qiagen (2 mentions) Farnesoid x receptor fxrβ inhibitor, by Merck Group (2 mentions) Chemical grade reagents, by Merck Group (2 mentions) Real time pcr materials, by Qiagen (2 mentions)

2 protocols using apical sodium bile acid transporter asbt inhibitor

1

Characterizing Liver Histamine Signaling

Cited 2 times
Check if the same lab product or an alternative is used in the 5 most similar protocols
Chemical grade reagents were purchased from Sigma-Aldrich Co (St. Louis, MO) unless stated otherwise. All mouse and human primers and real-time PCR materials were obtained from Qiagen (Fredrick, MD). Antibodies for immunohistochemistry and immunofluorescence were purchased from Abcam (Cambridge, MA) or Santa Cruz (Dallas, TX). Histamine EIA kits were purchased from Cayman Chemical (An Arbor, MI)5 (link)9 (link)10 (link). The apical sodium-bile acid transporter (ASBT) inhibitor was obtained from Tocris Bioscience (Minneapolis, MN) and the farnesoid X receptor (FXRβ) inhibitor was obtained from Sigma-Aldrich Co (St. Louis, MO). Kits to measure total bile acids (TBAs) were purchased from Crystal Chemical, Inc (Downers Grove, IL) 5 (link).
Meng F., Kennedy L., Hargrove L., Demieville J., Jones H., Madeka T., Karstens A., Chappell K., Alpini G., Sybenga A., Invernizzi P., Bernuzzi F., DeMorrow S, & Francis H. (2018). Ursodeoxycholate inhibits mast cell activation and reverses biliary injury and fibrosis in Mdr2−/− mice and human primary sclerosing cholangitis. Laboratory investigation; a journal of technical methods and pathology, 98(11), 1465-1477.
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2

Characterizing Liver Histamine Signaling

Cited 2 times
Check if the same lab product or an alternative is used in the 5 most similar protocols
Chemical grade reagents were purchased from Sigma-Aldrich Co (St. Louis, MO) unless stated otherwise. All mouse and human primers and real-time PCR materials were obtained from Qiagen (Fredrick, MD). Antibodies for immunohistochemistry and immunofluorescence were purchased from Abcam (Cambridge, MA) or Santa Cruz (Dallas, TX). Histamine EIA kits were purchased from Cayman Chemical (An Arbor, MI)5 (link)9 (link)10 (link). The apical sodium-bile acid transporter (ASBT) inhibitor was obtained from Tocris Bioscience (Minneapolis, MN) and the farnesoid X receptor (FXRβ) inhibitor was obtained from Sigma-Aldrich Co (St. Louis, MO). Kits to measure total bile acids (TBAs) were purchased from Crystal Chemical, Inc (Downers Grove, IL) 5 (link).
Meng F., Kennedy L., Hargrove L., Demieville J., Jones H., Madeka T., Karstens A., Chappell K., Alpini G., Sybenga A., Invernizzi P., Bernuzzi F., DeMorrow S, & Francis H. (2018). Ursodeoxycholate inhibits mast cell activation and reverses biliary injury and fibrosis in Mdr2−/− mice and human primary sclerosing cholangitis. Laboratory investigation; a journal of technical methods and pathology, 98(11), 1465-1477.
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