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  • Animal models of systemic lupus erythematosus (SLE) and ex vivo assay design for drug discovery.

Animal models of systemic lupus erythematosus (SLE) and ex vivo assay design for drug discovery.

Current protocols in pharmacology (2011-09-22)
Matthew M Seavey, Lily D Lu, Kristine L Stump
ANOTACE

Systemic Lupus Erythematosus (SLE) is a debilitating and often fatal autoimmune disease that involves multiple organ systems. It can develop for years before being diagnosed. Current treatments for SLE usually involve the use of cytotoxic or immunosuppressive agents that can lead to infection or cancer. The design of appropriate models and assays will determine the efficiency and speed with which an investigator can test a new chemical entity (NCE) or expect results to move a drug discovery program forward. This unit describes a series of preclinical assays for the identification of new agents for the treatment of SLE. Most importantly, this unit will guide the reader through a step-by-step process to select appropriate models, validation drugs, and readouts, depending on the objective of the study. The reader will acquire a working knowledge of what models are available and the potential advantages and disadvantages of each, including ex vivo assays relevant to the discovery of new SLE therapeutics.

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Sigma-Aldrich
Albumin from chicken egg white, lyophilized powder, ≥98% (agarose gel electrophoresis)
Millipore
Protease Inhibitor Cocktail Set IV, The Protease Inhibitor Cocktail Set IV controls the activity of Protease. This small molecule/inhibitor is primarily used for Protease Inhibitors applications.
Sigma-Aldrich
Anti-SMN antibody, Mouse monoclonal, clone 2B1, purified from hybridoma cell culture