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Titlebook: Calpain; Methods and Protocol Jeannette S. Messer Book 2019 Springer Science+Business Media, LLC, part of Springer Nature 2019 proteases.en

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11#
發(fā)表于 2025-3-23 13:44:07 | 只看該作者
12#
發(fā)表于 2025-3-23 15:20:07 | 只看該作者
Identification of Calpain-Activated Protein Functionsbstrates. The cleavage of some substrates can produce active fragments that perform functions that are different from those performed by the full-length proteins. Therefore, cleavage by calpains can operate as a posttranslational modification and increase the functional diversity of target proteins.
13#
發(fā)表于 2025-3-23 19:36:18 | 只看該作者
14#
發(fā)表于 2025-3-23 23:21:58 | 只看該作者
Isolation of Endogenous Calpastatinhibitory activity against calpain in the presence of Ca. to specifically identify the protein. Thus, the purification steps necessary to obtain the inhibitor protein were originally designed to obtain calpain from the same tissue. For this reason, in addition to calpastatin purification, we also inc
15#
發(fā)表于 2025-3-24 04:54:15 | 只看該作者
Immunoblotting for Calpastatin Expression calpastatin isoforms can vary by tissue, can be modified by partial digestion, and can undergo posttranslational modifications. Here we describe a method for more precise evaluation of calpastatin expression by combining immunoblot analysis with an assay for the inhibitory activity of a single calp
16#
發(fā)表于 2025-3-24 10:23:46 | 只看該作者
17#
發(fā)表于 2025-3-24 13:12:42 | 只看該作者
Single-Step Purification of Calpain-1, Calpain-2, and Calpastatin Using Anion-Exchange Chromatographs that effectively bind with the DEAE Sephacel and separate well using a stepwise, increasing gradient of NaCl to elute the proteins. Calpastatin binds most weakly with the column matrix, so it elutes first, followed by calpain-1 and, finally, calpain-2.
18#
發(fā)表于 2025-3-24 15:38:46 | 只看該作者
Casein Zymography for Analysis of Calpain-1 and Calpain-2 Activityvoid of dye when stained with Coomassie Brilliant Blue G-250. We describe here how calpains can be extracted from muscle tissue and assayed for activity using this technique. This technique is also generally applicable to lysates from other types of cells or tissues.
19#
發(fā)表于 2025-3-24 20:14:47 | 只看該作者
Mara B. Antonoff,Ashok K. Salujas that effectively bind with the DEAE Sephacel and separate well using a stepwise, increasing gradient of NaCl to elute the proteins. Calpastatin binds most weakly with the column matrix, so it elutes first, followed by calpain-1 and, finally, calpain-2.
20#
發(fā)表于 2025-3-25 01:41:37 | 只看該作者
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