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LIN28 phosphorylation by MAP/ERK couples signaling to the posttranscriptional control of pluripotencyThe Harvard community has made this article openly available. Please share how this access benefits
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Step 1: Start by gathering all the necessary materials, including the lin28 phosphorylation assay kit and a sample containing MAPK/ERK protein.
02
Step 2: Prepare a reaction mix by adding the necessary components according to the assay kit instructions. This typically includes a reaction buffer, ATP, and a substrate for MAPK/ERK.
03
Step 3: Add the lin28 protein to the reaction mix at the specified concentration. Mix gently to ensure proper distribution.
04
Step 4: Incubate the reaction mix at the appropriate temperature and duration as recommended by the assay kit instructions. This will allow the phosphorylation reaction to occur.
05
Step 5: Stop the reaction by adding a stopping buffer or by cooling the reaction mix to a low temperature. This will halt any further phosphorylation.
06
Step 6: Analyze the phosphorylation of lin28 by MAPK/ERK. This can be done through various techniques such as Western blotting or enzyme activity assays.
07
Step 7: Interpret the results obtained from the analysis and draw conclusions about the phosphorylation status of lin28 by MAPK/ERK.

Who needs lin28 phosphorylation by mapkerk?

01
Researchers studying the role of lin28 phosphorylation in cellular processes.
02
Scientists exploring the signaling pathways involving MAPK/ERK and lin28.
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Biomedical researchers interested in the regulation of lin28 protein activity.
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Pharmaceutical companies developing drugs targeting MAPK/ERK signaling and lin28 function.
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Anyone involved in understanding the molecular mechanisms and functional significance of lin28 phosphorylation by MAPK/ERK.

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