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Our Blog
Discover the latest blog posts from Peptide Works
Discover how researchers measure AMPK activity using methods including Thr172 phosphorylation analysis, downstream substrate phosphorylation and direct kinase activity assays to characterise AMPK-associated signalling.
Much of the laboratory research on LL-37 has focused on how the peptide behaves around microbial membranes, bacterial components, and biofilms.
The examination of Vilon has been carried out in controlled laboratory tissue models in order to find out how the various experimental preparations react to the short dipeptide. This review considers the results obtained from organotypic culture, the measured tissue responses, and the limitations of the existing evidence.
Explaining why accurate chemical classification matters in MK-677 research, establishing ibutamoren as a synthetic non-peptide small molecule and highlighting the importance of distinguishing its molecular form and nomenclature when interpreting scientific data.
This blog examines how Kisspeptin is investigated in reproductive endocrine signalling, focusing on GnRH-associated activity, LH pulsatility, endocrine feedback and coordinated hypothalamic–pituitary signalling.
Article & News
AMP-activated protein kinase, commonly referred to as AMPK, is a protein kinase that plays a role in how cells respond to changes in energy availability. Research concerning AMPK is directed towards understanding how cells detect changes in their energy status and then adjust the various intracellular pathways related to glucose handling, lipid metabolism, mitochondrial function, and autophagy.
AICAR is widely used as an experimental compound for investigating AMP-activated protein kinase (AMPK) signaling in cultured muscle cells. Research has examined how AICAR-associated AMPK activation relates to glucose transport, protein synthesis, mitochondrial metabolism, transcriptional regulation, and other intracellular pathways.
Adamax is referred to in research literature as a peptide that is chemically modified in relation to the Semax sequence. Yet scientific evidence on Adamax alone is very limited, especially compared with the extensive research on related peptide sequences.
This review looks at how researchers investigate myostatin signaling in skeletal muscle, comparing molecular approaches involving follistatin, ACE-031, and other strategies used to study the pathway.
