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Lipolysis-activating peptide

The heterodimer non-edited LVP1 induces lipolysis in rat adipocytes. Induction of lipolysis by LVP1 appears to be mediated through the beta-2 adrenergic receptor pathway (ADRB2) (By similarity).

Below are the list of possible Lipolysis-activating peptide products. If you cannot find the target and/or product is not available in our catalog, please click here to contact us and request the product or submit your request for custom elisa kit production, custom recombinant protein production or custom antibody production. Custom ELISA Kits, Recombinant Proteins and Antibodies can be designed, manufactured and produced according to the researcher's specifications.

Lipolysis-activating peptide 1-alpha chain

 Lipolysis-activating peptide 1-alpha chain ELISA Kit
 Lipolysis-activating peptide 1-alpha chain Recombinant
 Lipolysis-activating peptide 1-alpha chain Antibody
Also known as Lipolysis-activating peptide 1-alpha chain (BmLVP1-alpha) (LVP1-alpha).
The heterodimer non-edited LVP1 induces lipolysis in rat adipocytes. Induction of lipolysis by LVP1 appears to be mediated through the beta-2 adrenergic receptor pathway (ADRB2) ().
 LVP1a Recombinant
 LVP1a Antibody
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Lipolysis-activating peptide 1-beta chain

 Lipolysis-activating peptide 1-beta chain ELISA Kit
 Lipolysis-activating peptide 1-beta chain Recombinant
 Lipolysis-activating peptide 1-beta chain Antibody
Also known as Lipolysis-activating peptide 1-beta chain (BoiLVP1-beta) (LVP1-beta) (Putative beta-like toxin Tx457).
The homodimer inhibits HMG-CoA reductase (HMGCR) (32% of inhibition produced by
0.6 µM), a glycoprotein involved in the control of cholesterol biosynthesis. The inhibitory effects of bumarsin are seen at much lower concentrations (0.6 µM) than that for statins such as atorvastatin (5 mM) and simvastatin (10 µM). In addition to inhibition of HMG-CoA reductase, this protein lowers cholesterol levels by inducing steroid hormone synthesis via StAR, and by increasing reverse cholesterol transport mediated by the induction of ABCA1 and APOA1 ().
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