Rabbit Polyclonal PPP1R3C antibody. Suitable for IHC-P, WB and reacts with Human samples. Immunogen corresponding to Recombinant Fragment Protein within Human PPP1R3C aa 1-150.
pH: 7.2
Preservative: 0.02% Sodium azide
Constituents: PBS, 40% Glycerol (glycerin, glycerine)
IHC-P | WB | |
---|---|---|
Human | Tested | Tested |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 1/20.00000 - 1/50.00000 | Notes Perform heat-mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol. |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 0.04000-0.40000 µg/mL | Notes - |
Acts as a glycogen-targeting subunit for PP1 and regulates its activity. Activates glycogen synthase, reduces glycogen phosphorylase activity and limits glycogen breakdown. Dramatically increases basal and insulin-stimulated glycogen synthesis upon overexpression in a variety of cell types.
PPP1R5, PPP1R3C, Protein phosphatase 1 regulatory subunit 3C, Protein phosphatase 1 regulatory subunit 5, Protein targeting to glycogen, PP1 subunit R5, PTG
Rabbit Polyclonal PPP1R3C antibody. Suitable for IHC-P, WB and reacts with Human samples. Immunogen corresponding to Recombinant Fragment Protein within Human PPP1R3C aa 1-150.
pH: 7.2
Preservative: 0.02% Sodium azide
Constituents: PBS, 40% Glycerol (glycerin, glycerine)
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PPP1R3C also known as protein phosphatase 1 regulatory subunit 3C is a regulatory subunit of protein phosphatase 1 (PP1). This protein has a mass of approximately 34 kDa. PPP1R3C is mainly expressed in skeletal muscle and liver tissues. It acts by modulating glycogen metabolism where it impacts glycogen synthesis and breakdown. This regulation is achieved through altering the activity of PP1 which dephosphorylates diverse biological substrates to control various cellular functions.
The PPP1R3C protein binds to glycogen and PP1 forming a complex with these substrates. This interaction plays a role in the regulation of glucose homeostasis by controlling glycogen synthesis and breakdown. Such processes are important for energy storage and release in muscle and liver tissues. By integrating within this complex PPP1R3C influences the activity and localization of PP1 facilitating efficient glycogen regulation.
PPP1R3C participates in critical pathways like glycogen metabolism and insulin signaling. The protein is closely associated with key metabolic proteins such as glycogen synthase. Within these pathways PPP1R3C modifies the enzymatic activity of its pathway partners to balance glucose levels in response to insulin. This involvement supports metabolic flexibility and energy management in response to dietary changes.
PPP1R3C connects to insulin resistance and type 2 diabetes where its altered function may disrupt normal glycogen metabolism. The protein's dysfunction impacts glucose homeostasis and insulin signaling pathway contributing to the pathophysiology of these metabolic diseases. Additionally PPP1R3C interacts with proteins like glycogen synthase which play significant roles in the metabolic disturbances seen in such disorders. Understanding these interactions helps in devising strategies for targeted therapeutic interventions.
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Western blot analysis of RT-4 cell lysate labeling PPP1R3C with ab251771.
All lanes: Western blot - Anti-PPP1R3C antibody (ab251771) at 0.04 µg/mL
All lanes: RT-4 cell lysate
Predicted band size: 36 kDa
Formalin-fixed, paraffin-embedded human liver tissue stained for PP1R3C with ab251771 at a 1/50 dilution in immunohistochemical analysis.
Formalin-fixed, paraffin-embedded human lung tissue stained for PP1R3C with ab251771 at a 1/50 dilution in immunohistochemical analysis.
Formalin-fixed, paraffin-embedded human heart tissue stained for PP1R3C with ab251771 at a 1/50 dilution in immunohistochemical analysis.
Formalin-fixed, paraffin-embedded human skeletal muscle tissue stained for PP1R3C with ab251771 at a 1/50 dilution in immunohistochemical analysis.
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