Recombinant Human Caveolin-3 protein is a Human Fragment protein, in the 1 to 83 aa range, expressed in Wheat germ and suitable for SDS-PAGE, ELISA, WB.
Wheat germ
Tag free
SDS-PAGE, ELISA, WB
No
M M A E E H T D L E A Q I V K D I H C K E I D L V N R D P K N I N E D I V K V D F E D V I A E P V G T Y S F D G V W K V S Y T T F T V S K Y W C Y R L L S T L L G V P
Application | Reactivity | Dilution info | Notes |
---|---|---|---|
Application SDS-PAGE | Reactivity Reacts | Dilution info - | Notes - |
Application ELISA | Reactivity Reacts | Dilution info - | Notes - |
Application WB | Reactivity Reacts | Dilution info - | Notes - |
May act as a scaffolding protein within caveolar membranes. Interacts directly with G-protein alpha subunits and can functionally regulate their activity. May also regulate voltage-gated potassium channels. Plays a role in the sarcolemma repair mechanism of both skeletal muscle and cardiomyocytes that permits rapid resealing of membranes disrupted by mechanical stress (By similarity). Mediates the recruitment of CAVIN2 and CAVIN3 proteins to the caveolae (PubMed:19262564).
Caveolin-3, M-caveolin, CAV3
Recombinant Human Caveolin-3 protein is a Human Fragment protein, in the 1 to 83 aa range, expressed in Wheat germ and suitable for SDS-PAGE, ELISA, WB.
Caveolin-3, M-caveolin, CAV3
Wheat germ
Tag free
SDS-PAGE, ELISA, WB
No
No
Human
pH: 8
Constituents: 0.79% Tris HCl, 0.3% Glutathione
M M A E E H T D L E A Q I V K D I H C K E I D L V N R D P K N I N E D I V K V D F E D V I A E P V G T Y S F D G V W K V S Y T T F T V S K Y W C Y R L L S T L L G V P
Fragment
34.76 kDa
1 to 83
Recombinant
Liquid
May act as a scaffolding protein within caveolar membranes. Interacts directly with G-protein alpha subunits and can functionally regulate their activity. May also regulate voltage-gated potassium channels. Plays a role in the sarcolemma repair mechanism of both skeletal muscle and cardiomyocytes that permits rapid resealing of membranes disrupted by mechanical stress (By similarity). Mediates the recruitment of CAVIN2 and CAVIN3 proteins to the caveolae (PubMed:19262564).
Belongs to the caveolin family.
Sumoylation with SUMO3 by PIAS4 may reduce agonist-induced internalization and desensitization of adrenergic receptor ABRD2.
Dry Ice
-80°C
Upon delivery aliquot
Avoid freeze / thaw cycle
U+00A0;
U+00A0;
Caveolin-3 also referred to as 'caveolin' 'caveolae' and 'CAV3' is a protein with an approximate mass of 17 kDa. It acts as a structural component of caveolae small invaginations in the plasma membrane. Caveolin-3 is expressed majorly in muscle cells including cardiac skeletal and smooth muscle tissues. As a distinguishing marker for caveolae it plays an essential role in the formation and stabilization of these structures.
Caveolae perform vital functions in cellular signaling and endocytosis. Caveolin-3 assists in various signaling pathways within muscle cells and interacts with other caveolae markers to facilitate signal transduction. It often forms a complex with other caveolin proteins such as caveolin-1 creating an environment conducive for the embedding of signaling molecules. This protein also modulates the trafficking and function of certain ion channels and receptors impacting muscle physiology.
Caveolin-3 significantly influences pathways concerned with muscle function and signal transduction. In particular it involves itself with the nitric oxide (NO) signaling pathway and beta-adrenergic signaling both critical to the contractile functions of muscle tissues. It closely interacts with proteins such as endothelial nitric oxide synthase (eNOS) and components of the G-protein coupled receptor family indicating its pivotal role in mediating physiological responses to stimuli.
Caveolin-3 mutations have been associated with a range of muscle-related disorders including limb-girdle muscular dystrophy and hypertrophic cardiomyopathy. These conditions often arise due to alterations in muscle cell signaling and integrity. Caveolin-3 also shares connections with proteins like dystrophin an important player in maintaining muscle cell structure and its dysfunction can exacerbate these muscular disorders. Understanding these interactions offers insights into potential therapeutic targets for managing related pathologies.
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ab114265 analysed on a 12.5% SDS-PAGE gel stained with Coomassie Blue.
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