Anti-RYR2 antibody produced in rabbit

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RYR2 (ryanodine receptor 2) provides guidance to the release and transport of Ca²⁺ from sarcoplasmic reticulum (SR) to the cytoplasm during cardiac muscle excitation-contraction (EC) coupling. Protein kinase A (PKA) phosphorylated RYR2 separates (FKBP12.6) to regulate the channel open probability (Po). During the process, a small portion of Ca²⁺ enter into the cell through the L-type Ca²⁺ channel, which further activates the RyR2 channel upon membrane depolarization. The activated RyR2 channel releases a large amount of Ca²⁺ from the SR and subsequent muscle contraction. Missense mutations in this gene cause Kazakh idiopathic ventricular tachycardia and arrhythmogenic right ventricular dysplasia.

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Prestige Antibodies^® are highly characterized and extensively validated antibodies with the added benefit of all available characterization data for each target being accessible via the Human Protein Atlas portal linked just below the product name at the top of this page. The uniqueness and low cross-reactivity of the Prestige Antibodies^® to other proteins are due to a thorough selection of antigen regions, affinity purification, and stringent selection. Prestige antigen controls are available for every corresponding Prestige Antibody and can be found in the linkage section.

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• IHC tissue array of 44 normal human tissues and 20 of the most common cancer type tissues.
• Protein array of 364 human recombinant protein fragments.

RYR2 (ryanodine receptor 2) is an intracellular Ca²⁺ release channel present on the sarcoplasmic reticulum (SR).

RYR2 gene is located at the human chromosome location 1q43. It is majorly expressed in the brain and heart.

Ryanodine receptor 2 recombinant protein epitope signature tag (PrEST)

Corresponding Antigen APREST73317

Solution in phosphate-buffered saline, pH 7.2, containing 40% glycerol and 0.02% sodium azide

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