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ATP2A2 Antibody (Center) Blocking peptide

Synthetic peptide

Product Information
Primary Accession P16615
Clone Names 101008263
Peptide ID 101008263
Additional Information
Gene ID 488
Other Names Sarcoplasmic/endoplasmic reticulum calcium ATPase 2, SERCA2, SR Ca(2+)-ATPase 2, Calcium pump 2, Calcium-transporting ATPase sarcoplasmic reticulum type, slow twitch skeletal muscle isoform, Endoplasmic reticulum class 1/2 Ca(2+) ATPase, ATP2A2, ATP2B
Format Synthetic peptide was lyophilized with 100% acetonitrile and is supplied as a powder. Reconstitute with 0.1 ml DI water for a final concentration of 1 mg/ml.
StorageMaintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C.
PrecautionsThis product is for research use only. Not for use in diagnostic or therapeutic procedures.
Protein Information
Name ATP2A2
Synonyms ATP2B
Function This magnesium-dependent enzyme catalyzes the hydrolysis of ATP coupled with the translocation of calcium from the cytosol to the sarcoplasmic reticulum lumen. Isoform 2 is involved in the regulation of the contraction/relaxation cycle.
Cellular Location Endoplasmic reticulum membrane; Multi-pass membrane protein. Sarcoplasmic reticulum membrane; Multi-pass membrane protein
Tissue Location Isoform 1 is widely expressed in smooth muscle and nonmuscle tissues such as in adult skin epidermis, with highest expression in liver, pancreas and lung, and intermediate expression in brain, kidney and placenta. Also expressed at lower levels in heart and skeletal muscle. Isoforms 2 and 3 are highly expressed in the heart and slow twitch skeletal muscle. Expression of isoform 3 is predominantly restricted to cardiomyocytes and in close proximity to the sarcolemma. Both isoforms are mildly expressed in lung, kidney, liver, pancreas and placenta Expression of isoform 3 is amplified during monocytic differentiation and also observed in the fetal heart
Research Areas
Citations (0)

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This gene encodes one of the SERCA Ca(2+)-ATPases, whichare intracellular pumps located in the sarcoplasmic or endoplasmicreticula of muscle cells. This enzyme catalyzes the hydrolysis ofATP coupled with the translocation of calcium from the cytosol intothe sarcoplasmic reticulum lumen, and is involved in regulation ofthe contraction/relaxation cycle. Mutations in this gene causeDarier-White disease, also known as keratosis follicularis, anautosomal dominant skin disorder characterized by loss of adhesionbetween epidermal cells and abnormal keratinization. Alternativesplicing results in multiple transcript variants encoding differentisoforms.


Bailey, S.D., et al. Diabetes Care 33(10):2250-2253(2010)Tuusa, J.T., et al. FEBS J. 277(13):2815-2829(2010)Godic, A., et al. Eur J Dermatol 20(3):271-275(2010)Godic, A., et al. J. Am. Acad. Dermatol. 62(5):819-823(2010)Kiec-Wilk, B., et al. Prz. Lek. 67(3):151-156(2010)

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$ 80.00
Cat# BP12148c
(40 western blots)
Availability: In Stock
Bulk Size
Seasonal Special on Bulk Order
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