ATPase, Ca++ Transporting, Type 2C, Member 1 (ATP2C1) Peptide
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- Target See all ATP2C1 products
- ATP2C1 (ATPase, Ca++ Transporting, Type 2C, Member 1 (ATP2C1))
- Origin
- Human
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Source
- Synthetic
- Application
- Blocking Peptide (BP), Western Blotting (WB)
- Characteristics
- This is a synthetic peptide designed for use in combination with anti-ATP2C1 antibody (Catalog #: ARP44399_P050). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
- Purification
- Purified
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- Application Notes
- Each Investigator should determine their own optimal working dilution for specific applications.
- Restrictions
- For Research Use only
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- Format
- Lyophilized
- Reconstitution
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
- Concentration
- 1 mg/mL
- Buffer
- Final peptide concentration is 1 mg/mL in PBS.
- Handling Advice
- Avoid repeated freeze-thaw cycles.
- Storage
- -20 °C
- Storage Comment
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- Target
- ATP2C1 (ATPase, Ca++ Transporting, Type 2C, Member 1 (ATP2C1))
- Synonyms
- ATP2C1 Peptide, ATP2C1A Peptide, BCPM Peptide, HHD Peptide, PMR1 Peptide, SPCA1 Peptide, hSPCA1 Peptide, Spca1 Peptide, si:dkey-11p23.6 Peptide, SPCA Peptide, 1700121J11Rik Peptide, AW061228 Peptide, D930003G21Rik Peptide, pmr1 Peptide, ATPase secretory pathway Ca2+ transporting 1 Peptide, ATPase, Ca++ transporting, type 2C, member 1 Peptide, ATPase, Ca++-sequestering Peptide, ATP2C1 Peptide, atp2c1 Peptide, Atp2c1 Peptide
- Background
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ATP2C1 belongs to the family of P-type cation transport ATPases. This magnesium-dependent enzyme catalyzes the hydrolysis of ATP coupled with the transport of the calcium. Defects in this gene cause Hailey-Hailey disease, an autosomal dominant disorder. Alternatively spliced transcript variants encoding different isoforms have been identified.The protein encoded by this gene belongs to the family of P-type cation transport ATPases. This magnesium-dependent enzyme catalyzes the hydrolysis of ATP coupled with the transport of the calcium. Defects in this gene cause Hailey-Hailey disease, an autosomal dominant disorder. Alternatively spliced transcript variants encoding different isoforms have been identified.
Alias Symbols: ATP2C1A, BCPM, HHD, KIAA1347, PMR1, SPCA1, hSPCA1
Protein Size: 888 - Molecular Weight
- 98 kDa
- Gene ID
- 27032
- NCBI Accession
- NM_001001485, NP_001001485
- UniProt
- P98194
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