ATP2C1 antibody (C-Term)
Quick Overview for ATP2C1 antibody (C-Term) (ABIN2781847)
Target
See all ATP2C1 AntibodiesReactivity
Host
Clonality
Conjugate
Application
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Binding Specificity
- C-Term
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Sequence
- TKSVFEIGLC SNRMFCYAVL GSIMGQLLVI YFPPLQKVFQ TESLSILGLA
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Predicted Reactivity
- Cow: 100%, Dog: 100%, Guinea Pig: 100%, Horse: 100%, Human: 100%, Mouse: 100%, Rabbit: 100%, Rat: 100%, Zebrafish: 93%
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Characteristics
- This is a rabbit polyclonal antibody against ATP2C1. It was validated on Western Blot using a cell lysate as a positive control.
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Purification
- Affinity Purified
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Immunogen
- The immunogen is a synthetic peptide directed towards the C terminal region of human ATP2C1
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Application Notes
- Optimal working dilutions should be determined experimentally by the investigator.
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Comment
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Antigen size: 888 AA
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Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- Lot specific
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Buffer
- Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
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Preservative
- Sodium azide
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Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Handling Advice
- Avoid repeated freeze-thaw cycles.
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Storage
- -20 °C
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Storage Comment
- For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
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- ATP2C1 (ATPase, Ca++ Transporting, Type 2C, Member 1 (ATP2C1))
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Alternative Name
- ATP2C1
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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 Interaction Partner: UBC, RNF2, ELAVL1,
Protein Size: 888 -
Molecular Weight
- 98 kDa
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Gene ID
- 27032
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NCBI Accession
- NM_001001485, NP_001001485
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UniProt
- P98194
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Pathways
- Transition Metal Ion Homeostasis, Ribonucleoside Biosynthetic Process
Target
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