ATP7B antibody (Middle Region)
Quick Overview for ATP7B antibody (Middle Region) (ABIN5514518)
Target
See all ATP7B AntibodiesReactivity
Host
Clonality
Conjugate
Application
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Binding Specificity
- Middle Region
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Purpose
- ATP7B Antibody - middle region
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Sequence
- IIMSTLTLVV WIVIGFIDFG VVQRYFPNPN KHISQTEVII RFAFQTSITV
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Predicted Reactivity
- Dog: 82%, Guinea Pig: 82%, Horse: 82%, Human: 100%, Mouse: 91%, Rabbit: 92%, Rat: 91%
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Characteristics
- This is a rabbit polyclonal antibody against ATP7B. It was validated on Western Blot.
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Purification
- Affinity Purified
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Immunogen
- The immunogen is a synthetic peptide directed towards the middle region of human ATP7B
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Application Notes
- Optimal working dilution should be determined by the investigator.
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Comment
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We also sell a specific blocking peptide that can be used in combination with this antibody. You can find the blocking peptide under AAP44524-100UG
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Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 0.5 mg/mL
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Buffer
- 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
- prevent freeze-thaw cycles
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Storage
- 4 °C,-20 °C
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Storage Comment
- For short term use, store at 2-8C up to 1 week. For long term storage, store at -20 °C in small aliquots to prevent freeze-thaw cycles.
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- ATP7B (ATPase, Cu++ Transporting, beta Polypeptide (ATP7B))
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Alternative Name
- ATP7B
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Background
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Background Information: This gene is a member of the P-type cation transport ATPase family and encodes a protein with several membrane-spanning domains, an ATPase consensus sequence, a hinge domain, a phosphorylation site, and at least 2 putative copper-binding sites. This protein functions as a monomer, exporting copper out of the cells, such as the efflux of hepatic copper into the bile. Alternate transcriptional splice variants, encoding different isoforms with distinct cellular localizations, have been characterized. Mutations in this gene have been associated with Wilson disease (WD).
Gene Name: ATPase copper transporting beta
Alternative Symbols: WD, PWD, WC1, WND
Protein Name: copper-transporting ATPase 2
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Molecular Weight
- 74kDa
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Gene ID
- 540
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NCBI Accession
- NP_000044
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UniProt
- P35670
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Pathways
- Transition Metal Ion Homeostasis, Ribonucleoside Biosynthetic Process
Target
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