Peroxisomal Biogenesis Factor 10 (PEX10) Peptide
PEX10
Reactivity: Human
Host: Synthetic
BP, WB, IHC
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- Target See all PEX10 products
- PEX10 (Peroxisomal Biogenesis Factor 10 (PEX10))
- Origin
- Human
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Source
- Synthetic
- Application
- Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
- Characteristics
- This is a synthetic peptide designed for use in combination with anti-PEX10 antibody (Catalog #: ARP43442_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
- PEX10 (Peroxisomal Biogenesis Factor 10 (PEX10))
- Synonyms
- ATPEX10 Peptide, T9J22.2 Peptide, peroxin 10 Peptide, NALD Peptide, PBD6A Peptide, PBD6B Peptide, RNF69 Peptide, AV128229 Peptide, Gm142 Peptide, peroxin 10 Peptide, peroxisomal biogenesis factor 10 Peptide, PEX10 Peptide, Pex10 Peptide
- Background
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PEX10 is a protein involved in import of peroxisomal matrix proteins. This protein localizes to the peroxisomal membrane. Mutations in PEX10 gene result in phenotypes within the Zellweger spectrum of peroxisomal biogenesis disorders, ranging from neonatal adrenoleukodystrophy to Zellweger syndrome.This gene encodes a protein involved in import of peroxisomal matrix proteins. This protein localizes to the peroxisomal membrane. Mutations in this gene result in phenotypes within the Zellweger spectrum of peroxisomal biogenesis disorders, ranging from neonatal adrenoleukodystrophy to Zellweger syndrome. Alternative splicing results in two transcript variants encoding different isoforms.
Alias Symbols: MGC1998, NALD, RNF69
Protein Interaction Partner: PEX12,PEX19,PEX2,PEX5,PEX10,PEX12,PEX12,PEX19,PEX19,PEX2,PEX5
Protein Size: 346 - Molecular Weight
- 39 kDa
- Gene ID
- 5192
- NCBI Accession
- NM_153818, NP_722540
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