Arylsulfatase E (ARSE) (Middle Region) Peptide
ARSE
Reactivity: Human
Host: Synthetic
BP, WB
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- Target See all Arylsulfatase E (ARSE) products
- Arylsulfatase E (ARSE)
- Protein Region
- Middle Region
- 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-ARSE antibody (Catalog #: ARP41665_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
- Arylsulfatase E (ARSE)
- Synonyms
- ASE Peptide, CDPX Peptide, CDPX1 Peptide, CDPXR Peptide, ARSE Peptide, MGC155058 Peptide, arylsulfatase E (chondrodysplasia punctata 1) Peptide, arylsulfatase E Peptide, ARSE Peptide, Arse Peptide
- Background
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Arylsulfatase E is a member of the sulfatase family. It is glycosylated postranslationally and localized to the golgi apparatus. Sulfatases are essential for the correct composition of bone and cartilage matrix. X-linked chondrodysplasia punctata, a disease characterized by abnormalities in cartilage and bone development, has been linked to mutations in this gene.Arylsulfatase E is a member of the sulfatase family. It is glycosylated postranslationally and localized to the golgi apparatus. Sulfatases are essential for the correct composition of bone and cartilage matrix. X-linked chondrodysplasia punctata, a disease characterized by abnormalities in cartilage and bone development, has been linked to mutations in this gene. PRIMARYREFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-170 AC005295.1 87561-87730 c 171-744 AK223183.1 1-574 745-2036 AK223199.1 542-1833 2037-2220 AW779826.1 1-184 c
Alias Symbols: CDPX, CDPX1, CDPXR, MGC163310, ASE
Protein Interaction Partner: C19orf6,COQ6,NDN,TNK2,COQ6,NDN
Protein Size: 589 - Molecular Weight
- 62 kDa
- Gene ID
- 415
- NCBI Accession
- NM_000047, NP_000038
- UniProt
- P51690
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