Fucosidase, alpha-L- 1, Tissue (FUCA1) Peptide
FUCA1
Reactivity: Human
Host: Synthetic
BP, WB
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- Target See all FUCA1 products
- FUCA1 (Fucosidase, alpha-L- 1, Tissue (FUCA1))
- 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-FUCA1 antibody (Catalog #: ARP54293_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
- FUCA1 (Fucosidase, alpha-L- 1, Tissue (FUCA1))
- Synonyms
- FUCA Peptide, FUCA1 Peptide, 0610006A03Rik Peptide, 9530055J05Rik Peptide, Afuc Peptide, Fuca Peptide, fuca Peptide, fuca1 Peptide, ATFUC1 Peptide, F24D13.11 Peptide, F24D13_11 Peptide, alpha-L-fucosidase 1 Peptide, wu:fb02a09 Peptide, zgc:101116 Peptide, alpha-L-fucosidase 1 Peptide, fucosidase, alpha-L- 1, tissue Peptide, alpha-L-fucosidase 1 L homeolog Peptide, alpha-L-fucosidase 1, tandem duplicate 2 Peptide, FUCA1 Peptide, Fuca1 Peptide, fuca1.L Peptide, fuca1 Peptide, FUC1 Peptide, LOC9317020 Peptide, LOC100285202 Peptide, fuca1.2 Peptide
- Background
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Alpha-L-fucosidase (EC 3.2.1.51) is a lysosomal enzyme involved in the degradation of fucose-containing glycoproteins and glycolipids. At least 2 separate polymorphic alpha-L-fucosidases are recognized in man: that in tissues, FUCA1, which is deficient in fucosidosis, and that in plasma, FUCA2. Fucosidosis is an autosomal recessive lysosomal storage disease caused by defective alpha-L-fucosidase with accumulation of fucose in the tissues. Different phenotypes include clinical features such as neurologic deterioration, growth retardation, visceromegaly, and seizures in a severe early form, coarse facial features, angiokeratoma corporis diffusum, spasticity and delayed psychomotor development in a longer surviving form, and an unusual spondylometaphyseoepiphyseal dysplasia in yet another form.[supplied by OMIM]. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.
Alias Symbols: FUCA
Protein Interaction Partner: MARK2,USP21
Protein Size: 466 - Molecular Weight
- 54 kDa
- Gene ID
- 2517
- NCBI Accession
- NM_000147, NP_000138
- UniProt
- P04066
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