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SUMF1 Protein

SUMF1 Origin: Human Host: HEK-293 Cells Recombinant > 95 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Catalog No. ABIN2732974
  • Target See all SUMF1 Proteins
    SUMF1 (Sulfatase Modifying Factor 1 (SUMF1))
    Protein Type
    Recombinant
    Origin
    • 8
    • 1
    Human
    Source
    • 4
    • 2
    • 1
    • 1
    • 1
    HEK-293 Cells
    Application
    Antibody Production (AbP), Standard (STD)
    Characteristics
    • Recombinant human SUMF1 / FGE protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    Purity
    > 95 % as determined by SDS-PAGE and Coomassie blue staining
    Endotoxin Level
    < 0.1 EU per μg protein as determined by LAL test
    Top Product
    Discover our top product SUMF1 Protein
  • Application Notes
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    Restrictions
    For Research Use only
  • Concentration
    50 μg/mL
    Buffer
    20 mM Tris-HCl, 150 mM NaCl, 2 mM CaCl2, 10 % Glycerol, pH 7.5. Avoid repeated freeze-thaw cycles. Stable for at least 3 months from receipt of products under proper storage and handling conditions.
    Storage
    -80 °C
    Storage Comment
    Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
  • Target
    SUMF1 (Sulfatase Modifying Factor 1 (SUMF1))
    Alternative Name
    Sumf1,fge (SUMF1 Products)
    Synonyms
    AAPA3037 Protein, FGE Protein, AA543204 Protein, AI463102 Protein, AI851573 Protein, sulfatase modifying factor 1 Protein, SUMF1 Protein, Sumf1 Protein
    Background
    This gene encodes an enzyme that catalyzes the hydrolysis of sulfate esters by oxidizing a cysteine residue in the substrate sulfatase to an active site 3-oxoalanine residue, which is also known as C-alpha-formylglycine. Mutations in this gene cause multiple sulfatase deficiency, a lysosomal storage disorder. Alternative splicing results in multiple transcript variants.
    Molecular Weight
    38.3 kDa
    NCBI Accession
    NP_877437
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