Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

Arylsulfatase E Protein (ARSE) (Myc-DYKDDDDK Tag)

ARSE Origin: Human Host: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Catalog No. ABIN2714961
  • Target See all Arylsulfatase E (ARSE) Proteins
    Arylsulfatase E (ARSE)
    Protein Type
    Recombinant
    Origin
    Human
    Source
    • 1
    HEK-293 Cells
    Purification tag / Conjugate
    This Arylsulfatase E protein is labelled with Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Characteristics
    • Recombinant human Arylsulfatase E protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    Purity
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product ARSE Protein
  • Application Notes
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    Comment

    The tag is located at the C-terminal.

    Restrictions
    For Research Use only
  • Concentration
    50 μg/mL
    Buffer
    25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
    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
    Arylsulfatase E (ARSE)
    Alternative Name
    Arylsulfatase E (ARSE Products)
    Synonyms
    ASE Protein, CDPX Protein, CDPX1 Protein, CDPXR Protein, ARSE Protein, MGC155058 Protein, arylsulfatase E (chondrodysplasia punctata 1) Protein, arylsulfatase E Protein, ARSE Protein, Arse Protein
    Background
    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. Alternative splicing results in multiple transcript variants. A pseudogene related to this gene is located on the Y chromosome.
    Molecular Weight
    62.2 kDa
    NCBI Accession
    NP_000038
You are here:
Support