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Arylsulfatase A Protein (ARSA) (Transcript Variant 4) (Myc-DYKDDDDK Tag)

ARSA Spezies: Human Wirt: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Produktnummer ABIN2714956
$1,112.40
Zzgl. Versandkosten $45.00 und $20.00 Trockeneis
20 μg
Lieferung in 11 Werktagen
  • Target Alle Arylsulfatase A (ARSA) Proteine anzeigen
    Arylsulfatase A (ARSA)
    Protein-Typ
    Recombinant
    Proteineigenschaft
    Transcript Variant 4
    Spezies
    • 13
    • 2
    Human
    Quelle
    • 4
    • 4
    • 4
    • 2
    • 1
    HEK-293 Cells
    Aufreinigungstag / Konjugat
    Dieses Arylsulfatase A Protein ist gelabelt mit Myc-DYKDDDDK Tag.
    Applikation
    Antibody Production (AbP), Standard (STD)
    Produktmerkmale
    • Recombinant human Arylsulfatase A (transcript variant 4) protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    Reinheit
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
  • Applikationshinweise
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    Kommentare

    The tag is located at the C-terminal.

    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Konzentration
    50 μg/mL
    Buffer
    25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
    Lagerung
    -80 °C
    Informationen zur Lagerung
    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 A (ARSA)
    Andere Bezeichnung
    Arylsulfatase A (ARSA Produkte)
    Synonyme
    ARSA, zgc:101575, arsa, AS-A, ASA, AW212749, As-2, As2, TISP73, MLD, mld, arylsulfatase A, arylsulfatase, arylsulfatase A, gene 1 S homeolog, ARSA, arsa, arsA, RB6599, Arsa, arsa.1.S
    Hintergrund
    The protein encoded by this gene hydrolyzes cerebroside sulfate to cerebroside and sulfate. Defects in this gene lead to metachromatic leucodystrophy (MLD), a progressive demyelination disease which results in a variety of neurological symptoms and ultimately death. Alternatively spliced transcript variants have been described for this gene.
    Molekulargewicht
    51.9 kDa
    NCBI Accession
    NP_001078896
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