Telefon:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@antikoerper-online.de

Arylsulfatase A (ARSA) (Middle Region) Peptid

ARSA Reaktivität: Human Wirt: Synthetic BP, WB
Produktnummer ABIN973463
  • Target Alle Arylsulfatase A (ARSA) Produkte
    Arylsulfatase A (ARSA)
    Protein Region
    Middle Region
    Spezies
    Human
    Quelle
    • 6
    Synthetic
    Applikation
    Blocking Peptide (BP), Western Blotting (WB)
    Produktmerkmale
    This is a synthetic peptide designed for use in combination with anti-ARSA antibody (Catalog #: ARP54529_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.
    Aufreinigung
    Purified
  • Applikationshinweise
    Each Investigator should determine their own optimal working dilution for specific applications.
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Lyophilized
    Rekonstitution
    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
    Konzentration
    1 mg/mL
    Buffer
    Final peptide concentration is 1 mg/mL in PBS.
    Handhabung
    Avoid repeated freeze-thaw cycles.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Target
    Arylsulfatase A (ARSA)
    Synonyme
    ARSA Peptide, zgc:101575 Peptide, arsa Peptide, AS-A Peptide, ASA Peptide, AW212749 Peptide, As-2 Peptide, As2 Peptide, TISP73 Peptide, MLD Peptide, mld Peptide, arylsulfatase A Peptide, arylsulfatase Peptide, arylsulfatase A, gene 1 S homeolog Peptide, ARSA Peptide, arsa Peptide, arsA Peptide, RB6599 Peptide, Arsa Peptide, arsa.1.S Peptide
    Hintergrund
    ARSA hydrolyzes cerebroside sulfate. Defects in ARSA are a cause of leukodystrophy metachromatic (MLD).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. Multiple alternatively spliced transcript variants, one of which encodes a distinct protein, have been described for this gene.

    Alias Symbols: MLD

    Protein Interaction Partner: ARSA,BMPR2,CTSL1,GAL3ST1,ARSA

    Protein Size: 507
    Molekulargewicht
    52 kDa
    Gen-ID
    410
    NCBI Accession
    NM_001085427, NP_001078896
    UniProt
    P15289
Sie sind hier:
Kundenservice