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Major Facilitator Superfamily Domain Containing 8 (MFSD8) Peptid

MFSD8 Reaktivität: Säugetier Wirt: Synthetic BP, WB, IHC
Produktnummer ABIN938277
  • Target Alle MFSD8 Produkte
    MFSD8 (Major Facilitator Superfamily Domain Containing 8 (MFSD8))
    Protein-Typ
    Synthetic
    Spezies
    Säugetier
    Quelle
    • 1
    Synthetic
    Applikation
    Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
    Sequenz
    FFILLPWGNQ FPKIQWEDLH NNSIPNTTFG EIIIGLWKSP MEDDNERPTG
    Produktmerkmale
    A synthetic peptide for use as a blocking control in assays to test for specificity of MFSD8 antibody,
    Alternative Names: MFSD8 control peptide, MFSD8 antibody Blocking Peptide, Anti-MFSD8 Blocking Peptide, major facilitator superfamily domain containing 8 Blocking Peptide, CLN7 Blocking Peptide, MGC33302 Blocking Peptide, MFSD8, MFSD-8, MFSD 8, MFSD-8 Blocking Peptide, MFSD 8 Blocking Peptide
    Aufreinigung
    The antibody is affinity-purified from rabbit antiserum by affinity chromatography using epitope-specific phosphopeptide. The antibody against non-phosphopeptide is removed by chromatogramphy using non-phosphopeptide corresponding to the phosphorylation site.
  • Applikationshinweise
    Optimal conditions should be determined by the investigator
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Lyophilized
    Rekonstitution
    Add 100 µL of distilled water for a final peptide concentration is 1 mg/mL.
    Buffer
    PBS
    Handhabung
    Avoid repeated freeze/thaw cycles.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    Store at -20 °C long term.
  • Target
    MFSD8 (Major Facilitator Superfamily Domain Containing 8 (MFSD8))
    Hintergrund
    This gene encodes a ubiquitous integral membrane protein that contains a transporter domain and a major facilitator superfamily (MFS) domain. Other members of the major facilitator superfamily transport small solutes through chemiosmotic ion gradients. The substrate transported by this protein is unknown. The protein likely localizes to lysosomal membranes. Mutations in this gene are correlated with a variant form of late infantile-onset neuronal ceroid lipofuscinoses (vLINCL).
    Molekulargewicht
    57 kDa
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