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Major Facilitator Superfamily Domain Containing 8 (MFSD8) Peptide

MFSD8 Reactivity: Mammalian Host: Synthetic BP, WB, IHC
Catalog No. ABIN938277
  • Target See all MFSD8 products
    MFSD8 (Major Facilitator Superfamily Domain Containing 8 (MFSD8))
    Peptide Type
    Synthetic
    Origin
    Mammalian
    Source
    • 1
    Synthetic
    Application
    Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
    Sequence
    FFILLPWGNQ FPKIQWEDLH NNSIPNTTFG EIIIGLWKSP MEDDNERPTG
    Characteristics
    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
    Purification
    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.
  • Application Notes
    Optimal conditions should be determined by the investigator
    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Add 100 µL of distilled water for a final peptide concentration is 1 mg/mL.
    Buffer
    PBS
    Handling Advice
    Avoid repeated freeze/thaw cycles.
    Storage
    -20 °C
    Storage Comment
    Store at -20 °C long term.
  • Target
    MFSD8 (Major Facilitator Superfamily Domain Containing 8 (MFSD8))
    Background
    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).
    Molecular Weight
    57 kDa
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