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Major Facilitator Superfamily Domain Containing 8 (MFSD8) Peptide

MFSD8 Reactivity: Mammalian Host: Synthetic BP, WB, IHC
Catalog No. ABIN938277

Quick Overview for Major Facilitator Superfamily Domain Containing 8 (MFSD8) Peptide (ABIN938277)

Target

MFSD8 (Major Facilitator Superfamily Domain Containing 8 (MFSD8))

Origin

Mammalian

Source

  • 1
Synthetic

Application

Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
  • Peptide Type

    Synthetic

    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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