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Major Facilitator Superfamily Domain Containing 8 (MFSD8) (Middle Region) Peptid

MFSD8 Reaktivität: Human Wirt: Synthetic BP, WB
Produktnummer ABIN8104771
168,15 €
Zzgl. Versandkosten 20,00 € und MwSt
100 μg
Lieferung nach: Deutschland
Lieferung in 6 bis 9 Werktagen

Kurzübersicht für Major Facilitator Superfamily Domain Containing 8 (MFSD8) (Middle Region) Peptid (ABIN8104771)

Target

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

Spezies

Human

Quelle

  • 2
Synthetic

Applikation

Blocking Peptide (BP), Western Blotting (WB)
  • Protein Region

    Middle Region

    Verwendungszweck

    MFSD8 Peptide - middle region

    Sequenz

    FFILLPWGNQ FPKIQWEDLH NNSIPNTTFG EIIIGLWKSP MEDDNERPTG
  • Applikationshinweise

    Optimal working dilution should be determined by the investigator.

    Kommentare

    This is a synthetic peptide designed for use in combination with anti-MFSD8 Antibody(ARP55547_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. Please inquire for more details.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Rekonstitution

    Add 100 µL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.

    Buffer

    Lyophilized powder

    Lagerung

    -20 °C

    Informationen zur Lagerung

    For longer periods of storage, store at -20 °C. Avoid repeat freeze-thaw cycles.
  • Target

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

    Hintergrund

    Background Information: 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).

    Alternative Symbols: CLN7, MGC33302

    Molekulargewicht

    57kDa

    Gen-ID

    256471

    NCBI Accession

    NP_689991

    UniProt

    Q8NHS3
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