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Scavenger Receptor Class B, Member 2 (SCARB2) (Middle Region) Peptid

SCARB2 Reaktivität: Human Wirt: Synthetic BP, WB
Produktnummer ABIN5671489
  • Target Alle SCARB2 Produkte
    SCARB2 (Scavenger Receptor Class B, Member 2 (SCARB2))
    Protein Region
    Middle Region
    Spezies
    Human
    Quelle
    • 5
    Synthetic
    Applikation
    Blocking Peptide (BP), Western Blotting (WB)
    Sequenz
    EEILRGETPR VEEVGPYTYR ELRNKANIQF GDNGTTISAV SNKAYVFERD
    Produktmerkmale
    This is a synthetic peptide designed for use in combination with anti- SCARB2 Antibody. 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.
  • Applikationshinweise
    Optimal working dilution should be determined by the investigator.
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Lyophilized
    Rekonstitution
    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Target
    SCARB2 (Scavenger Receptor Class B, Member 2 (SCARB2))
    Hintergrund
    The protein encoded by this gene is a type III glycoprotein that is located primarily in limiting membranes of lysosomes and endosomes. Earlier studies in mice and rat suggested that this protein may participate in membrane transportation and the reorganization of endosomal/lysosomal compartment. The protein deficiency in mice was reported to impair cell membrane transport processes and cause pelvic junction obstruction, deafness, and peripheral neuropathy. Further studies in human showed that this protein is a ubiquitously expressed protein and that it is involved in the pathogenesis of HFMD (hand, foot, and mouth disease) caused by enterovirus-71 and possibly by coxsackievirus A16. Mutations in this gene caused an autosomal recessive progressive myoclonic epilepsy-4 (EPM4), also known as action myoclonus-renal failure syndrome (AMRF). Alternatively spliced transcript variants encoding different isoforms have been found for this gene.

    Alias Symbols: AMRF, EPM4, LGP85, CD36L2, HLGP85, LIMP-2, LIMPII, SR-BII

    Protein Size: 478
    Gen-ID
    950
    NCBI Accession
    NM_001204255, NP_001191184
    UniProt
    Q14108
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