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Loricrin (LOR) Peptid

LOR Reaktivität: Human Wirt: Synthetic BP, IHC, WB
Produktnummer ABIN979528
  • Target Alle LOR Produkte
    LOR (Loricrin (LOR))
    Spezies
    Human
    Quelle
    • 1
    Synthetic
    Applikation
    Blocking Peptide (BP), Immunohistochemistry (IHC), Western Blotting (WB)
    Produktmerkmale
    This is a synthetic peptide designed for use in combination with anti-LOR antibody (Catalog #: ARP41738_T100). 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.
    Aufreinigung
    Purified
  • Applikationshinweise
    Each Investigator should determine their own optimal working dilution for specific applications.
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Lyophilized
    Rekonstitution
    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
    Konzentration
    1 mg/mL
    Buffer
    Final peptide concentration is 1 mg/mL in PBS.
    Handhabung
    Avoid repeated freeze-thaw cycles.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Target
    LOR (Loricrin (LOR))
    Synonyme
    AI036317 Peptide, S77319 Peptide, RGD1559993 Peptide, LOR Peptide, loricrin Peptide, Loricrin Peptide, LOR Peptide, Lor Peptide, TVAG_146950 Peptide, TVAG_228830 Peptide, TVAG_228920 Peptide, TVAG_238290 Peptide, TVAG_035050 Peptide, TVAG_070680 Peptide, Bm1_52290 Peptide, LOC100281109 Peptide, LOC100281170 Peptide
    Substanzklasse
    Chemical
    Hintergrund
    LOR is a major protein component of the cornified cell envelope found in terminally differentiated epidermal cells. Mutations in this gene are associated with Vohwinkel's syndrome and progressive symmetric erythrokeratoderma, both inherited skin diseases.LOR encodes loricrin, a major protein component of the cornified cell envelope found in terminally differentiated epidermal cells. Mutations in LOR may be the cause of both Vohwinkel's syndrome and progressive symmetric erythrokeratoderma, both inherited skin diseases.

    Alias Symbols: MGC111513

    Protein Interaction Partner: EVPL,SPRR3,VIM,CSTA,IVL,KRT1,LOR,PI3,VIM

    Protein Size: 316
    Molekulargewicht
    35 kDa
    Gen-ID
    4014
    NCBI Accession
    NM_000427, NP_000418
    UniProt
    P23490
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