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Loricrin (LOR) Peptide

LOR Reactivité: Mammifères Hôte: Synthetic BP, IHC, WB
N° du produit ABIN939071
  • Antigène Tous les produits LOR
    LOR (Loricrin (LOR))
    Type de proteíne
    Synthetic
    Origine
    Mammifères
    Source
    • 1
    Synthetic
    Application
    Blocking Peptide (BP), Immunohistochemistry (IHC), Western Blotting (WB)
    Séquence
    GYSGGGCGGG SSGGGGGGGI GGCGGGSGGS VKYSGGGGSS GGGSGCFSSG
    Attributs du produit
    A synthetic peptide for use as a blocking control in assays to test for specificity of LOR antibody,
    Alternative Names: Loricrin control peptide, Loricrin antibody Blocking Peptide, Anti-Loricrin Blocking Peptide, MGC111513 Blocking Peptide, LOR Blocking Peptide
  • Indications d'application
    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
    Conseil sur la manipulation
    Avoid repeated freeze/thaw cycles.
    Stock
    -20 °C
    Stockage commentaire
    Store at -20 °C long term.
  • Antigène
    LOR (Loricrin (LOR))
    Synonymes
    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
    Classe de substances
    Chemical
    Sujet
    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.
    Poids moléculaire
    35 kDa
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