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Leber Congenital Amaurosis 5 (LCA5) Peptide

LCA5 Reactivité: Mammifères Hôte: Synthetic BP, WB, IHC
N° du produit ABIN938457
  • Antigène Tous les produits LCA5
    LCA5 (Leber Congenital Amaurosis 5 (LCA5))
    Type de proteíne
    Synthetic
    Origine
    Mammifères
    Source
    • 1
    Synthetic
    Application
    Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
    Séquence
    FSLQKLKEIS EARHLPERDD LAKKLVSAEL KLDDTERRIK ELSKNLELST
    Attributs du produit
    A synthetic peptide for use as a blocking control in assays to test for specificity of LCA5 antibody,
    Alternative Names: LCA5 control peptide, LCA5 antibody Blocking Peptide, Anti-LCA5 Blocking Peptide, Leber Congenital Amaurosis 5 Blocking Peptide, C6orf152 Blocking Peptide, LCA5, LCA-5, LCA 5, LCA-5 Blocking Peptide, LCA 5 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
    LCA5 (Leber Congenital Amaurosis 5 (LCA5))
    Synonymes
    C6orf152 Peptide, RGD1308555 Peptide, 4930431B11Rik Peptide, 5730406O13Rik Peptide, AV274874 Peptide, ORF64 Peptide, LCA5, lebercilin Peptide, Leber congenital amaurosis 5 Peptide, Leber congenital amaurosis 5 (human) Peptide, LCA5 Peptide, LOC787523 Peptide, Lca5 Peptide
    Sujet
    LCA5 is a protein that is thought to be involved in centrosomal or ciliary functions. Mutations in this gene cause Leber congenital amaurosis type V. Mutations in this gene cause Leber congenital amaurosis type V. Alternative splicing results in two transcript variants.
    Poids moléculaire
    80 kDa
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