Tel:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@anticorps-enligne.fr

Leber Congenital Amaurosis 5 (LCA5) Peptide

LCA5 Reactivité: Humain Hôte: Synthetic BP, WB
N° du produit ABIN979227
  • Antigène Tous les produits LCA5
    LCA5 (Leber Congenital Amaurosis 5 (LCA5))
    Origine
    Humain
    Source
    • 1
    Synthetic
    Application
    Blocking Peptide (BP), Western Blotting (WB)
    Attributs du produit
    This is a synthetic peptide designed for use in combination with anti-LCA5 antibody (Catalog #: ARP53410_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.
    Purification
    Purified
  • Indications d'application
    Each Investigator should determine their own optimal working dilution for specific applications.
    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
    Concentration
    1 mg/mL
    Buffer
    Final peptide concentration is 1 mg/mL in PBS.
    Conseil sur la manipulation
    Avoid repeated freeze-thaw cycles.
    Stock
    -20 °C
    Stockage commentaire
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • 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. This gene encodes a protein that is thought to be involved in centrosomal or ciliary functions. Mutations in this gene cause Leber congenital amaurosis type V. Alternative splicing results in two transcript variants.

    Alias Symbols: C6orf152

    Protein Size: 697
    Poids moléculaire
    80 kDa
    ID gène
    167691
    NCBI Accession
    NM_181714, NP_859065
    UniProt
    Q86VQ0
Vous êtes ici:
Support technique