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LCA5L anticorps

LCA5L Reactivité: Humain, Rat, Souris WB, IF (p), IHC (p) Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN1387233
  • Antigène Tous les produits LCA5L
    LCA5L (Leber Congenital Amaurosis 5-Like (LCA5L))
    Reactivité
    • 34
    • 29
    • 23
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Humain, Rat, Souris
    Hôte
    • 49
    Lapin
    Clonalité
    • 49
    Polyclonal
    Conjugué
    • 11
    • 4
    • 4
    • 4
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    Cet anticorp LCA5L est non-conjugé
    Application
    • 34
    • 25
    • 16
    • 13
    • 13
    • 8
    • 3
    • 1
    • 1
    Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
     Réactivité croisée
    Humain, Souris, Rat
    Purification
    Purified by Protein A.
    Immunogène
    KLH conjugated synthetic peptide derived from human LCA5L
    Isotype
    IgG
  • Indications d'application
    WB 1:300-5000
    IHC-P 1:200-400
    IF(IHC-P) 1:50-200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 μg/μL
    Buffer
    0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
    Agent conservateur
    ProClin
    Précaution d'utilisation
    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
    Stock
    4 °C,-20 °C
    Stockage commentaire
    Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
    Date de péremption
    12 months
  • Antigène
    LCA5L (Leber Congenital Amaurosis 5-Like (LCA5L))
    Autre désignation
    LCA5L (LCA5L Produits)
    Synonymes
    anticorps C21orf13, anticorps 4921526F01Rik, anticorps Lcca5l, anticorps Leber congenital amaurosis 5-like, anticorps LCA5L, lebercilin like, anticorps LCA5L, anticorps Lca5l
    Sujet

    Synonyms: C21ORF13, Chromosome 21 open reading frame 13, Lca5l, LCA5L_HUMAN, Leber congenital amaurosis 5 like, Leber congenital amaurosis 5 like protein, Leber congenital amaurosis 5-like protein, Lebercilin-like protein.

    Background: Leber congenital amaurosis (LCA) is one of the most common causes of hereditary blindness or severe visual impairment in infants. Mutations in several genes with diverse functions mapping to two loci have been implicated in LCA causation. These proteins are involved in processes such as photoreceptor development and maintenance, phototransduction, vitamin A metabolism and protein trafficking. LCA5, also known as Lebercilin, is a ciliary protein that is widely expressed during development and localizes to the connecting cilia of photoreceptors and to the microtubules, centrioles and primary cilia of cultured mammalian cells. The Leber congenital amaurosis 5-like protein (LCA5L) is a 670 amino acid protein that belongs to the LCA5 family.

    ID gène
    150082
    UniProt
    O95447
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