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LCA5L anticorps

Cet anticorps anti-LCA5L est un anticorps Lapin Polyclonal détectant LCA5L dans WB, IF (p) et IHC (p). Adapté pour Humain, Rat et Souris.
N° du produit ABIN1387233

Aperçu rapide pour LCA5L anticorps (ABIN1387233)

Antigène

LCA5L (Leber Congenital Amaurosis 5-Like (LCA5L))

Reactivité

  • 30
  • 29
  • 23
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Humain, Rat, Souris

Hôte

  • 45
Lapin

Clonalité

  • 45
Polyclonal

Conjugué

  • 12
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Cet anticorp LCA5L est non-conjugé

Application

  • 30
  • 25
  • 13
  • 11
  • 8
  • 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

    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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