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CLN3 anticorps

Cet anticorps Lapin Polyclonal détecte spécifiquement CLN3 dans WB. Il présente une réactivité envers Humain.
N° du produit ABIN7469280

Aperçu rapide pour CLN3 anticorps (ABIN7469280)

Antigène

Voir toutes CLN3 Anticorps
CLN3 (Ceroid-Lipofuscinosis, Neuronal 3 (CLN3))

Reactivité

  • 29
  • 25
  • 20
  • 3
  • 3
Humain

Hôte

  • 31
  • 2
Lapin

Clonalité

  • 31
  • 2
Polyclonal

Conjugué

  • 12
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp CLN3 est non-conjugé

Application

  • 24
  • 8
  • 4
  • 2
Western Blotting (WB)
  •  Réactivité croisée

    Humain

    Purification

    Purified by antigen-affinity chromatography.

    Immunogène

    Carrier-protein conjugated synthetic peptide encompassing a sequence within the center region of human CLN3. The exact sequence is proprietary.

    Isotype

    IgG
  • Indications d'application

    WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

    Commentaires

    Positive Control: NT2D1 , Jurkat , Raji , NCI-H929

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    1XPBS ( pH 7), 20 % Glycerol, 0.025 % ProClin 300

    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

    Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
  • Antigène

    CLN3 (Ceroid-Lipofuscinosis, Neuronal 3 (CLN3))

    Autre désignation

    CLN3

    Sujet

    Synonyms: CLN3 lysosomal/endosomal transmembrane protein, battenin , BTN1 , BTS , JNCL

    Background: This gene encodes a protein that is involved in lysosomal function. Mutations in this, as well as other neuronal ceroid-lipofuscinosis (CLN) genes, cause neurodegenerative diseases commonly known as Batten disease or collectively known as neuronal ceroid lipofuscinoses (NCLs). Many alternatively spliced transcript variants have been found for this gene. [provided by RefSeq]

    Poids moléculaire

    48 kDa

    ID gène

    1201

    UniProt

    Q13286
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