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ALS2 anticorps (AA 390-470)

Cet anticorps anti-ALS2 Polyclonal Lapin (ABIN8119717) détecte spécifiquement ALS2 dans WB et ELISA. L’anticorps est réactif avec des échantillons de Humain, Souris et Rat.
N° du produit ABIN8119717
276,00 €
Plus frais de livraison 40,00 € et TVA
50 μL
Destination: France
Envoi sous 6 à 9 jours ouvrables

Aperçu rapide pour ALS2 anticorps (AA 390-470) (ABIN8119717)

Antigène

Voir toutes ALS2 Anticorps
ALS2 (Amyotrophic Lateral Sclerosis 2 (Juvenile) (ALS2))

Reactivité

  • 44
  • 11
  • 6
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Humain, Souris, Rat

Hôte

  • 39
  • 4
  • 1
Lapin

Clonalité

  • 40
  • 3
Polyclonal

Conjugué

  • 24
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp ALS2 est non-conjugé

Application

  • 20
  • 13
  • 13
  • 10
  • 7
  • 5
  • 3
  • 3
  • 1
Western Blotting (WB), ELISA
  • Épitope

    • 15
    • 4
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 390-470

    Fonction

    ALS2 Antibody

    Specificité

    ALS2 Polyclonal Antibody detects endogenous levels of protein.

    Purification

    The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

    Immunogène

    Synthesized peptide derived from human protein . at AA range: 390-470

    Isotype

    IgG
  • Indications d'application

    WB 1:500-2000 ELISA 1:5000-20000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Liquid in PBS containing 50 % glycerol, and 0.02 % sodium azide.

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Stock

    -20 °C

    Stockage commentaire

    Store at -20°C/1 year

    Date de péremption

    12 months
  • Antigène

    ALS2 (Amyotrophic Lateral Sclerosis 2 (Juvenile) (ALS2))

    Autre désignation

    ALS2

    Sujet

    Background: The protein encoded by this gene contains an ATS1/RCC1-like domain, a RhoGEF domain, and a vacuolar protein sorting 9 (VPS9) domain, all of which are guanine-nucleotide exchange factors that activate members of the Ras superfamily of GTPases. The protein functions as a guanine nucleotide exchange factor for the small GTPase RAB5. The protein localizes with RAB5 on early endosomal compartments, and functions as a modulator for endosomal dynamics. Mutations in this gene result in several forms of juvenile lateral sclerosis and infantile-onset ascending spastic paralysis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2008],

    Gene Name: ALS2 ALS2CR6 KIAA1563

    Protein Name: Alsin (Amyotrophic lateral sclerosis 2 chromosomal region candidate gene 6 protein) (Amyotrophic lateral sclerosis 2 protein)

    ID gène

    57679

    UniProt

    Q96Q42

    Pathways

    Skeletal Muscle Fiber Development
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