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SEPN1 anticorps

Cet anticorps Lapin Polyclonal détecte spécifiquement SEPN1 dans WB, IHC et ELISA. Il présente une réactivité envers Humain.
N° du produit ABIN7192312

Aperçu rapide pour SEPN1 anticorps (ABIN7192312)

Antigène

Voir toutes SEPN1 Anticorps
SEPN1 (Selenoprotein N, 1 (SEPN1))

Reactivité

  • 25
  • 5
  • 4
  • 4
  • 3
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1
Humain

Hôte

  • 25
Lapin

Clonalité

  • 25
Polyclonal

Conjugué

  • 13
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp SEPN1 est non-conjugé

Application

  • 18
  • 12
  • 7
  • 4
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), ELISA
  • Fonction

    SEPN1 Antibody

    Purification

    Antigen affinity purification

    Immunogène

    Synthetic peptide of Human SEPN1

    Isotype

    IgG
  • Indications d'application

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

     pH 7.4 PBS, 0.05 % Sodium azide, 40 % Glycerol

    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,-80 °C

    Stockage commentaire

    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • Antigène

    SEPN1 (Selenoprotein N, 1 (SEPN1))

    Autre désignation

    SEPN1

    Sujet

    Background: This gene encodes a selenoprotein, which contains a selenocysteine (Sec) residue at its active site. The selenocysteine is encoded by the UGA codon that normally signals translation termination. The 3' UTR of selenoprotein genes have a common stem-loop structure, the sec insertion sequence (SECIS), that is necessary for the recognition of UGA as a Sec codon rather than as a stop signal. Mutations in this gene cause the classical phenotype of multiminicore disease and congenital muscular dystrophy with spinal rigidity and restrictive respiratory syndrome.

    Aliases: CFTD antibody, MDRS1 antibody, RSMD1 antibody, RSS antibody, Selenoprotein N antibody, Selenoprotein N, 1 antibody, SelN antibody, SELN_HUMAN antibody, sepn1 antibody

    UniProt

    Q9NZV5

    Pathways

    Skeletal Muscle Fiber Development
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