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SMNDC1 anticorps

SMNDC1 Reactivité: Humain, Souris, Rat ELISA, IHC Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7246922
  • Antigène Voir toutes SMNDC1 Anticorps
    SMNDC1 (Survival Motor Neuron Domain Containing 1 (SMNDC1))
    Reactivité
    • 42
    • 25
    • 15
    • 5
    • 5
    • 5
    • 4
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    Humain, Souris, Rat
    Hôte
    • 38
    • 5
    Lapin
    Clonalité
    • 40
    • 3
    Polyclonal
    Conjugué
    • 22
    • 4
    • 4
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp SMNDC1 est non-conjugé
    Application
    • 28
    • 18
    • 15
    • 6
    • 5
    • 4
    • 2
    • 1
    • 1
    ELISA, Immunohistochemistry (IHC)
    Attributs du produit
    Polyclonal Antibody
    Purification
    Antigen affinity purification
    Immunogène
    Fusion protein of human SMNDC1
    Isotype
    IgG
    Top Product
    Discover our top product SMNDC1 Anticorps primaire
  • Indications d'application
    IHC 1:40-1:200, ELISA 1:5000-1:10000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.6 mg/mL
    Buffer
    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
    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. Avoid freeze / thaw cycles.
  • Antigène
    SMNDC1 (Survival Motor Neuron Domain Containing 1 (SMNDC1))
    Autre désignation
    SMNDC1 (SMNDC1 Produits)
    Synonymes
    anticorps smnr, anticorps spf30, anticorps SMNDC1, anticorps SMNR, anticorps SPF30, anticorps TDRD16C, anticorps wu:fb37h07, anticorps wu:fc23a07, anticorps 2410004J23Rik, anticorps 4933440I19Rik, anticorps survival motor neuron domain containing 1, anticorps smndc1, anticorps SMNDC1, anticorps Bm1_41545, anticorps Smndc1
    Sujet
    This gene is a paralog of SMN1 gene, which encodes the survival motor neuron protein, mutations in which are cause of autosomal recessive proximal spinal muscular atrophy. The protein encoded by this gene is a nuclear protein that has been identified as a constituent of the spliceosome complex. This gene is differentially expressed, with abundant levels in skeletal muscle, and may share similar cellular function as the SMN1 gene.
    UniProt
    O75940
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