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SMN1 anticorps (AA 50-100)

Cet anticorps Lapin Polyclonal détecte spécifiquement SMN1 dans IP. Il présente une réactivité envers Humain.
N° du produit ABIN7452436

Aperçu rapide pour SMN1 anticorps (AA 50-100) (ABIN7452436)

Antigène

Voir toutes SMN1 Anticorps
SMN1 (Survival of Motor Neuron 1, Telomeric (SMN1))

Reactivité

  • 60
  • 34
  • 16
  • 6
  • 6
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
Humain

Hôte

  • 63
  • 12
Lapin

Clonalité

  • 54
  • 21
Polyclonal

Conjugué

  • 37
  • 5
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp SMN1 est non-conjugé

Application

  • 57
  • 28
  • 15
  • 13
  • 13
  • 13
  • 10
  • 8
  • 8
  • 3
  • 3
  • 1
  • 1
Immunoprecipitation (IP)
  • Épitope

    • 15
    • 9
    • 5
    • 5
    • 4
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 50-100

    Fonction

    Rabbit anti-SMN1 Antibody, Affinity Purified

    Purification

    Affinity Purified

    Immunogène

    between AA 50 and 100

    Isotype

    IgG
  • Indications d'application

    IP: 2 - 5 μg/mg lysate

    WB: Not recommended. Use rabbit anti-SMN1 antibody ABIN7452052.

    Restrictions

    For Research Use only
  • Concentration

    1000 μg/mL

    Buffer

    Tris-citrate/phosphate buffer, pH 7 to 8 containing 0.09 % 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

    4 °C

    Date de péremption

    12 months
  • Antigène

    SMN1 (Survival of Motor Neuron 1, Telomeric (SMN1))

    Autre désignation

    SMN1

    Sujet

    Background: Survival motor neuron protein (SMN1) has been identified as the gene that is defective in spinal muscular atrophy (SMA), a neurodegenerative autosomal recessive disease characterized by paralysis and muscular atrophy which results from the loss of motor neurons in the spinal cord. There are two closely related SMN genes that do not appear to be functionally redundant. SMN1 represents the telomeric copy while SMN2 represents the centromeric copy. In the cell, SMN1 is part of a large complex of proteins involved in snRNP biogenesis. The functional role of SMN1 is proposed to play a role in messenger and ribosomal RNA transcription and processing.

    ID gène

    6606

    NCBI Accession

    NP_000335

    UniProt

    Q16637

    Pathways

    Ribonucleoprotein Complex Subunit Organization
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