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SOX2 anticorps

Cet anticorps Lapin Monoclonal détecte spécifiquement SOX2 dans WB. Il présente une réactivité envers Humain.
N° du produit ABIN7270573

Aperçu rapide pour SOX2 anticorps (ABIN7270573)

Antigène

Voir toutes SOX2 Anticorps
SOX2 (SRY (Sex Determining Region Y)-Box 2 (SOX2))

Reactivité

  • 221
  • 119
  • 73
  • 21
  • 13
  • 11
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  • 10
  • 8
  • 8
  • 7
  • 7
  • 5
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  • 2
  • 2
  • 1
  • 1
  • 1
Humain

Hôte

  • 172
  • 58
  • 2
Lapin

Clonalité

  • 161
  • 71
Monoclonal

Conjugué

  • 114
  • 14
  • 12
  • 10
  • 6
  • 6
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 1
Cet anticorp SOX2 est non-conjugé

Application

  • 161
  • 97
  • 69
  • 49
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  • 40
  • 40
  • 29
  • 24
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  • 20
  • 20
  • 16
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  • 4
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  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Fonction

    SOX2 Rabbit mAb

     Réactivité croisée

    Humain, Souris, Rat

    Attributs du produit

    Monoclonal Antibodies

    Purification

    Affinity purification

    Immunogène

    A synthesized peptide derived from human SOX2

    Isotype

    IgG
  • Indications d'application

    WB,1:500 - 1:2000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,0.05 % BSA,50 % glycerol, pH 7.3.

    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

    SOX2 (SRY (Sex Determining Region Y)-Box 2 (SOX2))

    Autre désignation

    SOX2

    Sujet

    This intronless gene encodes a member of the SRY-related HMG-box (SOX) family of transcription factors involved in the regulation of embryonic development and in the determination of cell fate. The product of this gene is required for stem-cell maintenance in the central nervous system, and also regulates gene expression in the stomach. Mutations in this gene have been associated with optic nerve hypoplasia and with syndromic microphthalmia, a severe form of structural eye malformation. This gene lies within an intron of another gene called SOX2 overlapping transcript (SOX2OT). [provided by RefSeq, Jul 2008],ANOP3,MCOPS3,SOX2,SRY-box 2,Cell Biology & Developmental Biology,Cell Type Marker,Cell Type Marker_Neural Stem Cell marker,Embryonic Stem Cells,Epigenetics & Nuclear Signaling,ESC Pluripotency and Differentiation,Germline Stem Cells,Neuroscience,Signal Transduction,Stem Cells,Transcription Factors,SOX2

    Poids moléculaire

    34kDa

    ID gène

    6657

    UniProt

    P48431

    Pathways

    Dopaminergic Neurogenesis, Sensory Perception of Sound, Stem Cell Maintenance, Cell RedoxHomeostasis
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