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SOX2 Antikörper

Dieses Kaninchen Monoklonal-Antikörper erkennt spezifisch SOX2 in WB. Er zeigt eine Reaktivität gegenüber Human.
Produktnummer ABIN7270573

Kurzübersicht für SOX2 Antikörper (ABIN7270573)

Target

Alle SOX2 Antikörper anzeigen
SOX2 (SRY (Sex Determining Region Y)-Box 2 (SOX2))

Reaktivität

  • 246
  • 140
  • 73
  • 21
  • 13
  • 11
  • 10
  • 10
  • 8
  • 8
  • 7
  • 7
  • 5
  • 5
  • 2
  • 2
  • 1
  • 1
  • 1
Human

Wirt

  • 185
  • 70
  • 2
Kaninchen

Klonalität

  • 163
  • 94
Monoklonal

Konjugat

  • 122
  • 14
  • 14
  • 10
  • 6
  • 6
  • 6
  • 5
  • 5
  • 5
  • 5
  • 5
  • 5
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 1
Dieser SOX2 Antikörper ist unkonjugiert

Applikation

  • 165
  • 99
  • 93
  • 49
  • 45
  • 42
  • 40
  • 40
  • 30
  • 24
  • 22
  • 21
  • 16
  • 12
  • 4
  • 4
  • 4
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Verwendungszweck

    SOX2 Rabbit mAb

    Kreuzreaktivität

    Human, Maus, Ratte

    Produktmerkmale

    Monoclonal Antibodies

    Aufreinigung

    Affinity purification

    Immunogen

    A synthesized peptide derived from human SOX2

    Isotyp

    IgG
  • Applikationshinweise

    WB,1:500 - 1:2000

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Buffer

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

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

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

    Lagerung

    -20 °C

    Informationen zur Lagerung

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

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

    Andere Bezeichnung

    SOX2

    Hintergrund

    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

    Molekulargewicht

    34kDa

    Gen-ID

    6657

    UniProt

    P48431

    Pathways

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