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SOX2 Antikörper

Dieser 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

  • 230
  • 128
  • 72
  • 21
  • 13
  • 11
  • 10
  • 10
  • 8
  • 8
  • 7
  • 7
  • 5
  • 5
  • 2
  • 2
  • 1
  • 1
  • 1
Human

Wirt

  • 180
  • 58
  • 2
Kaninchen

Klonalität

  • 160
  • 80
Monoklonal

Konjugat

  • 113
  • 14
  • 13
  • 10
  • 6
  • 6
  • 4
  • 4
  • 4
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
Dieser SOX2 Antikörper ist unkonjugiert

Applikation

  • 169
  • 98
  • 76
  • 52
  • 49
  • 40
  • 40
  • 38
  • 24
  • 22
  • 20
  • 18
  • 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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