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SOX14 anticorps

Cet anticorps anti-SOX14 est un anticorps Lapin Polyclonal détectant SOX14 dans IHC et IF. Adapté pour Humain, Souris et Rat.
N° du produit ABIN6568117

Aperçu rapide pour SOX14 anticorps (ABIN6568117)

Antigène

Voir toutes SOX14 Anticorps
SOX14 (SRY (Sex Determining Region Y)-Box 14 (SOX14))

Reactivité

  • 29
  • 6
  • 5
  • 5
  • 4
  • 4
  • 4
  • 4
  • 3
  • 2
  • 2
  • 1
Humain, Souris, Rat

Hôte

  • 29
Lapin

Clonalité

  • 29
Polyclonal

Conjugué

  • 11
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp SOX14 est non-conjugé

Application

  • 24
  • 13
  • 13
  • 10
  • 3
  • 3
  • 2
  • 2
  • 1
Immunohistochemistry (IHC), Immunofluorescence (IF)
  • Purification

    Affinity purification

    Immunogène

    Recombinant protein of human SOX14

    Isotype

    IgG
  • Indications d'application

    IHC 1:50 - 1:200 IF 1:50 - 1:200

    Restrictions

    For Research Use only
  • Concentration

    1 mg/mL

    Buffer

    Buffer: PBS with 0.02 % sodium azide, 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

    SOX14 (SRY (Sex Determining Region Y)-Box 14 (SOX14))

    Autre désignation

    SOX14

    Sujet

    Synonyms: HMG box transcription factor SOX 14,MGC119898,MGC119899,SOX 14,SOX 28,Sox box protein 14,SOX28,SRY (sex determining region Y) box 14 ,SRY box 14,Transcription factor SOX 14

    Background: This intronless gene encodes a member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of the cell fate. The encoded protein may act as a transcriptional regulator after forming a protein complex with other proteins. Mutations in this gene are suggested to be responsible for the limb defects associated with blepharophimosis, ptosis, epicanthus inversus syndrome (BPES) and Mobius syndrome.

    Poids moléculaire

    Observed_MW: Refer to Figures

    Calculated_MW: 26kDa

    ID gène

    8403

    UniProt

    O95416
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