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ZIC1-3 anticorps (C-Term)

Cet anticorps anti-ZIC1-3 est un anticorps Lapin Polyclonal détectant ZIC1-3 dans IHC et WB. Adapté pour Humain.
N° du produit ABIN351417

Aperçu rapide pour ZIC1-3 anticorps (C-Term) (ABIN351417)

Antigène

ZIC1-3 (Zic1/2/3) (Zic Family Member 1/2/3 (Zic1/2/3))

Reactivité

Humain

Hôte

Lapin

Clonalité

Polyclonal

Application

Immunohistochemistry (IHC), Western Blotting (WB)
  • Épitope

    C-Term

    Fonction

    Rabbit antibody to ZIC1-3

    Specificité

    Specific for ZIC1 2 3.

     Réactivité croisée

    Humain, Souris, Rat

    Réactivité croisée (Details)

    Other species not yet tested.

    Purification

    IgG

    Immunogène

    A synthetic peptide from c-terminal region of human ZIC3 (Zinc finger protein ZIC 3) conjugated to an immunogenic carrier protein was used as the antigen. The peptide is homologous in many species including rat and mouse.

    Isotype

    IgG
  • Indications d'application

    IHC WB. A concentration of 10-50,micro,g,ml is recommended. The optimal concentration should be determined by the end user. Not yet tested in other applications.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Reconstitute in 500 µl of sterile water. Centrifuge to remove any insoluble material.

    Conseil sur la manipulation

    Avoid freeze and thaw cycles.

    Stock

    4 °C,-20 °C

    Stockage commentaire

    Maintain the lyophilised/reconstituted antibodies frozen at -20°C for long term storage and refrigerated at 2-8°C for a shorter term. When reconstituting glycerol (1:1) may be added for an additional stability. Avoid freeze and thaw cycles.

    Date de péremption

    12 months
  • Antigène

    ZIC1-3 (Zic1/2/3) (Zic Family Member 1/2/3 (Zic1/2/3))

    Autre désignation

    ZIC1-3

    Sujet

    Function: Probably functions as a transcription factor in the earliest stages of the left-right (LR) body axis formation. Defects in ZIC3 are the cause of X-linked visceral heterotaxy (HTX1). HTX1 is a disease characterized by congenital heart disease and alterations of visceral situs including asplenia or polysplenia symmetric liver intestinal malrotation and abnormal lung lobation.

    UniProt

    O60481
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