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LHX3 anticorps

L’anticorps anti-LHX3 Polyclonal Lapin est utilisé pour la détection de LHX3 dans des échantillons de Humain. Il a été validé pour WB, ELISA et IHC.
N° du produit ABIN2460776
699,88 €
Plus frais de livraison 40,00 € et TVA
100 μL
Destination: France
Envoi sous 6 à 8 jours ouvrables

Aperçu rapide pour LHX3 anticorps (ABIN2460776)

Antigène

Voir toutes LHX3 Anticorps
LHX3 (LIM Homeobox 3 (LHX3))

Reactivité

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  • 8
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  • 6
  • 6
  • 4
  • 4
  • 2
  • 2
  • 1
  • 1
  • 1
Humain

Hôte

  • 27
  • 2
Lapin

Clonalité

  • 15
  • 14
Polyclonal

Conjugué

  • 17
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp LHX3 est non-conjugé

Application

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Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
  • Purification

    Antibody is purified by protein A chromatography method.

    Immunogène

    Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human LHX3.
  • Indications d'application

    LHX3 antibody can be used for detection of LHX3 by ELISA at 1:312500. LHX3 antibody can be used for detection of LHX3 by western blot at 1.25 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Add 100 ?L of distilled water. Final antibody concentration is 1 mg/mL.

    Concentration

    1 mg/mL

    Buffer

    Antibody is lyophilized in PBS buffer with 2 % sucrose.

    Conseil sur la manipulation

    As with any antibody avoid repeat freeze-thaw cycles.

    Stock

    4 °C/-20 °C

    Stockage commentaire

    For short periods of storage (days) store at 4 °C. For longer periods of storage, store LHX3 antibody at -20 °C.
  • Antigène

    LHX3 (LIM Homeobox 3 (LHX3))

    Autre désignation

    LHX3

    Sujet

    LHX3 encodes a member a large protein family which carry the LIM domain, a unique cysteine-rich zinc-binding domain. The encoded protein is a transcription factor that is required for pituitary development and motor neuron specification. Mutations in this gene have been associated with a syndrome of combined pituitary hormone deficiency and rigid cervical spine.

    Poids moléculaire

    44 kDa

    ID gène

    8022

    NCBI Accession

    NP_055379
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