Anticorps Monoclonal anti-VSX2

VSX2 Monoclonal Antibody for WB, Indirect ELISA

Hôte / Isotype

Mouse / IgG2b

Réactivité testée

Humain, rat, souris

Applications

WB, Indirect ELISA

Conjugaison

Non conjugué

CloneNo.

2C7C1

N° de cat : 67626-1-PBS

Synonymes

CHX10, Homeobox protein CHX10, HOX10, MCOP2, MCOPCB3, RET1, visual system homeobox 2, VSX2

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Galerie de données de validation

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  WB analysis using 67626-1-Ig (same clone as 67626-1-PBS)

  Various lysates were subjected to SDS PAGE followed by western blot with 67626-1-Ig (VSX2 antibody) at dilution of 1:10000 incubated at room temperature for 1.5 hours. The membrane was stripped and reblotted with HRP-conjugated GAPDH Monoclonal antibody (HRP-60004) as loading control. This data was developed using the same antibody clone with 67626-1-PBS in a different storage buffer formulation.

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  WB analysis of rat eye using 67626-1-Ig (same clone as 67626-1-PBS)

  rat eye tissue were subjected to SDS PAGE followed by western blot with 67626-1-Ig (VSX2 antibody) at dilution of 1:10000 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 67626-1-PBS in a different storage buffer formulation.

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Informations sur le produit

67626-1-PBS cible VSX2 dans les applications de WB, Indirect ELISA et montre une réactivité avec des échantillons Humain, rat, souris

• Réactivité: Humain, rat, souris
• Hôte / Isotype: Mouse / IgG2b
• Clonalité: Monoclonal
• Type: Anticorps
• Immunogène: VSX2 Protéine recombinante Ag29867
• Nom complet: visual system homeobox 2
• Masse moléculaire calculée: 361 aa, 39 kDa
• Poids moléculaire observé: 45 kDa
• Numéro d’acquisition GenBank: BC128153
• Symbole du gène: VSX2
• Identification du gène (NCBI): 338917
• Conjugaison: Non conjugué
• Forme: Liquide
• Méthode de purification: Purification par protéine A
• Tampon de stockage: PBS only
• Conditions de stockage: Store at -80°C. 20ul contiennent 0,1% de BSA.

Informations générales

VSX2, also named as CHX10 and HOX10, belongs to the paired homeobox family. VSX2 plays a significant role in the specification and morphogenesis of the sensory retina. It may also participate in the development of the cells of the inner nuclear layer, particularly bipolar cells. Defects in VSX2 are the cause of microphthalmia isolated type 2 (MCOP2). Defects in VSX2 are the cause of microphthalmia with cataracts and iris abnormalities (MCOPCTI). Defects in VSX2 are the cause of microphthalmia isolated with coloboma type 3 (MCOPCB3). The antibody is specific to VSX2.

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