Anticorps Polyclonal de lapin anti-OPN1MW

OPN1MW Polyclonal Antibody for WB, Indirect ELISA

Hôte / Isotype

Lapin / IgG

Réactivité testée

Humain, rat, souris

Applications

WB, Indirect ELISA

Conjugaison

Non conjugué

N° de cat : 30975-1-PBS

Synonymes

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Galerie de données de validation

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  WB analysis of mouse brain using 30975-1-AP (same clone as 30975-1-PBS)

  mouse brain tissue were subjected to SDS PAGE followed by western blot with 30975-1-AP (OPN1MW antibody) at dilution of 1:1000 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 30975-1-PBS in a different storage buffer formulation.

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Informations sur le produit

30975-1-PBS cible OPN1MW dans les applications de WB, Indirect ELISA et montre une réactivité avec des échantillons Humain, rat, souris

• Réactivité: Humain, rat, souris
• Hôte / Isotype: Lapin / IgG
• Clonalité: Polyclonal
• Type: Anticorps
• Immunogène: OPN1MW Protéine recombinante Ag34169
• Nom complet: opsin 1 (cone pigments), medium-wave-sensitive
• Poids moléculaire observé: 38-40 kDa
• Numéro d’acquisition GenBank: BC156776
• Symbole du gène: OPN1MW
• Identification du gène (NCBI): 2652
• Conjugaison: Non conjugué
• Forme: Liquide
• Méthode de purification: Purification par affinité contre l'antigène
• Tampon de stockage: PBS only
• Conditions de stockage: Store at -80°C. 20ul contiennent 0,1% de BSA.

Informations générales

OPN1MW (opsin 1, medium wave sensitive), also known as CBD. It is expected to be located in cell membrane. This gene encodes for a light absorbing visual pigment of the opsin gene family. The encoded protein is called green cone photopigment or medium-wavelength sensitive opsin. Opsins are G-protein coupled receptors with seven transmembrane domains, an N-terminal extracellular domain, and a C-terminal cytoplasmic domain. The long-wavelength opsin gene and multiple copies of the medium-wavelength opsin gene are tandemly arrayed on the X chromosome and frequent unequal recombination and gene conversion may occur between these sequences. X chromosomes may have fusions of the medium- and long-wavelength opsin genes or may have more than one copy of these genes. Defects in this gene are the cause of deutanopic colorblindness. The calculated molecular weight of OPN1MW is 40 kDa.

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