Anticorps Polyclonal de lapin anti-C4orf26

C4orf26 Polyclonal Antibody for IHC, Indirect ELISA

Hôte / Isotype

Lapin / IgG

Réactivité testée

Humain

Applications

IHC, Indirect ELISA

Conjugaison

Non conjugué

N° de cat : 30132-1-PBS

Synonymes

ODAPH, FLJ23657

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Galerie de données de validation

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  IHC staining of human placenta using 30132-1-AP (same clone as 30132-1-PBS)

  Immunohistochemical analysis of paraffin-embedded human placenta tissue slide using 30132-1-AP (C4orf26 antibody) at dilution of 1:200 (under 10x lens). Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0). This data was developed using the same antibody clone with 30132-1-PBS in a different storage buffer formulation.

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  IHC staining of human placenta using 30132-1-AP (same clone as 30132-1-PBS)

  Immunohistochemical analysis of paraffin-embedded human placenta tissue slide using 30132-1-AP (C4orf26 antibody) at dilution of 1:200 (under 40x lens). Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0). This data was developed using the same antibody clone with 30132-1-PBS in a different storage buffer formulation.

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Informations sur le produit

30132-1-PBS cible C4orf26 dans les applications de IHC, Indirect ELISA et montre une réactivité avec des échantillons Humain

• Réactivité: Humain
• Hôte / Isotype: Lapin / IgG
• Clonalité: Polyclonal
• Type: Anticorps
• Immunogène: C4orf26 Protéine recombinante Ag32600
• Nom complet: chromosome 4 open reading frame 26
• Masse moléculaire calculée: 16kd
• Numéro d’acquisition GenBank: NM_001206981
• Symbole du gène: C4orf26
• Identification du gène (NCBI): 152816
• 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

Chromosome 4 open reading frame 26 (C4orf26), also known as odontogenesis associated phosphoprotein (ODAPH), is an enamel matrix protein at the maturation stage. It has been reported that mutations in C4orf26 gene are associated with autosomal recessive type of Amelogenesis Imperfecta (AI), a hereditary condition that affects enamel formation/mineralization (PMID: 33884476; PMID: 36163390).

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