Anticorps Polyclonal de lapin anti-COL9A1

COL9A1 Polyclonal Antibody for WB, Indirect ELISA

Hôte / Isotype

Lapin / IgG

Réactivité testée

Humain

Applications

WB, Indirect ELISA

Conjugaison

Non conjugué

N° de cat : 12507-1-PBS

Synonymes

COL9, Collagen alpha 1(IX) chain, Collagen alpha-1(IX) chain, Collagen Type IX, EDM6

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Galerie de données de validation

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  WB analysis using 12507-1-AP (same clone as 12507-1-PBS)

  Various lysates were subjected to SDS PAGE followed by western blot with 12507-1-AP (Collagen Type IX antibody) at dilution of 1:1000 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 12507-1-PBS in a different storage buffer formulation.

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Informations sur le produit

12507-1-PBS cible COL9A1 dans les applications de WB, Indirect ELISA et montre une réactivité avec des échantillons Humain

• Réactivité: Humain
• Hôte / Isotype: Lapin / IgG
• Clonalité: Polyclonal
• Type: Anticorps
• Immunogène: COL9A1 Protéine recombinante Ag3189
• Nom complet: collagen, type IX, alpha 1
• Masse moléculaire calculée: 921 aa 92 kDa
• Poids moléculaire observé: 64-67 kDa
• Numéro d’acquisition GenBank: BC015409
• Symbole du gène: COL9A1
• Identification du gène (NCBI): 1297
• 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

COL9A1 (collagen type IX alpha 1 chain), also known as MED. It is expected to be located in extracellular space, and the protein is enriched in the brain, choroid plexus and prostate. This gene encodes one of the three alpha chains of type IX collagen, which is a minor (5-20%) collagen component of hyaline cartilage. Type IX collagen is usually found in tissues containing type II collagen, a fibrillar collagen. Mutations in this gene are associated with osteoarthritis in humans, with multiple epiphyseal dysplasia, 6, a form of chondrodysplasia, and with Stickler syndrome, a disease characterized by ophthalmic, orofacial, articular, and auditory defects. The molecular weight of COL9A1 is 64 kDa, and it can recognize other isoforms.

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