Anticorps Recombinant de lapin anti-COL6A3

COL6A3 Recombinant Antibody for FC (Intra), Cytometric bead array, Indirect ELISA

Hôte / Isotype

Lapin / IgG

Réactivité testée

Humain

Applications

FC (Intra), Cytometric bead array, Indirect ELISA

Conjugaison

Non conjugué

CloneNo.

230540D3

N° de cat : 83010-3-PBS

Synonymes

COL6A3-Specific, 230540D3, Collagen alpha 3(VI) chain, Collagen alpha-3(VI) chain, Collagen Type VI



Informations sur le produit

83010-3-PBS cible COL6A3 dans les applications de FC (Intra), Cytometric bead array, Indirect ELISA et montre une réactivité avec des échantillons Humain

Réactivité Humain
Hôte / Isotype Lapin / IgG
Clonalité Recombinant
Type Anticorps
Immunogène COL6A3 Protéine recombinante Ag34752
Nom complet collagen, type VI, alpha 3
Masse moléculaire calculée 344 kDa
Poids moléculaire observé343 kDa
Numéro d’acquisition GenBankNM_004369
Symbole du gène COL6A3
Identification du gène (NCBI) 1293
Conjugaison Non conjugué
Forme Liquide
Méthode de purification Purification par protéine A
Tampon de stockage PBS only
Conditions de stockageStore at -80°C. 20ul contiennent 0,1% de BSA.

Informations générales

COL6A3 belongs to the type VI collagen family. Collagen VI acts as a cell-binding protein. It is expected to be expressed in smooth muscle. And the calculated molecular weight of COL6A3 is 343 kDa. The protein has similar expression in obese and T2DM (2 patients, and it regulates the chemotaxis and inflammation of macrophages in adipose tissue. Its expression is also related to weight gain. The expression of this protein in adipocytes is related to insulin resistance, which is believed to depend on PPAR (peroxisome proliferator-activated receptor) α-mediated adipocyte development (PMID: 25337653). Defects in COL6A3 are a cause of Bethlem myopathy (BM). Defects in COL6A3 are a cause of Ullrich congenital muscular dystrophy (UCMD) which also known as Ullrich scleroatonic muscular dystrophy. This antibody is specific to COL6A3.

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