Background:

COL4A5 encodes one of the six subunits of type IV collagen, the major structural component of basement membranes. Mutations in this gene are associated with X-linked Alport syndrome, also known as hereditary nephritis. Like the other members of the type IV collagen gene family, this gene is organized in a head-to-head conformation with another type IV collagen gene so that each gene pair shares a common promoter. Alternatively spliced transcript variants have been identified for this gene.

Classification:

Primary antibody

Alternative names:

COL4A5; Collagen alpha-5(IV) chain

Species reactivity:

Human;Mouse

Host:

Rabbit

Isotype:

IgG

Immunogen:

The antiserum was produced against synthesized peptide derived from human Collagen IV alpha5. AA range:21-70

Concentration:

1 mg/ml

Molecular weight:

161044

Applications:

IHC-p, IF, WB, ELISA

Storage:

-20°C for one year

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