COL4A5 rabbit pAb

• Background :

  This gene 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. [provided by RefSeq, Aug 2010]

• Description :

  This gene 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. [provided by RefSeq, Aug 2010],

• UniProt :

  P29400

• Swiss Prot :

  P29400

• Reactivity :

  Human; Mouse

• Immunogen :

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

• Clonality :

  Polyclonal

• Source :

  Rabbit

• Applications :

  IHC; IF; WB; ELISA

• Concentration :

  1 mg/ml

• Dilution :

  WB 1:500-2000 Immunohistochemistry: 1/100 - 1/300. Immunofluorescence: 1/200 - 1/1000. ELISA: 1/10000. Not yet tested in other applications.

• Molecular Weight :

  160kD

• Storage Conditions :

  -20°C/1 year

• Observed Molecular Weight :

  160kD

• Fragment :

  IgG

• Subcellular Location :

  Secreted, extracellular space, extracellular matrix, basement membrane.

• Other Product Names :

  COL4A5; Collagen alpha-5 (IV) chain

• Gene ID (Human) :

  1287