The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
1/800. Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.
FunctionMay play an integral structural role in elastic-fiber architectural organization and/or assembly.
Tissue specificityExpressed in lung, weakly expressed in heart, placenta, liver and skeletal muscle.
Involvement in diseaseDefects in LTBP2 are the cause of primary congenital glaucoma type 3D (GLC3D) [MIM:613086]. An autosomal recessive form of primary congenital glaucoma (PCG). PCG is characterized by marked increase of intraocular pressure at birth or early childhood, large ocular globes (buphthalmos) and corneal edema. It results from developmental defects of the trabecular meshwork and anterior chamber angle of the eye that prevent adequate drainage of aqueous humor. Defects in LTBP2 are the cause of microspherophakia (MCSPH) [MIM:251750]. It is a rare disease characterized by smaller and more spherical lenses than normal bilaterally, an increased anteroposterior thickness of the lens and highly myopic eyes. Lens dislocation or subluxation may occur, leading to defective accommodation.
Sequence similaritiesBelongs to the LTBP family. Contains 20 EGF-like domains. Contains 4 TB (TGF-beta binding) domains.
DomainAssociates covalently with small latent TGF-beta complex via Repeat B and Repeat C.