Human Latent Transforming Growth Factor Beta Binding Protein 2 (LTBP2) ELISA Kit | LTBP2 elisa kit
Human Latent Transforming Growth Factor Beta Binding Protein 2 (LTBP2) ELISA Kit
No significant cross-reactivity or interference between Latent Transforming Growth Factor Beta Binding Protein 2 (LTBP2) and analogues was observed.
To minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.
NCBI and Uniprot Product Information
NCBI Description
The protein encoded by this gene belongs to the family of latent transforming growth factor (TGF)-beta binding proteins (LTBP), which are extracellular matrix proteins with multi-domain structure. This protein is the largest member of the LTBP family possessing unique regions and with most similarity to the fibrillins. It has thus been suggested that it may have multiple functions: as a member of the TGF-beta latent complex, as a structural component of microfibrils, and a role in cell adhesion. [provided by RefSeq, Jul 2008]
Uniprot Description
LTBP2: May play an integral structural role in elastic-fiber architectural organization and/or assembly. Defects in LTBP2 are the cause of primary congenital glaucoma type 3D (GLC3D). 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). 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. Defects in LTBP2 are the cause of Weill-Marchesani syndrome 3 (WMS3). A rare connective tissue disorder characterized by short stature, brachydactyly, joint stiffness, and lens abnormalities. Belongs to the LTBP family.
Protein type: Secreted, signal peptide; Secreted
Chromosomal Location of Human Ortholog: 14q24
Cellular Component: extracellular matrix; extracellular space; proteinaceous extracellular matrix
Molecular Function: heparin binding; protein binding; growth factor binding; calcium ion binding
Biological Process: transforming growth factor beta receptor signaling pathway; protein secretion; protein targeting
Disease: Microspherophakia And/or Megalocornea, With Ectopia Lentis And With Or Without Secondary Glaucoma; Glaucoma 3, Primary Congenital, D; Glaucoma 3, Primary Infantile, B; Weill-marchesani Syndrome 3
Research Articles on LTBP2
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Product Notes
The Human LTBP2 ltbp2 (Catalog #AAA2020850) is an ELISA Kit and is intended for research purposes only. The product is available for immediate purchase. The AAA2020850 ELISA Kit recognizes Human LTBP2. It is sometimes possible for the material contained within the vial of "Latent Transforming Growth Factor Beta Binding Protein 2 (LTBP2), ELISA Kit" to become dispersed throughout the inside of the vial, particularly around the seal of said vial, during shipment and storage. We always suggest centrifuging these vials to consolidate all of the liquid away from the lid and to the bottom of the vial prior to opening. Please be advised that certain products may require dry ice for shipping and that, if this is the case, an additional dry ice fee may also be required.Precautions
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