|Description:||Rabbit polyclonal antibody to LRP4.|
|Dilutions:||WB 1:500 - 1:2000|
|Immunogen:||Recombinant protein of human LRP4|
|Formulation:||PBS with 0.02% sodium azide, 50% glycerol, pH7.3.|
|Storage:||Store at -20℃. Avoid freeze / thaw cycles.|
Target (Information from UniProt)
|Function:||Mediates SOST-dependent inhibition of bone formation. Functions as a specific facilitator of SOST-mediated inhibition of Wnt signaling. Plays a key role in the formation and the maintenance of the neuromuscular junction (NMJ), the synapse between motor neuron and skeletal muscle. Directly binds AGRIN and recruits it to the MUSK signaling complex. Mediates the AGRIN-induced phosphorylation of MUSK, the kinase of the complex. The activation of MUSK in myotubes induces the formation of NMJ by regulating different processes including the transcription of specific genes and the clustering of AChR in the postsynaptic membrane. Alternatively, may be involved in the negative regulation of the canonical Wnt signaling pathway, being able to antagonize the LRP6-mediated activation of this pathway. More generally, has been proposed to function as a cell surface endocytic receptor binding and internalizing extracellular ligands for degradation by lysosomes.|
|Tissue Specificity:||Expressed in bone; present in osteoblasts and osteocytes. No expression is observed in osteoclast. Expressed in several regions of the brain.|
|Involvement in Disease:||Cenani-Lenz syndactyly syndrome: A congenital malformation syndrome defined as complete and complex syndactyly of the hands combined with malformations of the forearm bones and similar manifestations in the lower limbs. It is characterized by fusion and disorganization of metacarpal and phalangeal bones, radius and ulnar shortening, radioulnar synostosis, and severe syndactyly of hands and feet.
Sclerosteosis 2: A sclerosing bone dysplasia characterized by a generalized hyperostosis and sclerosis leading to a markedly thickened skull, with mandible, ribs, clavicles and all long bones also being affected. Due to narrowing of the foramina of the cranial nerves, facial nerve palsy, hearing loss and atrophy of the optic nerves can occur. Sclerosteosis is clinically and radiologically very similar to van Buchem disease, mainly differentiated by hand malformations and a large stature in sclerosteosis patients.
Myasthenic syndrome, congenital, 17: A form of congenital myasthenic syndrome, a group of disorders characterized by failure of neuromuscular transmission, including pre-synaptic, synaptic, and post-synaptic disorders that are not of autoimmune origin. Clinical features are easy fatigability and muscle weakness affecting the axial and limb muscles (with hypotonia in early-onset forms), the ocular muscles (leading to ptosis and ophthalmoplegia), and the facial and bulbar musculature (affecting sucking and swallowing, and leading to dysphonia). The symptoms fluctuate and worsen with physical effort.
|Sequence Similarities:||Belongs to the LDLR family.|
|Synonyms:||activated protease fragment Antibody
ATC 2 Antibody
Atrial natriuretic peptide-converting enzyme Antibody
Atrial natriuteric peptide converting enzyme Antibody
Corin serine peptidase Antibody
Heart specific serine proteinase Antibody
Heart specific serine proteinase ATC2 Antibody
Heart-specific serine proteinase ATC2 Antibody
LDLR dan Antibody
Low density lipoprotein receptor related protein 4 Antibody
Low-density lipoprotein receptor-related protein 4 Antibody
Lrp 4 Antibody
Multiple epidermal growth factor like domains 7 Antibody
Multiple epidermal growth factor-like domains 7 Antibody
Pro ANP convertase Antibody
Pro ANP converting enzyme Antibody
Pro-ANP-converting enzyme Antibody
TMPRSS 10 Antibody
Transmembrane protease serine 10 Antibody
Western blot analysis of extracts of various cell lines, using LRP4 antibody.