TLR1 Polyclonal Antibody, 50ul[BT-AP15002] Miscellaneous Mutations in this gene cause

Mutations in this gene cause glycogen storage disease type 9A| also known as X-linked liver glycogenosis

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Mutations in this gene are associated with microphthalmia

and the protein is a type-1 transmembrane protein found at the slit diaphragm of glomerular podocytes

The synergy of this protein and the APP is required to mediate neuromuscular transmission

TLR1 Polyclonal Antibody, 50ul[BT-AP15002] Miscellaneous Mutations in this gene causeThe protein encoded by this gene is a member of the Toll like receptor (TLR) family which plays a fundamental role in pathogen recognition and activation of innate immunity. TLRs are highly conserved from Drosophila to humans and share structural and functional similarities. They recognize pathogen associated molecular patterns (PAMPs) that are expressed on infectious agents, and mediate the production of cytokines necessary for the development of