Tenascin-R Polyclonal Antibody, 20ul Filtration Mutations in PMS1 cause hereditary

Mutations in PMS1 cause hereditary nonpolyposis colorectal cancer type 3 (HNPCC3) either alone or in combination with mutations in other genes involved in the HNPCC phenotype

AQP2 encodes a water channel protein located in the kidney collecting tubule

The first is an energy-independent docking of the protein to the nuclear envelope and the second is an energy-dependent translocation through the nuclear pore complex

This gene encodes subunit 3 of the splicing factor 3a protein complex

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Tenascin-R Polyclonal Antibody, 20ul Filtration Mutations in PMS1 cause hereditaryThis gene encodes a member of the tenascin family of extracellular matrix glycoproteins. The encoded protein is restricted to the central nervous system. The protein may play a role in neurite outgrowth, neural cell adhesion and modulation of sodium channel function. It is a constituent of perineuronal nets.