RAP1B Polyclonal Antibody, 20ul Peripheral Blood Separation Tube A mutation in this gene

A mutation in this gene has been associated with hyperimmunoglobulin E syndrome (HIES) - a primary immunodeficiency characterized by elevated serum immunoglobulin E

are involved in the formation of gap junctions

and mRNA localization

This gene encodes a member of the CHD family of proteins which are characterized by the presence of chromo (chromatin organization modifier) domains and SNF2-related helicase/ATPase domains

Each product has a separate

RAP1B Polyclonal Antibody, 20ul Peripheral Blood Separation Tube A mutation in this geneThis gene encodes a member of the RAS like small GTP binding protein superfamily. Members of this family regulate multiple cellular processes including cell adhesion and growth and differentiation. This protein localizes to cellular membranes and has been shown to regulate integrin mediated cell signaling. This protein also plays a role in regulating outside in signaling in platelets. Alternate splicing results in multiple transcript variants.