C1QT5 Polyclonal Antibody, 20ul Immune Cell Analysis This gene is a member

This gene is a member of the protein-tyrosine kinase oncogene family

preventing over-aspiration and piston corrosion due to improper operation

Mutations in this gene are the cause of several cardiomyopathies and keratodermas| including skin fragility-woolly hair syndrome

a cytokine that acts on T and natural killer cells

FOXB1 is a gene on chromosome 15q22 that encodes a member of the forkhead class of DNA-binding proteins

C1QT5 Polyclonal Antibody, 20ul Immune Cell Analysis This gene is a memberThis gene encodes a member of a family of proteins that function as components of basement membranes and may play a role in cell adhesion. Mutations in this gene have been associated with late onset retinal degeneration. The protein may be encoded by either a bicistronic transcript including sequence from the upstream membrane frizzled related protein gene (MFRP), or by a monocistronic transcript expressed from an internal promoter.