FAP-1 Polyclonal Antibody, 100ul Protein Modification providing a molecular signature to

providing a molecular signature to distinguish between self and non-self mRNAs by the host during viral infection

The solute carrier family 39 member 2 functions as a zinc transporter

Mutations in the gene cause X-linked neurological syndromes known as CRASH (corpus callosum hypoplasia

CLDN8 (claudin 8) encodes a member of the claudin family

RAD51C is a member of the RAD51 family

FAP-1 Polyclonal Antibody, 100ul Protein Modification providing a molecular signature toThe protein encoded by this gene is a homodimeric integral membrane gelatinase belonging to the serine protease family. It is selectively expressed in reactive stromal fibroblasts of epithelial cancers, granulation tissue of healing wounds, and malignant cells of bone and soft tissue sarcomas. This protein is thought to be involved in the control of fibroblast growth or epithelial mesenchymal interactions during development, tissue repair, and