CD6 Polyclonal Antibody, 100ul[BT-AP01948] Reagent Reservoirs Mutations in this gene have

Mutations in this gene have been associated with transient neonatal diabetes mellitus type 1 (TNDM1)

Variations in this gene may be associated with susceptibility to systemic lupus erythematosus (SLE)

Diseases associated with REG4 include ulcerative colitis

Receptor-activated non-selective cation channel involved in detection of sensations such as coolness

BRE is upregulated in several types of cancer

CD6 Polyclonal Antibody, 100ul[BT-AP01948] Reagent Reservoirs Mutations in this gene haveMMP17 encodes a member of the peptidase M10 family and membrane type subfamily of matrix metalloproteinases (MMPs). Proteins in this family are involved in the breakdown of extracellular matrix in normal physiological processes, such as embryonic development, reproduction, and tissue remodeling, as well as in disease processes, such as arthritis and metastasis. Members of this subfamily contain a transmembrane domain suggesting that these proteins are