S-100P Polyclonal Antibody, 20ul Enzyme Activity Assays Individuals with certain allelic variants

Individuals with certain allelic variants are said to have a poor metabolizer phenotype

Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of this cadherin-like gene

The encoded protein interacts with specifc DNA structures including nicked Holliday junctions

This gene encodes the B-cell lineage specific activator protein that is expressed at early

LONP2 (Lon Peptidase 2

S-100P Polyclonal Antibody, 20ul Enzyme Activity Assays Individuals with certain allelic variantsThe protein encoded by S100P (S100 calcium binding protein P) is a member of the S100 family of proteins containing 2 EF hand calcium binding motifs. S100 proteins are localized in the cytoplasm and or nucleus of a wide range of cells, and involved in the regulation of a number of cellular processes such as cell cycle progression and differentiation. S100 genes include at least 13 members which are located as a cluster on chromosome 1q21; however,