LIN-28 Monoclonal Antibody, 50ul Serum & Sample Tubes The GSTT1 gene is haplotype-specific

The GSTT1 gene is haplotype-specific and is absent from 38% of the population

an autosomal recessive disorder characterized by palmoplantar keratosis and periodontitis

Mutation of this cleavage site causes autosomal dominant hypophosphatemic rickets (ADHR)

in normal adult tissues

Anykrin repeats and a GRK-interacting domain

LIN-28 Monoclonal Antibody, 50ul Serum & Sample Tubes The GSTT1 gene is haplotype-specificThis gene encodes a LIN 28 family RNA binding protein that acts as a posttranscriptional regulator of genes involved in developmental timing and self renewal in embryonic stem cells. The encoded protein functions through direct interaction with target mRNAs and by disrupting the maturation of certain miRNAs involved in embryonic development. This protein prevents the terminal processing of the LET7 family of microRNAs which are major regulators of