S26A4 Polyclonal Antibody, 20ul Molecular Biology delivering 20 Units of activity

delivering 20 Units of activity per μL in a 10 mL solution

Temperature self-calibration

as well as in chromatid cohesion during mitosis

particularly in the formation and maintanance of cilia

Both proteins are widely expressed and contain an amino-terminal kinase domain followed by a central proline/serine rich domain and a highly conserved carboxy-terminal domain

S26A4 Polyclonal Antibody, 20ul Molecular Biology delivering 20 Units of activityMutations in this gene are associated with Pendred syndrome, the most common form of syndromic deafness, an autosomal recessive disease. It is highly homologous to the SLC26A3 gene; they have similar genomic structures and this gene is located 3' of the SLC26A3 gene. The encoded protein has homology to sulfate transporters.