S12A3 Rabbit Polyclonal Antibody, 100ul Peptide Synthesis Don't let limitations hold you

Don't let limitations hold you back

tissue specificity:Preferentially detected in breast carcinoma tissue and mammary gland

Mutations in this gene may be associated with iron overload in human patients

where CENP-B is localized

This gene encodes a nuclear transcription factor that belongs to the NK-linked or NK-like (NKL) subfamily of homeobox genes

S12A3 Rabbit Polyclonal Antibody, 100ul Peptide Synthesis Don't let limitations hold youThis gene encodes a renal thiazide sensitive sodium chloride cotransporter that is important for electrolyte homeostasis. This cotransporter mediates sodium and chloride reabsorption in the distal convoluted tubule. Mutations in this gene cause Gitelman syndrome a disease similar to Bartter's syndrome that is characterized by hypokalemic alkalosis combined with hypomagnesemia low urinary calcium and increased renin activity associated with normal