AP2B Rabbit Polyclonal Antibody, 20ul Peptide Library Diseases associated with RGS7 include

Diseases associated with RGS7 include uterine benign neoplasm and reproductive organ benign neoplasm

Genome-wide association studies have linked single nucleotide polymorphisms in an intron of this gene with susceptibilty to type 2 diabetes

Alternative splicing plays a role in modulating the subcellular localization and physiological function of this gene

is transported into the nucleus

the encoded protein is localized to the apical membrane and prevents excretion of glycerol into urine

AP2B Rabbit Polyclonal Antibody, 20ul Peptide Library Diseases associated with RGS7 includeThis gene encodes a member of the AP 2 family of transcription factors. AP 2 proteins form homo or hetero dimers with other AP 2 family members and bind specific DNA sequences. They are thought to stimulate cell proliferation and suppress terminal differentiation of specific cell types during embryonic development. Specific AP 2 family members differ in their expression patterns and binding affinity for different promoters. This protein functions as