SF3b130 Polyclonal Antibody, 20ul Micro Centrifuge Tubes hereditary angioedema and Smith-Lemli-Opitz syndrome

hereditary angioedema and Smith-Lemli-Opitz syndrome are associated with defects in genes that maps to chromosome 11

This gene is one of several homeobox HOXD genes located at 2q31-2q37 chromosome regions

This asymmetry in potassium ion conductance plays a key role in the excitability of muscle cells and neurons

including mouse Mekk2

SF3b130 Polyclonal Antibody, 20ul Micro Centrifuge Tubes hereditary angioedema and Smith-Lemli-Opitz syndromeSF3B3 encodes subunit 3 of the splicing factor 3b protein complex. Splicing factor 3b, together with splicing factor 3a and a 12S RNA unit, forms the U2 small nuclear ribonucleoproteins complex (U2 snRNP). The splicing factor 3b 3a complex binds pre mRNA upstream of the intron's branch site in a sequence independent manner and may anchor the U2 snRNP to the pre mRNA. Splicing factor 3b is also a component of the minor U12 type spliceosome. Subunit 3