ORAOV1 Polyclonal Antibody, 100ul Dialysis cardiac defects and autonomic dysfunction

cardiac defects and autonomic dysfunction

With 30 rxns per unit and a concentration of 1 rxn/μl

It is an imprinted gene| expressed only from the paternal allele| and epigenetic changes at this locus are associated with Wilms tumour| Beckwith-Wiedemann syndrome| rhabdomyosarcoma| and Silver-Russell syndrome

It has been inferred by analogy with the strikingly similar 3' UTR sequence in mouse laminin gamma 1 cDNA

This protein is involved in central nervous system development

ORAOV1 Polyclonal Antibody, 100ul Dialysis cardiac defects and autonomic dysfunctionSLC22A18 is one of several tumor suppressing subtransferable fragments located in the imprinted gene domain of 11p15. , an important tumor suppressor gene region. Alterations in this region have been associated with the Beckwith Wiedemann syndrome, Wilms tumor, rhabdomyosarcoma, adrenocortical carcinoma, and lung, ovarian, and breast cancer. SLC22A18 is imprinted, with preferential expression from the maternal allele. Mutations in SLC22A18 have been