TSSC1 Polyclonal Antibody, 20ul Deep Well Plates Mutations in MYBPC3 are one

Mutations in MYBPC3 are one cause of familial hypertrophic cardiomyopathy

Polymorphisms resulting in amino acid substitutions in these two subunits have been associated with the regulation of blood pressure in an animal model of hypertension

preventing its association with target genes

Demethylation of Lys residue generates formaldehyde and succinate

Altered copy number and activity of this gene have been observed in a number of human cancers

TSSC1 Polyclonal Antibody, 20ul Deep Well Plates Mutations in MYBPC3 are oneTSSC1 (tumor suppressing subtransferable candidate 1) has been reported in PMID 9403053 as one of several tumor suppressing subtransferable fragments located in the imprinted gene domain of 11p15. 5, 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. Alignment of TSSC1 to genomic