ROAA Polyclonal Antibody, 100ul Syringe Filter Mutations in SMARCA4 cause rhabdoid

Mutations in SMARCA4 cause rhabdoid tumor predisposition syndrome type 2

NBPF1 is a member of the neuroblastoma breakpoint family (NBPF) which consists of dozens of recently duplicated genes primarily located in segmental duplications on human chromosome 1

tissue specificity:Widely expressed with highest levels in the heart

in addition

In mitosis RCC1 is phosphorylated at Ser11

ROAA Polyclonal Antibody, 100ul Syringe Filter Mutations in SMARCA4 cause rhabdoidThis gene belongs to the subfamily of ubiquitously expressed heterogeneous nuclear ribonucleoproteins (hnRNPs). The hnRNPs are produced by RNA polymerase II and are components of the heterogeneous nuclear RNA (hnRNA) complexes. They are associated with pre mRNAs in the nucleus and appear to influence pre mRNA processing and other aspects of mRNA metabolism and transport. While all of the hnRNPs are present in the nucleus, some seem to shuttle between