hnRNP K Polyclonal Antibody, 50ul Dialysis Mutations in this gene have

Mutations in this gene have been associated with primary autosomal recessive microcephaly 1 and premature chromosome condensation syndrome

and possesses ubiquitin ligase E3 activity

Mouse studies suggest that this gene functions during normal adipose tissue development and may play a role in human triglyceride metabolism

SERPINB7 (serpin family B member 7) encodes a member of a family of proteins which function as protease inhibitors

hnRNP K Polyclonal Antibody, 50ul Dialysis Mutations in this gene haveHNRNPK belongs to the subfamily of ubiquitously expressed heterogeneous nuclear ribonucleoproteins (hnRNPs). The hnRNPs are RNA binding proteins and they complex with heterogeneous nuclear RNA (hnRNA). These proteins 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 the nucleus and