Eme1 Polyclonal Antibody, 100ul Low retention tips Mutations in ADAMTS2 cause Ehlers-Danlos

Mutations in ADAMTS2 cause Ehlers-Danlos syndrome type VIIC

The protein can inhibit human sperm motility and exhibits antimicrobial activity against E

F2 also plays a role in maintaining vascular integrity during development and postnatal life

Its depletion enhances the cytotoxic action of the chemotherapeutic drugs

This gene encodes a glutamate decarboxylase that catalyzes the deglutamylation of polyglutamylated proteins

Eme1 Polyclonal Antibody, 100ul Low retention tips Mutations in ADAMTS2 cause Ehlers-DanlosEME1 encodes essential meiotic structure specific endonuclease 1 that complexes with methyl methanesulfonate sensitive UV sensitive 81 protein to form an endonuclease complex. The encoded protein interacts with specifc DNA structures including nicked Holliday junctions, 3' flap structures and aberrant replication fork structures. This protein may be involved in repairing DNA damage and in maintaining genomic stability. Alternative splicing results in