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

Mutations in ADAMTS2 cause Ehlers-Danlos syndrome type VIIC

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

The encoded protein functions as a chloride channel and controls the regulation of other transport pathways

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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