BTBD9 Rabbit Polyclonal Antibody, 100ul Oligo Pool Mutations in this gene may

Mutations in this gene may be associated with susceptibility to carotid artery disease

except during the early phase of chromosome condensation

Ectodomain cleavage of the encoded protein relieves inhibition of Tie2 and is mediated by multiple factors including vascular endothelial growth factor

• Maximum up to 4000rpm Speed can be set in RPM/RCF

Interacts with SMN1 AND GEMIN4

BTBD9 Rabbit Polyclonal Antibody, 100ul Oligo Pool Mutations in this gene mayThis locus encodes a BTB POZ domain containing protein. This domain is known to be involved in protein protein interactions. Polymorphisms at this locus have been reported to be associated with susceptibility to Restless Legs Syndrome and may also be associated with Tourette Syndrome. Alternatively spliced transcript variants have been described.