DQ2, Dystonia 1, Dystonia 1 protein, Dyt1, Tor1a, Torsin A, Torsin family 1 member A, TOR1A_HUMAN.
A mutation of the DYT1 gene, which codes for TorsinA, has been identified as the cause of one form of autosomal dominantly inherited dystonia. Early-onset torsion dystonia is a movement disorder, characterized by twisting muscle contractures, that begins
Clonality:
Polyclonal
Concentration:
1ug/ul
Buffer:
Aqueous buffered solution containing 0.01M TBS (pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
Source:
KLH conjugated synthetic peptide derived from human Torsin A
