TRPS1 Polyclonal Antibody, 100ul Cell Culture Flasks |subunit:Interacts with TXNL2/PICOT

|subunit:Interacts with TXNL2/PICOT

Defects in this gene are a cause of benign familial neonatal convulsions type 1 (BFNC)

which is a regulatory complex located on the thin filament of the sarcomere

which contains 6 ATPase subunits and 2 non-ATPase subunits

TRPS1 Polyclonal Antibody, 100ul Cell Culture Flasks |subunit:Interacts with TXNL2/PICOTTRPS1 (transcriptional repressor GATA binding 1) encodes a transcription factor that represses GATA regulated genes and binds to a dynein light chain protein. Binding of the encoded protein to the dynein light chain protein affects binding to GATA consensus sequences and suppresses its transcriptional activity. Defects in TRPS1 are a cause of tricho rhino phalangeal syndrome (TRPS) types I III.