RAI1 Antibody

Defects in Retinoic acid-induced protein 1 (RAI1) are a cause of Smith-Magenis syndrome (SMS) [MIM:182290]. SMS is characterized by congenital mental retardation associated with development and growth delays. The RAI1 has also been associated with schizophrenia [taken from the Universal Protein Resource (UniProt) www.uniprot.org/uniprot/Q7Z5J4].
RAI1
retinoic acid induced 1
Retinoic acid-induced protein 1
:  DKFZP434A139 KIAA1820 MGC12824 SMCR Smith-Magenis syndrome chromosome region SMS
Product
Specifications
Ordering Information
Human
WB, IP, IHC-P
Between 25 and 75
$339
$229
$99