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Recommended positive controls: 293T, A431, H1299, HeLa, HepG2, Molt-4, Raji.
Predicted reactivity: Mouse (90%), Rat (91%), Rhesus Monkey (99%).
Store product as a concentrated solution. Centrifuge briefly prior to opening the vial.
FKTN regulates the migration and assembly of neurons during cortical histogenesis. Fukuyama congenital muscular dystrophy results from mutations in its gene.
⚠WARNING: This product can expose you to chemicals including mercury, which is known to the State of California to cause birth defects or other reproductive harm. For more information go to www.P65Warnings.ca.gov.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: Fukutin; Fukuyama type congenital muscular dystrophy protein; Fukuyama-type congenital muscular dystrophy protein; patient fukutin; Ribitol-5-phosphate transferase; Ribitol-5-phosphate transferase FKTN; RP11-235C23.1
Gene Aliases: CMD1X; FCMD; FKTN; LGMD2M; MDDGA4; MDDGB4; MDDGC4
UniProt ID: (Human) O75072
Entrez Gene ID: (Human) 2218
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