This Antibody was verified by Relative expression to ensure that the antibody binds to the antigen stated. View Details
Immunogen sequence: YENKGTKQSA MAICQHFYKR GNIYPGNDTF DIDPEIETEC FFVEPDEPFH IGTPAENKLN LTLDFHRLLT VELQFKLKAI NLQTVRHQEL PDCYDFTLT
Highest antigen sequence identity to the following orthologs: Mouse - 89%, Rat - 87%.
Expressed in the cochlea; particularly in the inner and outer hair cells. Defects in Mcoln3 are the cause of the varitin-waddler (Va) phenotype. Classical Va mice exhibit early-onset hearing loss, vestibular defects, pigmentation abnormalities and perinatal lethality. The phenotype varitin-waddler Jackcon (Va-J), which arose in a cross segregating for Va, is similar but less severe. Belongs to the transient receptor family, polycystin subfamily.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: FLJ11006; FLJ36629; MCLN3; Mcoln3 mucolipin 3; MGC124245; MGC124246; MGC71509; Mucolipin-3; Transient receptor potential channel mucolipin 3; TRPML3
Gene Aliases: MCOLN3; TRP-ML3; TRPML3
UniProt ID: (Human) Q8TDD5
Entrez Gene ID: (Human) 55283