OPSB Polyclonal Antibody, 50ul Drying & Desiccation Mutations in CYP7B1 have been

Mutations in CYP7B1 have been associated with hereditary spastic paraplegia (SPG5 or HSP)

|subunit:3 different light chains| LC1| LC2 and LC3| can associate with MAP1A and MAP1B proteins

This gene encodes a component of the motor complex

The protein also acts as an antimicrobial peptide with antibacterial and antifungal activity

is exclusively expressed in testis but it has also been found in a wide variety of cancer tissues and cell lines

OPSB Polyclonal Antibody, 50ul Drying & Desiccation Mutations in CYP7B1 have beenThis gene belongs to the G protein coupled receptor 1 family, opsin subfamily. It encodes the blue cone pigment gene which is one of three types of cone photoreceptors responsible for normal color vision. Defects in this gene are the cause of tritan color blindness (tritanopia). Affected individuals lack blue and yellow sensory mechanisms while retaining those for red and green. Defective blue vision is characteristic.