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• Rocking motion angle 7°

a highly penetrant familial cancer phenotype usually associated with inherited mutations in TP53

Post-translational modifications such as phosphorylation

Mutations in this gene are associated with 2 neurologic disorders

OPSB Polyclonal Antibody, 20ul Vacuum Aspirator Take control of your experimentsThis 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.