SWS Rabbit Polyclonal Antibody, 20ul Glassware Diseases associated with SEPT2 include

Diseases associated with SEPT2 include gastrointestinal anthrax and acute orbital inflammation

supports the notion that it is a candidate gene for neuroblastoma

Defects in this gene have been linked to susceptibility to lung cancer type 2 (LNCR2)

sgRNA (single-guide RNA) is a key component in the CRISPR-Cas9 gene-editing system

SWS Rabbit Polyclonal Antibody, 20ul Glassware Diseases associated with SEPT2 includeThis 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.