PUR4 Rabbit Polyclonal Antibody, 100ul Protein Post-translational Modification A related pseudogene has been

A related pseudogene has been identified on chromosome 1

Defects in this gene can also cause cone-rod dystrophy type 11| a disease characterized by the initial degeneration of cone photoreceptor cells and resulting in loss of color vision and visual acuity| followed by the degeneration of rod photoreceptor cells| which progresses to night blindness and the loss of peripheral vision

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including USPs (ubiquitin specific peptidases)

GPR171 is a gene on chromosome 3q25

PUR4 Rabbit Polyclonal Antibody, 100ul Protein Post-translational Modification A related pseudogene has beenPurines are necessary for many cellular processes including DNA replication transcription and energy metabolism. Ten enzymatic steps are required to synthesize inosine monophosphate (IMP) in the de novo pathway of purine biosynthesis. The enzyme encoded by this gene catalyzes the fourth step of IMP biosynthesis.