P311 Polyclonal Antibody, 100ul Cellular Function Assays making them unavailable for display

making them unavailable for display on antigen-presenting cells

however its substrate specificity is currently unknown

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

is retained in cytoplasm by YWHAZ

P311 Polyclonal Antibody, 100ul Cellular Function Assays making them unavailable for displayP311, also known as C5orf13 (chromosome 5 open reading frame 13), D4S114, PTZ17 or PRO1873, is a 68 amino acid cytoplasmic protein involved in cellular differentiation, neural function and axonal regeneration. Found in the granular layer of the cerebellum, P311 is expressed at lower levels in hippocampus, olfactory bulb, kidney, liver and heart and when expressed ectopically, P311 augments giloma motility. P311 is enriched in mice within the