NUT Polyclonal Antibody, 20ul Enzyme-Linked Immunosorbent Assay (ELISA) PPFIA4| or liprin-alpha-4| belongs to

PPFIA4| or liprin-alpha-4| belongs to the liprin-alpha gene family

This disease is characterized by the lysosomal accumulation and urinary excretion of heparan sulfate

and suggested to be involved in the processes that regulate the differentiation of endothelial cells

providing a molecular signature to distinguish between self and non-self mRNAs by the host during viral infection

Leukocyte Immunoglobulin Like Receptor B3 belongs to the subfamily B class of LIR receptors which contain two or four extracellular immunoglobulin domains

NUT Polyclonal Antibody, 20ul Enzyme-Linked Immunosorbent Assay (ELISA) PPFIA4| or liprin-alpha-4| belongs toA chromosomal aberration involving NUT is found in a rare, aggressive, and lethal carcinoma arising in midline organs of young people. Translocation t(15; 19)(q14; p13) with BRD4 which produces a BRD4 NUT fusion protein.,disease: A chromosomal aberration involving NUT is found in a rare, aggressive, and lethal carcinoma arising in midline organs of young people. Translocation t(15; 9)(q14; q34) with BRD3 which produces a BRD3 NUT fusion protein.,PTM: