CD56 Polyclonal Antibody, 20ul[BT-AP01981] Culture Media Mutations in the corresponding AQP2

Mutations in the corresponding AQP2 gene cause a rare form of diabetes known as nephrogenic diabetes insipidus

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but the exact function of the encoded protein is unknown

a chromosomal region involved in both translocations and deletions in human malignancies

and may participate in the killing and digestion of engulfed pathogens

CD56 Polyclonal Antibody, 20ul[BT-AP01981] Culture Media Mutations in the corresponding AQP2CLK2 encodes a dual specificity protein kinase that phosphorylates serine threonine and tyrosine containing substrates. Activity of this protein regulates serine and arginine rich (SR) proteins of the spliceosomal complex, thereby influencing alternative transcript splicing. Chromosomal translocations have been characterized between this locus and the PAFAH1B3 (platelet activating factor acetylhydrolase 1b, catalytic subunit 3 (29kDa)) gene on