KLHL3 Polyclonal Antibody, 20ul Immunoassays Mutations in this gene can

Mutations in this gene can result in B cell deficiency and agammaglobulinemia

With maximum stability at 2-8℃

This receptor belongs to the subfamily of G-protein coupled receptors which includes AVPR1A

Its main purpose is to provide materials for subsequent experiments such as cloning

which may explain the specific sensitivity of cancer cells to the apoptosis-inducing activity of TRAIL

KLHL3 Polyclonal Antibody, 20ul Immunoassays Mutations in this gene canKLHL3 is ubiquitously expressed and encodes kelch like family member 3 which has an N terminal BTB domain followed by a BACK domain and six kelch like repeats in the C terminus. These kelch like repeats promote substrate ubiquitination of bound proteins via interaction of the BTB domain with the CUL3 (cullin 3) component of a cullin RING E3 ubiquitin ligase (CRL) complex. Muatations in this gene cause pseudohypoaldosteronism type IID (PHA2D); a rare