CD63 Polyclonal Antibody, 20ul[BT-AP02343] Hepatocytes Defects in CLDN19 are the

Defects in CLDN19 are the cause of hypomagnesemia renal with ocular involvement (HOMGO)

CLPTM1 (Cleft Lip And Palate Associated Transmembrane Protein 1) is a Protein Coding gene

including a specific mutation that changes an ATG start codon to AGG

Notch 2 is cleaved in the trans-Golgi network

autosomal dominant non-syndromic sensorineural type 13 deafness (DFNA13)

CD63 Polyclonal Antibody, 20ul[BT-AP02343] Hepatocytes Defects in CLDN19 are theCyclin B1 encoded by CCNB1 is a regulatory protein involved in mitosis. The gene product complexes with p34 (cdc2) to form the maturation promoting factor (MPF). Two alternative transcripts have been found, a constitutively expressed transcript and a cell cycle regulated transcript, that is expressed predominantly during G2 M phase. The different transcripts result from the use of alternate transcription initiation sites.