HBP1(Phospho Ser402) Polyclonal Antibody, 20ul Shakers Mutations in this gene have

Mutations in this gene have been associated with acral peeling skin syndrome

HNRNPA2B1 has been described to generate two alternatively spliced transcript variants which encode different isoforms

It is highly expressed in adrenal gland

Inward rectifier potassium channel 2

The protein encoded by this gene is an integral membrane protein and inward-rectifier type potassium channel

HBP1(Phospho Ser402) Polyclonal Antibody, 20ul Shakers Mutations in this gene haveTranscriptional repressor that binds to the promoter region of target genes. Plays a role in the regulation of the cell cycle and of the Wnt pathway. Binds preferentially to the sequence 5' TTCATTCATTCA 3'. Binding to the H1F0 promoter is enhanced by interaction with RB1. Disrupts the interaction between DNA and TCF4.,Contains 1 AXH domain.,Contains 1 HMG box DNA binding domain.,subunit: Binds the second PAH repeat of SIN3A (By similarity). Binds TCF4