GRCR1 Rabbit Polyclonal Antibody, 20ul In vitro Transcription Defects in this gene are

Defects in this gene are a cause of congenital secretory sodium diarrhea

Sumoylation may play a role in a wide variety of cellular processes

lung and placenta

May be one regulator of transcriptional events during hemopoietic development

Don't let storage or shipping limitations hold you back from your next scientific breakthrough

GRCR1 Rabbit Polyclonal Antibody, 20ul In vitro Transcription Defects in this gene areThis gene is one of 60 loci associated with autosomal recessive nonsyndromic hearing impairment. This gene encodes a protein which contains GRX like domains; these domains play a role in the S glutathionylation of proteins and may be involved in actin organization in hair cells.