KLF13 (Acetyl Lys166) Rabbit Polyclonal Antibody, 100ul Filtration Mutations in DCLRE1C can cause

Mutations in DCLRE1C can cause Athabascan-type severe combined immunodeficiency (SCIDA) and Omenn syndrome

as well as protein phosphatase calcineurin were found to be involved in the regulation of BCL2 associated agonist of cell death

it was observed that the 3' UTR of this transcript contains a target site for miR29 microRNA

Functions in a multi-protein complex in spermatid maturation

KLF13 (Acetyl Lys166) Rabbit Polyclonal Antibody, 100ul Filtration Mutations in DCLRE1C can causeKLF13 belongs to a family of transcription factors that contain 3 classical zinc finger DNA binding domains consisting of a zinc atom tetrahedrally coordinated by 2 cysteines and 2 histidines (C2H2 motif). These transcription factors bind to GC rich sequences and related GT and CACCC boxes (Scohy et al. 2000