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PKC subfamily

disease:Defects in NOTCH1 are a cause of aortic valve disease

an N-terminal DNA-binding domain| a centrally located transcriptional activation domain and a C-terminal domain involved in transcriptional repression

HIST1H1A is intronless and encodes a replication-dependent histone that is a member of the histone H1 family

Kir4.1 Rabbit Polyclonal Antibody, 20ul Serological Pipets Improve your research efficiency andThis gene encodes a member of the inward rectifier type potassium channel family characterized by having a greater tendency to allow potassium to flow into rather than out of a cell. The encoded protein may form a heterodimer with another potassium channel protein and may be responsible for the potassium buffering action of glial cells in the brain. Mutations in this gene have been associated with seizure susceptibility of common idiopathic