Phospho-C/EBP Alpha (S21) Polyclonal Antibody, 20ul Drying & Desiccation Mutations in OCRL cause oculocerebrorenal

Mutations in OCRL cause oculocerebrorenal syndrome of Lowe and also Dent disease

hematopoetic tumors such as B-cell lymphomas

and acts as a positive regulator of p53/TP53 stability

Nop56p is required for assembly of the 60S ribosomal subunit and is involved in pre-rRNA processing

which houses over 1000 genes and comprises nearly 5% of the human genome

Phospho-C/EBP Alpha (S21) Polyclonal Antibody, 20ul Drying & Desiccation Mutations in OCRL cause oculocerebrorenalThis intronless gene (CEBPA) encodes a transcription factor that contains a basic leucine zipper (bZIP) domain and recognizes the CCAAT motif in the promoters of target genes. The encoded protein (CCAAT enhancer binding protein alpha) functions in homodimers and also heterodimers with CCAAT enhancer binding proteins beta and gamma. Activity of this protein can modulate the expression of genes involved in cell cycle regulation as well as in body weight