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

May bind to nascent polypeptide chains as they emerge from the ribosome and block their interaction with the signal recognition particle (SRP)

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

C-type lectin domain family 4 member K encoded by CD207 is expressed only in Langerhans cells which are immature dendritic cells of the epidermis and mucosa

noninsulin-dependent

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