SNPC4 Polyclonal Antibody, 50ul Miscellaneous CSNB1 is a rare inherited

CSNB1 is a rare inherited retinal disorder characterized by impaired scotopic vision| myopia| hyperopia| nystagmus and reduced visual acuity

the EGF containing fibulin like extracellular matrix protein 1 contains tandemly repeated epidermal growth factor-like repeats followed by a C-terminus fibulin-type domain

members of which are involved in regulated exocytosis of neurotransmitters and hormones

across the plasma membrane

Members of this family are well known for their essential roles as master switches in cell cycle control

SNPC4 Polyclonal Antibody, 50ul Miscellaneous CSNB1 is a rare inheritedThis gene encodes the largest subunit of the small nuclear RNA activating protein (SNAP) complex. The encoded protein contains a Myb DNA binding domain, and is essential for RNA polymerase II and III polymerase transcription from small nuclear RNA promoters. A mutation in this gene is associated with ankylosing spondylitis.