NYX Rabbit Polyclonal Antibody, 100ul Apoptosis & Autophagy tyrosine-phosphorylated protein with multiple ubiquitin-interacting

tyrosine-phosphorylated protein with multiple ubiquitin-interacting domains

thereby contributing to the inotropic response elicited in heart by beta-agonists

Alternatively spliced transcript variants encoding different isoforms have been described for CNTROB

These isoforms are expressed in a tissue-specific manner and differ significantly in their structure

The SERPINA1 gene is also located on chromosome 14 and

NYX Rabbit Polyclonal Antibody, 100ul Apoptosis & Autophagy tyrosine-phosphorylated protein with multiple ubiquitin-interactingThe product of this gene belongs to the small leucine rich proteoglycan (SLRP) family of proteins. Defects in this gene are the cause of congenital stationary night blindness type 1 (CSNB1) also called X linked congenital stationary night blindness (XLCSNB). CSNB1 is a rare inherited retinal disorder characterized by impaired scotopic vision myopia hyperopia nystagmus and reduced visual acuity. The role of other SLRP proteins suggests that mutations