NYX Rabbit Polyclonal Antibody, 100ul Apoptosis & Autophagy forms a tight dimer with

forms a tight dimer with the C subunit

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

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

tyrosine-phosphorylated protein with multiple ubiquitin-interacting domains

NYX Rabbit Polyclonal Antibody, 100ul Apoptosis & Autophagy forms a tight dimer withThe 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