53BP1 Polyclonal Antibody, 100ul[BT-AP00041] Filtration It is a type I

It is a type I integral membrane protein with a heavily glycosylated extracellular domain and binds to tissue- and organ-specific lectins or selectins

The main features of this syndrome involve retinal abnormalities| so type XVIII collagen may play an important role in retinal structure and in neural tube closure

it has been shown to play a role in the regulation of embryonic and ocular development

which is an ubiquitin-conjugating enzyme involved in embryonic development

This gene encodes a regulatory subunit of the SMG1 complex

53BP1 Polyclonal Antibody, 100ul[BT-AP00041] Filtration It is a type ITP53BP1 (Tumor Protein P53 Binding Protein 1) is a Protein Coding gene. Diseases associated with TP53BP1 include riddle syndrome and ataxia telangiectasia. Among its related pathways are DNA Damage and ATM Pathway. GO annotations related to this gene include sequence specific DNA binding and p53 binding.