CD55 Polyclonal Antibody, 100ul[BT-AP01513] Antisense Oligonucleotides Heterozygous loss-of-function mutations in this

Heterozygous loss-of-function mutations in this gene result in the dominant In(Lu) blood phenotype

which plays a key role in the malate-aspartate shuttle that allows malate to pass through the mitochondrial membrane to be transformed into oxaloacetate for further cellular processes

This gene encodes an F-box-containing protein that is a component of an SCF-type E3 ubiquitin ligase complex that regulates the onset of cell division

which is the main inhibitory neurotransmitter in the mammalian central nervous system

It is an atypical calpain in that it lacks the calmodulin-like calcium-binding domain and instead has a divergent C-terminal domain

CD55 Polyclonal Antibody, 100ul[BT-AP01513] Antisense Oligonucleotides Heterozygous loss-of-function mutations in thisCD55 encodes a glycoprotein involved in the regulation of the complement cascade. Binding of the encoded protein to complement proteins accelerates their decay, thereby disrupting the cascade and preventing damage to host cells. Antigens present on this protein constitute the Cromer blood group system (CROM). Alternative splicing results in multiple transcript variants. The predominant transcript variant encodes a membrane bound protein, but