CD55 Polyclonal Antibody, 100ul[BT-AP01513] Antisense Oligonucleotides Mutations in this gene are

Mutations in this gene are the cause of hyperlipoproteinemia| type 1D

|PTM:TNF-alpha induces a caspase-mediated cleavage of p22 BID into a major p15 and minor p13 and p11 products

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

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

ACTBL2 (Actin

CD55 Polyclonal Antibody, 100ul[BT-AP01513] Antisense Oligonucleotides Mutations in this gene areCD55 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