NLRX1 Polyclonal Antibody, 20ul Culture Tubes Mutations in this gene cause

Mutations in this gene cause nemaline myopathy type 3

CD9 encodes a member of the transmembrane 4 superfamily

the ability of CCL4 to bind CCR5 inhibits the cellular entry of M-tropic HIV-1 which utilizes CCR5 as a co-receptor

Hyperphosphorylation of the serine-repeat motif of COL4A3BP/CERT leads to its inactivation by dissociation from the Golgi complex

COL4A1 encodes a type IV collagen alpha protein

NLRX1 Polyclonal Antibody, 20ul Culture Tubes Mutations in this gene causeThe protein encoded by NLRX1 (NLR family member X1) is a member of the NLR family and localizes to the outer mitochondrial membrane. The encoded protein is a regulator of mitochondrial antivirus responses. Three transcript variants encoding the same protein have been found for NLRX1.