Hsp60 mouse mAb

Heat shock protein family D (Hsp60) member 1 (HSPD1) Homo sapiens This gene encodes a member of the chaperonin family. The encoded mitochondrial protein may function as a signaling molecule in the innate immune system. This protein is essential for the folding and assembly of newly imported proteins in the mitochondria. This gene is adjacent to a related family member and the region between the 2 genes functions as a bidirectional promoter. Several pseudogenes have been associated with this gene. Two transcript variants encoding the same protein have been identified for this gene. Mutations associated with this gene cause autosomal recessive spastic paraplegia 13. [provided by RefSeq, Jun 2010]

60 kDa chaperonin; 60 kDa heat shock protein mitochondrial; 60 kDa heat shock protein, mitochondrial; 60kDa; cb863; CH60_HUMAN; Chaperonin 60; Chaperonin; Chaperonin, 60-KD; CPN 60; CPN60; fa04a05; fb22d10; fi27b05; GROEL; GroEL Homolog; GroEL, E. coli, homolog of; Heat shock 60kD protein 1 (chaperonin); Heat shock 60kD protein 1 chaperonin; heat shock 60kDa protein 1 (chaperonin); Heat shock 60kDa protein 1; Heat shock protein 1 (chaperonin); Heat Shock Protein 60; Heat shock protein 65; HLD4; Hsp 60; HSP 65; HSP-60; HSP60; HSP65; HSPD 1; HSPD1; HuCHA60; id:ibd2197; Mitochondrial matrix protein P1; P60 lymphocyte protein; sb:cb144; Short heat shock protein 60 Hsp60s1; Spastic paraplegia 13 (autosomal dominant); Spastic paraplegia 13; SPG 13; SPG13; wu:fa04a05; wu:fb22d10; wu:fi04a12; wu:fi27b05.