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Human HSP60 quantitates human HSP60 in serum, plasma, supernatant. The assay will exclusively recognize both natural and recombinant human HSP60.
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.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Gene aliases : CPN60, GROEL, HLD4, HSP-60, HSP60, HSP65, HSPD1, HuCHA60, SPG13
Gene ID : (Human) 3329
Gene symbol : HSPD1
Protein Aliases : 60 kDa chaperonin, 60 kDa heat shock protein, mitochondrial, Chaperonin 60, CPN60, heat shock 60kDa protein 1 (chaperonin), Heat shock protein 60, heat shock protein 65, Heat shock protein family D member 1, HSP-60, HuCHA60, Mitochondrial matrix protein P1, P60 lymphocyte protein, short heat shock protein 60 Hsp60s1
UniProt ID (Human) P10809
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