Recombinant protein products

Name Mouse HSPD1 / HSP60 Protein/重组小鼠HSPD1 / HSP60
Specifications 20ug
Serial number CZDB-011
The price Inquiry
Chinese name Mouse HSPD1 / HSP60 Protein/重组小鼠HSPD1 / HSP60
Molecular nickname HSPD1,, HSP60
Molecular species Mouse
Express label His,S
Express the host E. coli
Concentration > 95 % as determined by SDS-PAGE
Buffer Lyophilized from sterile PBS, pH 7.4
Storage conditions -70°C,应避免反复冻融。
Basic description HSPD1, also known as HSP60, is a member of the chaperonin family. HSPD1 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. It may also prevent misfolding and promote the refolding and proper assembly of unfolded polypeptides generated under stress conditions in the mitochondrial matrix. HSPD1 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. Mutations associated with this gene cause autosomal recessive spastic paraplegia 13.Defects in HSPD1 are a cause of spastic paraplegia autosomal dominant type 13 (SPG13). Spastic paraplegia is a degenerative spinal cord disorder characterized by a slow, gradual, progressive weakness and spasticity of the lower limbs. Defects in HSPD1 are the cause of leukodystrophy hypomyelinating type 4 (HLD4); also called mitochondrial HSP60 chaperonopathy or MitCHAP-60 disease. HLD4 is a severe autosomal recessive hypomyelinating leukodystrophy. HSPD1 is cinically characterized by infantile-onset rotary nystagmus, progressive spastic paraplegia, neurologic regression, motor impairment, profound mental retardation. Death usually occurrs within the first two decades of life.

Collect from

鄂ICP备19022221号-2 Trigoats Co., Ltd.