"HSPD1" Related Products


Recombinant Human HSPD1

Cat.No.: HSPD1-28422TH
Product Overview: Recombinant full length Human Hsp60, 573 amino acids, MWt: 61kDa;
Description: 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.
Protein length: 573 amino acids
Molecular Weight: 61.000kDa
Source: E. coli
Form: Liquid
Purity: >90% by SDS-PAGE
Storage buffer: Preservative:0.09% Sodium azideConstituents:99% PBS, Phosphate Buffer
Storage: Shipped on dry ice. Upon delivery aliquot and store at -80oC. Avoid freeze / thaw cycles.
Sequence Similarities: Belongs to the chaperonin (HSP60) family.
Gene Name: HSPD1 heat shock 60kDa protein 1 (chaperonin) [ Homo sapiens ]
Official Symbol: HSPD1
Synonyms: HSPD1; heat shock 60kDa protein 1 (chaperonin); heat shock 60kD protein 1 (chaperonin) , spastic paraplegia 13 (autosomal dominant) , SPG13; 60 kDa heat shock protein, mitochondrial; GROEL; HSP60;
Gene ID: 3329
mRNA Refseq: NM_002156
Protein Refseq: NP_002147
MIM: 118190
Uniprot ID: P10809
Chromosome Location: 2q33.1
Pathway: Legionellosis, organism-specific biosystem; Legionellosis, conserved biosystem; RNA degradation, organism-specific biosystem; RNA degradation, conserved biosystem; SIDS Susceptibility Pathways, organism-specific biosystem;
Function: ATP binding; ATPase activity; DNA replication origin binding; cell surface binding; chaperone binding;

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