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H7158

Sigma-Aldrich

Heat Shock Protein 60 human

recombinant, expressed in E. coli, buffered aqueous solution, ≥95% (SDS-GE)

Sinónimos:

HSP 60

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About This Item

Código UNSPSC:
12352202

origen biológico

human

recombinante

expressed in E. coli

Ensayo

≥95% (SDS-GE)

Formulario

buffered aqueous solution

Nº de acceso UniProt

Condiciones de envío

dry ice

temp. de almacenamiento

−70°C

Información sobre el gen

human ... HSPD1(3329)

Descripción general

The gene HSP60 (heat shock protein 60) is mapped to human chromosome 2q33.1. It is a mitochondrial protein. HSP60 is induced under various stress conditions, including DNA damage, oxidative stress and heat shock. HSP60 is also referred to as HSPD1 (heat shock protein family D member 1).

Acciones bioquímicas o fisiológicas

HSP60 (heat shock protein) works together with the cochaperonin HSP10 to allow protein folding of mitochondrial-imported proteins. It is involved in brain myelination and pathogenesis of hypomyelinating neurodegenerative disease. It also enhances proinflammatory response in cells, including macrophages, dendritic cells and endothelial cells. Mutation in HSP60 is linked with hereditary spastic paraplegia (SPG13).

Forma física

Solution in Dulbecco′s buffered saline

Código de clase de almacenamiento

12 - Non Combustible Liquids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable


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Piotr Bodzek et al.
Journal of ovarian research, 7, 30-30 (2014-03-13)
The aim of this study was to evaluate the concentrations of IgG antibodies against Hsp60 and Hsp65 in sera of patients with ovarian cancer at various stages of clinical progress and for different histopathological types of disease. Serum samples from
Antonella Marino Gammazza et al.
Scientific reports, 5, 9434-9434 (2015-03-25)
The mitochondrial chaperonin Hsp60 is a ubiquitous molecule with multiple roles, constitutively expressed and inducible by oxidative stress. In the brain, Hsp60 is widely distributed and has been implicated in neurological disorders, including epilepsy. A role for mitochondria and oxidative
S Jindal et al.
Molecular and cellular biology, 9(5), 2279-2283 (1989-05-01)
The complete cDNA for a human mitochondrial protein designated P1, which was previously identified as a microtubule-related protein, has been cloned and sequenced. The deduced amino acid sequence of P1 shows strong homology (40 to 50% identical residues and an
Daniella Magen et al.
American journal of human genetics, 83(1), 30-42 (2008-06-24)
Hypomyelinating leukodystrophies (HMLs) are disorders involving aberrant myelin formation. The prototype of primary HMLs is the X-linked Pelizaeus-Merzbacher disease (PMD) caused by mutations in PLP1. Recently, homozygous mutations in GJA12 encoding connexin 47 were found in patients with autosomal-recessive Pelizaeus-Merzbacher-like
Jens Jacob Hansen et al.
American journal of human genetics, 70(5), 1328-1332 (2002-03-19)
SPG13, an autosomal dominant form of pure hereditary spastic paraplegia, was recently mapped to chromosome 2q24-34 in a French family. Here we present genetic data indicating that SPG13 is associated with a mutation, in the gene encoding the human mitochondrial

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