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Key Documents

PLA0269

Sigma-Aldrich

Rabbit anti-HSP60 Antibody, Affinity Purified

Powered by Bethyl Laboratories, Inc.

Sinonimo/i:

60 kDa chaperonin, CPN60, GroEL, HLD4, HSP-60, HSP60, HSP65, Heat shock protein 60, HuCHA60, P60 lymphocyte protein, SPG13, chaperonin 60, heat shock 60kD protein 1 (chaperonin), heat shock 60kDa protein 1 (chaperonin), heat shock protein 65, mitochondrial matrix protein P1, short heat shock protein 60 Hsp60s1, spastic paraplegia 13 (autosomal dominant)

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About This Item

Codice UNSPSC:
12352203
NACRES:
NA.41

Origine biologica

rabbit

Livello qualitativo

Forma dell’anticorpo

affinity purified immunoglobulin

Tipo di anticorpo

primary antibodies

Grado

Powered by Bethyl Laboratories, Inc.

Reattività contro le specie

human, mouse

tecniche

immunohistochemistry: 1:200- 1:1,000
immunoprecipitation (IP): 2-5 μg/mg
western blot: 1:2,000- 1:10,000

Numero d’accesso

NP_002147.2

Condizioni di spedizione

wet ice

Temperatura di conservazione

2-8°C

Informazioni sul gene

rabbit ... HSP60(3329)

Descrizione generale

The HSPD1 (heat shock protein family D member 1) gene encodes the HSP60 (heat shock protein 60) subunit of the HSP60/HSP10 chaperonin complex. The HSPD1 gene consisting of 12 exons is localized to human chromosome 2q33.1.

Immunogeno

The epitope recognized by PLA0269 maps to a region between residue 250 and 300 of human Heat Shock Protein 60 using the numbering given in entry NP_002147.2 (GeneID 3329).

Azioni biochim/fisiol

The protein encoded by the HSPD1 (heat shock protein family D member 1) gene forms a double-barrel chaperonin complex with heat shock protein 10 (HSP10). This chaperonin complex facilitates folding of proteins to their native state in the mitochondrial matrix space. Missense mutation in the HSP60 gene has been associated with a rare dominant form of hereditary spastic paraplegia and a recessively inherited white matter disorder called MitCHAP60 disease.
HSP60 is also found to interact with the transcription factor interferon regulatory factor 3 (IRF3), which is involved in the induction of IFN-β (interferon- β) signaling pathway, a crucial host-protective response.

Stato fisico

Tris-buffered Saline containing 0.1% BSA containing 0.09% Sodium Azide

Altre note

Heat shock protein 60 (HSP60) is a member of the chaperonin family. HSP60 is a mitochondrial protein that may function as a signaling molecule in the innate immune system. It is essential for the folding and assembly of newly imported proteins in the mitochondria. [taken from NCBI Entrez Gene (GeneID: 3329)].

Esclusione di responsabilità

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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Codice della classe di stoccaggio

12 - Non Combustible Liquids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable


Certificati d'analisi (COA)

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Disease-associated mutations in the HSPD1 gene encoding the large subunit of the mitochondrial HSP60/HSP10 chaperonin complex.
Bross P and Paula F G
Frontiers in molecular biosciences, 3, 49-49 (2016)
Xiao-shan Li et al.
PloS one, 9(9), e107507-e107507 (2014-09-11)
Heat shock protein 60 (HSP60) is a chaperonin with essential functions for cell physiology and survival, and its expression correlates with prognosis in a number of malignancies. The aim of this study is to determine the relationship of HSP60 status
Lan Lin et al.
PloS one, 9(12), e114874-e114874 (2014-12-17)
The production of IFN- I (IFN-α/β) is one of the earliest and most important host-protective responses. Interferon regulatory factor 3 (IRF3) is a critical transcriptional factor in the IFN-β signaling pathway. Although significant progress has been achieved in the regulation
Sylvie Bannwarth et al.
Brain : a journal of neurology, 137(Pt 8), 2329-2345 (2014-06-18)
Mitochondrial DNA instability disorders are responsible for a large clinical spectrum, among which amyotrophic lateral sclerosis-like symptoms and frontotemporal dementia are extremely rare. We report a large family with a late-onset phenotype including motor neuron disease, cognitive decline resembling frontotemporal

Articoli

Loading controls in western blotting application.

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