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DJ-1, Recombinant, Human (PARK7, Parkinson Disease (Autosomal Recessive, Early Onset) 7, FLJ27376, Oncogene DJ1)

Cat no: D3790-02A


Supplier: United States Biological
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Parkinson's disease (PD) is the second most common neurodegenerative disorder after Alzheimer's disease, with a prevalence of 1-2% in population aged 65 years or older. PD is a complex, multifactorial disorder that typically manifests after the age of 50 years. The pathology involves the loss of dopaminergic neurons in the substantia nigra and the presence of Lewy bodies (intraneuronal accumulations of aggregated proteins), in surviving neurons in various areas of the brain. Alpha-synuclein and parkin are thought to be firmly associated with PD. The exact biological function of the DJ-1 protein is currently unknown. It may play a role in the oxidative stress response, and this function could be important in preventing the onset of PD. Defects in PARK7 are the cause of autosomal recessive early-onset Parkinson disease 7 (PARK7). The human DJ-1 protein contains 189aa. DJ-1 may possess an active site and could also be a protease/hydrolase similar to the PfpI proteases. The DJ-1 gene has been highly conserved in evolution. The structures of the mouse and human DJ-1 genes are similar, and human and mouse DJ-1 proteins display 90% aa identity. Source: Recombinant corresponding to 1-190aa from human DJ-1 expressed in E.coli. Molecular Weight: ~20kD Storage and Stability: Aliquot to avoid repeated freezing and thawing and store at -70 degrees C. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.
Catalogue number: D3790-02A
Size: 200ug
Form: Supplied as a lyophilized powder from 20mM Tris, pH8.0, 10mM sodium chloride.
Purity: ~95% (SDS-PAGE)
References: 1. Bonifati V et al. 2004, J. Mol. Med. 82 (3): 163-174. 2. Tao X and Tong L, 2003, J. Biol. Chem. 278 (33): 31372-31379. 3. Bonifati V et al. 2003, Science. 299:256-259.

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