• merck millipore,默克密理博,05-828,Anti-DJ-1 Antibody, clone E.2
  • merck millipore,默克密理博,05-828,Anti-DJ-1 Antibody, clone E.2

    产品名称:Anti-DJ-1 Antibody, clone E.2
    产品型号:05-828
    Detect DJ-1 using this Anti-DJ-1 Antibody, clone E.2 validated for use in WB & IC.

    merck millipore,默克密理博,05-828,Anti-DJ-1 Antibody, clone E.2

  • 产品介绍
  • merck millipore,默克密理博,05-828,Anti-DJ-1 Antibody, clone E.2

    重要规格表

    品种反应性 主要应用 宿主 格式 抗体类型
    HICC, WBMPurifiedMonoclonal Antibody
    描述
    产品目录编号 05-828
    品牌系列 Upstate
    商名
    • Upstate
    描述 Anti-DJ-1 Antibody, clone E.2
    产品信息
    格式 Purified
    演示 0.05% sodium azide before the addition of glycerol to 30%
    应用
    应用 Detect DJ-1 using this Anti-DJ-1 Antibody, clone E.2 validated for use in WB & IC.
    主要应用
    • Immunocytochemistry
    • Western Blotting
    生物信息
    免疫原品种 GST fusion protein corresponding to full length human DJ-1
    克隆 clone E.2
    宿主 Mouse
    特异性 DJ-1
    同种型 IgM
    品种反应性 Human
    抗体类型 Monoclonal Antibody
    Entrez基因编号
    • NM_007262
    Entrez基因汇总 The product of this gene belongs to the peptidase C56 family of proteins. It acts as a positive regulator of androgen receptor-dependent transcription. It may also function as a redox-sensitive chaperone, as a sensor for oxidative stress, and it apparently protects neurons against oxidative stress and cell death. Defects in this gene are the cause of autosomal recessive early-onset Parkinson disease 7. Two transcript variants encoding the same protein have been identified for this gene.
    基因符号
    • DJ-1
    • PARK7
    • FLJ27376
    • DJ1
    纯化方法 Ascites
    UniProt编号
    • Q99497
    UniProt汇总 FUNCTION: SwissProt: Q99497 # Acts as a positive regulator of androgen receptor- dependent transcription. May function as a redox-sensitive chaperone and as a sensor for oxidative stress. Prevents aggregation of SNCA. Protects neurons against oxidative stress and cell death. Plays a role in fertilization. Has no proteolytic activity. Has cell-growth promoting activity and transforming activity.
    SIZE: 189 amino acids; 19891 Da
    SUBUNIT: Homodimer. Binds EFCAB6/DJBP and PIAS2. Part of a ternary complex containing PARK7, EFCAB6/DJBP and AR.
    SUBCELLULAR LOCATION: Nucleus. Cytoplasm. Note=Associated with mitochondria in some cells, particularly after oxidative stress. Detected in tau inclusions in brains from neurodegenerative disease patients.
    TISSUE SPECIFICITY: Highly expressed in pancreas, kidney, skeletal muscle, liver, testis and heart. Detected at slightly lower levels in placenta and brain. Detected in astrocytes, Sertoli cells, spermatogonia, spermatids and spermatozoa.
    PTM: Sumoylated on Lys-130 by PIAS2 or PIAS4; which is enhanced after ultraviolet irradiation and essential for cell-growth promoting activity and transforming activity.
    DISEASE: "SwissProt: Q99497 # Defects in PARK7 are the cause of autosomal recessive early-onset Parkinson disease 7 (PARK7) [MIM:606324, 168600]. Parkinson disease (PD) is a complex, multifactorial disorder that typically manifests after the age of 50 years, although early- onset cases (before 50 years) are known. PD generally arises as a sporadic condition but is occasionally inherited as a simple mendelian trait. Although sporadic and familial PD are very similar, inherited forms of the disease usually begin at earlier ages and are associated with atypical clinical features. PD is characterized by bradykinesia, resting tremor, muscular rigidity and postural instability, as well as by a clinically significant response to treatment with levodopa. 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. PARK7 is characterized by onset before 40 years, slow progression and initial good response to levodopa. & Defects in PARK7 influences susceptibility to amyotrophic lateral sclerosis-parkinsonism/dementia complex type 2 [MIM:105500]; also called amyotrophic lateral sclerosis- parkinsonism/dementia complex of Guam or Guam disease. Amyotrophic lateral sclerosis-parkinsonism/dementia complex type 2 is a neurodengenerative disorder with unusually high incidence among the Chamorro people of the Western Pacific Islands of Guam. Both amyotrophic lateral sclerosis and parkinsonism-dementia are chronic, progressive, and uniformly fatal disorders in this population. Both diseases are known to occur in the same kindred, the same sibship, and even the same individual."
    SIMILARITY: SwissProt: Q99497 ## Belongs to the peptidase C56 family.
    MISCELLANEOUS: Cys-106 is easily oxidized to sulfinic acid.
    产品使用声明
    质量保证 routinely evaluated by immunoblot on RIPA lysates from MCF-7 and LNCaP cells
    使用声明
    • 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.
    储存和货运信息
    存储条件 2 years at -20°C
    包装信息
    数量 100 µL

    merck millipore,默克密理博,05-828,Anti-DJ-1 Antibody, clone E.2

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