Synphilin-1 Polyclonal Antibody

    • 货号:YT4492
    • 应用:WB;IHC;IF;ELISA
    • 种属:Human;Mouse
      • 靶点:
      • Synphilin-1
      • 简介:
      • >>Parkinson disease;>>Pathways of neurodegeneration - multiple diseases
      • 基因名称:
      • SNCAIP
      • 蛋白名称:
      • Synphilin-1
      • Human Gene Id:
      • 9627
      • Human Swiss Prot No:
      • Q9Y6H5
      • Mouse Swiss Prot No:
      • Q99ME3
      • 免疫原:
      • The antiserum was produced against synthesized peptide derived from human Synphilin-1. AA range:797-846
      • 特异性:
      • Synphilin-1 Polyclonal Antibody detects endogenous levels of Synphilin-1 protein.
      • 组成:
      • Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
      • 来源:
      • Polyclonal, Rabbit,IgG
      • 稀释:
      • WB 1:500 - 1:2000. IHC 1:100 - 1:300. ELISA: 1:10000.. IF 1:50-200
      • 纯化工艺:
      • The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
      • 浓度:
      • 1 mg/ml
      • 储存:
      • -15°C to -25°C/1 year(Do not lower than -25°C)
      • 其他名称:
      • SNCAIP;Synphilin-1;Sph1;Alpha-synuclein-interacting protein
      • 实测条带:
      • 100kD
      • 背景:
      • This gene encodes a protein containing several protein-protein interaction domains, including ankyrin-like repeats, a coiled-coil domain, and an ATP/GTP-binding motif. The encoded protein interacts with alpha-synuclein in neuronal tissue and may play a role in the formation of cytoplasmic inclusions and neurodegeneration. A mutation in this gene has been associated with Parkinson's disease. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2015],
      • 功能:
      • disease:Defects in SNCAIP are a cause of Parkinson disease (PD) [MIM:168600]. 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.,miscellaneous:
      • 细胞定位:
      • Cytoplasm . Detected in cytoplasmic inclusion bodies, together with SNCA.
      • 组织表达:
      • Detected in brain (at protein level). Widely expressed, with highest levels in brain, heart and placenta.
      • 产品图片
      • Western Blot analysis of various cells using Synphilin-1 Polyclonal Antibody
      • Immunohistochemical analysis of paraffin-embedded Human lung cancer. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.
      • Immunohistochemistry analysis of Synphilin-1 antibody in paraffin-embedded lung carcinoma. tissue.
      • Western blot analysis of lysate from COLO205, using Synphilin-1 antibody.