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品种反应性 主要应用 宿主 格式 抗体类型 R, H, M IHC, WB M Ascites Monoclonal Antibody 描述 产品目录编号 36-009 品牌系列 Upstate
商名 - Upstate
描述 Anti-β-Synuclein Antibody, clone Syn207 产品信息 格式 Ascites 演示 ascites with 0.05% sodium azide 应用 应用 Anti-β-Synuclein Antibody, clone Syn207 is an antibody against β-Synuclein for use in WB, IH. 主要应用 - Immunohistochemistry
- Western Blotting
生物信息 免疫原品种 full length recombinant human β-Synuclein 克隆 clone Syn207 宿主 Mouse 特异性 recombinant β-Synuclein 品种反应性 RatHumanMouse 抗体类型 Monoclonal Antibody Entrez基因编号 - NM_003085.3
- NM_001001502.1
Entrez基因汇总 The protein encoded by this gene is highly homologous to alpha-synuclein. These proteins are abundantly expressed in the brain and putatively inhibit phospholipase D2 selectively. The encoded protein, which may play a role in neuronal plasticity, is abundant in neurofibrillary lesions of patients with Alzheimer disease. This protein has been shown to be highly expressed in the substantia nigra of the brain, a region of neuronal degeneration in patients with Parkinson disease; however, no direct relation to Parkinson disease has been established. Two transcript variants encoding the same protein have been found for this gene. 基因符号 - Beta-synuclein.
- SNCB
- beta-synuclein
纯化方法 Ascites UniProt编号 - Q16143
UniProt汇总 FUNCTION: SwissProt: Q16143 # Non-amyloid component of senile plaques found in Alzheimer disease. Could act as a regulator of SNCA aggregation process. Protects neurons from staurosporine and 6 hydroxy dopamine (6OHDA)-stimulated caspase activation in a p53-dependent manner. Contributes to restore the SNCA anti-apoptotic function abolished by 6OHDA. Not found in the Lewy bodies associated with Parkinson disease.
SIZE: 134 amino acids; 14288 Da
SUBCELLULAR LOCATION: Cytoplasm.
TISSUE SPECIFICITY: Expressed predominantly in brain; concentrated in presynaptic nerve terminals.
PTM: Phosphorylated. Phosphorylation by G-protein coupled receptor kinases (GRK) is more efficient than phosphorylation by CK1, CK2 and CaM-kinase II.
DISEASE: SwissProt: Q16143 # Brain iron accumulation type 1 (NBIA1, also called Hallervorden-Spatz syndrome), a rare neuroaxonal dystrophy, is histologically characterized by axonal spheroids, iron deposition, Lewy body (LB)-like intraneuronal inclusions, glial inclusions and neurofibrillary tangles. SNCB is found in spheroids but not in inclusions.
SIMILARITY: SwissProt: Q16143 ## Belongs to the synuclein family.产品使用声明 质量保证 routinely evaluated by immunoblot lot detected β-Synuclein recombinant protein 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 200 µL
上一件merck millipore产品：merck millipore,默克密理博,MABT147,Anti-MMP-12 (CT) Antibody, clone EP1261Y, rabbit monoclonal
下一件merck millipore产品：merck millipore,默克密理博,AB3265,Anti-Actin γ Antibody
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