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merck millipore,默克密理博,MAB5294-30UL,Anti-Neurofilament 70 kDa Antibody, clone DP5 2.7.3
产品名称:Anti-Neurofilament 70 kDa Antibody, clone DP5 2.7.3
产品型号:MAB5294-30UL
This Anti-Neurofilament 70 kDa Antibody, clone DP5 2.7.3 is validated for use in IH, IH(P) for the detection of Neurofilament 70 kDa.
merck millipore,默克密理博,MAB5294-30UL,Anti-Neurofilament 70 kDa Antibody, clone DP5 2.7.3
- 产品介绍
重要规格表
品种反应性 主要应用 宿主 格式 抗体类型 Po, B, H IHC M Purified Monoclonal Antibody 描述 产品目录编号 MAB5294-30UL 品牌系列 Chemicon®
商名 - Chemicon
描述 Anti-Neurofilament 70 kDa Antibody, clone DP5 2.7.3 背景信息 Neurofilaments are a type of intermediate filament that serve as major elements of the cytoskeleton supporting the axon cytoplasm. They are the most abundant fibrillar components of the axon, being on average 3-10 times more frequent than axonal microtubules. Neurofilaments (10nm in dia.) are built from three intertwined protofibrils which are themselves composed of two tetrameric protofilament complexs of monomeric proteins. The neurofilament triplet proteins (68/70, 160, and 200 kDa) occur in both the central and peripheral nervous system and are usually neuron specific. The 68/70 kDa NF-L protein can self-assemble into a filamentous structure, however the 160 kDa NF-M and 200 kDa NF-H proteins require the presence of the 68/70 kDa NF-L protein to co-assemble. Neuromas, ganglioneuromas, gangliogliomas, ganglioneuroblastomas and neuroblastomas stain positively for neurofilaments. Although typically restricted to neurons, neurofilaments have been detected in paragangliomas and adrenal and extra-adrenal pheochromocytomas. Carcinoids, neuroendocrine carcinomas of the skin, and oat cell carcinomas of the lung also express neurofilaments. For more neurofilament information see Nervous System Cell Type Specific Marker chart online under the CHEMICON Technical Support section. 产品信息 格式 Purified 演示 Liquid. Immunoglobulin purified from ascites fluid. 应用 应用 This Anti-Neurofilament 70 kDa Antibody, clone DP5 2.7.3 is validated for use in IH, IH(P) for the detection of Neurofilament 70 kDa. 主要应用 - Immunohistochemistry
应用说明 Immunohistochemistry on frozen tissue or paraffin embedded tissue sections: 1:100. The antibody should be diluted in PBS containing 2% BSA, 2% normal horse serum and 0.1% Triton X-100.
Optimal working dilutions must be determined by the end user.生物信息 免疫原品种 Neurofilament purified from bovine spinal cord. 表位 Ideal for research on xenograft models 克隆 DP5 2.7.3 宿主 Mouse 特异性 Neurofilament 70 kDa. This antibody recognizes neuroblasts, neurons and peripheral nerves from human, bovine and porcine. It DOES NOT recognize neuroblasts, neurons or peripheral nerves from rodent origin (rat and mouse). 同种型 IgG1 品种反应性 PigBovineHuman 抗体类型 Monoclonal Antibody Entrez基因编号 - NM_006158.2
基因符号 - NF-L
- NEFL
- NF68
- CMT2E
- NFL
- CMT1F
非反应性品种 - Rat
- Mouse
UniProt编号 - P07196
UniProt汇总 FUNCTION: SwissProt: P07196 # Neurofilaments usually contain three intermediate filament proteins: L, M, and H which are involved in the maintenance of neuronal caliber.
SIZE: 543 amino acids; 61517 Da
DOMAIN: SwissProt: P07196 The extra mass and high charge density that distinguish the neurofilament proteins from all other intermediate filament proteins are due to the tailpiece extensions. This region may form a charged scaffolding structure suitable for interaction with other neuronal components or ions.
PTM: O-glycosylated (By similarity).
DISEASE: SwissProt: P07196 # Defects in NEFL are the cause of Charcot-Marie-Tooth disease type 1F (CMT1F) [MIM:607734]. CMT1F is a form of Charcot- Marie-Tooth disease, the most common inherited disorder of the peripheral nervous system. Charcot-Marie-Tooth disease is classified in two main groups on the basis of electrophysiologic properties and histopathology: primary peripheral demyelinating neuropathy or CMT1, and primary peripheral axonal neuropathy or CMT2. Neuropathies of the CMT1 group are characterized by severely reduced nerve conduction velocities (less than 38 m/sec), segmental demyelination and remyelination with onion bulb formations on nerve biopsy, slowly progressive distal muscle atrophy and weakness, absent deep tendon reflexes, and hollow feet. CMT1F is characterized by onset in infancy or childhood (range 1 to 13 years). & Defects in NEFL are the cause of Charcot-Marie-Tooth disease type 2E (CMT2E) [MIM:607684]. CMT2E is an autosomal dominant form of Charcot-Marie-Tooth disease type 2. Neuropathies of the CMT2 group are characterized by signs of axonal regeneration in the absence of obvious myelin alterations, normal or slightly reduced nerve conduction velocities, and progressive distal muscle weakness and atrophy.
SIMILARITY: Belongs to the intermediate filament family.
MISCELLANEOUS: NF-L is the most abundant of the three neurofilament proteins and, as the other nonepithelial intermediate filament proteins, it can form homopolymeric 10-nm filaments.产品使用声明 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 Maintain at -20°C in undiluted aliquots for up to 12 months from date of receipt. Avoid repeated freeze/thaw cycles. 包装信息 数量 30 µL
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