Neurofilament (ABT208) IHC kit

    • 货号:IHCM6895
    • 应用:IHC
    • 种属:Human;
      • 靶点:
      • NF-L
      • 简介:
      • >>Amyotrophic lateral sclerosis;>>Pathways of neurodegeneration - multiple diseases
      • 基因名称:
      • NEFL NF68 NFL
      • 蛋白名称:
      • Neurofilament
      • Human Gene Id:
      • 4747
      • Human Swiss Prot No:
      • P07196
      • 免疫原:
      • Synthesized peptide derived from human Neurofilament AA range: 400-543
      • 特异性:
      • The antibody can specifically recognize human Neurofilament protein, especilaly NF-L protein.
      • 来源:
      • Mouse, Monoclonal/IgG2b, Kappa
      • 纯化工艺:
      • The antibody was affinity-purified from mouse ascites by affinity-chromatography using specific immunogen.
      • 储存:
      • 2°C to 8°C/1 year
      • 其他名称:
      • Neurofilament light polypeptide (NF-L;68 kDa neurofilament protein;Neurofilament triplet L protein)
      • 背景:
      • Neurofilaments are type IV intermediate filament heteropolymers composed of light, medium, and heavy chains. Neurofilaments comprise the axoskeleton and they functionally maintain the neuronal caliber. They may also play a role in intracellular transport to axons and dendrites. This gene encodes the light chain neurofilament protein. Mutations in this gene cause Charcot-Marie-Tooth disease types 1F (CMT1F) and 2E (CMT2E), disorders of the peripheral nervous system that are characterized by distinct neuropathies. A pseudogene has been identified on chromosome Y. [provided by RefSeq, Oct 2008],
      • 功能:
      • caution:The sequence shown here is derived from an Ensembl automatic analysis pipeline and should be considered as preliminary data.,disease: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 charac
      • 细胞定位:
      • Cytoplasmic
      • 组织表达:
      • Cytoplasmic
      • 产品图片
      • Human appendix tissue was stained with Anti-Neurofilament (ABT208) Antibody
      • Human cerebrum tissue was stained with Anti-Neurofilament (ABT208) Antibody
      • Human hippocampus tissue was stained with Anti-Neurofilament (ABT208) Antibody
      • Human prostatic adenocarcinoma tissue was stained with Anti-Neurofilament (ABT208) Antibody