储存: -15°C to -25°C/1 year(Do not lower than -25°C)
克隆性: Monoclonal
克隆号: PT1146R
特异性: Endogenous
基因名称: NEFL NF68 NFL
蛋白名称: Neurofilament light polypeptide;NF-L;Neurofilament triplet L protein;68 kDa neurofilament protein;
别名: Neurofilament light polypeptide;NF-L;68 kDa neurofilament protein;Neurofilament triplet L protein;
Organism-1: Human
基因ID-1: 4747
SwissProt-1: P07196
Organism-2: Mouse
基因ID-2: 18039
SwissProt-2: P08551
Organism-3: Rat
基因ID-3: 83613
SwissProt-3: P19527
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],
储存: -15°C to -25°C/1 year(Do not lower than -25°C)
克隆性: Monoclonal
克隆号: PT1146R
特异性: Endogenous
基因名称: NEFL NF68 NFL
蛋白名称: Neurofilament light polypeptide;NF-L;Neurofilament triplet L protein;68 kDa neurofilament protein;
别名: Neurofilament light polypeptide;NF-L;68 kDa neurofilament protein;Neurofilament triplet L protein;
Organism-1: Human
基因ID-1: 4747
SwissProt-1: P07196
Organism-2: Mouse
基因ID-2: 18039
SwissProt-2: P08551
Organism-3: Rat
基因ID-3: 83613
SwissProt-3: P19527
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],