Source: | Mouse | Gene Id: | 4747 |
Isotype: | IgG1 | Swiss Prot: | P07196 |
purity: | Affinity purification |
Background: |
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 |
Reactivity | Human |
Tested applications | WB IHC ELISA IF FC |
Clonality | Monoclonal Antibody |
Calculated MW | 70 kDa |
Recommended Dilutions |
WB 1:500-1:2000
IHC 1:200-1:1000
IF 1:200-1:1000
FC 1:200-1:400
|
Immunogen | A recombinant protein corresponding to human NEFL |
Storage | Store at 4°C. For long term storage store at -20°C in PBS (0.5% protein stabilizer, 0.05% sodium azide). Avoid freeze/thaw cycles. |
Synonym | CMT1F, CMT2E, FLJ53642, NF-L, NF68, NFL |
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