Recombinant Neurofilament (NF-L) Monoclonal Antibody (AN301288L)

For research use only.
Verified Samples | Verified Samples in IHC: Human brain |
Dilution | IHC 1:2000-1:10000 |
Isotype | IgG,κ |
Host | Rabbit |
Reactivity | Human, Mouse, Rat |
Applications | WB, IHC |
Clonality | Monoclonal;Recombinant |
Immunogen | Recombinant Human Neurofilament (NF-L) protein |
Abbre | Neurofilament |
Synonyms | PPP1R, NEFL, CMT1F, CMT2E, NF-L, NF68, NFL, PPP1R110, 68 kDa neurofilament protein, CMTDIG, light polypeptide, neurofilament, neurofilament light, FLJ53642, Neurofilament Light Polypeptide, Neurofilament triplet L protein, 68kDa Neurofilament, 68kDa Neurofilament, CMT1F, CMT2E, FLJ53642, Neurofilament Light Polypeptide, Neurofilament triplet L protein, NFL, NF-L, NF-L |
Swissprot | |
Cellular Localization | Cytoplasmic |
Concentration | 0.2 mg/mL |
Buffer | PBS, 50% glycerol, 0.05% Proclin 300, 0.05% protein protectant. |
Purification Method | Protein A |
Research Areas | Neuroscience, Signal Transduction, Stem Cells, Developmental Biology |
Clone No. | 4D5 |
Conjugation | Unconjugated |
Storage | Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles. |
Shipping | Ice bag |
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. |
Other Clones
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Other Formats
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Unconjugated
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