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Anti neurofilament l

Manufactured by Cell Signaling Technology
Sourced in United States

Anti-Neurofilament-L is a primary antibody product developed by Cell Signaling Technology. It is designed to detect neurofilament light chain (NF-L), a structural protein found in neurons. The antibody can be used in various laboratory techniques, such as western blotting and immunohistochemistry, to study the expression and distribution of NF-L in biological samples.

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4 protocols using anti neurofilament l

1

Ubiquitin Regulation in Neurodegeneration

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15dPGJ2 was purchased from Cayman Chemical (Ann Arbor, MI, USA). Antibody sources were as follows: mouse monoclonal anti-mono- and poly-ubiquitinated proteins antibody (clone FK2) and anti-poly-ubiquitinated proteins antibody (clone FK1) were from Enzo Life Sciences (Plymouth Meeting, PA, USA). Monoclonal anti-ubiquitin antibody was from Covance (Berkeley, CA, USA) and anti-ubiquitin Lys48-specific antibody was from Millipore (Temecula, CA, USA), anti-ubiquitin Lys63-specific antibody was from Abcam (Cambridge, MA, USA); anti-PARP, anti-caspase-3, and anti-Neurofilament-L antibodies were from Cell Signaling (Boston, MA, USA); anti-β-actin antibody and anti-UCH-L1 antibody were from Sigma-Aldrich (St Louis, MO, USA); anti-NeuN antibody was from Millipore; and anti-GAPDH antibody was from Ambion (Grand Island, NY, USA). Cy3- and Alexafluor 488-conjugated secondary antibodies were from Jackson Immunoresearch Lab (West Grove, PA, USA). Ultra performance liquid chromatography organic solvents and water were from VWR (West Chester, PA, USA). The lentiviral expression vector, pLVX-IRES-ZsGreen1 vector, and Lenti-X HTX concentrator and packaging system were purchased from Clontech Laboratories (Mountain View, CA, USA). WST-1 cell proliferation assay kit and Lenti-X 293 T cell line were purchased from Clontech.
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2

In Situ Hybridization and Immunohistochemistry

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In situ hybridization was carried out as described previously (He and Soriano, 2013 (link)). Pten antisense RNA probes was generated using primers: 5-TTACAGTTGGGCCCCGTACA-3 and 5- TAAAACACCCACACAATGACAAGA-3. For immunohistochemistry, samples were sectioned at 10μm and subjected to standard protocols using primary antibodies to anti-phospho-Akt (1:25, Cell Signaling Technology 9271), anti-Neurofilament-L (1:100, Cell Signaling Technology 2837), HRP-conjugated secondary antibody (1:100, Cell Signaling Technology 7074), anti-Sp7(1:200, Abcam ab94744) and AP-conjugated secondary antibody (1:100, Novus Biologicals, NB7157).)
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3

Herbal Material Screening for Neuroprotective Effects

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Herbal materials were purchased from Lee Hoong Kee Limited (Hong Kong) and Eu Yan Sang (Hong Kong). Antibodies including anti-neurofilament-L, anti-neurofilament-M, anti-neurofilament-H, anti-GFAP, anti-βIII-tubulin, anti-β-actin, anti-ChAT, anti-phospho-ERK, anti-ERK, anti-phospho-CREB, and anti-CREB were obtained from Cell Signaling Technology (MA, USA). Chemical markers for high-performance liquid chromatography (HPLC) reference were purchased from Cheungdu Biopurify Phytochemicals Ltd. (China), Fujifilm Wako Chemical Corporation (Japan), and Aobious Inc. (MA, USA). ReNcell culture materials including ReNcell VM neural progenitor cell line (Cat# SCC008) and ReNcell NSC maintenance medium (Cat#SCM005) were purchased from EMD Millipore. Other cell culture materials were purchased from Thermo Fisher Scientific (OH, USA) and Millipore Sigma (MA, USA). SensoLyte®Thioflavin T Aβ42 Aggregation kit (Cat# AS-72214) were purchased from AnaSpec (CA, USA). COX-1 and COX-2 inhibitor screening kits were from BioVision Inc. (CA, USA).
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4

Antibody Panel for Alpha-Synuclein Pathology

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Antibodies used in the present study were as follows. Anti-phospho-α-synuclein antibodies against pSer129 were 81A (Bio Legend) and EP1536Y (abcam). An anti-α-synuclein antibody was Syn202 (Santa Cruz). Anti-NeuN (abcam), anti-synapsin I (abcam), anti-tau (tauC, in house), anti-synaptoporin (Synaptic Syatems), anti-MAP2 (abcam), anti-Neurofilament L (Cell Signaling Technology), anti-inoinized calcium-binding adapter molecule 1 (Iba1) (Wako), anti-glial fibrillary acidic protein (GFAP) (abcam) or anti-2',3'-Cyclic-nucleotide 3'-phosphodiesterase (CNPase) (Cell Signaling Technology) were also used. Alexa488- or Alexa568-conjugated secondary antibodies (Thermo) were used.
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