Arthritis Research: Methods and Protocols by Shunichi Shiozawa
By Shunichi Shiozawa
Arthritis study: tools and Protocols, moment variation expands upon thefirst variation to provide new and present concepts for the learn of arthritis and similar stipulations. A compendium of leaders within the box give a contribution chapters that disguise functional learn tools comparable to the intravital multiphoton microscopy procedure, thoughts for comparing exhausted CD8 T phone and for learning nucleic acid sensors and their results, tools for in vivo tetracycline-controlled transgenic mice and T telephone receptor transgenic mice, protocols to discover V(D)J recombination items and microRNA, and the strategy to make bleomycin-induced dermal fibrosis. Written within the winning Methods in Molecular Biology sequence structure, chapters contain introductions to their respective themes, lists of the mandatory fabrics and reagents, step by step, quite simply reproducible protocols, and notes on troubleshooting and warding off recognized pitfalls.
Authoritative and simply obtainable, Arthritis learn: equipment and Protocols, moment variation will serve either execs and newbies with state of the art strategies touching on this attention-grabbing learn field.
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Extra resources for Arthritis Research: Methods and Protocols
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Human IL-1β: IL-1β, Human, ELISA Kit (R&D Systems). 3 Methods Carry out all procedures at room temperature unless otherwise specified. 1 Extracellular RNA/DNA Stimulation 1. 7 cells) or 5–10 × 105 cells (primary CD14+ monocytes) in 12-well plate in 500 μl of culture medium with serum but without antibiotics and grown overnight. 2. 5–50 μg of RNA/DNA ligands are suspended in 500 μl of culture medium (see Note 5). IFNA1 IFNA4 IFNB1 CXCL10 TNF IL6 OAS2 ISG15 ACTB GAPDH Ifna4 Ifnb1 Cxcl10 Tnf Il6 Oas1 Isg15 Actb Gapdh Human Murine TGATGAGCTACTACTGGTCAGC GAGCTCCAAGAAAGGACGAAC CCAAGTGCTGCCGTCATTTTC CCCTCACACTCAGATCATCTTCT TAGTCCTTCCTACCCCAATTTCC TGTCCTGGGTCATGTTAATAC AGCAATGGCCTGGGACCTAAA GCTCCCCGGGCTGTATTCC AGGTCGGTGTGAACGGATTTG GCCTCGCCCTTTGCTTTACT ACCTGGTTCAACATGGAAATG ATGACCAACAAGTGTCTCCTCC GTGGCATTCAAGGAGTACCTC ATGAGCACTGAAAGCATGATCC AACCTGAACCTTCCAAAGATGG AACTGCTTCCGACAATCAAC GAGAGGCAGCGAACTCATCT CATGTACGTTGCTATCCAGGC CATGAGAAGTATGACAACAGCCT Gene symbol Forward primer (5′–3′) Species GATCTCTTAGCACAAGGATGGC GGCAGTGTAACTCTTCTGCAT GGCTCGCAGGGATGATTTCAA GCTACGACGTGGGCTACAG TTGGTCCTTAGCCACTCCTTC CCGTGAAGCAGGTAGAGA AGCCGGCACACCAATCTT CTCTCTTGCTCTGGGCCTCGT TGTAGACCATGTAGTTGAGGTCA CTGTGGGTCTCAGGGAGATCA ACCAAGCTTCTTCACACTGCT GCTCATGGAAAGAGCTGTAGTG GCCTTCGATTCTGGATTCAGACA GAGGGCTGATTAGAGAGAGGTC TCTGGCTTGTTCCTCACTACT CCTCCTTCTCCCTCCAAAA CTTCAGCTCTGACACCGACA CTCCTTAATGTCACGCACGAT AGTCCTTCCACGATACCAAAGT Reverse primer (5′–3′) Table 2 Oligonucleotides used for the amplification of human and murine genes J Immunol 2010, 185:6146–6156 J Immunol 2010, 185:6146–6156 Nucl Acid Res 2012, 40:D1144–D1149 Infect Immun 2005, 73:3990–3998 J Immunol 2008, 181:2723–2731 J Immunol 2008, 180:2474–2485 J Virol 2006, 80:4501–4509 J Virol 2006, 80:4501–4509 J Immunol 2010, 185:6146–6156 Nat Immunol 2011, 12:37–44 Nat Immunol 2011, 12:37–44 Nat Immunol 2011, 12:37–44 Nat Immunol 2011, 12:37–44 Nat Immunol 2011, 12:37–44 Nat Immunol 2011, 12:37–44 J Immunol 2003, 170:749–756 Breast Cancer Res 2008, 10:R58 Nat Immunol 2011, 12:37–44 Nat Immunol 2011, 12:37–44 References Characterization of Innate Immune Signalings Stimulated by Ligands for Pattern… 27 28 Takeshi Kameyama and Akinori Takaoka 3.
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