rt2 profiler pcr array for mouse nf-κb signaling pathway  (Qiagen)

Journal: Cell reports

Article Title: Persistence of Integrase-Deficient Lentiviral Vectors correlates with the induction of STING-independent CD8 + T cell responses

doi: 10.1016/j.celrep.2019.01.025

Figure Lengend Snippet: (A) C57BL/6 mice were injected i.v. with PBS or 5×106 TUs IDLV-GFP. Four hours after injection, CD11c+ splenic cells were sorted, and the pathways involved in antiviral responses and NF-κB signaling were analyzed using the RT2 profiler PCR array. The results are expressed as the means ± SEM of fold regulation compared to PBS-injected mice, and represent the cumulative data from two mice from two independent experiments. The green dashed line represents a threshold of two-fold downregulation and the red dashed line represents a threshold of two-fold upregulation. C57BL/6 (B), MAVS−/− (C), STING−/− (D) and CD11c-Cre × Nemo flox (E) mice were injected i.v. with PBS, 106 TUs IDLV-OVA, OVA/5’ppp-dsRNA or OVA/CpG. Seven days (B-E) or one month (B) later, anti-OVA CTL responses were assessed by an in vivo killing assay (left panels) and IFN-γ ELISPOT (right panels). The results are expressed as the percentage of specific lysis for the in vivo killing assay and IFN-γ SFC per 106 splenocytes for ELISPOT. Each dot represents an individual mouse. The results represent the means ± SEM of cumulative data from 3 to 9 mice from two to three independent experiments (B-D) or 2 to 6 mice from two independent experiments (E). Nemo+ mice were born from the crossing of CD11c-Cre littermate non transgenic mice × Nemo flox mice. In contrast, Nemo− mice were born from the crossing of CD11c-Cre transgenic mice × Nemo flox mice. Statistical analysis was performed by unpaired Student’s t-test in comparison with PBS-treated mice or between control and deficient mice, as indicated by the horizontal bars (ns p > 0.05, * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001). See also Figures S7, S8 and S9.

Article Snippet: RNA from purified CD11c + cells was extracted from cell lysates with the RNeasy Plus microkit (QIAGEN, Courtaboeuf, France). cDNA was generated using a RT2 First Strand Kit and quantified using the RT2 Profiler Mouse antiviral responses and NF-κB signaling pathway PCR arrays (SABiosciences, QIAGEN, Courtaboeuf, France), according to the manufacturer’s instructions.

Techniques: Injection, In Vivo, Enzyme-linked Immunospot, Lysis, Transgenic Assay, Mouse Assay

Journal:

Article Title: pVHL acts as an Adapter to Promote the Inhibitory Phosphorylation of the NF-κB Agonist Card9 by CK2

doi: 10.1016/j.molcel.2007.09.010

Figure Lengend Snippet: Table 1

Article Snippet: 2 μg of RNA was used to generate the first strand cDNA using a SuperArray kit (SuperArray Bioscience), which was analyzed by real-time RT-PCR using the SuperArray's RT2 Profiler PCR Array Mouse NF-κB Signaling Pathway plates according to the manufacturer's instructions.

Techniques: