Anti-UBC4 antibody [EPR11031(B)]

2 product images

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  Western blot - Anti-UBC4 antibody [EPR11031(B)] (ab155088)

  All lanes: Western blot - Anti-UBC4 antibody [EPR11031(B)] (ab155088) at 1/1000 dilution

  Lane 1: MCF7 cell lysate at 10 µg

  Lane 2: HeLa cell lysate at 10 µg

  Lane 3: 293T cell lysate at 10 µg

  Lane 4: Human fetal brain lysate at 10 µg

  Secondary

  All lanes: Goat anti-rabbit HRP at 1/2000 dilution

  Predicted band size: 16 kDa

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  Image collected and cropped by CiteAb under a CC-BY license from the publication

  Western blot - Anti-UBC4 antibody [EPR11031(B)] (ab155088)

  UBC4 western blot using anti-UBC4 antibody [EPR11031(B)] ab155088. Publication image and figure legend from Shi, Y., Yuan, B., et al., 2017, Nat Commun, PubMed 28469175.

  
  

  ab155088 was used in this publication in western blot. This may not be the same as the application(s) guaranteed by Abcam. For a full list of applications guaranteed by Abcam for ab155088 please see the product overview.

  Ub2D3 and Ube2N are required for RIG-I and MAVS activation on virus infection in HEK293T cells.(a,b) The cell-free assay containing vRNA and purified components (E1, Ub, RIG-I and Riplet) was performed as described in Fig. 2b, except that S100 fraction was substituted with purified E2 recombinant proteins as indicated. Each E2 protein was analysed at three different concentrations. Lane 13 did not contain E2 proteins (−E2). (c) HEK293T cells (wild-type and knockout lines) were transfected with or without si-Ube2D3 RNAs. Seventy two hours after transfection, the cells were infected with VSV. Twelve hours post virus infection, the cells were collected for measuring IFN induction by qPCR. *P<0.05 and ***P<0.001. (d,e) Cells were treated as described in c. P5 fractions were isolated to examine MAVS aggregation (d), and whole cell lysate were used to analyse knockdown or knockout effect in genes as indicated (e). The original full blot for (e) can be found in Supplementary Fig. 8d. (f) si-Ube2D3 RNAs were transfected into HEK293T (Ube2N−/−) cells. Seventy two hours after siRNA transfection, the cells were further transfected with pcDNA-flag-Ube2D3 or pcDNA-flag-Ube2N as indicated. Twenty four hours after transfection of pcDNA plasmids, the cells were infected with VSV for another twelve hours. The cells were then collected for analysis of MAVS aggregation. See also Supplementary Fig. 3f.