Update README.md

README.md

@@ -33,37 +33,7 @@ model-index:
       type: f1
       value: 0.9282082570673175
 widgets:
-- text: >-
-    Figure 2A. HEK293T cells were transfected with MYC-FOXP3 and FLAG-USP44
-    encoding expression constructs using Polyethylenimine. 48hrs
-    post-transfection, cells were harvested, lysed, and anti-FLAG or anti-MYC
-    antibody coated beads were used to immunoprecipitate the given labeled
-    protein along with its binding partner. Co-IP' ed proteins were subjected to
-    SDS PAGE followed by immunoblot analysis. Antibodies recognizing FLAG or MYC
-    tags were used to probe for USP44 and FOXP3, respectively. B. Endogenous
-    co-IP of USP44 and FOXP3 in murine iTregs. iTregs were generated as in Fig.
-    1 from naïve CD4+T cells FACS isolated from pooled suspensions of the lymph
-    node and spleen cells of wild type C57BL/6 mice (n = 2-3 / experiment).
-    iTregs were lysed and key proteins were immunoprecipitated using either
-    anti-USP44 (right panel) or anti-FOXP3 (left panel) antibody. Proteins
-    pulled-down in this experiment were then resolved and analyzed by immunoblot
-    using anti-FOXP3 or anti-USP44 antibodies. C. Endogenous co-IP of USP44 and
-    FOXP3 in murine nTregs. nTregs (CD4+CD25high) isolated by FACS were
-    activated by anti-CD3 and anti-CD28 (1 and 4 ug/ml, respectively) overnight
-    in the presence of IL-2 (100 U/ml). The cells were lysed and proteins were
-    immunoprecipitated using either anti-Foxp3 (left panel) or anti-Usp44 (right
-    panel). Proteins pulled down in this experiment were then resolved and
-    identified with the indicated antibodies. D . Naïve murine CD4+T cells were
-    isolated by FACS from lymph node and spleen cell suspension of USP44fl/fl
-    CD4Cre+ mice and that of their wild type littermates (USP44fl/fl
-    CD4Cre-mice; n = 2-3 / group / experiment) . iTreg cells were generated from
-    these mice as described for Fig. 1 before incubation on a microscope slide
-    pre-coated with poly-L lysine for 1h. Adhered cells were then fixed by PFA
-    for 0.5 followed by blocking with 1% BSA for 1h, then incubation with the
-    specified antibodies. Representative confocal microscopy images (40X) were
-    visualized for endogenous USP44 (red) and FOXP3 Baxter et al (). DAPI was
-    used to visualize cell nuclei (blue); scale bar 50μm.
-language:
+- text: "Figure 2A. HEK293T cells were transfected with MYC-FOXP3 and FLAG-USP44 encoding expression constructs using Polyethylenimine. 48hrs post-transfection, cells were harvested, lysed, and anti-FLAG or anti-MYC antibody coated beads were used to immunoprecipitate the given labeled protein along with its binding partner. Co-IP' ed proteins were subjected to SDS PAGE followed by immunoblot analysis. Antibodies recognizing FLAG or MYC tags were used to probe for USP44 and FOXP3, respectively. B. Endogenous co-IP of USP44 and FOXP3 in murine iTregs. iTregs were generated as in Fig. 1 from naïve CD4+T cells FACS isolated from pooled suspensions of the lymph node and spleen cells of wild type C57BL/6 mice (n = 2-3 / experiment). iTregs were lysed and key proteins were immunoprecipitated using either anti-USP44 (right panel) or anti-FOXP3 (left panel) antibody. Proteins pulled-down in this experiment were then resolved and analyzed by immunoblot using anti-FOXP3 or anti-USP44 antibodies. C. Endogenous co-IP of USP44 and FOXP3 in murine nTregs. nTregs (CD4+CD25high) isolated by FACS were activated by anti-CD3 and anti-CD28 (1 and 4 ug/ml, respectively) overnight in the presence of IL-2 (100 U/ml). The cells were lysed and proteins were immunoprecipitated using either anti-Foxp3 (left panel) or anti-Usp44 (right panel). Proteins pulled down in this experiment were then resolved and identified with the indicated antibodies. D . Naïve murine CD4+T cells were isolated by FACS from lymph node and spleen cell suspension of USP44fl/fl CD4Cre+ mice and that of their wild type littermates (USP44fl/fl CD4Cre-mice; n = 2-3 / group / experiment) . iTreg cells were generated from these mice as described for Fig. 1 before incubation on a microscope slide pre-coated with poly-L lysine for 1h. Adhered cells were then fixed by PFA for 0.5 followed by blocking with 1% BSA for 1h, then incubation with the specified antibodies. Representative confocal microscopy images (40X) were visualized for endogenous USP44 (red) and FOXP3 Baxter et al (). DAPI was used to visualize cell nuclei (blue); scale bar 50μm."
 - en
 pipeline_tag: token-classification
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