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antibodies against tsp1 a6 1  (Boster Bio)
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<t>TSP1</t> levels in plasma, ascites, and peritoneal exudate cells from mice with ovarian cancer. HM-1 cells were transplanted into the peritoneal cavities of female mice as in , and samples of plasma, ascites, and PECs were collected at the indicated times post-transplantation. A , TSP1 levels in plasma, ascites, and PECs were examined using an immunoblot analysis with the anti-TSP1 antibody. Total proteins on the membranes were stained as described in the , and used for the loading controls. B , TSP1 levels in plasma and ascites were quantified and shown. NS1, not significant versus plasma (day 0). NS2, not significant versus ascites (day 3). C , TSP1 levels in PECs were quantified and shown. ∗ p < 0.01 versus day 0. TSP1, thrombospondin 1.
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<t>TSP1</t> levels in plasma, ascites, and peritoneal exudate cells from mice with ovarian cancer. HM-1 cells were transplanted into the peritoneal cavities of female mice as in , and samples of plasma, ascites, and PECs were collected at the indicated times post-transplantation. A , TSP1 levels in plasma, ascites, and PECs were examined using an immunoblot analysis with the anti-TSP1 antibody. Total proteins on the membranes were stained as described in the , and used for the loading controls. B , TSP1 levels in plasma and ascites were quantified and shown. NS1, not significant versus plasma (day 0). NS2, not significant versus ascites (day 3). C , TSP1 levels in PECs were quantified and shown. ∗ p < 0.01 versus day 0. TSP1, thrombospondin 1.
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mouse anti tsp1 antibody  (Santa Cruz Biotechnology)
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<t>TSP1</t> levels in plasma, ascites, and peritoneal exudate cells from mice with ovarian cancer. HM-1 cells were transplanted into the peritoneal cavities of female mice as in , and samples of plasma, ascites, and PECs were collected at the indicated times post-transplantation. A , TSP1 levels in plasma, ascites, and PECs were examined using an immunoblot analysis with the anti-TSP1 antibody. Total proteins on the membranes were stained as described in the , and used for the loading controls. B , TSP1 levels in plasma and ascites were quantified and shown. NS1, not significant versus plasma (day 0). NS2, not significant versus ascites (day 3). C , TSP1 levels in PECs were quantified and shown. ∗ p < 0.01 versus day 0. TSP1, thrombospondin 1.
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mouse anti tsp1 antibody - by Bioz Stars, 2026-07
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b6 129s2 thbs1 tmlhyn j tsp1 mice  (Jackson Laboratory)
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<t>TSP1</t> levels in plasma, ascites, and peritoneal exudate cells from mice with ovarian cancer. HM-1 cells were transplanted into the peritoneal cavities of female mice as in , and samples of plasma, ascites, and PECs were collected at the indicated times post-transplantation. A , TSP1 levels in plasma, ascites, and PECs were examined using an immunoblot analysis with the anti-TSP1 antibody. Total proteins on the membranes were stained as described in the , and used for the loading controls. B , TSP1 levels in plasma and ascites were quantified and shown. NS1, not significant versus plasma (day 0). NS2, not significant versus ascites (day 3). C , TSP1 levels in PECs were quantified and shown. ∗ p < 0.01 versus day 0. TSP1, thrombospondin 1.
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<t>TSP1</t> levels in plasma, ascites, and peritoneal exudate cells from mice with ovarian cancer. HM-1 cells were transplanted into the peritoneal cavities of female mice as in , and samples of plasma, ascites, and PECs were collected at the indicated times post-transplantation. A , TSP1 levels in plasma, ascites, and PECs were examined using an immunoblot analysis with the anti-TSP1 antibody. Total proteins on the membranes were stained as described in the , and used for the loading controls. B , TSP1 levels in plasma and ascites were quantified and shown. NS1, not significant versus plasma (day 0). NS2, not significant versus ascites (day 3). C , TSP1 levels in PECs were quantified and shown. ∗ p < 0.01 versus day 0. TSP1, thrombospondin 1.
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anti tsp1  (Cell Signaling Technology Inc)
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<t>TSP1</t> levels in plasma, ascites, and peritoneal exudate cells from mice with ovarian cancer. HM-1 cells were transplanted into the peritoneal cavities of female mice as in , and samples of plasma, ascites, and PECs were collected at the indicated times post-transplantation. A , TSP1 levels in plasma, ascites, and PECs were examined using an immunoblot analysis with the anti-TSP1 antibody. Total proteins on the membranes were stained as described in the , and used for the loading controls. B , TSP1 levels in plasma and ascites were quantified and shown. NS1, not significant versus plasma (day 0). NS2, not significant versus ascites (day 3). C , TSP1 levels in PECs were quantified and shown. ∗ p < 0.01 versus day 0. TSP1, thrombospondin 1.
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<t>TSP1</t> levels in plasma, ascites, and peritoneal exudate cells from mice with ovarian cancer. HM-1 cells were transplanted into the peritoneal cavities of female mice as in , and samples of plasma, ascites, and PECs were collected at the indicated times post-transplantation. A , TSP1 levels in plasma, ascites, and PECs were examined using an immunoblot analysis with the anti-TSP1 antibody. Total proteins on the membranes were stained as described in the , and used for the loading controls. B , TSP1 levels in plasma and ascites were quantified and shown. NS1, not significant versus plasma (day 0). NS2, not significant versus ascites (day 3). C , TSP1 levels in PECs were quantified and shown. ∗ p < 0.01 versus day 0. TSP1, thrombospondin 1.
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TSP1 levels in plasma, ascites, and peritoneal exudate cells from mice with ovarian cancer. HM-1 cells were transplanted into the peritoneal cavities of female mice as in , and samples of plasma, ascites, and PECs were collected at the indicated times post-transplantation. A , TSP1 levels in plasma, ascites, and PECs were examined using an immunoblot analysis with the anti-TSP1 antibody. Total proteins on the membranes were stained as described in the , and used for the loading controls. B , TSP1 levels in plasma and ascites were quantified and shown. NS1, not significant versus plasma (day 0). NS2, not significant versus ascites (day 3). C , TSP1 levels in PECs were quantified and shown. ∗ p < 0.01 versus day 0. TSP1, thrombospondin 1.

Journal: The Journal of Biological Chemistry

Article Title: C -mannosyl tryptophan dynamics in a mouse model of the peritoneal dissemination of ovarian cancer

doi: 10.1016/j.jbc.2026.111359

Figure Lengend Snippet: TSP1 levels in plasma, ascites, and peritoneal exudate cells from mice with ovarian cancer. HM-1 cells were transplanted into the peritoneal cavities of female mice as in , and samples of plasma, ascites, and PECs were collected at the indicated times post-transplantation. A , TSP1 levels in plasma, ascites, and PECs were examined using an immunoblot analysis with the anti-TSP1 antibody. Total proteins on the membranes were stained as described in the , and used for the loading controls. B , TSP1 levels in plasma and ascites were quantified and shown. NS1, not significant versus plasma (day 0). NS2, not significant versus ascites (day 3). C , TSP1 levels in PECs were quantified and shown. ∗ p < 0.01 versus day 0. TSP1, thrombospondin 1.

Article Snippet: Antibodies against TSP1 (A6.1) (sc-59887) and CFP (A00852-2) were from Santa Cruz Biotechnology Inc. and BOSTER Biological Technology, respectively.

Techniques: Clinical Proteomics, Transplantation Assay, Western Blot, Staining

C -Man-Trp production in ex vivo -cultured macrophages and myeloid-derived suppressor cells from peritoneal exudate cells of mice with ovarian cancer. HM-1 cells were transplanted into the peritoneal cavities of female mice as in , and PECs were collected 3 days later. Macrophages and MDSCs were isolated from PECs using a fluorescence-activated cell sorter with several specific antibodies as described in the . A , isolated macrophages (CD11b + F4/80 + ) and MDSCs (CD11b + Gr-1 + ) were cultured ex vivo for 8 h as described in the . C -Man-Trp levels were measured in the cell (Cell) and conditioned medium ( Medium ) at the indicated time points. ∗∗ p < 0.05 versus Time (0 h). B , the level of TSP1 secreted into the conditioned medium was examined using an immunoblot analysis at the indicated time points. Band intensity of TSP1 was quantified as described in the . The change of TSP1 level in medium (ΔTSP1) was calculated based on the TSP1 level in preconditioned medium as described in the . ∗ p < 0.01 versus CD11b + GR-1 + (4 and 8 h). ∗∗ p < 0.05 versus CD11b + F4/80 + (4 h). MDSC, myeloid-derived suppressor cell; TSP1, thrombospondin 1.

Journal: The Journal of Biological Chemistry

Article Title: C -mannosyl tryptophan dynamics in a mouse model of the peritoneal dissemination of ovarian cancer

doi: 10.1016/j.jbc.2026.111359

Figure Lengend Snippet: C -Man-Trp production in ex vivo -cultured macrophages and myeloid-derived suppressor cells from peritoneal exudate cells of mice with ovarian cancer. HM-1 cells were transplanted into the peritoneal cavities of female mice as in , and PECs were collected 3 days later. Macrophages and MDSCs were isolated from PECs using a fluorescence-activated cell sorter with several specific antibodies as described in the . A , isolated macrophages (CD11b + F4/80 + ) and MDSCs (CD11b + Gr-1 + ) were cultured ex vivo for 8 h as described in the . C -Man-Trp levels were measured in the cell (Cell) and conditioned medium ( Medium ) at the indicated time points. ∗∗ p < 0.05 versus Time (0 h). B , the level of TSP1 secreted into the conditioned medium was examined using an immunoblot analysis at the indicated time points. Band intensity of TSP1 was quantified as described in the . The change of TSP1 level in medium (ΔTSP1) was calculated based on the TSP1 level in preconditioned medium as described in the . ∗ p < 0.01 versus CD11b + GR-1 + (4 and 8 h). ∗∗ p < 0.05 versus CD11b + F4/80 + (4 h). MDSC, myeloid-derived suppressor cell; TSP1, thrombospondin 1.

Article Snippet: Antibodies against TSP1 (A6.1) (sc-59887) and CFP (A00852-2) were from Santa Cruz Biotechnology Inc. and BOSTER Biological Technology, respectively.

Techniques: Ex Vivo, Cell Culture, Derivative Assay, Isolation, Fluorescence, Western Blot