s 1000 dapi Search Results


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Proteintech antibodies against dlgap5
Fig. 10 Validation of the role of <t>DLGAP5</t> in PC in vitro. A Expression of DLGAP5 in PC tissues and adjacent normal tissues based on the data from the HPA; B RT-qPCR analysis of DLGAP5 in PC tissues and adjacent normal tissues; C Western blotting analysis of DLGAP5 in PC tis- sues and adjacent normal tissues; D Expression of DLGAP5 in PC cell lines; E RT-qPCR analysis of DLGAP5 in PC cells after transfection with si-circHIF-1α; F Western blotting analysis of DLGAP5 in PC cells after transfection with si-circHIF-1α; G The CCK-8 assay was used to deter- mine the rate of PC cell proliferation after DLGAP5 knockdown; H The changes in cell migration ability were determined through wound healing assays after DLGAP5 knockdown. PC, pancreatic cancer; HPA, human protein atls. *, p < 0.05; **, p < 0.01
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Cell Signaling Technology Inc dapi
Fig. 10 Validation of the role of <t>DLGAP5</t> in PC in vitro. A Expression of DLGAP5 in PC tissues and adjacent normal tissues based on the data from the HPA; B RT-qPCR analysis of DLGAP5 in PC tissues and adjacent normal tissues; C Western blotting analysis of DLGAP5 in PC tis- sues and adjacent normal tissues; D Expression of DLGAP5 in PC cell lines; E RT-qPCR analysis of DLGAP5 in PC cells after transfection with si-circHIF-1α; F Western blotting analysis of DLGAP5 in PC cells after transfection with si-circHIF-1α; G The CCK-8 assay was used to deter- mine the rate of PC cell proliferation after DLGAP5 knockdown; H The changes in cell migration ability were determined through wound healing assays after DLGAP5 knockdown. PC, pancreatic cancer; HPA, human protein atls. *, p < 0.05; **, p < 0.01
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Beijing Solarbio Science dapi
Fig. 10 Validation of the role of <t>DLGAP5</t> in PC in vitro. A Expression of DLGAP5 in PC tissues and adjacent normal tissues based on the data from the HPA; B RT-qPCR analysis of DLGAP5 in PC tissues and adjacent normal tissues; C Western blotting analysis of DLGAP5 in PC tis- sues and adjacent normal tissues; D Expression of DLGAP5 in PC cell lines; E RT-qPCR analysis of DLGAP5 in PC cells after transfection with si-circHIF-1α; F Western blotting analysis of DLGAP5 in PC cells after transfection with si-circHIF-1α; G The CCK-8 assay was used to deter- mine the rate of PC cell proliferation after DLGAP5 knockdown; H The changes in cell migration ability were determined through wound healing assays after DLGAP5 knockdown. PC, pancreatic cancer; HPA, human protein atls. *, p < 0.05; **, p < 0.01
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Ribobio co dapi
Fig. 10 Validation of the role of <t>DLGAP5</t> in PC in vitro. A Expression of DLGAP5 in PC tissues and adjacent normal tissues based on the data from the HPA; B RT-qPCR analysis of DLGAP5 in PC tissues and adjacent normal tissues; C Western blotting analysis of DLGAP5 in PC tis- sues and adjacent normal tissues; D Expression of DLGAP5 in PC cell lines; E RT-qPCR analysis of DLGAP5 in PC cells after transfection with si-circHIF-1α; F Western blotting analysis of DLGAP5 in PC cells after transfection with si-circHIF-1α; G The CCK-8 assay was used to deter- mine the rate of PC cell proliferation after DLGAP5 knockdown; H The changes in cell migration ability were determined through wound healing assays after DLGAP5 knockdown. PC, pancreatic cancer; HPA, human protein atls. *, p < 0.05; **, p < 0.01
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Image Search Results


Fig. 10 Validation of the role of DLGAP5 in PC in vitro. A Expression of DLGAP5 in PC tissues and adjacent normal tissues based on the data from the HPA; B RT-qPCR analysis of DLGAP5 in PC tissues and adjacent normal tissues; C Western blotting analysis of DLGAP5 in PC tis- sues and adjacent normal tissues; D Expression of DLGAP5 in PC cell lines; E RT-qPCR analysis of DLGAP5 in PC cells after transfection with si-circHIF-1α; F Western blotting analysis of DLGAP5 in PC cells after transfection with si-circHIF-1α; G The CCK-8 assay was used to deter- mine the rate of PC cell proliferation after DLGAP5 knockdown; H The changes in cell migration ability were determined through wound healing assays after DLGAP5 knockdown. PC, pancreatic cancer; HPA, human protein atls. *, p < 0.05; **, p < 0.01

Journal: Discover oncology

Article Title: Identification of exosome-related genes associated with prognosis and immune infiltration features in pancreatic cancer.

doi: 10.1007/s12672-025-01961-1

Figure Lengend Snippet: Fig. 10 Validation of the role of DLGAP5 in PC in vitro. A Expression of DLGAP5 in PC tissues and adjacent normal tissues based on the data from the HPA; B RT-qPCR analysis of DLGAP5 in PC tissues and adjacent normal tissues; C Western blotting analysis of DLGAP5 in PC tis- sues and adjacent normal tissues; D Expression of DLGAP5 in PC cell lines; E RT-qPCR analysis of DLGAP5 in PC cells after transfection with si-circHIF-1α; F Western blotting analysis of DLGAP5 in PC cells after transfection with si-circHIF-1α; G The CCK-8 assay was used to deter- mine the rate of PC cell proliferation after DLGAP5 knockdown; H The changes in cell migration ability were determined through wound healing assays after DLGAP5 knockdown. PC, pancreatic cancer; HPA, human protein atls. *, p < 0.05; **, p < 0.01

Article Snippet: The study utilized antibodies against DLGAP5 (1:1000, Cat No: 12038–1-AP, Proteintech, Wuhan, China) and GAPDH (1:50,000, cat no. 60004–1-Ig, Proteintech, Wuhan, China) antibodies were obtained from ABclonal Technology, Wuhan, China.

Techniques: Biomarker Discovery, In Vitro, Expressing, Quantitative RT-PCR, Western Blot, Transfection, CCK-8 Assay, Knockdown, Migration