Review



cell transfection pdac cells  (ATCC)


Bioz Verified Symbol ATCC is a verified supplier
Bioz Manufacturer Symbol ATCC manufactures this product  
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
    • 99
      Buy from Supplier

    Structured Review

    ATCC cell transfection pdac cells
    Cell Transfection Pdac Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 8175 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/human+pdac+tissue+array/PANC-1/pm36781839-48-5-27
    Average 99 stars, based on 8175 article reviews
    cell transfection pdac cells - by Bioz Stars, 2026-11
    99/100 stars

    Images

    Related Articles

    Cell Culture:

    Article Title: Targeting IGF2BP1 Creates a Mitotic Vulnerability in Colorectal Carcinoma
    Article Snippet: PrePrint: ining the highest absolute ranking score. Gene sets containing 15–500 genes were tested, and Benjamini–Hochberg-adjusted P values below 0.05 were considered significant. Cell lines were purchased from ATCC in 2024. Cells were tested regularly for mycoplasma by PCR. SW480 (CCL-228) and HT-29 (HTB-38) cells were cultured in RPMI-1640, SW1463 (CCL-234) in DMEM/Ham’s F-12, and PANC-1 (CRL-1469) and HEK

    Article Title: Intratumoral Fusobacterium nucleatum promotes ferroptosis resistance and a disulfide-stress-associated vulnerability under glucose restriction.
    Article Snippet: The human ESCC cell line E109 (CCTCC, Cat. No. GDC0207), kyse30 (a gift from Professor Musheng Zheng, SYSUCC, Guangzhou, China), the human breast cancer cell line 231 (ATCC, Cat. No. HTB-26), and the human pancreatic cancer cell line PANC-1 (ATCC, Cat. No. CRL-1469) were maintained at 37 °C in a humidified atmosphere containing 5% CO2.. E109 and kyse30 cells were cultured in RPMI 1640 medium, whereas 231 and PANC-1 cells were cultured in DMEM medium.E109 and kyse30 cells were cultured in RPMI 1640 medium, whereas 231 and PANC-1 cells were cultured in DMEM medium.

    Article Title: Nanoparticles improve targeting and efficacy of endocytosis inhibitors
    Article Snippet: SH-SY5Y cells were maintained in DMEM/F-12 medium (Gibco, New York, NY) supplemented with 10% fetal bovine serum (FBS; Gibco, New York, NY) and 1% Penicillin-Streptomycin (Corning, Kennebunk, ME), whereas A549 and BEAS-2B cells were cultured in DMEM (Gibco, New York, NY) containing 10% FBS and 1% Penicillin-Streptomycin under standard conditions.maintained in DMEM/F-12 medium (Gibco, New York, NY) supplemented with 10% fetal bovine serum (FBS; Gibco, New York, NY) and 1% Penicillin-Streptomycin (Corning, Kennebunk, ME), whereas A549 and BEAS-2B cells were cultured in DMEM (Gibco, New York, NY) containing 10% FBS and 1% Penicillin-Streptomycin under standard conditions. ... In addition, glioblastoma cell lines A-172 (ATCC, CRL-1620) and U-87 MG (ATCC, HTB-14), as well as the pancreatic carcinoma cell line PANC-1 (ATCC, CRL-1469), were included to broaden the cellular models of cytotoxicity.. Cells were cultured in cell culture flasks (Sarstedt, Numbrecht, Germany) at 37 °C, in an atmosphere containing 5% CO 2 , until they reached 90–95% subconfluence.Cells were cultured in cell culture flasks (Sarstedt, Numbrecht, Germany) at 37 °C, in an atmosphere containing 5% CO 2 , until they reached 90–95% subconfluence.

    Article Title: Targeting SERPINB5 and MSLN for Pancreatic Cancer Therapy.
    Article Snippet: HEK293T cells (RRID: CVCL_0063), BxPC-3 (RRID: CVCL_0186), CFPAC-1 (RRID: CVCL_1119), PANC-1 (RRID: CVCL_0480), and MIA PaCa-2 (RRID: CVCL_0428) cell lines were purchased from the American Type Culture Collection (ATCC) (Manassas, VA, USA).. Hs766T (RRID: CVCL_0334), AsPC-1 (RRID: CVCL_0152), and Capan-1 (RRID: CVCL_0237) were purchased from the Tissue Culture Facility (TCF) at MUSC.Hs766T (RRID: CVCL_0334), AsPC-1 (RRID: CVCL_0152), and Capan-1 (RRID: CVCL_0237) were purchased from the Tissue Culture Facility (TCF) at MUSC.

    Article Title: Macrophage-Fibroblast Crosstalk Governs Tumor Mechanics, as Revealed by Spatiotemporal Force Mapping in 3D Spheroids.
    Article Snippet: Materials andMethods .1 Cell Culture ouse CT26 colorectal carcinoma cells were a kind gift from r. Hawinkels, Leiden University Medical Centre, The Netherands.Materials andMethods .1 Cell Culture ouse CT26 colorectal carcinoma cells were a kind gift from r. Hawinkels, Leiden University Medical Centre, The Netherands.. 3T3 fibroblasts (#ATCC CRL-1658), murine macrophages AW264.7 (#ATCC TIB-71), human PANC-1 PDAC cells (#ATCC RL-1469), and THP-1 cells (#ATCCTIB-202) were obtained from he American Type Culture Collection (ATCC, Manassas, VA, SA).. Human pancreatic stellate cells (hPSCs) were obtained rom ScienCell (Carlsbad, USA).Human pancreatic stellate cells (hPSCs) were obtained rom ScienCell (Carlsbad, USA).

    Article Title: p38α Signaling Is Associated with Pancreatic Ductal Adenocarcinoma Progression and Represents a Potential Therapeutic Vulnerability.
    Article Snippet: Human pancreatic cancer cell lines AsPC-1, Mia PaCa-2, BxPC3, Capan-1, and PANC1 were obtained from the American Type Culture Collection (ATCC, Manassas, VA, USA).. HPDE was purchased from Sigma (SCC442, Sigma-Aldrich, Milan, Italy).HPDE was purchased from Sigma (SCC442, Sigma-Aldrich, Milan, Italy).

    Article Title: An intron retention-derived secreted Endoglin Isoform as a circulating biomarker in pancreatic ductal adenocarcinoma.
    Article Snippet: Human PDAC cell lines Mia PaCa-2, Capan-1, and Panc1 were purchased from ATCC, while murine KPC-derived PDAC cells, were a generous gift from Dr. David Kashatus (University of Virginia).. Cell lines were maintained in DMEM or RPMI 1640 supplemented with 10% fetal bovine serum and cultured at 37 C in 5% CO2.Cell lines were maintained in DMEM or RPMI 1640 supplemented with 10% fetal bovine serum and cultured at 37 C in 5% CO2.

    Polymerase Chain Reaction:

    Article Title: Targeting IGF2BP1 Creates a Mitotic Vulnerability in Colorectal Carcinoma
    Article Snippet: PrePrint: ining the highest absolute ranking score. Gene sets containing 15–500 genes were tested, and Benjamini–Hochberg-adjusted P values below 0.05 were considered significant. Cell lines were purchased from ATCC in 2024. Cells were tested regularly for mycoplasma by PCR. SW480 (CCL-228) and HT-29 (HTB-38) cells were cultured in RPMI-1640, SW1463 (CCL-234) in DMEM/Ham’s F-12, and PANC-1 (CRL-1469) and HEK

    Article Title: Intratumoral Fusobacterium nucleatum promotes ferroptosis resistance and a disulfide-stress-associated vulnerability under glucose restriction.
    Article Snippet: The human ESCC cell line E109 (CCTCC, Cat. No. GDC0207), kyse30 (a gift from Professor Musheng Zheng, SYSUCC, Guangzhou, China), the human breast cancer cell line 231 (ATCC, Cat. No. HTB-26), and the human pancreatic cancer cell line PANC-1 (ATCC, Cat. No. CRL-1469) were maintained at 37 °C in a humidified atmosphere containing 5% CO2.. E109 and kyse30 cells were cultured in RPMI 1640 medium, whereas 231 and PANC-1 cells were cultured in DMEM medium.E109 and kyse30 cells were cultured in RPMI 1640 medium, whereas 231 and PANC-1 cells were cultured in DMEM medium.

    Article Title: Nanoparticles improve targeting and efficacy of endocytosis inhibitors
    Article Snippet: SH-SY5Y cells were maintained in DMEM/F-12 medium (Gibco, New York, NY) supplemented with 10% fetal bovine serum (FBS; Gibco, New York, NY) and 1% Penicillin-Streptomycin (Corning, Kennebunk, ME), whereas A549 and BEAS-2B cells were cultured in DMEM (Gibco, New York, NY) containing 10% FBS and 1% Penicillin-Streptomycin under standard conditions.maintained in DMEM/F-12 medium (Gibco, New York, NY) supplemented with 10% fetal bovine serum (FBS; Gibco, New York, NY) and 1% Penicillin-Streptomycin (Corning, Kennebunk, ME), whereas A549 and BEAS-2B cells were cultured in DMEM (Gibco, New York, NY) containing 10% FBS and 1% Penicillin-Streptomycin under standard conditions. ... In addition, glioblastoma cell lines A-172 (ATCC, CRL-1620) and U-87 MG (ATCC, HTB-14), as well as the pancreatic carcinoma cell line PANC-1 (ATCC, CRL-1469), were included to broaden the cellular models of cytotoxicity.. Cells were cultured in cell culture flasks (Sarstedt, Numbrecht, Germany) at 37 °C, in an atmosphere containing 5% CO 2 , until they reached 90–95% subconfluence.Cells were cultured in cell culture flasks (Sarstedt, Numbrecht, Germany) at 37 °C, in an atmosphere containing 5% CO 2 , until they reached 90–95% subconfluence.

    Article Title: Targeting SERPINB5 and MSLN for Pancreatic Cancer Therapy.
    Article Snippet: HEK293T cells (RRID: CVCL_0063), BxPC-3 (RRID: CVCL_0186), CFPAC-1 (RRID: CVCL_1119), PANC-1 (RRID: CVCL_0480), and MIA PaCa-2 (RRID: CVCL_0428) cell lines were purchased from the American Type Culture Collection (ATCC) (Manassas, VA, USA).. Hs766T (RRID: CVCL_0334), AsPC-1 (RRID: CVCL_0152), and Capan-1 (RRID: CVCL_0237) were purchased from the Tissue Culture Facility (TCF) at MUSC.Hs766T (RRID: CVCL_0334), AsPC-1 (RRID: CVCL_0152), and Capan-1 (RRID: CVCL_0237) were purchased from the Tissue Culture Facility (TCF) at MUSC.

    Article Title: Macrophage-Fibroblast Crosstalk Governs Tumor Mechanics, as Revealed by Spatiotemporal Force Mapping in 3D Spheroids.
    Article Snippet: Materials andMethods .1 Cell Culture ouse CT26 colorectal carcinoma cells were a kind gift from r. Hawinkels, Leiden University Medical Centre, The Netherands.Materials andMethods .1 Cell Culture ouse CT26 colorectal carcinoma cells were a kind gift from r. Hawinkels, Leiden University Medical Centre, The Netherands.. 3T3 fibroblasts (#ATCC CRL-1658), murine macrophages AW264.7 (#ATCC TIB-71), human PANC-1 PDAC cells (#ATCC RL-1469), and THP-1 cells (#ATCCTIB-202) were obtained from he American Type Culture Collection (ATCC, Manassas, VA, SA).. Human pancreatic stellate cells (hPSCs) were obtained rom ScienCell (Carlsbad, USA).Human pancreatic stellate cells (hPSCs) were obtained rom ScienCell (Carlsbad, USA).

    Article Title: p38α Signaling Is Associated with Pancreatic Ductal Adenocarcinoma Progression and Represents a Potential Therapeutic Vulnerability.
    Article Snippet: Human pancreatic cancer cell lines AsPC-1, Mia PaCa-2, BxPC3, Capan-1, and PANC1 were obtained from the American Type Culture Collection (ATCC, Manassas, VA, USA).. HPDE was purchased from Sigma (SCC442, Sigma-Aldrich, Milan, Italy).HPDE was purchased from Sigma (SCC442, Sigma-Aldrich, Milan, Italy).

    Article Title: An intron retention-derived secreted Endoglin Isoform as a circulating biomarker in pancreatic ductal adenocarcinoma.
    Article Snippet: Human PDAC cell lines Mia PaCa-2, Capan-1, and Panc1 were purchased from ATCC, while murine KPC-derived PDAC cells, were a generous gift from Dr. David Kashatus (University of Virginia).. Cell lines were maintained in DMEM or RPMI 1640 supplemented with 10% fetal bovine serum and cultured at 37 C in 5% CO2.Cell lines were maintained in DMEM or RPMI 1640 supplemented with 10% fetal bovine serum and cultured at 37 C in 5% CO2.

    Food & Beverages:

    Article Title: Targeting IGF2BP1 Creates a Mitotic Vulnerability in Colorectal Carcinoma
    Article Snippet: PrePrint: ining the highest absolute ranking score. Gene sets containing 15–500 genes were tested, and Benjamini–Hochberg-adjusted P values below 0.05 were considered significant. Cell lines were purchased from ATCC in 2024. Cells were tested regularly for mycoplasma by PCR. SW480 (CCL-228) and HT-29 (HTB-38) cells were cultured in RPMI-1640, SW1463 (CCL-234) in DMEM/Ham’s F-12, and PANC-1 (CRL-1469) and HEK

    Article Title: Intratumoral Fusobacterium nucleatum promotes ferroptosis resistance and a disulfide-stress-associated vulnerability under glucose restriction.
    Article Snippet: The human ESCC cell line E109 (CCTCC, Cat. No. GDC0207), kyse30 (a gift from Professor Musheng Zheng, SYSUCC, Guangzhou, China), the human breast cancer cell line 231 (ATCC, Cat. No. HTB-26), and the human pancreatic cancer cell line PANC-1 (ATCC, Cat. No. CRL-1469) were maintained at 37 °C in a humidified atmosphere containing 5% CO2.. E109 and kyse30 cells were cultured in RPMI 1640 medium, whereas 231 and PANC-1 cells were cultured in DMEM medium.E109 and kyse30 cells were cultured in RPMI 1640 medium, whereas 231 and PANC-1 cells were cultured in DMEM medium.

    Article Title: Nanoparticles improve targeting and efficacy of endocytosis inhibitors
    Article Snippet: SH-SY5Y cells were maintained in DMEM/F-12 medium (Gibco, New York, NY) supplemented with 10% fetal bovine serum (FBS; Gibco, New York, NY) and 1% Penicillin-Streptomycin (Corning, Kennebunk, ME), whereas A549 and BEAS-2B cells were cultured in DMEM (Gibco, New York, NY) containing 10% FBS and 1% Penicillin-Streptomycin under standard conditions.maintained in DMEM/F-12 medium (Gibco, New York, NY) supplemented with 10% fetal bovine serum (FBS; Gibco, New York, NY) and 1% Penicillin-Streptomycin (Corning, Kennebunk, ME), whereas A549 and BEAS-2B cells were cultured in DMEM (Gibco, New York, NY) containing 10% FBS and 1% Penicillin-Streptomycin under standard conditions. ... In addition, glioblastoma cell lines A-172 (ATCC, CRL-1620) and U-87 MG (ATCC, HTB-14), as well as the pancreatic carcinoma cell line PANC-1 (ATCC, CRL-1469), were included to broaden the cellular models of cytotoxicity.. Cells were cultured in cell culture flasks (Sarstedt, Numbrecht, Germany) at 37 °C, in an atmosphere containing 5% CO 2 , until they reached 90–95% subconfluence.Cells were cultured in cell culture flasks (Sarstedt, Numbrecht, Germany) at 37 °C, in an atmosphere containing 5% CO 2 , until they reached 90–95% subconfluence.

    Article Title: Targeting SERPINB5 and MSLN for Pancreatic Cancer Therapy.
    Article Snippet: HEK293T cells (RRID: CVCL_0063), BxPC-3 (RRID: CVCL_0186), CFPAC-1 (RRID: CVCL_1119), PANC-1 (RRID: CVCL_0480), and MIA PaCa-2 (RRID: CVCL_0428) cell lines were purchased from the American Type Culture Collection (ATCC) (Manassas, VA, USA).. Hs766T (RRID: CVCL_0334), AsPC-1 (RRID: CVCL_0152), and Capan-1 (RRID: CVCL_0237) were purchased from the Tissue Culture Facility (TCF) at MUSC.Hs766T (RRID: CVCL_0334), AsPC-1 (RRID: CVCL_0152), and Capan-1 (RRID: CVCL_0237) were purchased from the Tissue Culture Facility (TCF) at MUSC.

    Article Title: Macrophage-Fibroblast Crosstalk Governs Tumor Mechanics, as Revealed by Spatiotemporal Force Mapping in 3D Spheroids.
    Article Snippet: Materials andMethods .1 Cell Culture ouse CT26 colorectal carcinoma cells were a kind gift from r. Hawinkels, Leiden University Medical Centre, The Netherands.Materials andMethods .1 Cell Culture ouse CT26 colorectal carcinoma cells were a kind gift from r. Hawinkels, Leiden University Medical Centre, The Netherands.. 3T3 fibroblasts (#ATCC CRL-1658), murine macrophages AW264.7 (#ATCC TIB-71), human PANC-1 PDAC cells (#ATCC RL-1469), and THP-1 cells (#ATCCTIB-202) were obtained from he American Type Culture Collection (ATCC, Manassas, VA, SA).. Human pancreatic stellate cells (hPSCs) were obtained rom ScienCell (Carlsbad, USA).Human pancreatic stellate cells (hPSCs) were obtained rom ScienCell (Carlsbad, USA).

    Article Title: p38α Signaling Is Associated with Pancreatic Ductal Adenocarcinoma Progression and Represents a Potential Therapeutic Vulnerability.
    Article Snippet: Human pancreatic cancer cell lines AsPC-1, Mia PaCa-2, BxPC3, Capan-1, and PANC1 were obtained from the American Type Culture Collection (ATCC, Manassas, VA, USA).. HPDE was purchased from Sigma (SCC442, Sigma-Aldrich, Milan, Italy).HPDE was purchased from Sigma (SCC442, Sigma-Aldrich, Milan, Italy).

    Article Title: An intron retention-derived secreted Endoglin Isoform as a circulating biomarker in pancreatic ductal adenocarcinoma.
    Article Snippet: Human PDAC cell lines Mia PaCa-2, Capan-1, and Panc1 were purchased from ATCC, while murine KPC-derived PDAC cells, were a generous gift from Dr. David Kashatus (University of Virginia).. Cell lines were maintained in DMEM or RPMI 1640 supplemented with 10% fetal bovine serum and cultured at 37 C in 5% CO2.Cell lines were maintained in DMEM or RPMI 1640 supplemented with 10% fetal bovine serum and cultured at 37 C in 5% CO2.

    Sterility:

    Article Title: Targeting IGF2BP1 Creates a Mitotic Vulnerability in Colorectal Carcinoma
    Article Snippet: PrePrint: ining the highest absolute ranking score. Gene sets containing 15–500 genes were tested, and Benjamini–Hochberg-adjusted P values below 0.05 were considered significant. Cell lines were purchased from ATCC in 2024. Cells were tested regularly for mycoplasma by PCR. SW480 (CCL-228) and HT-29 (HTB-38) cells were cultured in RPMI-1640, SW1463 (CCL-234) in DMEM/Ham’s F-12, and PANC-1 (CRL-1469) and HEK

    Article Title: Intratumoral Fusobacterium nucleatum promotes ferroptosis resistance and a disulfide-stress-associated vulnerability under glucose restriction.
    Article Snippet: The human ESCC cell line E109 (CCTCC, Cat. No. GDC0207), kyse30 (a gift from Professor Musheng Zheng, SYSUCC, Guangzhou, China), the human breast cancer cell line 231 (ATCC, Cat. No. HTB-26), and the human pancreatic cancer cell line PANC-1 (ATCC, Cat. No. CRL-1469) were maintained at 37 °C in a humidified atmosphere containing 5% CO2.. E109 and kyse30 cells were cultured in RPMI 1640 medium, whereas 231 and PANC-1 cells were cultured in DMEM medium.E109 and kyse30 cells were cultured in RPMI 1640 medium, whereas 231 and PANC-1 cells were cultured in DMEM medium.

    Article Title: Nanoparticles improve targeting and efficacy of endocytosis inhibitors
    Article Snippet: SH-SY5Y cells were maintained in DMEM/F-12 medium (Gibco, New York, NY) supplemented with 10% fetal bovine serum (FBS; Gibco, New York, NY) and 1% Penicillin-Streptomycin (Corning, Kennebunk, ME), whereas A549 and BEAS-2B cells were cultured in DMEM (Gibco, New York, NY) containing 10% FBS and 1% Penicillin-Streptomycin under standard conditions.maintained in DMEM/F-12 medium (Gibco, New York, NY) supplemented with 10% fetal bovine serum (FBS; Gibco, New York, NY) and 1% Penicillin-Streptomycin (Corning, Kennebunk, ME), whereas A549 and BEAS-2B cells were cultured in DMEM (Gibco, New York, NY) containing 10% FBS and 1% Penicillin-Streptomycin under standard conditions. ... In addition, glioblastoma cell lines A-172 (ATCC, CRL-1620) and U-87 MG (ATCC, HTB-14), as well as the pancreatic carcinoma cell line PANC-1 (ATCC, CRL-1469), were included to broaden the cellular models of cytotoxicity.. Cells were cultured in cell culture flasks (Sarstedt, Numbrecht, Germany) at 37 °C, in an atmosphere containing 5% CO 2 , until they reached 90–95% subconfluence.Cells were cultured in cell culture flasks (Sarstedt, Numbrecht, Germany) at 37 °C, in an atmosphere containing 5% CO 2 , until they reached 90–95% subconfluence.

    Article Title: Targeting SERPINB5 and MSLN for Pancreatic Cancer Therapy.
    Article Snippet: HEK293T cells (RRID: CVCL_0063), BxPC-3 (RRID: CVCL_0186), CFPAC-1 (RRID: CVCL_1119), PANC-1 (RRID: CVCL_0480), and MIA PaCa-2 (RRID: CVCL_0428) cell lines were purchased from the American Type Culture Collection (ATCC) (Manassas, VA, USA).. Hs766T (RRID: CVCL_0334), AsPC-1 (RRID: CVCL_0152), and Capan-1 (RRID: CVCL_0237) were purchased from the Tissue Culture Facility (TCF) at MUSC.Hs766T (RRID: CVCL_0334), AsPC-1 (RRID: CVCL_0152), and Capan-1 (RRID: CVCL_0237) were purchased from the Tissue Culture Facility (TCF) at MUSC.

    Article Title: Macrophage-Fibroblast Crosstalk Governs Tumor Mechanics, as Revealed by Spatiotemporal Force Mapping in 3D Spheroids.
    Article Snippet: Materials andMethods .1 Cell Culture ouse CT26 colorectal carcinoma cells were a kind gift from r. Hawinkels, Leiden University Medical Centre, The Netherands.Materials andMethods .1 Cell Culture ouse CT26 colorectal carcinoma cells were a kind gift from r. Hawinkels, Leiden University Medical Centre, The Netherands.. 3T3 fibroblasts (#ATCC CRL-1658), murine macrophages AW264.7 (#ATCC TIB-71), human PANC-1 PDAC cells (#ATCC RL-1469), and THP-1 cells (#ATCCTIB-202) were obtained from he American Type Culture Collection (ATCC, Manassas, VA, SA).. Human pancreatic stellate cells (hPSCs) were obtained rom ScienCell (Carlsbad, USA).Human pancreatic stellate cells (hPSCs) were obtained rom ScienCell (Carlsbad, USA).

    Article Title: p38α Signaling Is Associated with Pancreatic Ductal Adenocarcinoma Progression and Represents a Potential Therapeutic Vulnerability.
    Article Snippet: Human pancreatic cancer cell lines AsPC-1, Mia PaCa-2, BxPC3, Capan-1, and PANC1 were obtained from the American Type Culture Collection (ATCC, Manassas, VA, USA).. HPDE was purchased from Sigma (SCC442, Sigma-Aldrich, Milan, Italy).HPDE was purchased from Sigma (SCC442, Sigma-Aldrich, Milan, Italy).

    Article Title: An intron retention-derived secreted Endoglin Isoform as a circulating biomarker in pancreatic ductal adenocarcinoma.
    Article Snippet: Human PDAC cell lines Mia PaCa-2, Capan-1, and Panc1 were purchased from ATCC, while murine KPC-derived PDAC cells, were a generous gift from Dr. David Kashatus (University of Virginia).. Cell lines were maintained in DMEM or RPMI 1640 supplemented with 10% fetal bovine serum and cultured at 37 C in 5% CO2.Cell lines were maintained in DMEM or RPMI 1640 supplemented with 10% fetal bovine serum and cultured at 37 C in 5% CO2.



    Similar Products

    human pdac tissue array  (Biomax Inc)
    86
    Biomax Inc human pdac tissue array
    (A) Representative IHC staining <t>of</t> <t>ITGB3</t> in <t>PDAC</t> tissue microarrays (TMA) showing varying expression levels in non-cancer and cancer tissue sections. (B). High magnification IHC images demonstrating the expression of ITGB3 on normal pancreas and cancer cells with stromal regions. (D-I) . Scatter plots depicting the correlation between ITGB3 and key tumor-associated markers such as HIF-1α (D) , GLUT-1 (E) , VEGFA (F) , Vimentin (G) , COL1A1 (H) , and PECAM1 (I) . Pearson correlation coefficients (R) and p -values indicate statistically significant positive correlation between ITGB3 and these markers. Statistical significance was assessed using a two-tailed unpaired Student’s t-test. All quantitative data represent the mean ± SEM. ∗∗∗∗p < 0.0001.
    Human Pdac Tissue Array, supplied by Biomax Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/human+pdac+tissue+array/array+slides+tissue/bio_rxiv__64898__2026__01__15__699725-59-16-21
    Average 86 stars, based on 1 article reviews
    human pdac tissue array - by Bioz Stars, 2026-11
    86/100 stars
    		  Buy from Supplier
    human pdac tissue array  (TissueArray.com LLC)
    90
    TissueArray.com LLC human pdac tissue array
    (A) Representative IHC staining <t>of</t> <t>ITGB3</t> in <t>PDAC</t> tissue microarrays (TMA) showing varying expression levels in non-cancer and cancer tissue sections. (B). High magnification IHC images demonstrating the expression of ITGB3 on normal pancreas and cancer cells with stromal regions. (D-I) . Scatter plots depicting the correlation between ITGB3 and key tumor-associated markers such as HIF-1α (D) , GLUT-1 (E) , VEGFA (F) , Vimentin (G) , COL1A1 (H) , and PECAM1 (I) . Pearson correlation coefficients (R) and p -values indicate statistically significant positive correlation between ITGB3 and these markers. Statistical significance was assessed using a two-tailed unpaired Student’s t-test. All quantitative data represent the mean ± SEM. ∗∗∗∗p < 0.0001.
    Human Pdac Tissue Array, supplied by TissueArray.com LLC, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/human+pdac+tissue+array/human+pancreatic+cancer+tissue+array/pm39048609-54-1-9
    Average 90 stars, based on 1 article reviews
    human pdac tissue array - by Bioz Stars, 2026-11
    90/100 stars
    		  Buy from Supplier
    the human pdac tissue array  (TissueArray.com LLC)
    90
    TissueArray.com LLC the human pdac tissue array
    STING expression in <t>human</t> <t>PDAC</t> stroma and CAFs. ( a ) Groups categorized by positive, weakly positive, and negative STING expression in PDAC stroma. Representative IHC analysis of STING using a human PDAC tissue array (scale bar, 100 μm). ( b ) Percentages of the indicated groups in 40 PDAC samples. ( c ) Co-immunofluorescence staining for α-SMA (red) and STING (green) in STING positive or weakly positive or negative in stroma. ( d ) 5-AZA (0.1 nM) was administered to CAF1 and CAF2 derived from murine PDACs and incubated for 24 h.
    The Human Pdac Tissue Array, supplied by TissueArray.com LLC, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/human+pdac+tissue+array/human+pancreatic+cancer+tissue+array/pmc11269671-39-1-9
    Average 90 stars, based on 1 article reviews
    the human pdac tissue array - by Bioz Stars, 2026-11
    90/100 stars
    		  Buy from Supplier
    human pdac tissue array  (U.S Biomax Inc)
    90
    U.S Biomax Inc human pdac tissue array
    <t>a,</t> <t>Immunohistochemistry</t> staining of LPAR4 in a <t>PDAC</t> tissue array consisted of 15 PDAC samples and 4 samples of normal pancreas. Scale bar is 50 μM. Representative images showing normal pancreas (n=4 biological samples), low-LPAR4 PDAC (n=9 biological samples), and high-LPAR4 PDAC (n=6 biological samples). Bar graph shows the relative percentage of LPAR4-low and LPAR4-high patients in the PDAC tissue array. b, Quantitative RT-PCR confirming the manipulation of LPAR4 expression in 2 pancreatic cancer cell lines (Colo-357, MIA PaCa-2) and 2 patient-derived cancer cells (79E, 34E). Data were shown as mean ± s.d. (n=4 independent experiments for Colo-357 and 79E cells with LPAR4 stable knockdown, n=3 for Colo-357, 79E, and MiaPaCa2 cells with LPAR4 ectopic expression, n=3 for 34E cells with LPAR4 stable knockdown, and n=4 for 34E with LPAR4 ectopic expression). c, Non-invasive Bioluminescence images showing tumors formed at day 10 for Colo-357+sh-CTRL+luciferase or Colo-357+sh-R4.1+luciferase of various number implanted in the pancreas of nu/nu mice. Right panel showing the luminescence intensity in a blue-to-red spectrum. d, f, Trypan blue exclusion assay showing the relative number of viable cells with or without LPAR4 expression manipulation grown in 10% serum and 2D at day 4 and day 7. e, Tumor growth rates for 1 million Colo-357 cells with or without LPAR4 expression manipulation in a subcutaneous tumor model. Data were presented as mean ± s.d. for n=8 independent samples for each group. g, Quantitative RT-PCR confirming the knockdown of LPAR1 in Colo-357 cells. h, Effects of LPAR1 knockdown using siRNA on 2D or 3D (methylcellulose sphere forming) cell growth. Data were presented as mean ± s.d. for n=3 independent experiments (d,f,g, and h). Statistical analyses were performed using two tailed unpaired one sample t-test (b,g, and h) and one-way ANOVA (d-f). Source numerical data are available in source data.
    Human Pdac Tissue Array, supplied by U.S Biomax Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/human+pdac+tissue+array/human+pancreatic+cancer+tissue+arrays/pmc10280815-636-7-11
    Average 90 stars, based on 1 article reviews
    human pdac tissue array - by Bioz Stars, 2026-11
    90/100 stars
    		  Buy from Supplier
    human pancreas cancer tissue array including 20 pdacs  (Pantomics Inc)
    90
    Pantomics Inc human pancreas cancer tissue array including 20 pdacs
    <t>a,</t> <t>Immunohistochemistry</t> staining of LPAR4 in a <t>PDAC</t> tissue array consisted of 15 PDAC samples and 4 samples of normal pancreas. Scale bar is 50 μM. Representative images showing normal pancreas (n=4 biological samples), low-LPAR4 PDAC (n=9 biological samples), and high-LPAR4 PDAC (n=6 biological samples). Bar graph shows the relative percentage of LPAR4-low and LPAR4-high patients in the PDAC tissue array. b, Quantitative RT-PCR confirming the manipulation of LPAR4 expression in 2 pancreatic cancer cell lines (Colo-357, MIA PaCa-2) and 2 patient-derived cancer cells (79E, 34E). Data were shown as mean ± s.d. (n=4 independent experiments for Colo-357 and 79E cells with LPAR4 stable knockdown, n=3 for Colo-357, 79E, and MiaPaCa2 cells with LPAR4 ectopic expression, n=3 for 34E cells with LPAR4 stable knockdown, and n=4 for 34E with LPAR4 ectopic expression). c, Non-invasive Bioluminescence images showing tumors formed at day 10 for Colo-357+sh-CTRL+luciferase or Colo-357+sh-R4.1+luciferase of various number implanted in the pancreas of nu/nu mice. Right panel showing the luminescence intensity in a blue-to-red spectrum. d, f, Trypan blue exclusion assay showing the relative number of viable cells with or without LPAR4 expression manipulation grown in 10% serum and 2D at day 4 and day 7. e, Tumor growth rates for 1 million Colo-357 cells with or without LPAR4 expression manipulation in a subcutaneous tumor model. Data were presented as mean ± s.d. for n=8 independent samples for each group. g, Quantitative RT-PCR confirming the knockdown of LPAR1 in Colo-357 cells. h, Effects of LPAR1 knockdown using siRNA on 2D or 3D (methylcellulose sphere forming) cell growth. Data were presented as mean ± s.d. for n=3 independent experiments (d,f,g, and h). Statistical analyses were performed using two tailed unpaired one sample t-test (b,g, and h) and one-way ANOVA (d-f). Source numerical data are available in source data.
    Human Pancreas Cancer Tissue Array Including 20 Pdacs, supplied by Pantomics Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/human+pdac+tissue+array/pancreatic+cancer+tissue+array/pmc09763154-101-8-15
    Average 90 stars, based on 1 article reviews
    human pancreas cancer tissue array including 20 pdacs - by Bioz Stars, 2026-11
    90/100 stars
    		  Buy from Supplier
    human pdac tissue array  (BioChain Institute)
    90
    BioChain Institute human pdac tissue array
    <t>a,</t> <t>Immunohistochemistry</t> staining of LPAR4 in a <t>PDAC</t> tissue array consisted of 15 PDAC samples and 4 samples of normal pancreas. Scale bar is 50 μM. Representative images showing normal pancreas (n=4 biological samples), low-LPAR4 PDAC (n=9 biological samples), and high-LPAR4 PDAC (n=6 biological samples). Bar graph shows the relative percentage of LPAR4-low and LPAR4-high patients in the PDAC tissue array. b, Quantitative RT-PCR confirming the manipulation of LPAR4 expression in 2 pancreatic cancer cell lines (Colo-357, MIA PaCa-2) and 2 patient-derived cancer cells (79E, 34E). Data were shown as mean ± s.d. (n=4 independent experiments for Colo-357 and 79E cells with LPAR4 stable knockdown, n=3 for Colo-357, 79E, and MiaPaCa2 cells with LPAR4 ectopic expression, n=3 for 34E cells with LPAR4 stable knockdown, and n=4 for 34E with LPAR4 ectopic expression). c, Non-invasive Bioluminescence images showing tumors formed at day 10 for Colo-357+sh-CTRL+luciferase or Colo-357+sh-R4.1+luciferase of various number implanted in the pancreas of nu/nu mice. Right panel showing the luminescence intensity in a blue-to-red spectrum. d, f, Trypan blue exclusion assay showing the relative number of viable cells with or without LPAR4 expression manipulation grown in 10% serum and 2D at day 4 and day 7. e, Tumor growth rates for 1 million Colo-357 cells with or without LPAR4 expression manipulation in a subcutaneous tumor model. Data were presented as mean ± s.d. for n=8 independent samples for each group. g, Quantitative RT-PCR confirming the knockdown of LPAR1 in Colo-357 cells. h, Effects of LPAR1 knockdown using siRNA on 2D or 3D (methylcellulose sphere forming) cell growth. Data were presented as mean ± s.d. for n=3 independent experiments (d,f,g, and h). Statistical analyses were performed using two tailed unpaired one sample t-test (b,g, and h) and one-way ANOVA (d-f). Source numerical data are available in source data.
    Human Pdac Tissue Array, supplied by BioChain Institute, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/human+pdac+tissue+array/Monkey+Tissue+Array+-+22+types+of+cyno+monkey+normal+tissues+covering+all+major+organs/pmc07766822-273-13-17
    Average 90 stars, based on 1 article reviews
    human pdac tissue array - by Bioz Stars, 2026-11
    90/100 stars
    		  Buy from Supplier

    Image Search Results


    (A) Representative IHC staining of ITGB3 in PDAC tissue microarrays (TMA) showing varying expression levels in non-cancer and cancer tissue sections. (B). High magnification IHC images demonstrating the expression of ITGB3 on normal pancreas and cancer cells with stromal regions. (D-I) . Scatter plots depicting the correlation between ITGB3 and key tumor-associated markers such as HIF-1α (D) , GLUT-1 (E) , VEGFA (F) , Vimentin (G) , COL1A1 (H) , and PECAM1 (I) . Pearson correlation coefficients (R) and p -values indicate statistically significant positive correlation between ITGB3 and these markers. Statistical significance was assessed using a two-tailed unpaired Student’s t-test. All quantitative data represent the mean ± SEM. ∗∗∗∗p < 0.0001.

    Journal: bioRxiv

    Article Title: ProAgio, a Novel Integrin αvβ3 Targeted Cytotoxin, Suppresses Tumor Growth and Reprograms the PDAC Microenvironment

    doi: 10.64898/2026.01.15.699725

    Figure Lengend Snippet: (A) Representative IHC staining of ITGB3 in PDAC tissue microarrays (TMA) showing varying expression levels in non-cancer and cancer tissue sections. (B). High magnification IHC images demonstrating the expression of ITGB3 on normal pancreas and cancer cells with stromal regions. (D-I) . Scatter plots depicting the correlation between ITGB3 and key tumor-associated markers such as HIF-1α (D) , GLUT-1 (E) , VEGFA (F) , Vimentin (G) , COL1A1 (H) , and PECAM1 (I) . Pearson correlation coefficients (R) and p -values indicate statistically significant positive correlation between ITGB3 and these markers. Statistical significance was assessed using a two-tailed unpaired Student’s t-test. All quantitative data represent the mean ± SEM. ∗∗∗∗p < 0.0001.

    Article Snippet: To evaluate the role of ITGB3 in PDAC, we analyzed its expression using IHC in a human PDAC tissue array (PA483-L97, Biomax) that contains 40 cancer and eight non-cancer tissues ( Supplementary Table 1 ).

    Techniques: Immunohistochemistry, Expressing, Two Tailed Test

    STING expression in human PDAC stroma and CAFs. ( a ) Groups categorized by positive, weakly positive, and negative STING expression in PDAC stroma. Representative IHC analysis of STING using a human PDAC tissue array (scale bar, 100 μm). ( b ) Percentages of the indicated groups in 40 PDAC samples. ( c ) Co-immunofluorescence staining for α-SMA (red) and STING (green) in STING positive or weakly positive or negative in stroma. ( d ) 5-AZA (0.1 nM) was administered to CAF1 and CAF2 derived from murine PDACs and incubated for 24 h.

    Journal: Scientific Reports

    Article Title: Activation of STING in pancreatic cancer-associated fibroblasts exerts an antitumor effect by enhancing tumor immunity

    doi: 10.1038/s41598-024-68061-y

    Figure Lengend Snippet: STING expression in human PDAC stroma and CAFs. ( a ) Groups categorized by positive, weakly positive, and negative STING expression in PDAC stroma. Representative IHC analysis of STING using a human PDAC tissue array (scale bar, 100 μm). ( b ) Percentages of the indicated groups in 40 PDAC samples. ( c ) Co-immunofluorescence staining for α-SMA (red) and STING (green) in STING positive or weakly positive or negative in stroma. ( d ) 5-AZA (0.1 nM) was administered to CAF1 and CAF2 derived from murine PDACs and incubated for 24 h.

    Article Snippet: The human PDAC tissue array was purchased commercially from TissueArray.com (No.PA482a).

    Techniques: Expressing, Immunofluorescence, Staining, Derivative Assay, Incubation

    a, Immunohistochemistry staining of LPAR4 in a PDAC tissue array consisted of 15 PDAC samples and 4 samples of normal pancreas. Scale bar is 50 μM. Representative images showing normal pancreas (n=4 biological samples), low-LPAR4 PDAC (n=9 biological samples), and high-LPAR4 PDAC (n=6 biological samples). Bar graph shows the relative percentage of LPAR4-low and LPAR4-high patients in the PDAC tissue array. b, Quantitative RT-PCR confirming the manipulation of LPAR4 expression in 2 pancreatic cancer cell lines (Colo-357, MIA PaCa-2) and 2 patient-derived cancer cells (79E, 34E). Data were shown as mean ± s.d. (n=4 independent experiments for Colo-357 and 79E cells with LPAR4 stable knockdown, n=3 for Colo-357, 79E, and MiaPaCa2 cells with LPAR4 ectopic expression, n=3 for 34E cells with LPAR4 stable knockdown, and n=4 for 34E with LPAR4 ectopic expression). c, Non-invasive Bioluminescence images showing tumors formed at day 10 for Colo-357+sh-CTRL+luciferase or Colo-357+sh-R4.1+luciferase of various number implanted in the pancreas of nu/nu mice. Right panel showing the luminescence intensity in a blue-to-red spectrum. d, f, Trypan blue exclusion assay showing the relative number of viable cells with or without LPAR4 expression manipulation grown in 10% serum and 2D at day 4 and day 7. e, Tumor growth rates for 1 million Colo-357 cells with or without LPAR4 expression manipulation in a subcutaneous tumor model. Data were presented as mean ± s.d. for n=8 independent samples for each group. g, Quantitative RT-PCR confirming the knockdown of LPAR1 in Colo-357 cells. h, Effects of LPAR1 knockdown using siRNA on 2D or 3D (methylcellulose sphere forming) cell growth. Data were presented as mean ± s.d. for n=3 independent experiments (d,f,g, and h). Statistical analyses were performed using two tailed unpaired one sample t-test (b,g, and h) and one-way ANOVA (d-f). Source numerical data are available in source data.

    Journal: Nature cell biology

    Article Title: Pancreatic cancer cells upregulate LPAR4 in response to isolation stress to promote an ECM-enriched niche and support tumor initiation

    doi: 10.1038/s41556-022-01055-y

    Figure Lengend Snippet: a, Immunohistochemistry staining of LPAR4 in a PDAC tissue array consisted of 15 PDAC samples and 4 samples of normal pancreas. Scale bar is 50 μM. Representative images showing normal pancreas (n=4 biological samples), low-LPAR4 PDAC (n=9 biological samples), and high-LPAR4 PDAC (n=6 biological samples). Bar graph shows the relative percentage of LPAR4-low and LPAR4-high patients in the PDAC tissue array. b, Quantitative RT-PCR confirming the manipulation of LPAR4 expression in 2 pancreatic cancer cell lines (Colo-357, MIA PaCa-2) and 2 patient-derived cancer cells (79E, 34E). Data were shown as mean ± s.d. (n=4 independent experiments for Colo-357 and 79E cells with LPAR4 stable knockdown, n=3 for Colo-357, 79E, and MiaPaCa2 cells with LPAR4 ectopic expression, n=3 for 34E cells with LPAR4 stable knockdown, and n=4 for 34E with LPAR4 ectopic expression). c, Non-invasive Bioluminescence images showing tumors formed at day 10 for Colo-357+sh-CTRL+luciferase or Colo-357+sh-R4.1+luciferase of various number implanted in the pancreas of nu/nu mice. Right panel showing the luminescence intensity in a blue-to-red spectrum. d, f, Trypan blue exclusion assay showing the relative number of viable cells with or without LPAR4 expression manipulation grown in 10% serum and 2D at day 4 and day 7. e, Tumor growth rates for 1 million Colo-357 cells with or without LPAR4 expression manipulation in a subcutaneous tumor model. Data were presented as mean ± s.d. for n=8 independent samples for each group. g, Quantitative RT-PCR confirming the knockdown of LPAR1 in Colo-357 cells. h, Effects of LPAR1 knockdown using siRNA on 2D or 3D (methylcellulose sphere forming) cell growth. Data were presented as mean ± s.d. for n=3 independent experiments (d,f,g, and h). Statistical analyses were performed using two tailed unpaired one sample t-test (b,g, and h) and one-way ANOVA (d-f). Source numerical data are available in source data.

    Article Snippet: Immunohistochemistry staining of LPAR4 or FN1 in human PDAC tissue array (US Biomax PA484a) or formalin-fixed, paraffin-embedded xenograft tumors were performed using the LPAR4 antibody (Thermo Fisher, #PA5–49727) or FN1 antibody (CST, #26836, E5H6X) following the manufacturer’s protocol.

    Techniques: Immunohistochemistry, Staining, Quantitative RT-PCR, Expressing, Derivative Assay, Luciferase, Trypan Blue Exclusion Assay, Two Tailed Test