Review



primary antibodies against crt  (Abcam)

 
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
    • 96
      Buy from Supplier

    Structured Review

    Abcam primary antibodies against crt
    Induction of damage-associated molecular patterns (DAMPs) by TS-PDT in vitro (A) Flow cytometric analysis of cell-surface calreticulin <t>(CRT).</t> Negative controls, without TS addition or irradiation, are shown in red. The treated groups are shown in blue. (B) CRT translocation from the endoplasmic reticulum (ER) to the cell surface assessed by immunofluorescence staining. Images were obtained using a confocal microscope (original magnification ×350; scale bar, 5 μm). (C) Extracellular release of high-mobility group protein <t>B1</t> <t>(HMGB1)</t> induced by TS-PDT assessed by the enzyme-linked immunosorbent assay (ELISA) (n = 3). (D) HMGB1 translocation from the ER to the cell surface was assessed by immunofluorescence staining. Images were obtained using a confocal microscope (original magnification ×350; scale bar, 5 μm). (E) Heat-shock protein (HSP)-90 expression on the cell surface induced by TS-PDT assessed by flow cytometry. Negative controls, without TS addition nor irradiation, are shown in red. The treated groups are shown in blue. (F) Extracellular release of ATP induced by TS-PDT assessed by ELISA. ATP concentration in the culture medium after TS-PDT was detected by ELISA (n = 3).
    Primary Antibodies Against Crt, supplied by Abcam, used in various techniques. Bioz Stars score: 96/100, based on 729 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/primary antibodies against crt/product/Abcam
    Average 96 stars, based on 729 article reviews
    primary antibodies against crt - by Bioz Stars, 2026-03
    96/100 stars

    Images

    1) Product Images from "Anti-tumor immunity enhancement by photodynamic therapy with talaporfin sodium and anti-programmed death 1 antibody"

    Article Title: Anti-tumor immunity enhancement by photodynamic therapy with talaporfin sodium and anti-programmed death 1 antibody

    Journal: Molecular Therapy Oncolytics

    doi: 10.1016/j.omto.2022.12.009

    Induction of damage-associated molecular patterns (DAMPs) by TS-PDT in vitro (A) Flow cytometric analysis of cell-surface calreticulin (CRT). Negative controls, without TS addition or irradiation, are shown in red. The treated groups are shown in blue. (B) CRT translocation from the endoplasmic reticulum (ER) to the cell surface assessed by immunofluorescence staining. Images were obtained using a confocal microscope (original magnification ×350; scale bar, 5 μm). (C) Extracellular release of high-mobility group protein B1 (HMGB1) induced by TS-PDT assessed by the enzyme-linked immunosorbent assay (ELISA) (n = 3). (D) HMGB1 translocation from the ER to the cell surface was assessed by immunofluorescence staining. Images were obtained using a confocal microscope (original magnification ×350; scale bar, 5 μm). (E) Heat-shock protein (HSP)-90 expression on the cell surface induced by TS-PDT assessed by flow cytometry. Negative controls, without TS addition nor irradiation, are shown in red. The treated groups are shown in blue. (F) Extracellular release of ATP induced by TS-PDT assessed by ELISA. ATP concentration in the culture medium after TS-PDT was detected by ELISA (n = 3).
    Figure Legend Snippet: Induction of damage-associated molecular patterns (DAMPs) by TS-PDT in vitro (A) Flow cytometric analysis of cell-surface calreticulin (CRT). Negative controls, without TS addition or irradiation, are shown in red. The treated groups are shown in blue. (B) CRT translocation from the endoplasmic reticulum (ER) to the cell surface assessed by immunofluorescence staining. Images were obtained using a confocal microscope (original magnification ×350; scale bar, 5 μm). (C) Extracellular release of high-mobility group protein B1 (HMGB1) induced by TS-PDT assessed by the enzyme-linked immunosorbent assay (ELISA) (n = 3). (D) HMGB1 translocation from the ER to the cell surface was assessed by immunofluorescence staining. Images were obtained using a confocal microscope (original magnification ×350; scale bar, 5 μm). (E) Heat-shock protein (HSP)-90 expression on the cell surface induced by TS-PDT assessed by flow cytometry. Negative controls, without TS addition nor irradiation, are shown in red. The treated groups are shown in blue. (F) Extracellular release of ATP induced by TS-PDT assessed by ELISA. ATP concentration in the culture medium after TS-PDT was detected by ELISA (n = 3).

    Techniques Used: In Vitro, Irradiation, Translocation Assay, Immunofluorescence, Staining, Microscopy, Enzyme-linked Immunosorbent Assay, Expressing, Flow Cytometry, Concentration Assay



    Similar Products

    primary antibodies against crt  (R&D Systems)
    93
    R&D Systems primary antibodies against crt
    Representative photomicrographs of immunohistochemical staining of endometrial cancer specimens <t>with</t> <t>anti-CRT,</t> p-eIF2a, and Ki67 antibody. Immunostaining for (A) CRT, (B) p-eIF2a, and (C) Ki67 in endometrial cancer cells. CRT, calreticulin; p-eIF2α, phosphorylated eukaryotic initiation factor 2α.
    Primary Antibodies Against Crt, supplied by R&D Systems, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/primary antibodies against crt/product/R&D Systems
    Average 93 stars, based on 1 article reviews
    primary antibodies against crt - by Bioz Stars, 2026-03
    93/100 stars
    		  Buy from Supplier
    primary antibodies against crt and hmgb1  (Servicebio Inc)
    90
    Servicebio Inc primary antibodies against crt and hmgb1
    Representative photomicrographs of immunohistochemical staining of endometrial cancer specimens <t>with</t> <t>anti-CRT,</t> p-eIF2a, and Ki67 antibody. Immunostaining for (A) CRT, (B) p-eIF2a, and (C) Ki67 in endometrial cancer cells. CRT, calreticulin; p-eIF2α, phosphorylated eukaryotic initiation factor 2α.
    Primary Antibodies Against Crt And Hmgb1, supplied by Servicebio 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/result/primary antibodies against crt and hmgb1/product/Servicebio Inc
    Average 90 stars, based on 1 article reviews
    primary antibodies against crt and hmgb1 - by Bioz Stars, 2026-03
    90/100 stars
    		  Buy from Supplier
    primary antibodies against crt yt0620  (ImmunoWay Biotechnology Company)
    90
    ImmunoWay Biotechnology Company primary antibodies against crt yt0620
    Representative photomicrographs of immunohistochemical staining of endometrial cancer specimens <t>with</t> <t>anti-CRT,</t> p-eIF2a, and Ki67 antibody. Immunostaining for (A) CRT, (B) p-eIF2a, and (C) Ki67 in endometrial cancer cells. CRT, calreticulin; p-eIF2α, phosphorylated eukaryotic initiation factor 2α.
    Primary Antibodies Against Crt Yt0620, supplied by ImmunoWay Biotechnology Company, 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/result/primary antibodies against crt yt0620/product/ImmunoWay Biotechnology Company
    Average 90 stars, based on 1 article reviews
    primary antibodies against crt yt0620 - by Bioz Stars, 2026-03
    90/100 stars
    		  Buy from Supplier
    primary antibody against crt  (ImmunoWay Biotechnology Company)
    90
    ImmunoWay Biotechnology Company primary antibody against crt
    Representative photomicrographs of immunohistochemical staining of endometrial cancer specimens <t>with</t> <t>anti-CRT,</t> p-eIF2a, and Ki67 antibody. Immunostaining for (A) CRT, (B) p-eIF2a, and (C) Ki67 in endometrial cancer cells. CRT, calreticulin; p-eIF2α, phosphorylated eukaryotic initiation factor 2α.
    Primary Antibody Against Crt, supplied by ImmunoWay Biotechnology Company, 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/result/primary antibody against crt/product/ImmunoWay Biotechnology Company
    Average 90 stars, based on 1 article reviews
    primary antibody against crt - by Bioz Stars, 2026-03
    90/100 stars
    		  Buy from Supplier
    primary antibodies against crt  (Beyotime)
    90
    Beyotime primary antibodies against crt
    Representative photomicrographs of immunohistochemical staining of endometrial cancer specimens <t>with</t> <t>anti-CRT,</t> p-eIF2a, and Ki67 antibody. Immunostaining for (A) CRT, (B) p-eIF2a, and (C) Ki67 in endometrial cancer cells. CRT, calreticulin; p-eIF2α, phosphorylated eukaryotic initiation factor 2α.
    Primary Antibodies Against Crt, supplied by Beyotime, 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/result/primary antibodies against crt/product/Beyotime
    Average 90 stars, based on 1 article reviews
    primary antibodies against crt - by Bioz Stars, 2026-03
    90/100 stars
    		  Buy from Supplier
    primary antibodies against crt  (Abcam)
    96
    Abcam primary antibodies against crt
    Induction of damage-associated molecular patterns (DAMPs) by TS-PDT in vitro (A) Flow cytometric analysis of cell-surface calreticulin <t>(CRT).</t> Negative controls, without TS addition or irradiation, are shown in red. The treated groups are shown in blue. (B) CRT translocation from the endoplasmic reticulum (ER) to the cell surface assessed by immunofluorescence staining. Images were obtained using a confocal microscope (original magnification ×350; scale bar, 5 μm). (C) Extracellular release of high-mobility group protein <t>B1</t> <t>(HMGB1)</t> induced by TS-PDT assessed by the enzyme-linked immunosorbent assay (ELISA) (n = 3). (D) HMGB1 translocation from the ER to the cell surface was assessed by immunofluorescence staining. Images were obtained using a confocal microscope (original magnification ×350; scale bar, 5 μm). (E) Heat-shock protein (HSP)-90 expression on the cell surface induced by TS-PDT assessed by flow cytometry. Negative controls, without TS addition nor irradiation, are shown in red. The treated groups are shown in blue. (F) Extracellular release of ATP induced by TS-PDT assessed by ELISA. ATP concentration in the culture medium after TS-PDT was detected by ELISA (n = 3).
    Primary Antibodies Against Crt, supplied by Abcam, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/primary antibodies against crt/product/Abcam
    Average 96 stars, based on 1 article reviews
    primary antibodies against crt - by Bioz Stars, 2026-03
    96/100 stars
    		  Buy from Supplier
    primary antibodies against crt  (Cell Signaling Technology Inc)
    96
    Cell Signaling Technology Inc primary antibodies against crt
    Induction of damage-associated molecular patterns (DAMPs) by TS-PDT in vitro (A) Flow cytometric analysis of cell-surface calreticulin <t>(CRT).</t> Negative controls, without TS addition or irradiation, are shown in red. The treated groups are shown in blue. (B) CRT translocation from the endoplasmic reticulum (ER) to the cell surface assessed by immunofluorescence staining. Images were obtained using a confocal microscope (original magnification ×350; scale bar, 5 μm). (C) Extracellular release of high-mobility group protein <t>B1</t> <t>(HMGB1)</t> induced by TS-PDT assessed by the enzyme-linked immunosorbent assay (ELISA) (n = 3). (D) HMGB1 translocation from the ER to the cell surface was assessed by immunofluorescence staining. Images were obtained using a confocal microscope (original magnification ×350; scale bar, 5 μm). (E) Heat-shock protein (HSP)-90 expression on the cell surface induced by TS-PDT assessed by flow cytometry. Negative controls, without TS addition nor irradiation, are shown in red. The treated groups are shown in blue. (F) Extracellular release of ATP induced by TS-PDT assessed by ELISA. ATP concentration in the culture medium after TS-PDT was detected by ELISA (n = 3).
    Primary Antibodies Against Crt, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/primary antibodies against crt/product/Cell Signaling Technology Inc
    Average 96 stars, based on 1 article reviews
    primary antibodies against crt - by Bioz Stars, 2026-03
    96/100 stars
    		  Buy from Supplier
    primary antibodies against bax, bcl2, crt or pd-l1  (Santa Cruz Biotechnology)
    90
    Santa Cruz Biotechnology primary antibodies against bax, bcl2, crt or pd-l1
    Induction of damage-associated molecular patterns (DAMPs) by TS-PDT in vitro (A) Flow cytometric analysis of cell-surface calreticulin <t>(CRT).</t> Negative controls, without TS addition or irradiation, are shown in red. The treated groups are shown in blue. (B) CRT translocation from the endoplasmic reticulum (ER) to the cell surface assessed by immunofluorescence staining. Images were obtained using a confocal microscope (original magnification ×350; scale bar, 5 μm). (C) Extracellular release of high-mobility group protein <t>B1</t> <t>(HMGB1)</t> induced by TS-PDT assessed by the enzyme-linked immunosorbent assay (ELISA) (n = 3). (D) HMGB1 translocation from the ER to the cell surface was assessed by immunofluorescence staining. Images were obtained using a confocal microscope (original magnification ×350; scale bar, 5 μm). (E) Heat-shock protein (HSP)-90 expression on the cell surface induced by TS-PDT assessed by flow cytometry. Negative controls, without TS addition nor irradiation, are shown in red. The treated groups are shown in blue. (F) Extracellular release of ATP induced by TS-PDT assessed by ELISA. ATP concentration in the culture medium after TS-PDT was detected by ELISA (n = 3).
    Primary Antibodies Against Bax, Bcl2, Crt Or Pd L1, supplied by Santa Cruz Biotechnology, 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/result/primary antibodies against bax, bcl2, crt or pd-l1/product/Santa Cruz Biotechnology
    Average 90 stars, based on 1 article reviews
    primary antibodies against bax, bcl2, crt or pd-l1 - by Bioz Stars, 2026-03
    90/100 stars
    		  Buy from Supplier
    primary antibodies against crt  (Proteintech)
    96
    Proteintech primary antibodies against crt
    Induction of damage-associated molecular patterns (DAMPs) by TS-PDT in vitro (A) Flow cytometric analysis of cell-surface calreticulin <t>(CRT).</t> Negative controls, without TS addition or irradiation, are shown in red. The treated groups are shown in blue. (B) CRT translocation from the endoplasmic reticulum (ER) to the cell surface assessed by immunofluorescence staining. Images were obtained using a confocal microscope (original magnification ×350; scale bar, 5 μm). (C) Extracellular release of high-mobility group protein <t>B1</t> <t>(HMGB1)</t> induced by TS-PDT assessed by the enzyme-linked immunosorbent assay (ELISA) (n = 3). (D) HMGB1 translocation from the ER to the cell surface was assessed by immunofluorescence staining. Images were obtained using a confocal microscope (original magnification ×350; scale bar, 5 μm). (E) Heat-shock protein (HSP)-90 expression on the cell surface induced by TS-PDT assessed by flow cytometry. Negative controls, without TS addition nor irradiation, are shown in red. The treated groups are shown in blue. (F) Extracellular release of ATP induced by TS-PDT assessed by ELISA. ATP concentration in the culture medium after TS-PDT was detected by ELISA (n = 3).
    Primary Antibodies Against Crt, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/primary antibodies against crt/product/Proteintech
    Average 96 stars, based on 1 article reviews
    primary antibodies against crt - by Bioz Stars, 2026-03
    96/100 stars
    		  Buy from Supplier
    primary antibodies against crt  (Santa Cruz Biotechnology)
    90
    Santa Cruz Biotechnology primary antibodies against crt
    Induction of damage-associated molecular patterns (DAMPs) by TS-PDT in vitro (A) Flow cytometric analysis of cell-surface calreticulin <t>(CRT).</t> Negative controls, without TS addition or irradiation, are shown in red. The treated groups are shown in blue. (B) CRT translocation from the endoplasmic reticulum (ER) to the cell surface assessed by immunofluorescence staining. Images were obtained using a confocal microscope (original magnification ×350; scale bar, 5 μm). (C) Extracellular release of high-mobility group protein <t>B1</t> <t>(HMGB1)</t> induced by TS-PDT assessed by the enzyme-linked immunosorbent assay (ELISA) (n = 3). (D) HMGB1 translocation from the ER to the cell surface was assessed by immunofluorescence staining. Images were obtained using a confocal microscope (original magnification ×350; scale bar, 5 μm). (E) Heat-shock protein (HSP)-90 expression on the cell surface induced by TS-PDT assessed by flow cytometry. Negative controls, without TS addition nor irradiation, are shown in red. The treated groups are shown in blue. (F) Extracellular release of ATP induced by TS-PDT assessed by ELISA. ATP concentration in the culture medium after TS-PDT was detected by ELISA (n = 3).
    Primary Antibodies Against Crt, supplied by Santa Cruz Biotechnology, 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/result/primary antibodies against crt/product/Santa Cruz Biotechnology
    Average 90 stars, based on 1 article reviews
    primary antibodies against crt - by Bioz Stars, 2026-03
    90/100 stars
    		  Buy from Supplier

    Image Search Results


    Representative photomicrographs of immunohistochemical staining of endometrial cancer specimens with anti-CRT, p-eIF2a, and Ki67 antibody. Immunostaining for (A) CRT, (B) p-eIF2a, and (C) Ki67 in endometrial cancer cells. CRT, calreticulin; p-eIF2α, phosphorylated eukaryotic initiation factor 2α.

    Journal: Oncology Letters

    Article Title: Significance of calreticulin as a prognostic factor in endometrial cancer

    doi: 10.3892/ol.2018.8495

    Figure Lengend Snippet: Representative photomicrographs of immunohistochemical staining of endometrial cancer specimens with anti-CRT, p-eIF2a, and Ki67 antibody. Immunostaining for (A) CRT, (B) p-eIF2a, and (C) Ki67 in endometrial cancer cells. CRT, calreticulin; p-eIF2α, phosphorylated eukaryotic initiation factor 2α.

    Article Snippet: Primary antibodies against CRT (MAB3898), p-eIF2a (AF705) and PERK (AF3999) were purchased from R&D systems.

    Techniques: Immunohistochemical staining, Staining, Immunostaining

    Assessment of CRT, PERK, eIF2α, and p-eIF2α protein content by Western blot analysis. The protein content of CRT, PERK, eIF2α, and p-eIF2α in 12 pairs of DOX-resistant endometrial cancer patients and DOX-sensitive endometrial cancer patients was assessed. In the DOX-resistant endometrial cancer samples, the CRT, PERK, eIF2α, and p-eIF2α protein content was not significantly different between the pre-NAC and post-NAC. (A) In the DOX-sensitive endometrial cancer samples, the CRT, PERK, and p-eIF2α protein content was significantly increased in the post-NAC group compared with the pre-NAC group. (C) There was not a significant change in the eIF2α protein content in the DOX-sensitive endometrial cancer samples. The expression levels were normalized to the actin/pan-cadherin expression values. (B and D) The data are expressed as the means ± standard deviations, which were calculated from three parallel experiments. *P<0.05. CRT; calreticulin; PERK, PKR-like endoplasmic reticulum kinase.

    Journal: Oncology Letters

    Article Title: Significance of calreticulin as a prognostic factor in endometrial cancer

    doi: 10.3892/ol.2018.8495

    Figure Lengend Snippet: Assessment of CRT, PERK, eIF2α, and p-eIF2α protein content by Western blot analysis. The protein content of CRT, PERK, eIF2α, and p-eIF2α in 12 pairs of DOX-resistant endometrial cancer patients and DOX-sensitive endometrial cancer patients was assessed. In the DOX-resistant endometrial cancer samples, the CRT, PERK, eIF2α, and p-eIF2α protein content was not significantly different between the pre-NAC and post-NAC. (A) In the DOX-sensitive endometrial cancer samples, the CRT, PERK, and p-eIF2α protein content was significantly increased in the post-NAC group compared with the pre-NAC group. (C) There was not a significant change in the eIF2α protein content in the DOX-sensitive endometrial cancer samples. The expression levels were normalized to the actin/pan-cadherin expression values. (B and D) The data are expressed as the means ± standard deviations, which were calculated from three parallel experiments. *P<0.05. CRT; calreticulin; PERK, PKR-like endoplasmic reticulum kinase.

    Article Snippet: Primary antibodies against CRT (MAB3898), p-eIF2a (AF705) and PERK (AF3999) were purchased from R&D systems.

    Techniques: Western Blot, Expressing

    Induction of damage-associated molecular patterns (DAMPs) by TS-PDT in vitro (A) Flow cytometric analysis of cell-surface calreticulin (CRT). Negative controls, without TS addition or irradiation, are shown in red. The treated groups are shown in blue. (B) CRT translocation from the endoplasmic reticulum (ER) to the cell surface assessed by immunofluorescence staining. Images were obtained using a confocal microscope (original magnification ×350; scale bar, 5 μm). (C) Extracellular release of high-mobility group protein B1 (HMGB1) induced by TS-PDT assessed by the enzyme-linked immunosorbent assay (ELISA) (n = 3). (D) HMGB1 translocation from the ER to the cell surface was assessed by immunofluorescence staining. Images were obtained using a confocal microscope (original magnification ×350; scale bar, 5 μm). (E) Heat-shock protein (HSP)-90 expression on the cell surface induced by TS-PDT assessed by flow cytometry. Negative controls, without TS addition nor irradiation, are shown in red. The treated groups are shown in blue. (F) Extracellular release of ATP induced by TS-PDT assessed by ELISA. ATP concentration in the culture medium after TS-PDT was detected by ELISA (n = 3).

    Journal: Molecular Therapy Oncolytics

    Article Title: Anti-tumor immunity enhancement by photodynamic therapy with talaporfin sodium and anti-programmed death 1 antibody

    doi: 10.1016/j.omto.2022.12.009

    Figure Lengend Snippet: Induction of damage-associated molecular patterns (DAMPs) by TS-PDT in vitro (A) Flow cytometric analysis of cell-surface calreticulin (CRT). Negative controls, without TS addition or irradiation, are shown in red. The treated groups are shown in blue. (B) CRT translocation from the endoplasmic reticulum (ER) to the cell surface assessed by immunofluorescence staining. Images were obtained using a confocal microscope (original magnification ×350; scale bar, 5 μm). (C) Extracellular release of high-mobility group protein B1 (HMGB1) induced by TS-PDT assessed by the enzyme-linked immunosorbent assay (ELISA) (n = 3). (D) HMGB1 translocation from the ER to the cell surface was assessed by immunofluorescence staining. Images were obtained using a confocal microscope (original magnification ×350; scale bar, 5 μm). (E) Heat-shock protein (HSP)-90 expression on the cell surface induced by TS-PDT assessed by flow cytometry. Negative controls, without TS addition nor irradiation, are shown in red. The treated groups are shown in blue. (F) Extracellular release of ATP induced by TS-PDT assessed by ELISA. ATP concentration in the culture medium after TS-PDT was detected by ELISA (n = 3).

    Article Snippet: Primary antibodies against CRT (1:1,000 dilution; ab2907; Abcam) or HMGB1 (1:250 dilution; ab79823; Abcam) were used.

    Techniques: In Vitro, Irradiation, Translocation Assay, Immunofluorescence, Staining, Microscopy, Enzyme-linked Immunosorbent Assay, Expressing, Flow Cytometry, Concentration Assay