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Procell Inc murine macrophage cell line raw 264 7
A) Live/Dead staining of RAW 264.7 macrophages cultured on different material surfaces for 72 h, where dead cells were stained red and live cells were stained green. B) Cytoskeleton staining morphology of RAW 264.7 grown on different material surfaces for 72 h. C, D, F) Fluorescence images and flow cytometry analysis of intracellular ROS in RAW 264.7 cells with DCFH-DA probe. E) Proliferation of RAW 264.7 macrophages on different material surfaces assessed by CCK-8 assay. n = 3. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001. Created in BioRender.
Murine Macrophage Cell Line Raw 264 7, supplied by Procell Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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ATCC murine macrophage cell line raw264 7
A) Live/Dead staining of RAW 264.7 macrophages cultured on different material surfaces for 72 h, where dead cells were stained red and live cells were stained green. B) Cytoskeleton staining morphology of RAW 264.7 grown on different material surfaces for 72 h. C, D, F) Fluorescence images and flow cytometry analysis of intracellular ROS in RAW 264.7 cells with DCFH-DA probe. E) Proliferation of RAW 264.7 macrophages on different material surfaces assessed by CCK-8 assay. n = 3. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001. Created in BioRender.
Murine Macrophage Cell Line Raw264 7, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/murine+raw+264+7+cell+line/RAW+264%2E7/pmc13059125-142-1-6
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ATCC raw 264 7 murine macrophage cell line
A) Live/Dead staining of RAW 264.7 macrophages cultured on different material surfaces for 72 h, where dead cells were stained red and live cells were stained green. B) Cytoskeleton staining morphology of RAW 264.7 grown on different material surfaces for 72 h. C, D, F) Fluorescence images and flow cytometry analysis of intracellular ROS in RAW 264.7 cells with DCFH-DA probe. E) Proliferation of RAW 264.7 macrophages on different material surfaces assessed by CCK-8 assay. n = 3. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001. Created in BioRender.
Raw 264 7 Murine Macrophage Cell Line, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Korean Cell Line Bank murine macrophage cell line raw 264 7
A) Live/Dead staining of RAW 264.7 macrophages cultured on different material surfaces for 72 h, where dead cells were stained red and live cells were stained green. B) Cytoskeleton staining morphology of RAW 264.7 grown on different material surfaces for 72 h. C, D, F) Fluorescence images and flow cytometry analysis of intracellular ROS in RAW 264.7 cells with DCFH-DA probe. E) Proliferation of RAW 264.7 macrophages on different material surfaces assessed by CCK-8 assay. n = 3. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001. Created in BioRender.
Murine Macrophage Cell Line Raw 264 7, supplied by Korean Cell Line Bank, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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ATCC murine monocytic macrophage leukemia cell line raw264 7
A) Live/Dead staining of RAW 264.7 macrophages cultured on different material surfaces for 72 h, where dead cells were stained red and live cells were stained green. B) Cytoskeleton staining morphology of RAW 264.7 grown on different material surfaces for 72 h. C, D, F) Fluorescence images and flow cytometry analysis of intracellular ROS in RAW 264.7 cells with DCFH-DA probe. E) Proliferation of RAW 264.7 macrophages on different material surfaces assessed by CCK-8 assay. n = 3. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001. Created in BioRender.
Murine Monocytic Macrophage Leukemia Cell Line Raw264 7, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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ATCC murine macrophage cell line raw 264 7
A) Live/Dead staining of RAW 264.7 macrophages cultured on different material surfaces for 72 h, where dead cells were stained red and live cells were stained green. B) Cytoskeleton staining morphology of RAW 264.7 grown on different material surfaces for 72 h. C, D, F) Fluorescence images and flow cytometry analysis of intracellular ROS in RAW 264.7 cells with DCFH-DA probe. E) Proliferation of RAW 264.7 macrophages on different material surfaces assessed by CCK-8 assay. n = 3. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001. Created in BioRender.
Murine Macrophage Cell Line Raw 264 7, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/murine+raw+264+7+cell+line/RAW+264%2E7/pm42308787-326-15-25
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ATCC raw264 7 murine macrophage cell lines
Preparation and characterization of BM@MnO 2 @AB680 nanoparticles. (a) The TEM image of SiO 2 @MnO 2 nanoparticles. (b) The TEM image of hollow MnO 2 (MnO 2 ) nanoparticles. (c) The TEM image of hollow MnO 2 loaded with AB680 (MnO 2 @AB680) nanoparticles. (d) The TEM image of bacterial membrane (BM)-coated hollow MnO 2 loaded with AB680 (BM@MnO 2 @AB680) nanoparticles. (e) The particle sizes of different MnO 2 based nanoparticles. (f) The zeta potentials of BM and different nanoparticles. (g) The PDI of different MnO 2 based nanoparticles. (h) The particle size stability of BM@MnO 2 @AB680 nanoparticles. (i) The zeta potential stability of BM@MnO 2 @AB680 nanoparticles. (j) The PDI stability of BM@MnO 2 @AB680 nanoparticles. (k) Relative oxygen level in different groups within PBS added with H 2 O 2 . (l) CLSM images <t>of</t> <t>RAW264.7</t> cells incubated with Cy5.5 labeled MnO 2 @AB680 (left) and BM@MnO 2 @AB680 (right) nanoparticles. Scale bar: 100 μm. (m) Mean fluorescence intensity (MFI) of RAW264.7 cells after incubation with MnO 2 @AB680 (Mac@AMn) and BM@MnO 2 @AB680 (Mac@ABMn) nanoparticles. (n) MFI of RAW264.7 cells after incubation with BM@MnO 2 @AB680 with different time.
Raw264 7 Murine Macrophage Cell Lines, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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raw264 7 murine macrophage cell lines - by Bioz Stars, 2026-09
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A) Live/Dead staining of RAW 264.7 macrophages cultured on different material surfaces for 72 h, where dead cells were stained red and live cells were stained green. B) Cytoskeleton staining morphology of RAW 264.7 grown on different material surfaces for 72 h. C, D, F) Fluorescence images and flow cytometry analysis of intracellular ROS in RAW 264.7 cells with DCFH-DA probe. E) Proliferation of RAW 264.7 macrophages on different material surfaces assessed by CCK-8 assay. n = 3. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001. Created in BioRender.

Journal: Bioactive Materials

Article Title: Bioengineered titanium implants functionalized with aptamer-valproic acid conjugates orchestrate macrophage programming and mesenchymal stem cell homing for improved osseointegration

doi: 10.1016/j.bioactmat.2026.05.055

Figure Lengend Snippet: A) Live/Dead staining of RAW 264.7 macrophages cultured on different material surfaces for 72 h, where dead cells were stained red and live cells were stained green. B) Cytoskeleton staining morphology of RAW 264.7 grown on different material surfaces for 72 h. C, D, F) Fluorescence images and flow cytometry analysis of intracellular ROS in RAW 264.7 cells with DCFH-DA probe. E) Proliferation of RAW 264.7 macrophages on different material surfaces assessed by CCK-8 assay. n = 3. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001. Created in BioRender.

Article Snippet: The murine macrophage cell line RAW 264.7 (Procell Life Science, China) was cultured in high-glucose DMEM (Gibco, USA) containing 10% FBS and employed for immunomodulation studies.

Techniques: Staining, Cell Culture, Fluorescence, Flow Cytometry, CCK-8 Assay

A, F) IF staining of iNOS and CD206 in RAW 264.7 macrophages. B-E) Secretion of inflammation-related proteins in RAW 264.7 macrophages. G-J) Relative mRNA expression of inflammation-related genes in RAW 264.7 macrophages. n = 3. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001.

Journal: Bioactive Materials

Article Title: Bioengineered titanium implants functionalized with aptamer-valproic acid conjugates orchestrate macrophage programming and mesenchymal stem cell homing for improved osseointegration

doi: 10.1016/j.bioactmat.2026.05.055

Figure Lengend Snippet: A, F) IF staining of iNOS and CD206 in RAW 264.7 macrophages. B-E) Secretion of inflammation-related proteins in RAW 264.7 macrophages. G-J) Relative mRNA expression of inflammation-related genes in RAW 264.7 macrophages. n = 3. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001.

Article Snippet: The murine macrophage cell line RAW 264.7 (Procell Life Science, China) was cultured in high-glucose DMEM (Gibco, USA) containing 10% FBS and employed for immunomodulation studies.

Techniques: Staining, Expressing

Preparation and characterization of BM@MnO 2 @AB680 nanoparticles. (a) The TEM image of SiO 2 @MnO 2 nanoparticles. (b) The TEM image of hollow MnO 2 (MnO 2 ) nanoparticles. (c) The TEM image of hollow MnO 2 loaded with AB680 (MnO 2 @AB680) nanoparticles. (d) The TEM image of bacterial membrane (BM)-coated hollow MnO 2 loaded with AB680 (BM@MnO 2 @AB680) nanoparticles. (e) The particle sizes of different MnO 2 based nanoparticles. (f) The zeta potentials of BM and different nanoparticles. (g) The PDI of different MnO 2 based nanoparticles. (h) The particle size stability of BM@MnO 2 @AB680 nanoparticles. (i) The zeta potential stability of BM@MnO 2 @AB680 nanoparticles. (j) The PDI stability of BM@MnO 2 @AB680 nanoparticles. (k) Relative oxygen level in different groups within PBS added with H 2 O 2 . (l) CLSM images of RAW264.7 cells incubated with Cy5.5 labeled MnO 2 @AB680 (left) and BM@MnO 2 @AB680 (right) nanoparticles. Scale bar: 100 μm. (m) Mean fluorescence intensity (MFI) of RAW264.7 cells after incubation with MnO 2 @AB680 (Mac@AMn) and BM@MnO 2 @AB680 (Mac@ABMn) nanoparticles. (n) MFI of RAW264.7 cells after incubation with BM@MnO 2 @AB680 with different time.

Journal: Materials Today Bio

Article Title: Nano-bionic bacteria armed adoptive macrophage therapy against bladder cancer

doi: 10.1016/j.mtbio.2026.103130

Figure Lengend Snippet: Preparation and characterization of BM@MnO 2 @AB680 nanoparticles. (a) The TEM image of SiO 2 @MnO 2 nanoparticles. (b) The TEM image of hollow MnO 2 (MnO 2 ) nanoparticles. (c) The TEM image of hollow MnO 2 loaded with AB680 (MnO 2 @AB680) nanoparticles. (d) The TEM image of bacterial membrane (BM)-coated hollow MnO 2 loaded with AB680 (BM@MnO 2 @AB680) nanoparticles. (e) The particle sizes of different MnO 2 based nanoparticles. (f) The zeta potentials of BM and different nanoparticles. (g) The PDI of different MnO 2 based nanoparticles. (h) The particle size stability of BM@MnO 2 @AB680 nanoparticles. (i) The zeta potential stability of BM@MnO 2 @AB680 nanoparticles. (j) The PDI stability of BM@MnO 2 @AB680 nanoparticles. (k) Relative oxygen level in different groups within PBS added with H 2 O 2 . (l) CLSM images of RAW264.7 cells incubated with Cy5.5 labeled MnO 2 @AB680 (left) and BM@MnO 2 @AB680 (right) nanoparticles. Scale bar: 100 μm. (m) Mean fluorescence intensity (MFI) of RAW264.7 cells after incubation with MnO 2 @AB680 (Mac@AMn) and BM@MnO 2 @AB680 (Mac@ABMn) nanoparticles. (n) MFI of RAW264.7 cells after incubation with BM@MnO 2 @AB680 with different time.

Article Snippet: RAW264.7 murine macrophage cell lines were purchased from ATCC, which were cultured in Dulbecco's modified Eagle's medium (DMEM) -high glucose medium.

Techniques: Membrane, Zeta Potential Analyzer, Incubation, Labeling, Fluorescence