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fitc-anti-cd44 antibody (im7)  (Thermo Fisher)


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    Thermo Fisher fitc-anti-cd44 antibody (im7)
    Fitc Anti Cd44 Antibody (Im7), supplied by Thermo Fisher, 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/cd44-fitc+(im7)/anti+cd44/pmc10104559__pnas__2217562120__sapp-11-35-38
    Average 90 stars, based on 1 article reviews
    fitc-anti-cd44 antibody (im7) - by Bioz Stars, 2026-10
    90/100 stars

    Images

    Related Articles

    Flow Cytometry:

    Article Title: MSC-Derived Small Extracellular Vesicles Attenuate Autoimmune Dacryoadenitis by Promoting M2 Macrophage Polarization and Inducing Tregs via miR-100-5p
    Article Snippet: The phenotype of hUC-MSCs was determined by flow cytometry using specific antibodies as follows: CD29-FITC (clone TS2/16), CD34-FITC (clone 4H11), CD44-FITC (clone IM7), CD45-FITC (clone HI30) and CD105-PE (clone SN6) (eBioscienceTM, USA); CD73-FITC (clone AD2), CD90-FITC (clone 5E10), CD11b-FITC (clone M1/70) and HLA-DR-PE (clone LN3) (Biolegend, USA).

    Marker:

    Article Title: MSC-Derived Small Extracellular Vesicles Attenuate Autoimmune Dacryoadenitis by Promoting M2 Macrophage Polarization and Inducing Tregs via miR-100-5p
    Article Snippet: The phenotype of hUC-MSCs was determined by flow cytometry using specific antibodies as follows: CD29-FITC (clone TS2/16), CD34-FITC (clone 4H11), CD44-FITC (clone IM7), CD45-FITC (clone HI30) and CD105-PE (clone SN6) (eBioscienceTM, USA); CD73-FITC (clone AD2), CD90-FITC (clone 5E10), CD11b-FITC (clone M1/70) and HLA-DR-PE (clone LN3) (Biolegend, USA).

    Staining:

    Article Title: MSC-Derived Small Extracellular Vesicles Attenuate Autoimmune Dacryoadenitis by Promoting M2 Macrophage Polarization and Inducing Tregs via miR-100-5p
    Article Snippet: The phenotype of hUC-MSCs was determined by flow cytometry using specific antibodies as follows: CD29-FITC (clone TS2/16), CD34-FITC (clone 4H11), CD44-FITC (clone IM7), CD45-FITC (clone HI30) and CD105-PE (clone SN6) (eBioscienceTM, USA); CD73-FITC (clone AD2), CD90-FITC (clone 5E10), CD11b-FITC (clone M1/70) and HLA-DR-PE (clone LN3) (Biolegend, USA).

    Differentiation Assay:

    Article Title: MSC-Derived Small Extracellular Vesicles Attenuate Autoimmune Dacryoadenitis by Promoting M2 Macrophage Polarization and Inducing Tregs via miR-100-5p
    Article Snippet: The phenotype of hUC-MSCs was determined by flow cytometry using specific antibodies as follows: CD29-FITC (clone TS2/16), CD34-FITC (clone 4H11), CD44-FITC (clone IM7), CD45-FITC (clone HI30) and CD105-PE (clone SN6) (eBioscienceTM, USA); CD73-FITC (clone AD2), CD90-FITC (clone 5E10), CD11b-FITC (clone M1/70) and HLA-DR-PE (clone LN3) (Biolegend, USA).

    Transmission Assay:

    Article Title: MSC-Derived Small Extracellular Vesicles Attenuate Autoimmune Dacryoadenitis by Promoting M2 Macrophage Polarization and Inducing Tregs via miR-100-5p
    Article Snippet: The phenotype of hUC-MSCs was determined by flow cytometry using specific antibodies as follows: CD29-FITC (clone TS2/16), CD34-FITC (clone 4H11), CD44-FITC (clone IM7), CD45-FITC (clone HI30) and CD105-PE (clone SN6) (eBioscienceTM, USA); CD73-FITC (clone AD2), CD90-FITC (clone 5E10), CD11b-FITC (clone M1/70) and HLA-DR-PE (clone LN3) (Biolegend, USA).

    Western Blot:

    Article Title: MSC-Derived Small Extracellular Vesicles Attenuate Autoimmune Dacryoadenitis by Promoting M2 Macrophage Polarization and Inducing Tregs via miR-100-5p
    Article Snippet: The phenotype of hUC-MSCs was determined by flow cytometry using specific antibodies as follows: CD29-FITC (clone TS2/16), CD34-FITC (clone 4H11), CD44-FITC (clone IM7), CD45-FITC (clone HI30) and CD105-PE (clone SN6) (eBioscienceTM, USA); CD73-FITC (clone AD2), CD90-FITC (clone 5E10), CD11b-FITC (clone M1/70) and HLA-DR-PE (clone LN3) (Biolegend, USA).



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    Chronic T cell-mediated colitis was induced in B6.B6.RAG1−/− mice by intraperitoneal injection (0.5 × 106) of naïve CD4+ CD45RBhigh or CD45RBlow T cells. Identification of 2-nitroimidazole EF5 hypoxic adducts in B6.B6.RAG1−/− mice injected with C57BL/6J/6JT cells. 6 weeks post-treatment spleens, lymph nodes and collagenase-digested colon tissues were assessed. a Flow cytometric sub-analysis of cellular profile within Cy5-labeled EF5 (nitroimidazole; injected IP-3h) naïve and effector memory CD4+ T cells from the spleen, mesenteric lymph nodes and the colons, ( n = 3–4, one-way ANOVA). b Effector memory CD4+ T cells from the spleen, mesenteric lymph node (MLN) and collagenase digested colons (gated on <t>CD44</t> + CD62L−) and labeled with EF5-Cy5. Identification of stabilized HIF in dissected colons by IVIS imaging from mice adoptively transferred with 0.5 × 106 B6.ΔODD.luc CD4+ T cells. Prior to euthanizing, mice were injected with Luciferase substrate for 10 min. Freshly dissected colons were flushed and imaged using IVIS. Representative IVIS photograph and corresponding colon micrograph sections were stained with H&E, n = 4. c Healthy colons from CD45RBlow transferred mice, with low luciferase activity in the upper panel. Colon histological sections (lower panel, Scale bar: 184.4 mm). d High luciferase activity in whole colon (upper panel) and histology micrograph with lymphocyte infiltrates in CD45RBhigh transferred mice at 6-week post transfer (lower panel, Scale bar: 184.4 mm). e Image radiance was quantified using IVIS and expressed as photons/sec/cm2/sr. ( n = 3, two-tailed T test). f Colon inflammation score (weight/length) in adoptively transferred animals from ( c ) and ( d ) ( n = 4, two-tailed T test). Male and female mice used in ( a ) and ( b ), male recipients and male and female donors used in ( c )–( f ). Radiance of IVIS image was quantified and expressed as photons/sec/cm2/sr. Data expressed as Mean ±S.E.M., * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001 vs. indicated.
    Anti Cd44 Fitc Im7, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Thermo Fisher anti-cd44 fitc (clone im7)
    Chronic T cell-mediated colitis was induced in B6.B6.RAG1−/− mice by intraperitoneal injection (0.5 × 106) of naïve CD4+ CD45RBhigh or CD45RBlow T cells. Identification of 2-nitroimidazole EF5 hypoxic adducts in B6.B6.RAG1−/− mice injected with C57BL/6J/6JT cells. 6 weeks post-treatment spleens, lymph nodes and collagenase-digested colon tissues were assessed. a Flow cytometric sub-analysis of cellular profile within Cy5-labeled EF5 (nitroimidazole; injected IP-3h) naïve and effector memory CD4+ T cells from the spleen, mesenteric lymph nodes and the colons, ( n = 3–4, one-way ANOVA). b Effector memory CD4+ T cells from the spleen, mesenteric lymph node (MLN) and collagenase digested colons (gated on <t>CD44</t> + CD62L−) and labeled with EF5-Cy5. Identification of stabilized HIF in dissected colons by IVIS imaging from mice adoptively transferred with 0.5 × 106 B6.ΔODD.luc CD4+ T cells. Prior to euthanizing, mice were injected with Luciferase substrate for 10 min. Freshly dissected colons were flushed and imaged using IVIS. Representative IVIS photograph and corresponding colon micrograph sections were stained with H&E, n = 4. c Healthy colons from CD45RBlow transferred mice, with low luciferase activity in the upper panel. Colon histological sections (lower panel, Scale bar: 184.4 mm). d High luciferase activity in whole colon (upper panel) and histology micrograph with lymphocyte infiltrates in CD45RBhigh transferred mice at 6-week post transfer (lower panel, Scale bar: 184.4 mm). e Image radiance was quantified using IVIS and expressed as photons/sec/cm2/sr. ( n = 3, two-tailed T test). f Colon inflammation score (weight/length) in adoptively transferred animals from ( c ) and ( d ) ( n = 4, two-tailed T test). Male and female mice used in ( a ) and ( b ), male recipients and male and female donors used in ( c )–( f ). Radiance of IVIS image was quantified and expressed as photons/sec/cm2/sr. Data expressed as Mean ±S.E.M., * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001 vs. indicated.
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    Image Search Results


    Journal: iScience

    Article Title: Lymphopoiesis is attenuated upon hepatocyte-specific deletion of the cytochrome c oxidase assembly factor Sco1

    doi: 10.1016/j.isci.2025.112151

    Figure Lengend Snippet:

    Article Snippet: CD44-FITC (Clone: IM7) , ThermoFisher Scientific , Cat# 11-0441-82; RRID: AB_465045.

    Techniques: Control, Enzyme-linked Immunosorbent Assay, Functional Assay, Western Blot, Recombinant, Protease Inhibitor, Diagnostic Assay, Staining, Software

    Chronic T cell-mediated colitis was induced in B6.B6.RAG1−/− mice by intraperitoneal injection (0.5 × 106) of naïve CD4+ CD45RBhigh or CD45RBlow T cells. Identification of 2-nitroimidazole EF5 hypoxic adducts in B6.B6.RAG1−/− mice injected with C57BL/6J/6JT cells. 6 weeks post-treatment spleens, lymph nodes and collagenase-digested colon tissues were assessed. a Flow cytometric sub-analysis of cellular profile within Cy5-labeled EF5 (nitroimidazole; injected IP-3h) naïve and effector memory CD4+ T cells from the spleen, mesenteric lymph nodes and the colons, ( n = 3–4, one-way ANOVA). b Effector memory CD4+ T cells from the spleen, mesenteric lymph node (MLN) and collagenase digested colons (gated on CD44 + CD62L−) and labeled with EF5-Cy5. Identification of stabilized HIF in dissected colons by IVIS imaging from mice adoptively transferred with 0.5 × 106 B6.ΔODD.luc CD4+ T cells. Prior to euthanizing, mice were injected with Luciferase substrate for 10 min. Freshly dissected colons were flushed and imaged using IVIS. Representative IVIS photograph and corresponding colon micrograph sections were stained with H&E, n = 4. c Healthy colons from CD45RBlow transferred mice, with low luciferase activity in the upper panel. Colon histological sections (lower panel, Scale bar: 184.4 mm). d High luciferase activity in whole colon (upper panel) and histology micrograph with lymphocyte infiltrates in CD45RBhigh transferred mice at 6-week post transfer (lower panel, Scale bar: 184.4 mm). e Image radiance was quantified using IVIS and expressed as photons/sec/cm2/sr. ( n = 3, two-tailed T test). f Colon inflammation score (weight/length) in adoptively transferred animals from ( c ) and ( d ) ( n = 4, two-tailed T test). Male and female mice used in ( a ) and ( b ), male recipients and male and female donors used in ( c )–( f ). Radiance of IVIS image was quantified and expressed as photons/sec/cm2/sr. Data expressed as Mean ±S.E.M., * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001 vs. indicated.

    Journal: Nature Communications

    Article Title: HIF-2α- dependent induction of miR-29a restrains T H 1 activity during T cell dependent colitis

    doi: 10.1038/s41467-024-52113-y

    Figure Lengend Snippet: Chronic T cell-mediated colitis was induced in B6.B6.RAG1−/− mice by intraperitoneal injection (0.5 × 106) of naïve CD4+ CD45RBhigh or CD45RBlow T cells. Identification of 2-nitroimidazole EF5 hypoxic adducts in B6.B6.RAG1−/− mice injected with C57BL/6J/6JT cells. 6 weeks post-treatment spleens, lymph nodes and collagenase-digested colon tissues were assessed. a Flow cytometric sub-analysis of cellular profile within Cy5-labeled EF5 (nitroimidazole; injected IP-3h) naïve and effector memory CD4+ T cells from the spleen, mesenteric lymph nodes and the colons, ( n = 3–4, one-way ANOVA). b Effector memory CD4+ T cells from the spleen, mesenteric lymph node (MLN) and collagenase digested colons (gated on CD44 + CD62L−) and labeled with EF5-Cy5. Identification of stabilized HIF in dissected colons by IVIS imaging from mice adoptively transferred with 0.5 × 106 B6.ΔODD.luc CD4+ T cells. Prior to euthanizing, mice were injected with Luciferase substrate for 10 min. Freshly dissected colons were flushed and imaged using IVIS. Representative IVIS photograph and corresponding colon micrograph sections were stained with H&E, n = 4. c Healthy colons from CD45RBlow transferred mice, with low luciferase activity in the upper panel. Colon histological sections (lower panel, Scale bar: 184.4 mm). d High luciferase activity in whole colon (upper panel) and histology micrograph with lymphocyte infiltrates in CD45RBhigh transferred mice at 6-week post transfer (lower panel, Scale bar: 184.4 mm). e Image radiance was quantified using IVIS and expressed as photons/sec/cm2/sr. ( n = 3, two-tailed T test). f Colon inflammation score (weight/length) in adoptively transferred animals from ( c ) and ( d ) ( n = 4, two-tailed T test). Male and female mice used in ( a ) and ( b ), male recipients and male and female donors used in ( c )–( f ). Radiance of IVIS image was quantified and expressed as photons/sec/cm2/sr. Data expressed as Mean ±S.E.M., * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001 vs. indicated.

    Article Snippet: Antibodies used were as follows: anti-CD62L-APC (Clone: MEL-14, Cat#: 17-0621-82, Invitrogen), 1:500, anti-CD44-FITC (Clone: IM7, Cat#: 11-0441-82, Invitrogen), 1:200, anti-CD25-PB (Clone PC61.5 Cat#: 404-0251-82, Invitrogen), 1:400, anti-CD4-FITC (Clone: GK1.5, Cat#: 11-0041-82, Invitrogen), 1:400, anti-CD45RB-PE (Clone: C363.16A, Cat#: 12-0455-82, Invitrogen), 1:600, anti-CD62L-APC (Clone: MEL-14, Cat#: 17-0621-82, Invitrogen), 1:500.

    Techniques: Injection, Labeling, Imaging, Luciferase, Staining, Activity Assay, Two Tailed Test