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fgf21 ko mice  (Cyagen Biosciences)


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    Cyagen Biosciences fgf21 ko mice
    Figure 4 Healthy plasma increased <t>FGF21</t> and its' receptors expression in the tMCAO mouse brain photomicrograph showed that Western blot images of FGF21 bands (A) and bar graph (B) showed semiquantification of FGF21 protein expression in sham, saline-injected and plasma-injected mouse brain at 3 days of tMCAO. Data are mean±SD, n=3 per group. *p<0.05, plasma-injected versus control mice. RT-PCR quantification of FGF21 (C), β-klotho (D), FGFR1 (E), FGFR2 (F) and FGFR3 (G) mRNA expression in the sham, saline-injected and plasma-injected mouse brain at 3 days of tMCAO. Data are mean±SD, n=4 per group. *p<0.05; ** p<0.01, plasma-injected versus control. FGF21, fibroblast growth factor 21; FGFR1, fibroblast growth factor receptor; tMCAO, transient middle cerebral artery occlusion.
    Fgf21 Ko Mice, supplied by Cyagen Biosciences, used in various techniques. Bioz Stars score: 93/100, based on 9 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/fgf21/Fgf21/pm33785536-31-0-7
    Average 93 stars, based on 9 article reviews
    fgf21 ko mice - by Bioz Stars, 2026-10
    93/100 stars

    Images

    1) Product Images from "Plasma from healthy donors protects blood-brain barrier integrity via FGF21 and improves the recovery in a mouse model of cerebral ischaemia."

    Article Title: Plasma from healthy donors protects blood-brain barrier integrity via FGF21 and improves the recovery in a mouse model of cerebral ischaemia.

    Journal: Stroke and vascular neurology

    doi: 10.1136/svn-2020-000774

    Figure 4 Healthy plasma increased FGF21 and its' receptors expression in the tMCAO mouse brain photomicrograph showed that Western blot images of FGF21 bands (A) and bar graph (B) showed semiquantification of FGF21 protein expression in sham, saline-injected and plasma-injected mouse brain at 3 days of tMCAO. Data are mean±SD, n=3 per group. *p<0.05, plasma-injected versus control mice. RT-PCR quantification of FGF21 (C), β-klotho (D), FGFR1 (E), FGFR2 (F) and FGFR3 (G) mRNA expression in the sham, saline-injected and plasma-injected mouse brain at 3 days of tMCAO. Data are mean±SD, n=4 per group. *p<0.05; ** p<0.01, plasma-injected versus control. FGF21, fibroblast growth factor 21; FGFR1, fibroblast growth factor receptor; tMCAO, transient middle cerebral artery occlusion.
    Figure Legend Snippet: Figure 4 Healthy plasma increased FGF21 and its' receptors expression in the tMCAO mouse brain photomicrograph showed that Western blot images of FGF21 bands (A) and bar graph (B) showed semiquantification of FGF21 protein expression in sham, saline-injected and plasma-injected mouse brain at 3 days of tMCAO. Data are mean±SD, n=3 per group. *p<0.05, plasma-injected versus control mice. RT-PCR quantification of FGF21 (C), β-klotho (D), FGFR1 (E), FGFR2 (F) and FGFR3 (G) mRNA expression in the sham, saline-injected and plasma-injected mouse brain at 3 days of tMCAO. Data are mean±SD, n=4 per group. *p<0.05; ** p<0.01, plasma-injected versus control. FGF21, fibroblast growth factor 21; FGFR1, fibroblast growth factor receptor; tMCAO, transient middle cerebral artery occlusion.

    Techniques Used: Clinical Proteomics, Expressing, Western Blot, Saline, Injection, Control, Reverse Transcription Polymerase Chain Reaction

    Figure 5 Depletion of FGF21 in plasma reversed the beneficial effect of healthy plasma in the tMCAO mice bar graphs showed that neurological severity score (A), rotarod test (B), EBST (C) and corner test (D) in wild-type mice that treated with plasma from wild-type mice (WT+WT); wild-type mice that treated with plasma from FGF21-/- mice (WT+ FGF21-/- plasma); and FGF21- /- mice that treated with wild-type plasma (FGF21-/-+ WT plasma) at 1, 3, 7 and 14 days after tMCAO. (E, F) Images of cresyl violet-stained brain sections of WT+ saline group, WT+WT group, WT+ FGF21-/- plasma group, and FGF21-/-+ WT plasma group at 3 and 14 days of tMCAO. Dashed line showed infarct area in the ipsilateral hemisphere of the brain. Semiquantification of brain oedema and infarct volume in WT+ saline group, WT+WT group, WT+ FGF21-/- plasma group, and FGF21-/-+ WT plasma group at 3 days of tMCAO (G, H). Bbar graph showed that the brain atrophy volume and the volume ratio of the ipsilateral hemisphere and contralateral hemisphere in the WT+ saline group, WT+WT group, WT+ FGF21-/- plasma group and FGF21-/-+ WT plasma group at 14 days in the tMCAO mouse brain (I, J). Data are mean±SD, n=10 per group. *p<0.05, **p<0.01, ***p<0.001, FGF21-treated versus control mice. EBST, elevated body swing test; FGF21, fibroblast growth factor 21; tMCAO, transient middle cerebral artery occlusion.
    Figure Legend Snippet: Figure 5 Depletion of FGF21 in plasma reversed the beneficial effect of healthy plasma in the tMCAO mice bar graphs showed that neurological severity score (A), rotarod test (B), EBST (C) and corner test (D) in wild-type mice that treated with plasma from wild-type mice (WT+WT); wild-type mice that treated with plasma from FGF21-/- mice (WT+ FGF21-/- plasma); and FGF21- /- mice that treated with wild-type plasma (FGF21-/-+ WT plasma) at 1, 3, 7 and 14 days after tMCAO. (E, F) Images of cresyl violet-stained brain sections of WT+ saline group, WT+WT group, WT+ FGF21-/- plasma group, and FGF21-/-+ WT plasma group at 3 and 14 days of tMCAO. Dashed line showed infarct area in the ipsilateral hemisphere of the brain. Semiquantification of brain oedema and infarct volume in WT+ saline group, WT+WT group, WT+ FGF21-/- plasma group, and FGF21-/-+ WT plasma group at 3 days of tMCAO (G, H). Bbar graph showed that the brain atrophy volume and the volume ratio of the ipsilateral hemisphere and contralateral hemisphere in the WT+ saline group, WT+WT group, WT+ FGF21-/- plasma group and FGF21-/-+ WT plasma group at 14 days in the tMCAO mouse brain (I, J). Data are mean±SD, n=10 per group. *p<0.05, **p<0.01, ***p<0.001, FGF21-treated versus control mice. EBST, elevated body swing test; FGF21, fibroblast growth factor 21; tMCAO, transient middle cerebral artery occlusion.

    Techniques Used: Clinical Proteomics, Staining, Saline, Control

    Figure 6 Depletion of FGF21 in plasma diminished the beneficial effects of plasma-induced BBB protection in mice after 3 days of tMCAO coimmunostaining of endothelial cell marker CD31(red) with BBB (green) ZO-1(A), occludin (C) and claudin-5 (E) in the peri-infarct area of the striatum in wild-type mice that treated with saline (WT+ saline), wild-type mice that treated with wild mouse plasma (WT+WT), wild-type mice that treated with plasma from FGF21-/- mice (WT+ FGF21-/- plasma) and FGF21- /- KO mice that treated with wild-type plasma (FGF21-/- + WT plasma) at 3 days of tMCAO. Arrows indicate the gaps in BBB tight junction proteins, scale bar=10 μm. Quantification of gaps that formed on BBB tight junction proteins ZO-1(B), occludin (D) and claudin-5 (F) in the WT+ saline group, WT+WT group, WT+ FGF21-/- plasma group, and FGF21-/-+ WT plasma group at 3 days of tMCAO. Data are mean±SD, n=3 per group. **p<0.01. ***p<0.001. (G) Photomicrographs of IgG in the perifocal area of WT+ saline group, WT+WT group, WT+ FGF21-/- plasma group and FGF21-/-+ WT plasma group at 3 days after stroke. Scale bar=75 μm. (H) Bar graph showed semiquantification of IgG extravasation in the WT+ Saline group, WT+WT group, WT+FGF21-/- plasma group and FGF21-/-+WT plasma group. Data are presented as mean±SD, n=5 per group. * p<0.05; ****p<0.001, plasma versus control. BBB, blood-brain barrier; FGF21, fibroblast growth factor 21; tMCAO, transient middle cerebral artery occlusion; ZO-1, zonula occludens-1.
    Figure Legend Snippet: Figure 6 Depletion of FGF21 in plasma diminished the beneficial effects of plasma-induced BBB protection in mice after 3 days of tMCAO coimmunostaining of endothelial cell marker CD31(red) with BBB (green) ZO-1(A), occludin (C) and claudin-5 (E) in the peri-infarct area of the striatum in wild-type mice that treated with saline (WT+ saline), wild-type mice that treated with wild mouse plasma (WT+WT), wild-type mice that treated with plasma from FGF21-/- mice (WT+ FGF21-/- plasma) and FGF21- /- KO mice that treated with wild-type plasma (FGF21-/- + WT plasma) at 3 days of tMCAO. Arrows indicate the gaps in BBB tight junction proteins, scale bar=10 μm. Quantification of gaps that formed on BBB tight junction proteins ZO-1(B), occludin (D) and claudin-5 (F) in the WT+ saline group, WT+WT group, WT+ FGF21-/- plasma group, and FGF21-/-+ WT plasma group at 3 days of tMCAO. Data are mean±SD, n=3 per group. **p<0.01. ***p<0.001. (G) Photomicrographs of IgG in the perifocal area of WT+ saline group, WT+WT group, WT+ FGF21-/- plasma group and FGF21-/-+ WT plasma group at 3 days after stroke. Scale bar=75 μm. (H) Bar graph showed semiquantification of IgG extravasation in the WT+ Saline group, WT+WT group, WT+FGF21-/- plasma group and FGF21-/-+WT plasma group. Data are presented as mean±SD, n=5 per group. * p<0.05; ****p<0.001, plasma versus control. BBB, blood-brain barrier; FGF21, fibroblast growth factor 21; tMCAO, transient middle cerebral artery occlusion; ZO-1, zonula occludens-1.

    Techniques Used: Clinical Proteomics, Marker, Saline, Control

    Related Articles

    Microscopy:

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    Enzyme-linked Immunosorbent Assay:

    Article Title: Cancer-associated adipocytes mediate CD8 + T cell dysfunction via FGF21-driven lipolysis.
    Article Snippet: .. REAGENT or RESOURCE SOURCE IDENTIFIER Electron microscope fixative buffer Servicebio Cat#G1102 Human FGF21 ELISA Kit Sangon Biotech Cat#D711036-0096 Mouse FGF21 ELISA Kit Sangon Biotech Cat#D721010-0096 Stemcell EasySep TM Mouse Pan-Naive T Cell Isolation Kit Stemcell Cat#19848 Stemcell EasySep TM Mouse Naı̈ve CD8 + T Cell Isolation Kit Stemcell Cat#19858 All-in one RT SuperМix Perfect for qPCR kit Vazyme Cat#R333-01 SYBR Green qPCR Master Mix Vazyme Cat#Q711-03 Deposited data The Bulk RNA-Seq data This paper Sequence Read Archive (SRA) data: PRJNA1170421 Experimental models: Cell lines MC38 Laboratory of Bin Ma N/A E0771 ATCC CRL-3461 Experimental models: Organisms/strains C57BL/6 mice Shanghai Model Organisms Center SM-001 Fgf21 flox/+ mice Cyagen CKOCMP-56636-Fgf21-B6N-VA, C57BL/6N Adipoq-cre mice Cyagen C001042 Oligonucleotides shRNA and sgRNA sequences Method N/A RT-qPCR primer sequences Table S2 N/A Recombinant DNA pMD2.G Laboratory of Qi Wang N/A psPAX2 Laboratory of Qi Wang N/A pLenti-CRISPRv2/Cas9 Laboratory of Qi Wang N/A Software and algorithms FlowJo_V10 software TreeStar N/A Graphpad prism_V10 GraphPad Software N/A Image J NIH N/A 20 Cell Reports 44, 116526, November 25, 2025 reported abnormalities. ..

    Cell Isolation:

    Article Title: Cancer-associated adipocytes mediate CD8 + T cell dysfunction via FGF21-driven lipolysis.
    Article Snippet: .. REAGENT or RESOURCE SOURCE IDENTIFIER Electron microscope fixative buffer Servicebio Cat#G1102 Human FGF21 ELISA Kit Sangon Biotech Cat#D711036-0096 Mouse FGF21 ELISA Kit Sangon Biotech Cat#D721010-0096 Stemcell EasySep TM Mouse Pan-Naive T Cell Isolation Kit Stemcell Cat#19848 Stemcell EasySep TM Mouse Naı̈ve CD8 + T Cell Isolation Kit Stemcell Cat#19858 All-in one RT SuperМix Perfect for qPCR kit Vazyme Cat#R333-01 SYBR Green qPCR Master Mix Vazyme Cat#Q711-03 Deposited data The Bulk RNA-Seq data This paper Sequence Read Archive (SRA) data: PRJNA1170421 Experimental models: Cell lines MC38 Laboratory of Bin Ma N/A E0771 ATCC CRL-3461 Experimental models: Organisms/strains C57BL/6 mice Shanghai Model Organisms Center SM-001 Fgf21 flox/+ mice Cyagen CKOCMP-56636-Fgf21-B6N-VA, C57BL/6N Adipoq-cre mice Cyagen C001042 Oligonucleotides shRNA and sgRNA sequences Method N/A RT-qPCR primer sequences Table S2 N/A Recombinant DNA pMD2.G Laboratory of Qi Wang N/A psPAX2 Laboratory of Qi Wang N/A pLenti-CRISPRv2/Cas9 Laboratory of Qi Wang N/A Software and algorithms FlowJo_V10 software TreeStar N/A Graphpad prism_V10 GraphPad Software N/A Image J NIH N/A 20 Cell Reports 44, 116526, November 25, 2025 reported abnormalities. ..

    Real-time Polymerase Chain Reaction:

    Article Title: Cancer-associated adipocytes mediate CD8 + T cell dysfunction via FGF21-driven lipolysis.
    Article Snippet: .. REAGENT or RESOURCE SOURCE IDENTIFIER Electron microscope fixative buffer Servicebio Cat#G1102 Human FGF21 ELISA Kit Sangon Biotech Cat#D711036-0096 Mouse FGF21 ELISA Kit Sangon Biotech Cat#D721010-0096 Stemcell EasySep TM Mouse Pan-Naive T Cell Isolation Kit Stemcell Cat#19848 Stemcell EasySep TM Mouse Naı̈ve CD8 + T Cell Isolation Kit Stemcell Cat#19858 All-in one RT SuperМix Perfect for qPCR kit Vazyme Cat#R333-01 SYBR Green qPCR Master Mix Vazyme Cat#Q711-03 Deposited data The Bulk RNA-Seq data This paper Sequence Read Archive (SRA) data: PRJNA1170421 Experimental models: Cell lines MC38 Laboratory of Bin Ma N/A E0771 ATCC CRL-3461 Experimental models: Organisms/strains C57BL/6 mice Shanghai Model Organisms Center SM-001 Fgf21 flox/+ mice Cyagen CKOCMP-56636-Fgf21-B6N-VA, C57BL/6N Adipoq-cre mice Cyagen C001042 Oligonucleotides shRNA and sgRNA sequences Method N/A RT-qPCR primer sequences Table S2 N/A Recombinant DNA pMD2.G Laboratory of Qi Wang N/A psPAX2 Laboratory of Qi Wang N/A pLenti-CRISPRv2/Cas9 Laboratory of Qi Wang N/A Software and algorithms FlowJo_V10 software TreeStar N/A Graphpad prism_V10 GraphPad Software N/A Image J NIH N/A 20 Cell Reports 44, 116526, November 25, 2025 reported abnormalities. ..

    SYBR Green Assay:

    Article Title: Cancer-associated adipocytes mediate CD8 + T cell dysfunction via FGF21-driven lipolysis.
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    RNA sequencing:

    Article Title: Cancer-associated adipocytes mediate CD8 + T cell dysfunction via FGF21-driven lipolysis.
    Article Snippet: .. REAGENT or RESOURCE SOURCE IDENTIFIER Electron microscope fixative buffer Servicebio Cat#G1102 Human FGF21 ELISA Kit Sangon Biotech Cat#D711036-0096 Mouse FGF21 ELISA Kit Sangon Biotech Cat#D721010-0096 Stemcell EasySep TM Mouse Pan-Naive T Cell Isolation Kit Stemcell Cat#19848 Stemcell EasySep TM Mouse Naı̈ve CD8 + T Cell Isolation Kit Stemcell Cat#19858 All-in one RT SuperМix Perfect for qPCR kit Vazyme Cat#R333-01 SYBR Green qPCR Master Mix Vazyme Cat#Q711-03 Deposited data The Bulk RNA-Seq data This paper Sequence Read Archive (SRA) data: PRJNA1170421 Experimental models: Cell lines MC38 Laboratory of Bin Ma N/A E0771 ATCC CRL-3461 Experimental models: Organisms/strains C57BL/6 mice Shanghai Model Organisms Center SM-001 Fgf21 flox/+ mice Cyagen CKOCMP-56636-Fgf21-B6N-VA, C57BL/6N Adipoq-cre mice Cyagen C001042 Oligonucleotides shRNA and sgRNA sequences Method N/A RT-qPCR primer sequences Table S2 N/A Recombinant DNA pMD2.G Laboratory of Qi Wang N/A psPAX2 Laboratory of Qi Wang N/A pLenti-CRISPRv2/Cas9 Laboratory of Qi Wang N/A Software and algorithms FlowJo_V10 software TreeStar N/A Graphpad prism_V10 GraphPad Software N/A Image J NIH N/A 20 Cell Reports 44, 116526, November 25, 2025 reported abnormalities. ..

    Sequencing:

    Article Title: Cancer-associated adipocytes mediate CD8 + T cell dysfunction via FGF21-driven lipolysis.
    Article Snippet: .. REAGENT or RESOURCE SOURCE IDENTIFIER Electron microscope fixative buffer Servicebio Cat#G1102 Human FGF21 ELISA Kit Sangon Biotech Cat#D711036-0096 Mouse FGF21 ELISA Kit Sangon Biotech Cat#D721010-0096 Stemcell EasySep TM Mouse Pan-Naive T Cell Isolation Kit Stemcell Cat#19848 Stemcell EasySep TM Mouse Naı̈ve CD8 + T Cell Isolation Kit Stemcell Cat#19858 All-in one RT SuperМix Perfect for qPCR kit Vazyme Cat#R333-01 SYBR Green qPCR Master Mix Vazyme Cat#Q711-03 Deposited data The Bulk RNA-Seq data This paper Sequence Read Archive (SRA) data: PRJNA1170421 Experimental models: Cell lines MC38 Laboratory of Bin Ma N/A E0771 ATCC CRL-3461 Experimental models: Organisms/strains C57BL/6 mice Shanghai Model Organisms Center SM-001 Fgf21 flox/+ mice Cyagen CKOCMP-56636-Fgf21-B6N-VA, C57BL/6N Adipoq-cre mice Cyagen C001042 Oligonucleotides shRNA and sgRNA sequences Method N/A RT-qPCR primer sequences Table S2 N/A Recombinant DNA pMD2.G Laboratory of Qi Wang N/A psPAX2 Laboratory of Qi Wang N/A pLenti-CRISPRv2/Cas9 Laboratory of Qi Wang N/A Software and algorithms FlowJo_V10 software TreeStar N/A Graphpad prism_V10 GraphPad Software N/A Image J NIH N/A 20 Cell Reports 44, 116526, November 25, 2025 reported abnormalities. ..

    shRNA:

    Article Title: Cancer-associated adipocytes mediate CD8 + T cell dysfunction via FGF21-driven lipolysis.
    Article Snippet: .. REAGENT or RESOURCE SOURCE IDENTIFIER Electron microscope fixative buffer Servicebio Cat#G1102 Human FGF21 ELISA Kit Sangon Biotech Cat#D711036-0096 Mouse FGF21 ELISA Kit Sangon Biotech Cat#D721010-0096 Stemcell EasySep TM Mouse Pan-Naive T Cell Isolation Kit Stemcell Cat#19848 Stemcell EasySep TM Mouse Naı̈ve CD8 + T Cell Isolation Kit Stemcell Cat#19858 All-in one RT SuperМix Perfect for qPCR kit Vazyme Cat#R333-01 SYBR Green qPCR Master Mix Vazyme Cat#Q711-03 Deposited data The Bulk RNA-Seq data This paper Sequence Read Archive (SRA) data: PRJNA1170421 Experimental models: Cell lines MC38 Laboratory of Bin Ma N/A E0771 ATCC CRL-3461 Experimental models: Organisms/strains C57BL/6 mice Shanghai Model Organisms Center SM-001 Fgf21 flox/+ mice Cyagen CKOCMP-56636-Fgf21-B6N-VA, C57BL/6N Adipoq-cre mice Cyagen C001042 Oligonucleotides shRNA and sgRNA sequences Method N/A RT-qPCR primer sequences Table S2 N/A Recombinant DNA pMD2.G Laboratory of Qi Wang N/A psPAX2 Laboratory of Qi Wang N/A pLenti-CRISPRv2/Cas9 Laboratory of Qi Wang N/A Software and algorithms FlowJo_V10 software TreeStar N/A Graphpad prism_V10 GraphPad Software N/A Image J NIH N/A 20 Cell Reports 44, 116526, November 25, 2025 reported abnormalities. ..

    Quantitative RT-PCR:

    Article Title: Cancer-associated adipocytes mediate CD8 + T cell dysfunction via FGF21-driven lipolysis.
    Article Snippet: .. REAGENT or RESOURCE SOURCE IDENTIFIER Electron microscope fixative buffer Servicebio Cat#G1102 Human FGF21 ELISA Kit Sangon Biotech Cat#D711036-0096 Mouse FGF21 ELISA Kit Sangon Biotech Cat#D721010-0096 Stemcell EasySep TM Mouse Pan-Naive T Cell Isolation Kit Stemcell Cat#19848 Stemcell EasySep TM Mouse Naı̈ve CD8 + T Cell Isolation Kit Stemcell Cat#19858 All-in one RT SuperМix Perfect for qPCR kit Vazyme Cat#R333-01 SYBR Green qPCR Master Mix Vazyme Cat#Q711-03 Deposited data The Bulk RNA-Seq data This paper Sequence Read Archive (SRA) data: PRJNA1170421 Experimental models: Cell lines MC38 Laboratory of Bin Ma N/A E0771 ATCC CRL-3461 Experimental models: Organisms/strains C57BL/6 mice Shanghai Model Organisms Center SM-001 Fgf21 flox/+ mice Cyagen CKOCMP-56636-Fgf21-B6N-VA, C57BL/6N Adipoq-cre mice Cyagen C001042 Oligonucleotides shRNA and sgRNA sequences Method N/A RT-qPCR primer sequences Table S2 N/A Recombinant DNA pMD2.G Laboratory of Qi Wang N/A psPAX2 Laboratory of Qi Wang N/A pLenti-CRISPRv2/Cas9 Laboratory of Qi Wang N/A Software and algorithms FlowJo_V10 software TreeStar N/A Graphpad prism_V10 GraphPad Software N/A Image J NIH N/A 20 Cell Reports 44, 116526, November 25, 2025 reported abnormalities. ..

    Recombinant:

    Article Title: Cancer-associated adipocytes mediate CD8 + T cell dysfunction via FGF21-driven lipolysis.
    Article Snippet: .. REAGENT or RESOURCE SOURCE IDENTIFIER Electron microscope fixative buffer Servicebio Cat#G1102 Human FGF21 ELISA Kit Sangon Biotech Cat#D711036-0096 Mouse FGF21 ELISA Kit Sangon Biotech Cat#D721010-0096 Stemcell EasySep TM Mouse Pan-Naive T Cell Isolation Kit Stemcell Cat#19848 Stemcell EasySep TM Mouse Naı̈ve CD8 + T Cell Isolation Kit Stemcell Cat#19858 All-in one RT SuperМix Perfect for qPCR kit Vazyme Cat#R333-01 SYBR Green qPCR Master Mix Vazyme Cat#Q711-03 Deposited data The Bulk RNA-Seq data This paper Sequence Read Archive (SRA) data: PRJNA1170421 Experimental models: Cell lines MC38 Laboratory of Bin Ma N/A E0771 ATCC CRL-3461 Experimental models: Organisms/strains C57BL/6 mice Shanghai Model Organisms Center SM-001 Fgf21 flox/+ mice Cyagen CKOCMP-56636-Fgf21-B6N-VA, C57BL/6N Adipoq-cre mice Cyagen C001042 Oligonucleotides shRNA and sgRNA sequences Method N/A RT-qPCR primer sequences Table S2 N/A Recombinant DNA pMD2.G Laboratory of Qi Wang N/A psPAX2 Laboratory of Qi Wang N/A pLenti-CRISPRv2/Cas9 Laboratory of Qi Wang N/A Software and algorithms FlowJo_V10 software TreeStar N/A Graphpad prism_V10 GraphPad Software N/A Image J NIH N/A 20 Cell Reports 44, 116526, November 25, 2025 reported abnormalities. ..

    Software:

    Article Title: Cancer-associated adipocytes mediate CD8 + T cell dysfunction via FGF21-driven lipolysis.
    Article Snippet: .. REAGENT or RESOURCE SOURCE IDENTIFIER Electron microscope fixative buffer Servicebio Cat#G1102 Human FGF21 ELISA Kit Sangon Biotech Cat#D711036-0096 Mouse FGF21 ELISA Kit Sangon Biotech Cat#D721010-0096 Stemcell EasySep TM Mouse Pan-Naive T Cell Isolation Kit Stemcell Cat#19848 Stemcell EasySep TM Mouse Naı̈ve CD8 + T Cell Isolation Kit Stemcell Cat#19858 All-in one RT SuperМix Perfect for qPCR kit Vazyme Cat#R333-01 SYBR Green qPCR Master Mix Vazyme Cat#Q711-03 Deposited data The Bulk RNA-Seq data This paper Sequence Read Archive (SRA) data: PRJNA1170421 Experimental models: Cell lines MC38 Laboratory of Bin Ma N/A E0771 ATCC CRL-3461 Experimental models: Organisms/strains C57BL/6 mice Shanghai Model Organisms Center SM-001 Fgf21 flox/+ mice Cyagen CKOCMP-56636-Fgf21-B6N-VA, C57BL/6N Adipoq-cre mice Cyagen C001042 Oligonucleotides shRNA and sgRNA sequences Method N/A RT-qPCR primer sequences Table S2 N/A Recombinant DNA pMD2.G Laboratory of Qi Wang N/A psPAX2 Laboratory of Qi Wang N/A pLenti-CRISPRv2/Cas9 Laboratory of Qi Wang N/A Software and algorithms FlowJo_V10 software TreeStar N/A Graphpad prism_V10 GraphPad Software N/A Image J NIH N/A 20 Cell Reports 44, 116526, November 25, 2025 reported abnormalities. ..

    Knock-Out:

    Article Title: FGF21 Blunts Cardiac Ischemia/Reperfusion Injury by Promoting Autophagic Flux Via Stat1/Irgm1 Pathway.
    Article Snippet: This study aimed to investigate the underlying mechanisms of Fibroblast Growth Factor 21 (FGF21) in myocardial ischemia/ reperfusion (I/R) injury.. First, FGF21 was upregulated in the serum of patients with myocardial I/R injury as well as in I/R hearts of mice and hypoxia/reoxygenation (H/R) neonatal rat cardiomyocytes (NRCMs).. While FGF21 knockout exacerbated such injury, which was mitigated by rhFGF21.

    Article Title: Fibroblast growth factor 21 attenuates ventilator-induced lung injury by inhibiting the NLRP3/caspase-1/GSDMD pyroptotic pathway.
    Article Snippet: .. FGF21 global knockout mice (C57BL/6N-Fgf21em1Cyagen, NCBI ID 56,636) were obtained from Cyagen Biosciences Inc (Santa Clara, CA, USA). ..

    Article Title: Endurance Exercise-Induced Fgf21 Promotes Skeletal Muscle Fiber Conversion through TGF-β1 and p38 MAPK Signaling Pathway.
    Article Snippet: .. The Fgf21 conventional knockout mouse model used in this study was designed and developed with high-throughput electroporation of zygotes by Cyagen Biosciences Inc (Suzhou, China). ..

    Article Title: Investigation of the effects and mechanisms of endogenous deletion of FGF21 on cognitive functions.
    Article Snippet: Cognitive impairment is characterized by reduced cognitive abilities in one or more areas such as language, memory, and reasoning.. It is a common problem in various neurological diseases and the aging process, seriously affecting people’s quality of life and overall health.. Fibroblast growth factor 21 (FGF21), a hormone regulating glucose/lipid metabolism and energy homeostasis, exhibits neuroprotective properties.

    Generated:

    Article Title: FGF21 Blunts Cardiac Ischemia/Reperfusion Injury by Promoting Autophagic Flux Via Stat1/Irgm1 Pathway.
    Article Snippet: This study aimed to investigate the underlying mechanisms of Fibroblast Growth Factor 21 (FGF21) in myocardial ischemia/ reperfusion (I/R) injury.. First, FGF21 was upregulated in the serum of patients with myocardial I/R injury as well as in I/R hearts of mice and hypoxia/reoxygenation (H/R) neonatal rat cardiomyocytes (NRCMs).. While FGF21 knockout exacerbated such injury, which was mitigated by rhFGF21.

    CRISPR:

    Article Title: Endurance Exercise-Induced Fgf21 Promotes Skeletal Muscle Fiber Conversion through TGF-β1 and p38 MAPK Signaling Pathway.
    Article Snippet: Wild-type male C57BL/6 mice aged about 12 weeks were purchased from the Experimental Animal Center of Shanxi Provincial People’s Hospital (Taiyuan, Shanxi, China). .. Fgf21 KO mice (named C57BL/6N-Fgf21em1cyage) were created via CRISPR/Cas-mediated genome engineering (KOCMP-56636-Fgf21-B6N-VA, Cyagen, Suzhou, China). ..

    Electroporation:

    Article Title: Endurance Exercise-Induced Fgf21 Promotes Skeletal Muscle Fiber Conversion through TGF-β1 and p38 MAPK Signaling Pathway.
    Article Snippet: .. The Fgf21 conventional knockout mouse model used in this study was designed and developed with high-throughput electroporation of zygotes by Cyagen Biosciences Inc (Suzhou, China). ..

    other:

    Article Title: Cancer-associated adipocytes mediate CD8 + T cell dysfunction via FGF21-driven lipolysis.
    Article Snippet: Adipoq-Cre (C001042, C57BL/6N) and Fgf21 flox/+ mice (CKOCMP-56636-Fgf21-B6N-VA, C57BL/6N) were purchased from Cyagen Biosciences.



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    Circulating biomarkers levels in chronic heart failure patients and controls

    Journal: ESC Heart Failure

    Article Title: Integrated miRNA-cytokine profiling reveals a molecular signature of cachexia in patients with chronic heart failure

    doi: 10.1093/eschf/xvag229

    Figure Lengend Snippet: Circulating biomarkers levels in chronic heart failure patients and controls

    Article Snippet: Serum concentrations of GDF-15 (#ELH-GDF15-1) and FGF-21 (#ELH-FGF21-1) were measured using ELISA (RayBiotech, Norcross, GA, USA) according to manufacturers’ instructions.

    Techniques:

    Circulating miRNAs and cytokines as molecular signatures of heart failure. Differences in serum levels of GDF-15 and FGF-21 in CHF patients and controls. Serum levels of GDF-15 by ELISA assay in patients with heart failure (HF) ( n = 25) and the control group ( n = 10). ( A ) Data showed significant upregulation of GDF-15 in CHF vs controls ( P < .001). ( B ) FGF-21 levels did not differ significantly between groups. Correlations between GDF-15 and selected miRNAs in CHF patients. ( C , D ) In CHF patients, GDF-15 levels were positively associated with miR-29b ( ρ = 0.42, P = .037) and miR-486 ( ρ = 0.42, P = .039). Data are expressed as fold change and are presented as mean ± SEM. Student's t -test or Mann–Whitney test was used for normally distributed data or non-normally distributed data, respectively. *** P ≤ .001.

    Journal: ESC Heart Failure

    Article Title: Integrated miRNA-cytokine profiling reveals a molecular signature of cachexia in patients with chronic heart failure

    doi: 10.1093/eschf/xvag229

    Figure Lengend Snippet: Circulating miRNAs and cytokines as molecular signatures of heart failure. Differences in serum levels of GDF-15 and FGF-21 in CHF patients and controls. Serum levels of GDF-15 by ELISA assay in patients with heart failure (HF) ( n = 25) and the control group ( n = 10). ( A ) Data showed significant upregulation of GDF-15 in CHF vs controls ( P < .001). ( B ) FGF-21 levels did not differ significantly between groups. Correlations between GDF-15 and selected miRNAs in CHF patients. ( C , D ) In CHF patients, GDF-15 levels were positively associated with miR-29b ( ρ = 0.42, P = .037) and miR-486 ( ρ = 0.42, P = .039). Data are expressed as fold change and are presented as mean ± SEM. Student's t -test or Mann–Whitney test was used for normally distributed data or non-normally distributed data, respectively. *** P ≤ .001.

    Article Snippet: Serum concentrations of GDF-15 (#ELH-GDF15-1) and FGF-21 (#ELH-FGF21-1) were measured using ELISA (RayBiotech, Norcross, GA, USA) according to manufacturers’ instructions.

    Techniques: Enzyme-linked Immunosorbent Assay, Control, MANN-WHITNEY

    Molecular profiles in CHF patients. Differences in serum levels of GDF-15 and FGF-21 among heart failure patients with and without cardiac cachexia. Circulating levels of GDF-15 and FGF-21 were analyzed in CHF patients with cardiac cachexia (CC) ( n = 10) and without cardiac cachexia (nCC) ( n = 15), and a control group ( n = 10). ( A ) Significant difference in GDF-15 levels was observed between patients with CC or nCC vs controls (all P < .001). ( B ) Levels of FGF-21 were significantly higher in CHF with CC compared with nCC ( P = .012) and vs controls ( P = .010) ( C ). Spearman’s correlation analysis revealed that in CHF patients with CC, GDF-15 negatively correlated with miR-21 ( ρ = −0.81, P = .007). ( D ) In the same group, FGF-21 negatively correlated with miR-486 ( ρ = −0.69, P = .035). Data are expressed as fold change and are presented as mean ± SEM. One-way ANOVA test or Kruskal–Wallis test was used for normally distributed data or non-normally distributed data, respectively. * P < .05, *** P ≤ .001.

    Journal: ESC Heart Failure

    Article Title: Integrated miRNA-cytokine profiling reveals a molecular signature of cachexia in patients with chronic heart failure

    doi: 10.1093/eschf/xvag229

    Figure Lengend Snippet: Molecular profiles in CHF patients. Differences in serum levels of GDF-15 and FGF-21 among heart failure patients with and without cardiac cachexia. Circulating levels of GDF-15 and FGF-21 were analyzed in CHF patients with cardiac cachexia (CC) ( n = 10) and without cardiac cachexia (nCC) ( n = 15), and a control group ( n = 10). ( A ) Significant difference in GDF-15 levels was observed between patients with CC or nCC vs controls (all P < .001). ( B ) Levels of FGF-21 were significantly higher in CHF with CC compared with nCC ( P = .012) and vs controls ( P = .010) ( C ). Spearman’s correlation analysis revealed that in CHF patients with CC, GDF-15 negatively correlated with miR-21 ( ρ = −0.81, P = .007). ( D ) In the same group, FGF-21 negatively correlated with miR-486 ( ρ = −0.69, P = .035). Data are expressed as fold change and are presented as mean ± SEM. One-way ANOVA test or Kruskal–Wallis test was used for normally distributed data or non-normally distributed data, respectively. * P < .05, *** P ≤ .001.

    Article Snippet: Serum concentrations of GDF-15 (#ELH-GDF15-1) and FGF-21 (#ELH-FGF21-1) were measured using ELISA (RayBiotech, Norcross, GA, USA) according to manufacturers’ instructions.

    Techniques: Control, Analysis

    Molecular profiles in cachectic patients with severe CHF. FGF-21 concentrations and their associations with NYHA functional class in patients with CHF. ( A ) Data show higher FGF-21 levels in NYHA class III-IV ( n = 13) compared with class I-II ( n = 9) ( P = .050) and the control group ( n = 10) ( P = .050). ( B ) In NYHA class III-IV, FGF-21 positively correlated with miR-15b ( r = 0.68, P = .014). Data are expressed as fold change and are presented as mean ± SEM. One-way ANOVA test or Kruskal–Wallis test was used for normally distributed data or non-normally distributed data, respectively. * P < .05.

    Journal: ESC Heart Failure

    Article Title: Integrated miRNA-cytokine profiling reveals a molecular signature of cachexia in patients with chronic heart failure

    doi: 10.1093/eschf/xvag229

    Figure Lengend Snippet: Molecular profiles in cachectic patients with severe CHF. FGF-21 concentrations and their associations with NYHA functional class in patients with CHF. ( A ) Data show higher FGF-21 levels in NYHA class III-IV ( n = 13) compared with class I-II ( n = 9) ( P = .050) and the control group ( n = 10) ( P = .050). ( B ) In NYHA class III-IV, FGF-21 positively correlated with miR-15b ( r = 0.68, P = .014). Data are expressed as fold change and are presented as mean ± SEM. One-way ANOVA test or Kruskal–Wallis test was used for normally distributed data or non-normally distributed data, respectively. * P < .05.

    Article Snippet: Serum concentrations of GDF-15 (#ELH-GDF15-1) and FGF-21 (#ELH-FGF21-1) were measured using ELISA (RayBiotech, Norcross, GA, USA) according to manufacturers’ instructions.

    Techniques: Functional Assay, Control

    Schematic representation of the circulating molecular profile associated with chronic heart failure and cardiac cachexia, characterized by dysregulation of muscle- and remodelling-related miRNAs and increased stress-responsive cytokines. CHF patients showed reduced miR-15b, miR-29b, miR-133a, and miR-486 and increased GDF-15, while cardiac cachexia was further associated with lower miR-29b and higher FGF-21 levels.

    Journal: ESC Heart Failure

    Article Title: Integrated miRNA-cytokine profiling reveals a molecular signature of cachexia in patients with chronic heart failure

    doi: 10.1093/eschf/xvag229

    Figure Lengend Snippet: Schematic representation of the circulating molecular profile associated with chronic heart failure and cardiac cachexia, characterized by dysregulation of muscle- and remodelling-related miRNAs and increased stress-responsive cytokines. CHF patients showed reduced miR-15b, miR-29b, miR-133a, and miR-486 and increased GDF-15, while cardiac cachexia was further associated with lower miR-29b and higher FGF-21 levels.

    Article Snippet: Serum concentrations of GDF-15 (#ELH-GDF15-1) and FGF-21 (#ELH-FGF21-1) were measured using ELISA (RayBiotech, Norcross, GA, USA) according to manufacturers’ instructions.

    Techniques: