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rat anti ccl1  (R&D Systems)


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    Structured Review

    R&D Systems rat anti ccl1
    Rat Anti Ccl1, supplied by R&D Systems, used in various techniques. Bioz Stars score: 91/100, based on 5 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/anti+ccl1/Human+Bax+Minus+C-Terminus+Antibody/pmc12002127-258-43-46
    Average 91 stars, based on 5 article reviews
    rat anti ccl1 - by Bioz Stars, 2026-10
    91/100 stars

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    Related Articles

    Recombinant:

    Article Title: Protumoral TSP50 Regulates Macrophage Activities and Polarization via Production of TNF-α and IL-1β, and Activation of the NF-κB Signaling Pathway
    Article Snippet: Anti-Phosphors-IκBα (9246), anti-phosphor-IKKα/β (2697), and anti-Phosphors-p65-Ser536 (3033) were obtained from Cell Signaling (Beverly, MA, USA). .. Anti-CCL1 (AF272 and AF845) (1:1000), anti-CCL5 (AF278 and AF478), human recombinant TNF-α, and human recombinant IL-1β were obtained from R&D systems (Boston, MA, USA). ..

    Incubation:

    Article Title: The chemokine binding protein M3 prevents diabetes induced by multiple low doses of streptozotocin.
    Article Snippet: .. Slides were incubated for 1 h at room temperature with purified primary Abs followed by incubation with the appropriate labeled secondary Abs for 30 min. Primary Abs used were anti-CD45 (catalog no. 550539), CD3 (catalog no. 553058), CD11c (catalog no. 553799), CD11b (catalog no. 553308), and CD31 (catalog no. 550274) from BD Biosciences, rat anti-insulin (catalog no. MAB1417), anti-CCL1 (catalog no. MAB845), anti-CCL21 (catalog no. AF455) from R&D Systems, anti-CXCL9 (provided by J. Farber and H. Zhang, National Institute of Allergy and Infectious Diseases), and guinea pig polyclonal anti-insulin (catalog no. A0564) from DakoCytomation. .. The secondary Abs used were Alexa Fluor 488 goat anti-rat IgG (catalog no. A-11006), Alexa Fluor 594 goat anti-rat IgG (catalog no. A-11007), and Alexa Fluor 594 goat anti-rabbit IgG (catalog no. A-11037) from Molecular Probes and FITC anti-Guinea Pig IgG (catalog no. 127065160) from Jackson ImmunoResearch Laboratories.

    Purification:

    Article Title: The chemokine binding protein M3 prevents diabetes induced by multiple low doses of streptozotocin.
    Article Snippet: .. Slides were incubated for 1 h at room temperature with purified primary Abs followed by incubation with the appropriate labeled secondary Abs for 30 min. Primary Abs used were anti-CD45 (catalog no. 550539), CD3 (catalog no. 553058), CD11c (catalog no. 553799), CD11b (catalog no. 553308), and CD31 (catalog no. 550274) from BD Biosciences, rat anti-insulin (catalog no. MAB1417), anti-CCL1 (catalog no. MAB845), anti-CCL21 (catalog no. AF455) from R&D Systems, anti-CXCL9 (provided by J. Farber and H. Zhang, National Institute of Allergy and Infectious Diseases), and guinea pig polyclonal anti-insulin (catalog no. A0564) from DakoCytomation. .. The secondary Abs used were Alexa Fluor 488 goat anti-rat IgG (catalog no. A-11006), Alexa Fluor 594 goat anti-rat IgG (catalog no. A-11007), and Alexa Fluor 594 goat anti-rabbit IgG (catalog no. A-11037) from Molecular Probes and FITC anti-Guinea Pig IgG (catalog no. 127065160) from Jackson ImmunoResearch Laboratories.

    Labeling:

    Article Title: The chemokine binding protein M3 prevents diabetes induced by multiple low doses of streptozotocin.
    Article Snippet: .. Slides were incubated for 1 h at room temperature with purified primary Abs followed by incubation with the appropriate labeled secondary Abs for 30 min. Primary Abs used were anti-CD45 (catalog no. 550539), CD3 (catalog no. 553058), CD11c (catalog no. 553799), CD11b (catalog no. 553308), and CD31 (catalog no. 550274) from BD Biosciences, rat anti-insulin (catalog no. MAB1417), anti-CCL1 (catalog no. MAB845), anti-CCL21 (catalog no. AF455) from R&D Systems, anti-CXCL9 (provided by J. Farber and H. Zhang, National Institute of Allergy and Infectious Diseases), and guinea pig polyclonal anti-insulin (catalog no. A0564) from DakoCytomation. .. The secondary Abs used were Alexa Fluor 488 goat anti-rat IgG (catalog no. A-11006), Alexa Fluor 594 goat anti-rat IgG (catalog no. A-11007), and Alexa Fluor 594 goat anti-rabbit IgG (catalog no. A-11037) from Molecular Probes and FITC anti-Guinea Pig IgG (catalog no. 127065160) from Jackson ImmunoResearch Laboratories.



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    ( A ) Il1a , Ccl5 , and <t>Ccl1</t> mRNA levels in the dorsal horn of female mice. n = 5 to 8. ( B ) Immunofluorescence image of IL-1α (green) in vascular endothelial cells (red). Scale bars, 50 μm (low) or 20 μm (high). ( C ) Double immunofluorescence staining of CCL1 (green) and vascular endothelial cells (red). Scale bars, 50 μm (low) or 20 μm (high). ( D and E ) Coimmunostaining image of F4/80 (green) and CD31 (red) in the spinal dorsal horn and the statistical graph. Scale bar, 200 μm. n = 5. ( F ) Intrathecal injection of IL-1α siRNA attenuated the mechanical allodynia induced by BTZ. n = 5. ( G ) Immunofluorescence image shows IL-1R1 (red) expression in macrophages (green). Scale bar, 10 μm. ( H and I ) Intrathecal IL-1R1 injection inhibited the up-regulation of F4/80 (green) and CD31 (red) in the near vascular of the spinal dorsal horn. Scale bar, 200 μm (H). The number of F4/80 high cells in the dorsal horn of the spinal cord [(I), left]. The percentage of F4/80 high area among CD31 + area [(I), right]. n = 4 to 5. ( J and K ) Immunostaining shows F4/80 (green) and CD31 (red) expression in the spinal dorsal horn. Scale bar, 200 μm (J). The number of F4/80 high cells in the dorsal horn of the spinal cord [(K), left]. The percentage of F4/80 high area among CD31 + area [(K), right]. n = 5. ( L ) Intrathecal injection of IL-1α siRNA attenuated the mechanical allodynia induced by BTZ. n = 5. Significance: * P < 0.05, # P < 0.05, ** P < 0.01, and ## P < 0.01.
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    Novus Biologicals anti mouse v450 conjugated ccl1
    ( A ) Il1a , Ccl5 , and <t>Ccl1</t> mRNA levels in the dorsal horn of female mice. n = 5 to 8. ( B ) Immunofluorescence image of IL-1α (green) in vascular endothelial cells (red). Scale bars, 50 μm (low) or 20 μm (high). ( C ) Double immunofluorescence staining of CCL1 (green) and vascular endothelial cells (red). Scale bars, 50 μm (low) or 20 μm (high). ( D and E ) Coimmunostaining image of F4/80 (green) and CD31 (red) in the spinal dorsal horn and the statistical graph. Scale bar, 200 μm. n = 5. ( F ) Intrathecal injection of IL-1α siRNA attenuated the mechanical allodynia induced by BTZ. n = 5. ( G ) Immunofluorescence image shows IL-1R1 (red) expression in macrophages (green). Scale bar, 10 μm. ( H and I ) Intrathecal IL-1R1 injection inhibited the up-regulation of F4/80 (green) and CD31 (red) in the near vascular of the spinal dorsal horn. Scale bar, 200 μm (H). The number of F4/80 high cells in the dorsal horn of the spinal cord [(I), left]. The percentage of F4/80 high area among CD31 + area [(I), right]. n = 4 to 5. ( J and K ) Immunostaining shows F4/80 (green) and CD31 (red) expression in the spinal dorsal horn. Scale bar, 200 μm (J). The number of F4/80 high cells in the dorsal horn of the spinal cord [(K), left]. The percentage of F4/80 high area among CD31 + area [(K), right]. n = 5. ( L ) Intrathecal injection of IL-1α siRNA attenuated the mechanical allodynia induced by BTZ. n = 5. Significance: * P < 0.05, # P < 0.05, ** P < 0.01, and ## P < 0.01.
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    ( A ) Il1a , Ccl5 , and <t>Ccl1</t> mRNA levels in the dorsal horn of female mice. n = 5 to 8. ( B ) Immunofluorescence image of IL-1α (green) in vascular endothelial cells (red). Scale bars, 50 μm (low) or 20 μm (high). ( C ) Double immunofluorescence staining of CCL1 (green) and vascular endothelial cells (red). Scale bars, 50 μm (low) or 20 μm (high). ( D and E ) Coimmunostaining image of F4/80 (green) and CD31 (red) in the spinal dorsal horn and the statistical graph. Scale bar, 200 μm. n = 5. ( F ) Intrathecal injection of IL-1α siRNA attenuated the mechanical allodynia induced by BTZ. n = 5. ( G ) Immunofluorescence image shows IL-1R1 (red) expression in macrophages (green). Scale bar, 10 μm. ( H and I ) Intrathecal IL-1R1 injection inhibited the up-regulation of F4/80 (green) and CD31 (red) in the near vascular of the spinal dorsal horn. Scale bar, 200 μm (H). The number of F4/80 high cells in the dorsal horn of the spinal cord [(I), left]. The percentage of F4/80 high area among CD31 + area [(I), right]. n = 4 to 5. ( J and K ) Immunostaining shows F4/80 (green) and CD31 (red) expression in the spinal dorsal horn. Scale bar, 200 μm (J). The number of F4/80 high cells in the dorsal horn of the spinal cord [(K), left]. The percentage of F4/80 high area among CD31 + area [(K), right]. n = 5. ( L ) Intrathecal injection of IL-1α siRNA attenuated the mechanical allodynia induced by BTZ. n = 5. Significance: * P < 0.05, # P < 0.05, ** P < 0.01, and ## P < 0.01.
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    Image Search Results


    ( A ) Il1a , Ccl5 , and Ccl1 mRNA levels in the dorsal horn of female mice. n = 5 to 8. ( B ) Immunofluorescence image of IL-1α (green) in vascular endothelial cells (red). Scale bars, 50 μm (low) or 20 μm (high). ( C ) Double immunofluorescence staining of CCL1 (green) and vascular endothelial cells (red). Scale bars, 50 μm (low) or 20 μm (high). ( D and E ) Coimmunostaining image of F4/80 (green) and CD31 (red) in the spinal dorsal horn and the statistical graph. Scale bar, 200 μm. n = 5. ( F ) Intrathecal injection of IL-1α siRNA attenuated the mechanical allodynia induced by BTZ. n = 5. ( G ) Immunofluorescence image shows IL-1R1 (red) expression in macrophages (green). Scale bar, 10 μm. ( H and I ) Intrathecal IL-1R1 injection inhibited the up-regulation of F4/80 (green) and CD31 (red) in the near vascular of the spinal dorsal horn. Scale bar, 200 μm (H). The number of F4/80 high cells in the dorsal horn of the spinal cord [(I), left]. The percentage of F4/80 high area among CD31 + area [(I), right]. n = 4 to 5. ( J and K ) Immunostaining shows F4/80 (green) and CD31 (red) expression in the spinal dorsal horn. Scale bar, 200 μm (J). The number of F4/80 high cells in the dorsal horn of the spinal cord [(K), left]. The percentage of F4/80 high area among CD31 + area [(K), right]. n = 5. ( L ) Intrathecal injection of IL-1α siRNA attenuated the mechanical allodynia induced by BTZ. n = 5. Significance: * P < 0.05, # P < 0.05, ** P < 0.01, and ## P < 0.01.

    Journal: Science Advances

    Article Title: Earlier onset of chemotherapy-induced neuropathic pain in females by ICAM-1–mediated accumulation of perivascular macrophages

    doi: 10.1126/sciadv.adu2159

    Figure Lengend Snippet: ( A ) Il1a , Ccl5 , and Ccl1 mRNA levels in the dorsal horn of female mice. n = 5 to 8. ( B ) Immunofluorescence image of IL-1α (green) in vascular endothelial cells (red). Scale bars, 50 μm (low) or 20 μm (high). ( C ) Double immunofluorescence staining of CCL1 (green) and vascular endothelial cells (red). Scale bars, 50 μm (low) or 20 μm (high). ( D and E ) Coimmunostaining image of F4/80 (green) and CD31 (red) in the spinal dorsal horn and the statistical graph. Scale bar, 200 μm. n = 5. ( F ) Intrathecal injection of IL-1α siRNA attenuated the mechanical allodynia induced by BTZ. n = 5. ( G ) Immunofluorescence image shows IL-1R1 (red) expression in macrophages (green). Scale bar, 10 μm. ( H and I ) Intrathecal IL-1R1 injection inhibited the up-regulation of F4/80 (green) and CD31 (red) in the near vascular of the spinal dorsal horn. Scale bar, 200 μm (H). The number of F4/80 high cells in the dorsal horn of the spinal cord [(I), left]. The percentage of F4/80 high area among CD31 + area [(I), right]. n = 4 to 5. ( J and K ) Immunostaining shows F4/80 (green) and CD31 (red) expression in the spinal dorsal horn. Scale bar, 200 μm (J). The number of F4/80 high cells in the dorsal horn of the spinal cord [(K), left]. The percentage of F4/80 high area among CD31 + area [(K), right]. n = 5. ( L ) Intrathecal injection of IL-1α siRNA attenuated the mechanical allodynia induced by BTZ. n = 5. Significance: * P < 0.05, # P < 0.05, ** P < 0.01, and ## P < 0.01.

    Article Snippet: For neutralizing antibodies CCL1 (20 μg/kg; R&D Systems, MAB845) and IL-1R1 (20 μg/kg; Bio X Cell, BE0256), mice were administered intrathecally 30 min before the injection of BTZ or the IL-1R1 ligand, IL-1α.

    Techniques: Immunofluorescence, Double Immunofluorescence Staining, Injection, Expressing, Immunostaining

    ( A ) Coimmunofluorescence of CCL1 (green) and macrophages (purple) on day 3 following BTZ treatment in female mice. Scale bar, 50 μm. ( B ) Quantification of CCL1 fluorescence intensity in macrophages. n = 5. ( C ) Coimmunofluorescence of CCR8 (red) and NeuN (marker of neuron, green). Scale bars, 20 μm. ( D ) Coimmunofluorescence of CCR8 (red) and glial fibrillary acidic protein (GFAP; a marker of astrocyte, green). Scale bars, 20 μm. ( E ) Representative traces (left) and statistical data (right) for the action potential firing recorded in spinal cord lamina II neurons. n = 4 mice. ( F ) Intrathecal injection of CCL1-neutralizing antibody attenuated the mechanical allodynia induced by BTZ. n = 5 to 7. ( G ) CCL1 increased the action potentials of neurons in female mouse spinal slices. n = 6. ( H ) Intraspinal CCL1 injection reduced the mechanical withdrawal threshold. n = 5. ( I ) R243 preincubation blocked the CCL1-induced action potential increase in female mouse spinal slices. n = 6. ( J ) Intrathecal injection of R243 attenuated the mechanical allodynia induced by BTZ. n = 5. ( K ) Intrathecal injection of R243 attenuated the mechanical allodynia induced by recombinant CCL1. n = 5. ( L ) Recombinant CCL1 increased the action potentials in astrocyte CCR8 knockdown mouse spinal slices. n = 5. ( M ) Intraspinal CCL1 injection reduced the mechanical withdrawal threshold in astrocyte CCR8 knockdown female mice. n = 5. Significance: not significant (n.s.), * P < 0.05 and ** P < 0.01.

    Journal: Science Advances

    Article Title: Earlier onset of chemotherapy-induced neuropathic pain in females by ICAM-1–mediated accumulation of perivascular macrophages

    doi: 10.1126/sciadv.adu2159

    Figure Lengend Snippet: ( A ) Coimmunofluorescence of CCL1 (green) and macrophages (purple) on day 3 following BTZ treatment in female mice. Scale bar, 50 μm. ( B ) Quantification of CCL1 fluorescence intensity in macrophages. n = 5. ( C ) Coimmunofluorescence of CCR8 (red) and NeuN (marker of neuron, green). Scale bars, 20 μm. ( D ) Coimmunofluorescence of CCR8 (red) and glial fibrillary acidic protein (GFAP; a marker of astrocyte, green). Scale bars, 20 μm. ( E ) Representative traces (left) and statistical data (right) for the action potential firing recorded in spinal cord lamina II neurons. n = 4 mice. ( F ) Intrathecal injection of CCL1-neutralizing antibody attenuated the mechanical allodynia induced by BTZ. n = 5 to 7. ( G ) CCL1 increased the action potentials of neurons in female mouse spinal slices. n = 6. ( H ) Intraspinal CCL1 injection reduced the mechanical withdrawal threshold. n = 5. ( I ) R243 preincubation blocked the CCL1-induced action potential increase in female mouse spinal slices. n = 6. ( J ) Intrathecal injection of R243 attenuated the mechanical allodynia induced by BTZ. n = 5. ( K ) Intrathecal injection of R243 attenuated the mechanical allodynia induced by recombinant CCL1. n = 5. ( L ) Recombinant CCL1 increased the action potentials in astrocyte CCR8 knockdown mouse spinal slices. n = 5. ( M ) Intraspinal CCL1 injection reduced the mechanical withdrawal threshold in astrocyte CCR8 knockdown female mice. n = 5. Significance: not significant (n.s.), * P < 0.05 and ** P < 0.01.

    Article Snippet: For neutralizing antibodies CCL1 (20 μg/kg; R&D Systems, MAB845) and IL-1R1 (20 μg/kg; Bio X Cell, BE0256), mice were administered intrathecally 30 min before the injection of BTZ or the IL-1R1 ligand, IL-1α.

    Techniques: Fluorescence, Marker, Injection, Recombinant, Knockdown

    ( A ) Immunofluorescence imaging showed BTZ-activated astrocytes (turquoise) in close proximity to macrophages (green) and vascular endothelial cells (red). Scale bars, 20 μm. ( B ) Schematic of two-photon imaging configuration. ( C ) Representative image showed the increased GCaMP6s (green) in spinal cord astrocytes (SR101, red) following CCL1 incubation. Scale bar, 150 μm. ( D ) Example signal trace (left) and histogram of area under the curve (AUC) (right) of calcium signaling value from the spinal dorsal horn astrocyte in mice treated with CCL1. n = 3. ( E to G ) R243 incubation prevented CCL1-induced calcium signaling increase in GCaMP6s + astrocytes. Representative image (E) and signal trace (F) show R243 blocked CCL1-induced calcium up-regulation. Scale bar, 20 μm. AUC quantification (G). n = 3. ( H to J ) Response of astrocytes to recombinant CCL1 during bath application of TTX (1 μM). Representative image (H) and signal trace (I) showed that TTX did not inhibit the increase in intracellular calcium signaling induced by CCL1. Scale bar, 20 μm. AUC quantification (J). n = 3. ( K to M ) Application of CNO increased the astrocyte intracellular calcium signaling in the female with injection of AAV2/5-GfaABC1D-CRE and AAV-DIO-hM3Dq-mCherry. Scale bar, 20 μm. ( N ) The action potential number in female mouse spinal cord slice was increased by CNO application. Representative trace (left) and statistical data (right) were shown. n = 3. ( O ) Application with CNO decreased the paw withdrawal threshold in female mice with intraspinal injection of AAV2/5-GfaABC1D-CRE and AAV-DIO-hM3Dq-mCherry. n = 5. Significance: not significant (n.s.) and * P < 0.05.

    Journal: Science Advances

    Article Title: Earlier onset of chemotherapy-induced neuropathic pain in females by ICAM-1–mediated accumulation of perivascular macrophages

    doi: 10.1126/sciadv.adu2159

    Figure Lengend Snippet: ( A ) Immunofluorescence imaging showed BTZ-activated astrocytes (turquoise) in close proximity to macrophages (green) and vascular endothelial cells (red). Scale bars, 20 μm. ( B ) Schematic of two-photon imaging configuration. ( C ) Representative image showed the increased GCaMP6s (green) in spinal cord astrocytes (SR101, red) following CCL1 incubation. Scale bar, 150 μm. ( D ) Example signal trace (left) and histogram of area under the curve (AUC) (right) of calcium signaling value from the spinal dorsal horn astrocyte in mice treated with CCL1. n = 3. ( E to G ) R243 incubation prevented CCL1-induced calcium signaling increase in GCaMP6s + astrocytes. Representative image (E) and signal trace (F) show R243 blocked CCL1-induced calcium up-regulation. Scale bar, 20 μm. AUC quantification (G). n = 3. ( H to J ) Response of astrocytes to recombinant CCL1 during bath application of TTX (1 μM). Representative image (H) and signal trace (I) showed that TTX did not inhibit the increase in intracellular calcium signaling induced by CCL1. Scale bar, 20 μm. AUC quantification (J). n = 3. ( K to M ) Application of CNO increased the astrocyte intracellular calcium signaling in the female with injection of AAV2/5-GfaABC1D-CRE and AAV-DIO-hM3Dq-mCherry. Scale bar, 20 μm. ( N ) The action potential number in female mouse spinal cord slice was increased by CNO application. Representative trace (left) and statistical data (right) were shown. n = 3. ( O ) Application with CNO decreased the paw withdrawal threshold in female mice with intraspinal injection of AAV2/5-GfaABC1D-CRE and AAV-DIO-hM3Dq-mCherry. n = 5. Significance: not significant (n.s.) and * P < 0.05.

    Article Snippet: For neutralizing antibodies CCL1 (20 μg/kg; R&D Systems, MAB845) and IL-1R1 (20 μg/kg; Bio X Cell, BE0256), mice were administered intrathecally 30 min before the injection of BTZ or the IL-1R1 ligand, IL-1α.

    Techniques: Immunofluorescence, Imaging, Incubation, Recombinant, Injection

    ( A ) Increased ICAM-1 promotes monocyte adhesion to vascular endothelial cells following BTZ treatment. ( B ) IL-1α/ICAM-1 collaboratively promote monocyte transmigration across the vascular wall. ( C ) Infiltrated macrophage-released CCL1 enhances neuron excitability directly or indirectly via the activated astrocytes.

    Journal: Science Advances

    Article Title: Earlier onset of chemotherapy-induced neuropathic pain in females by ICAM-1–mediated accumulation of perivascular macrophages

    doi: 10.1126/sciadv.adu2159

    Figure Lengend Snippet: ( A ) Increased ICAM-1 promotes monocyte adhesion to vascular endothelial cells following BTZ treatment. ( B ) IL-1α/ICAM-1 collaboratively promote monocyte transmigration across the vascular wall. ( C ) Infiltrated macrophage-released CCL1 enhances neuron excitability directly or indirectly via the activated astrocytes.

    Article Snippet: For neutralizing antibodies CCL1 (20 μg/kg; R&D Systems, MAB845) and IL-1R1 (20 μg/kg; Bio X Cell, BE0256), mice were administered intrathecally 30 min before the injection of BTZ or the IL-1R1 ligand, IL-1α.

    Techniques: Transmigration Assay