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drg cell marker  (Proteintech)


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    Structured Review

    Proteintech drg cell marker
    Pulsed radiofrequency (PRF) impaired axonal transport in dorsal root ganglion <t>(DRG)</t> small neurons. ( a ) Experimental schedule. Fast Blue was injected on day 13 after MIA administration, and the tissue was collected on day 14. ( b ) Illustration of Neurotracer injection into the mouse knee joint using a Hamilton syringe. The next day, the L4 DRGs were collected. ( c ) Representative micrographs of Nissl staining (upper) and Fast Blue retrograde tracer (FB: bottom) in the L4 DRG of the sham (left) and PRF (right) groups. The yellow arrow indicates FB-positive neurons. Scale bar: 100 μm. ( d ) Bar graph of the mean percentage of FB-positive cells among total cells (top), FB-positive large cells among total large cell counts (bottom left), and FB-positive small cells among total small cell counts (bottom right) in the sham (white) and PRF groups (gray). Data are presented as mean ± SD. Statistical analysis was performed using unpaired t-test. * p < 0.05, vs. the sham group on the same day, n.s.: no significant. ( e ) Representative images of FB staining (upper panel) and immunostaining <t>with</t> <t>anti-peripherin</t> antibody (bottom) in the L4 DRG of the sham (left) and PRF (right) groups. Yellow arrowheads indicate FB- and peripherin-positive cells; red arrowheads indicate FB-positive and peripherin-negative cells. Scale bar: 100 μm. ( f ) The bar graph shows the average percentage of both FB- and peripherin-positive cells among peripherin-positive cells. Data are presented as mean ± SD. Statistical analysis was performed using unpaired t-test. ** p < 0.01 vs. the sham group on the same day.
    Drg Cell Marker, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 2373 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/drg+cell+marker/pmc12480965-298-15-24?v=Proteintech
    Average 96 stars, based on 2373 article reviews
    drg cell marker - by Bioz Stars, 2026-08
    96/100 stars

    Images

    1) Product Images from "Elucidation of the treatment mechanism of pulsed radiofrequency based on its antiinflammatory effects"

    Article Title: Elucidation of the treatment mechanism of pulsed radiofrequency based on its antiinflammatory effects

    Journal: Scientific Reports

    doi: 10.1038/s41598-025-19045-z

    Pulsed radiofrequency (PRF) impaired axonal transport in dorsal root ganglion (DRG) small neurons. ( a ) Experimental schedule. Fast Blue was injected on day 13 after MIA administration, and the tissue was collected on day 14. ( b ) Illustration of Neurotracer injection into the mouse knee joint using a Hamilton syringe. The next day, the L4 DRGs were collected. ( c ) Representative micrographs of Nissl staining (upper) and Fast Blue retrograde tracer (FB: bottom) in the L4 DRG of the sham (left) and PRF (right) groups. The yellow arrow indicates FB-positive neurons. Scale bar: 100 μm. ( d ) Bar graph of the mean percentage of FB-positive cells among total cells (top), FB-positive large cells among total large cell counts (bottom left), and FB-positive small cells among total small cell counts (bottom right) in the sham (white) and PRF groups (gray). Data are presented as mean ± SD. Statistical analysis was performed using unpaired t-test. * p < 0.05, vs. the sham group on the same day, n.s.: no significant. ( e ) Representative images of FB staining (upper panel) and immunostaining with anti-peripherin antibody (bottom) in the L4 DRG of the sham (left) and PRF (right) groups. Yellow arrowheads indicate FB- and peripherin-positive cells; red arrowheads indicate FB-positive and peripherin-negative cells. Scale bar: 100 μm. ( f ) The bar graph shows the average percentage of both FB- and peripherin-positive cells among peripherin-positive cells. Data are presented as mean ± SD. Statistical analysis was performed using unpaired t-test. ** p < 0.01 vs. the sham group on the same day.
    Figure Legend Snippet: Pulsed radiofrequency (PRF) impaired axonal transport in dorsal root ganglion (DRG) small neurons. ( a ) Experimental schedule. Fast Blue was injected on day 13 after MIA administration, and the tissue was collected on day 14. ( b ) Illustration of Neurotracer injection into the mouse knee joint using a Hamilton syringe. The next day, the L4 DRGs were collected. ( c ) Representative micrographs of Nissl staining (upper) and Fast Blue retrograde tracer (FB: bottom) in the L4 DRG of the sham (left) and PRF (right) groups. The yellow arrow indicates FB-positive neurons. Scale bar: 100 μm. ( d ) Bar graph of the mean percentage of FB-positive cells among total cells (top), FB-positive large cells among total large cell counts (bottom left), and FB-positive small cells among total small cell counts (bottom right) in the sham (white) and PRF groups (gray). Data are presented as mean ± SD. Statistical analysis was performed using unpaired t-test. * p < 0.05, vs. the sham group on the same day, n.s.: no significant. ( e ) Representative images of FB staining (upper panel) and immunostaining with anti-peripherin antibody (bottom) in the L4 DRG of the sham (left) and PRF (right) groups. Yellow arrowheads indicate FB- and peripherin-positive cells; red arrowheads indicate FB-positive and peripherin-negative cells. Scale bar: 100 μm. ( f ) The bar graph shows the average percentage of both FB- and peripherin-positive cells among peripherin-positive cells. Data are presented as mean ± SD. Statistical analysis was performed using unpaired t-test. ** p < 0.01 vs. the sham group on the same day.

    Techniques Used: Injection, Staining, Immunostaining



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    Pulsed radiofrequency (PRF) impaired axonal transport in dorsal root ganglion <t>(DRG)</t> small neurons. ( a ) Experimental schedule. Fast Blue was injected on day 13 after MIA administration, and the tissue was collected on day 14. ( b ) Illustration of Neurotracer injection into the mouse knee joint using a Hamilton syringe. The next day, the L4 DRGs were collected. ( c ) Representative micrographs of Nissl staining (upper) and Fast Blue retrograde tracer (FB: bottom) in the L4 DRG of the sham (left) and PRF (right) groups. The yellow arrow indicates FB-positive neurons. Scale bar: 100 μm. ( d ) Bar graph of the mean percentage of FB-positive cells among total cells (top), FB-positive large cells among total large cell counts (bottom left), and FB-positive small cells among total small cell counts (bottom right) in the sham (white) and PRF groups (gray). Data are presented as mean ± SD. Statistical analysis was performed using unpaired t-test. * p < 0.05, vs. the sham group on the same day, n.s.: no significant. ( e ) Representative images of FB staining (upper panel) and immunostaining <t>with</t> <t>anti-peripherin</t> antibody (bottom) in the L4 DRG of the sham (left) and PRF (right) groups. Yellow arrowheads indicate FB- and peripherin-positive cells; red arrowheads indicate FB-positive and peripherin-negative cells. Scale bar: 100 μm. ( f ) The bar graph shows the average percentage of both FB- and peripherin-positive cells among peripherin-positive cells. Data are presented as mean ± SD. Statistical analysis was performed using unpaired t-test. ** p < 0.01 vs. the sham group on the same day.
    Drg Cell Marker, 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/product/drg+cell+marker/pmc12480965-298-15-24?v=Proteintech
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    anti-gfap drg satellite cell marker  (Millipore)
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    Pulsed radiofrequency (PRF) impaired axonal transport in dorsal root ganglion <t>(DRG)</t> small neurons. ( a ) Experimental schedule. Fast Blue was injected on day 13 after MIA administration, and the tissue was collected on day 14. ( b ) Illustration of Neurotracer injection into the mouse knee joint using a Hamilton syringe. The next day, the L4 DRGs were collected. ( c ) Representative micrographs of Nissl staining (upper) and Fast Blue retrograde tracer (FB: bottom) in the L4 DRG of the sham (left) and PRF (right) groups. The yellow arrow indicates FB-positive neurons. Scale bar: 100 μm. ( d ) Bar graph of the mean percentage of FB-positive cells among total cells (top), FB-positive large cells among total large cell counts (bottom left), and FB-positive small cells among total small cell counts (bottom right) in the sham (white) and PRF groups (gray). Data are presented as mean ± SD. Statistical analysis was performed using unpaired t-test. * p < 0.05, vs. the sham group on the same day, n.s.: no significant. ( e ) Representative images of FB staining (upper panel) and immunostaining <t>with</t> <t>anti-peripherin</t> antibody (bottom) in the L4 DRG of the sham (left) and PRF (right) groups. Yellow arrowheads indicate FB- and peripherin-positive cells; red arrowheads indicate FB-positive and peripherin-negative cells. Scale bar: 100 μm. ( f ) The bar graph shows the average percentage of both FB- and peripherin-positive cells among peripherin-positive cells. Data are presented as mean ± SD. Statistical analysis was performed using unpaired t-test. ** p < 0.01 vs. the sham group on the same day.
    Anti Gfap Drg Satellite Cell Marker, supplied by Millipore, 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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    Image Search Results


    Pulsed radiofrequency (PRF) impaired axonal transport in dorsal root ganglion (DRG) small neurons. ( a ) Experimental schedule. Fast Blue was injected on day 13 after MIA administration, and the tissue was collected on day 14. ( b ) Illustration of Neurotracer injection into the mouse knee joint using a Hamilton syringe. The next day, the L4 DRGs were collected. ( c ) Representative micrographs of Nissl staining (upper) and Fast Blue retrograde tracer (FB: bottom) in the L4 DRG of the sham (left) and PRF (right) groups. The yellow arrow indicates FB-positive neurons. Scale bar: 100 μm. ( d ) Bar graph of the mean percentage of FB-positive cells among total cells (top), FB-positive large cells among total large cell counts (bottom left), and FB-positive small cells among total small cell counts (bottom right) in the sham (white) and PRF groups (gray). Data are presented as mean ± SD. Statistical analysis was performed using unpaired t-test. * p < 0.05, vs. the sham group on the same day, n.s.: no significant. ( e ) Representative images of FB staining (upper panel) and immunostaining with anti-peripherin antibody (bottom) in the L4 DRG of the sham (left) and PRF (right) groups. Yellow arrowheads indicate FB- and peripherin-positive cells; red arrowheads indicate FB-positive and peripherin-negative cells. Scale bar: 100 μm. ( f ) The bar graph shows the average percentage of both FB- and peripherin-positive cells among peripherin-positive cells. Data are presented as mean ± SD. Statistical analysis was performed using unpaired t-test. ** p < 0.01 vs. the sham group on the same day.

    Journal: Scientific Reports

    Article Title: Elucidation of the treatment mechanism of pulsed radiofrequency based on its antiinflammatory effects

    doi: 10.1038/s41598-025-19045-z

    Figure Lengend Snippet: Pulsed radiofrequency (PRF) impaired axonal transport in dorsal root ganglion (DRG) small neurons. ( a ) Experimental schedule. Fast Blue was injected on day 13 after MIA administration, and the tissue was collected on day 14. ( b ) Illustration of Neurotracer injection into the mouse knee joint using a Hamilton syringe. The next day, the L4 DRGs were collected. ( c ) Representative micrographs of Nissl staining (upper) and Fast Blue retrograde tracer (FB: bottom) in the L4 DRG of the sham (left) and PRF (right) groups. The yellow arrow indicates FB-positive neurons. Scale bar: 100 μm. ( d ) Bar graph of the mean percentage of FB-positive cells among total cells (top), FB-positive large cells among total large cell counts (bottom left), and FB-positive small cells among total small cell counts (bottom right) in the sham (white) and PRF groups (gray). Data are presented as mean ± SD. Statistical analysis was performed using unpaired t-test. * p < 0.05, vs. the sham group on the same day, n.s.: no significant. ( e ) Representative images of FB staining (upper panel) and immunostaining with anti-peripherin antibody (bottom) in the L4 DRG of the sham (left) and PRF (right) groups. Yellow arrowheads indicate FB- and peripherin-positive cells; red arrowheads indicate FB-positive and peripherin-negative cells. Scale bar: 100 μm. ( f ) The bar graph shows the average percentage of both FB- and peripherin-positive cells among peripherin-positive cells. Data are presented as mean ± SD. Statistical analysis was performed using unpaired t-test. ** p < 0.01 vs. the sham group on the same day.

    Article Snippet: The macrophage marker, F4/80 rat monoclonal antibody (1:100; ab6640, Abcam, Cambridge, UK) or the small DRG cell marker, peripherin rabbit polyclonal antibody (1:100; 17399-1-AP, Proteintech, Rosemont, IL, USA) were used as the primary antibody.

    Techniques: Injection, Staining, Immunostaining