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matrix metalloprotein 9 mmp 9  (Boster Bio)


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    Boster Bio matrix metalloprotein 9 mmp 9
    Au treatment reduced brain edema and improved neurologic functions. a , b Effects of TBI and Au on water content ( a ) and neurologic deficits ( b ). c , d Representative western blot bands ( c ) and quantification of relative protein expression ( d ) for <t>MMP-9.</t> e Effects of Au on the latency to fall in the rotarod test were analyzed using two-way ANOVA. The Bonferroni post hoc test was used to compare differences among several groups at 14 days post-TBI. f Typical swimming path of mice in all groups during the training days (upper) and the probe trial period (lower) of the MWM test. i Effects of Au on the latency to find platform in the MWM test. The two-way ANOVA was performed, and the Bonferroni post hoc test was utilized to compare differences among several groups on day 28. j , k Au did not affect the average swimming speed during the training days ( j ) or during the probe trial period ( k ). l Time spent in the correct quadrant during the probe trail. m Number of crossings over the platform position during the probe trail. Bars represent the mean ± SD. * P < 0.05 versus indicated groups
    Matrix Metalloprotein 9 Mmp 9, supplied by Boster Bio, 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/pb10008/Anti-MMP9+Antibody+Picoband/pmc07294631-82-56-62
    Average 90 stars, based on 1 article reviews
    matrix metalloprotein 9 mmp 9 - by Bioz Stars, 2026-09
    90/100 stars

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    1) Product Images from "Aucubin alleviates oxidative stress and inflammation via Nrf2-mediated signaling activity in experimental traumatic brain injury"

    Article Title: Aucubin alleviates oxidative stress and inflammation via Nrf2-mediated signaling activity in experimental traumatic brain injury

    Journal: Journal of Neuroinflammation

    doi: 10.1186/s12974-020-01863-9

    Au treatment reduced brain edema and improved neurologic functions. a , b Effects of TBI and Au on water content ( a ) and neurologic deficits ( b ). c , d Representative western blot bands ( c ) and quantification of relative protein expression ( d ) for MMP-9. e Effects of Au on the latency to fall in the rotarod test were analyzed using two-way ANOVA. The Bonferroni post hoc test was used to compare differences among several groups at 14 days post-TBI. f Typical swimming path of mice in all groups during the training days (upper) and the probe trial period (lower) of the MWM test. i Effects of Au on the latency to find platform in the MWM test. The two-way ANOVA was performed, and the Bonferroni post hoc test was utilized to compare differences among several groups on day 28. j , k Au did not affect the average swimming speed during the training days ( j ) or during the probe trial period ( k ). l Time spent in the correct quadrant during the probe trail. m Number of crossings over the platform position during the probe trail. Bars represent the mean ± SD. * P < 0.05 versus indicated groups
    Figure Legend Snippet: Au treatment reduced brain edema and improved neurologic functions. a , b Effects of TBI and Au on water content ( a ) and neurologic deficits ( b ). c , d Representative western blot bands ( c ) and quantification of relative protein expression ( d ) for MMP-9. e Effects of Au on the latency to fall in the rotarod test were analyzed using two-way ANOVA. The Bonferroni post hoc test was used to compare differences among several groups at 14 days post-TBI. f Typical swimming path of mice in all groups during the training days (upper) and the probe trial period (lower) of the MWM test. i Effects of Au on the latency to find platform in the MWM test. The two-way ANOVA was performed, and the Bonferroni post hoc test was utilized to compare differences among several groups on day 28. j , k Au did not affect the average swimming speed during the training days ( j ) or during the probe trial period ( k ). l Time spent in the correct quadrant during the probe trail. m Number of crossings over the platform position during the probe trail. Bars represent the mean ± SD. * P < 0.05 versus indicated groups

    Techniques Used: Western Blot, Expressing

    Related Articles

    Incubation:

    Article Title: Aucubin alleviates oxidative stress and inflammation via Nrf2-mediated signaling activity in experimental traumatic brain injury
    Article Snippet: .. Then, the membranes were incubated with primary antibodies against Nrf2 (1:1000, cat# ab137550, Abcam), Histone H3 (H3) (1:5000, cat# AF0009, Beyotime, China), NQO-1 (1:1000, cat# ab34173, Abcam), HO-1 (1:1000, cat# ab13248, Abcam), B-cell lymphoma-2 (Bcl2) (1:200, cat# 196495, Abcam), Bcl-2 Associated X Protein (Bax) (1:200, cat# ab32503, Abcam), cleaved-caspase 3 (CC3) (1:1000, cat# 9664, Cell Signaling), matrix metalloprotein-9 (MMP-9) (1:1000, cat# PB10008, Boster), glutathione peroxidase 1 (GPx1) (1:1000, cat# ab22604, Abcam), superoxide dismutase 1 (SOD1) (1:200, cat# sc-101523, Santa Cruz), Iba-1 (1:1000, cat# ab178846, Abcam), HMGB1 (1:100, cat# sc-56698, Santa Cruz), TLR4 (1:200, cat# sc-30002, Santa Cruz), MyD88 (1:200, cat# sc-74532, Santa Cruz), NF-κB p65 (1:1000, cat# 8242, Cell Signaling), inducible Nitric Oxide Synthase (iNOS) (1:1000, cat# 13120, Cell Signaling), Cyclooxygenase-2 (COX2) (1:500, cat# sc-19999, Santa Cruz), Interleukin-1β (IL-1β) (1:500, cat# 12242, Cell Signaling), or β-actin (1:3000, cat# BS6007M, Bioword) overnight at 4 °C. .. After washing 3 times for 15 min with Tris-buffered saline with Tween 20, the membranes were incubated with corresponding HRP conjugated secondary antibodies (1:5000, Bioword) for 1 h at room temperature.

    Article Title: Aucubin alleviates oxidative stress and inflammation via Nrf2-mediated signaling activity in experimental traumatic brain injury
    Article Snippet: .. Then, the membranes were incubated with primary antibodies against Nrf2 (1:1000, cat# ab137550, Abcam), Histone H3 (H3) (1:5000, cat# AF0009, Beyotime, China), NQO-1 (1:1000, cat# ab34173, Abcam), HO-1 (1:1000, cat# ab13248, Abcam), B-cell lymphoma-2 (Bcl2) (1:200, cat# 196495, Abcam), Bcl-2 Associated X Protein (Bax) (1:200, cat# ab32503, Abcam), cleaved-caspase 3 (CC3) (1:1000, cat# 9664, Cell Signaling), matrix metalloprotein-9 (MMP-9) (1:1000, cat# PB10008, Boster), glutathione peroxidase 1 (GPx1) (1:1000, cat# ab22604, Abcam), superoxide dismutase 1 (SOD1) (1:200, cat# sc-101523, Santa Cruz), Iba-1 (1:1000, cat# ab178846, Abcam), HMGB1 (1:100, cat# sc-56698, Santa Cruz), TLR4 (1:200, cat# sc-30002, Santa Cruz), MyD88 (1:200, cat# sc-74532, Santa Cruz), NF-κB p65 (1:1000, cat# 8242, Cell Signaling), inducible Nitric Oxide Synthase (iNOS) (1:1000, cat# 13120, Cell Signaling), Cyclooxygenase-2 (COX2) (1:500, cat# sc-19999, Santa Cruz), Interleukin-1β (IL-1β) (1:500, cat# 12242, Cell Signaling) or β-actin (1:3000, cat# BS6007M, Bioword) overnight at 4 °C. .. After washing 3 times for 15 min with Tris-buffered saline with Tween 20, the membranes were incubated with corresponding HRP conjugated secondary antibodies (1:5000, Bioword) for 1 h at room temperature.



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    Au treatment reduced brain edema and improved neurologic functions. a , b Effects of TBI and Au on water content ( a ) and neurologic deficits ( b ). c , d Representative western blot bands ( c ) and quantification of relative protein expression ( d ) for <t>MMP-9.</t> e Effects of Au on the latency to fall in the rotarod test were analyzed using two-way ANOVA. The Bonferroni post hoc test was used to compare differences among several groups at 14 days post-TBI. f Typical swimming path of mice in all groups during the training days (upper) and the probe trial period (lower) of the MWM test. i Effects of Au on the latency to find platform in the MWM test. The two-way ANOVA was performed, and the Bonferroni post hoc test was utilized to compare differences among several groups on day 28. j , k Au did not affect the average swimming speed during the training days ( j ) or during the probe trial period ( k ). l Time spent in the correct quadrant during the probe trail. m Number of crossings over the platform position during the probe trail. Bars represent the mean ± SD. * P < 0.05 versus indicated groups
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    https://www.bioz.com/product/pb10008/Anti-MMP9+Antibody+Picoband/pmc07294631-82-56-62
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    Au treatment reduced brain edema and improved neurologic functions. a , b Effects of TBI and Au on water content ( a ) and neurologic deficits ( b ). c , d Representative western blot bands ( c ) and quantification of relative protein expression ( d ) for <t>MMP-9.</t> e Effects of Au on the latency to fall in the rotarod test were analyzed using two-way ANOVA. The Bonferroni post hoc test was used to compare differences among several groups at 14 days post-TBI. f Typical swimming path of mice in all groups during the training days (upper) and the probe trial period (lower) of the MWM test. i Effects of Au on the latency to find platform in the MWM test. The two-way ANOVA was performed, and the Bonferroni post hoc test was utilized to compare differences among several groups on day 28. j , k Au did not affect the average swimming speed during the training days ( j ) or during the probe trial period ( k ). l Time spent in the correct quadrant during the probe trail. m Number of crossings over the platform position during the probe trail. Bars represent the mean ± SD. * P < 0.05 versus indicated groups
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    Image Search Results


    Au treatment reduced brain edema and improved neurologic functions. a , b Effects of TBI and Au on water content ( a ) and neurologic deficits ( b ). c , d Representative western blot bands ( c ) and quantification of relative protein expression ( d ) for MMP-9. e Effects of Au on the latency to fall in the rotarod test were analyzed using two-way ANOVA. The Bonferroni post hoc test was used to compare differences among several groups at 14 days post-TBI. f Typical swimming path of mice in all groups during the training days (upper) and the probe trial period (lower) of the MWM test. i Effects of Au on the latency to find platform in the MWM test. The two-way ANOVA was performed, and the Bonferroni post hoc test was utilized to compare differences among several groups on day 28. j , k Au did not affect the average swimming speed during the training days ( j ) or during the probe trial period ( k ). l Time spent in the correct quadrant during the probe trail. m Number of crossings over the platform position during the probe trail. Bars represent the mean ± SD. * P < 0.05 versus indicated groups

    Journal: Journal of Neuroinflammation

    Article Title: Aucubin alleviates oxidative stress and inflammation via Nrf2-mediated signaling activity in experimental traumatic brain injury

    doi: 10.1186/s12974-020-01863-9

    Figure Lengend Snippet: Au treatment reduced brain edema and improved neurologic functions. a , b Effects of TBI and Au on water content ( a ) and neurologic deficits ( b ). c , d Representative western blot bands ( c ) and quantification of relative protein expression ( d ) for MMP-9. e Effects of Au on the latency to fall in the rotarod test were analyzed using two-way ANOVA. The Bonferroni post hoc test was used to compare differences among several groups at 14 days post-TBI. f Typical swimming path of mice in all groups during the training days (upper) and the probe trial period (lower) of the MWM test. i Effects of Au on the latency to find platform in the MWM test. The two-way ANOVA was performed, and the Bonferroni post hoc test was utilized to compare differences among several groups on day 28. j , k Au did not affect the average swimming speed during the training days ( j ) or during the probe trial period ( k ). l Time spent in the correct quadrant during the probe trail. m Number of crossings over the platform position during the probe trail. Bars represent the mean ± SD. * P < 0.05 versus indicated groups

    Article Snippet: Then, the membranes were incubated with primary antibodies against Nrf2 (1:1000, cat# ab137550, Abcam), Histone H3 (H3) (1:5000, cat# AF0009, Beyotime, China), NQO-1 (1:1000, cat# ab34173, Abcam), HO-1 (1:1000, cat# ab13248, Abcam), B-cell lymphoma-2 (Bcl2) (1:200, cat# 196495, Abcam), Bcl-2 Associated X Protein (Bax) (1:200, cat# ab32503, Abcam), cleaved-caspase 3 (CC3) (1:1000, cat# 9664, Cell Signaling), matrix metalloprotein-9 (MMP-9) (1:1000, cat# PB10008, Boster), glutathione peroxidase 1 (GPx1) (1:1000, cat# ab22604, Abcam), superoxide dismutase 1 (SOD1) (1:200, cat# sc-101523, Santa Cruz), Iba-1 (1:1000, cat# ab178846, Abcam), HMGB1 (1:100, cat# sc-56698, Santa Cruz), TLR4 (1:200, cat# sc-30002, Santa Cruz), MyD88 (1:200, cat# sc-74532, Santa Cruz), NF-κB p65 (1:1000, cat# 8242, Cell Signaling), inducible Nitric Oxide Synthase (iNOS) (1:1000, cat# 13120, Cell Signaling), Cyclooxygenase-2 (COX2) (1:500, cat# sc-19999, Santa Cruz), Interleukin-1β (IL-1β) (1:500, cat# 12242, Cell Signaling), or β-actin (1:3000, cat# BS6007M, Bioword) overnight at 4 °C.

    Techniques: Western Blot, Expressing