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rabbit anti-cbd-28k  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc rabbit anti-cbd-28k
    Rabbit Anti Cbd 28k, supplied by Cell Signaling Technology Inc, 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/rabbit+anti+cbd+28k/rabbit+anti+cbd+28k/pm36552657-87-20-24
    Average 90 stars, based on 1 article reviews
    rabbit anti-cbd-28k - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    Immunohistochemistry:

    Article Title: Therapeutic Administration of Oxcarbazepine Saves Cerebellar Purkinje Cells from Ischemia and Reperfusion Injury Induced by Cardiac Arrest through Attenuation of Oxidative Stress
    Article Snippet: To examine the mechanisms of cell damage or death in the cerebellum after CA/RoSC, according to our method as previously described [ ], the cerebellar sections (which were collected as described above) were examined using immunohistochemistry for anti-calbindin D-28kDa (CBD-28k, a marker for cerebellar Purkinje cells), anti-4-hydroxy-2-nonenal (4HNE, an end-product by lipid peroxidation) and anti-SOD1 and -SOD2 (endogenous antioxidant enzymes).[ ], the cerebellar sections (which were collected as described above) were examined using immunohistochemistry for anti-calbindin D-28kDa (CBD-28k, a marker for cerebellar Purkinje cells), anti-4-hydroxy-2-nonenal (4HNE, an end-product by lipid peroxidation) and anti-SOD1 and -SOD2 (endogenous antioxidant enzymes). ... In short, the cerebellar sections were blocked with 20% normal goat serum (in 0.05 M PBS) and immunoreacted with primary rabbit anti-CBD-28k (diluted 1:1100; Cell Signaling Technology, Danvers, MA, USA), mouse anti-4HNE (diluted 1:450; Alexis Biochemicals, San Diego, CA, USA), sheep anti-SOD1 (1:1500; Calbiochem, Darmstadt, Germany) and sheep anti-SOD2 (1:1500; Calbiochem) at 4 °C for eight hours.. Next, the sections were reacted with biotinylated goat anti-mouse IgG (diluted 1:200; Vector Laboratories Inc., Burlingame, CA, USA), goat anti-rabbit IgG (diluted 1:200; Vector Laboratories Inc.) and goat anti-sheep IgG (diluted 1:200; Vector Laboratories Inc.), then developed using Vectastain ABC (Vector Laboratories Inc., Burlingame, CA, USA).Next, the sections were reacted with biotinylated goat anti-mouse IgG (diluted 1:200; Vector Laboratories Inc., Burlingame, CA, USA), goat anti-rabbit IgG (diluted 1:200; Vector Laboratories Inc.) and goat anti-sheep IgG (diluted 1:200; Vector Laboratories Inc.), then developed using Vectastain..



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    ( A , C ) <t>CBD-28k</t> immunohistochemistry ( A ) and FJB histofluorescence ( C ) in the cerebellar vermis of the sham + vehicle ( A a, C a). The CA + vehicle ( A b–d, C b–d), sham + OXC ( A e, C e) and CA + OXC ( A f–h, C f–h) groups at 12 h and one and two days after CA/RoSC. In the CA + vehicle group, the numbers of CBD-28k-Purkinje cells are apparently reduced (arrows) in the Purkinje cell layer (PCL) two days after CA/RoSC, and FJB-cells are apparently increased (arrows) in the PCL at 12 h after CA/PCR. In the CA + OXC group, CBD-28k- and the number of FJB-Purkinje cells are markedly saved and reduced, respectively, two days after CA/RoSC. GCL, granular cell layer; MCL, molecular cell layer. Scale bar = 50 µm. ( B , D ). Numbers of CBD-28k-Purkinje cells ( B ) and FJB-Purkinje cells ( D ). The bars determine the means ± SEM ( n = 7, respectively; * p < 0.05 versus sham, † vehicle group; # p < 0.05 versus CA, † vehicle group).
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    Image Search Results


    ( A , C ) CBD-28k immunohistochemistry ( A ) and FJB histofluorescence ( C ) in the cerebellar vermis of the sham + vehicle ( A a, C a). The CA + vehicle ( A b–d, C b–d), sham + OXC ( A e, C e) and CA + OXC ( A f–h, C f–h) groups at 12 h and one and two days after CA/RoSC. In the CA + vehicle group, the numbers of CBD-28k-Purkinje cells are apparently reduced (arrows) in the Purkinje cell layer (PCL) two days after CA/RoSC, and FJB-cells are apparently increased (arrows) in the PCL at 12 h after CA/PCR. In the CA + OXC group, CBD-28k- and the number of FJB-Purkinje cells are markedly saved and reduced, respectively, two days after CA/RoSC. GCL, granular cell layer; MCL, molecular cell layer. Scale bar = 50 µm. ( B , D ). Numbers of CBD-28k-Purkinje cells ( B ) and FJB-Purkinje cells ( D ). The bars determine the means ± SEM ( n = 7, respectively; * p < 0.05 versus sham, † vehicle group; # p < 0.05 versus CA, † vehicle group).

    Journal: Antioxidants

    Article Title: Therapeutic Administration of Oxcarbazepine Saves Cerebellar Purkinje Cells from Ischemia and Reperfusion Injury Induced by Cardiac Arrest through Attenuation of Oxidative Stress

    doi: 10.3390/antiox11122450

    Figure Lengend Snippet: ( A , C ) CBD-28k immunohistochemistry ( A ) and FJB histofluorescence ( C ) in the cerebellar vermis of the sham + vehicle ( A a, C a). The CA + vehicle ( A b–d, C b–d), sham + OXC ( A e, C e) and CA + OXC ( A f–h, C f–h) groups at 12 h and one and two days after CA/RoSC. In the CA + vehicle group, the numbers of CBD-28k-Purkinje cells are apparently reduced (arrows) in the Purkinje cell layer (PCL) two days after CA/RoSC, and FJB-cells are apparently increased (arrows) in the PCL at 12 h after CA/PCR. In the CA + OXC group, CBD-28k- and the number of FJB-Purkinje cells are markedly saved and reduced, respectively, two days after CA/RoSC. GCL, granular cell layer; MCL, molecular cell layer. Scale bar = 50 µm. ( B , D ). Numbers of CBD-28k-Purkinje cells ( B ) and FJB-Purkinje cells ( D ). The bars determine the means ± SEM ( n = 7, respectively; * p < 0.05 versus sham, † vehicle group; # p < 0.05 versus CA, † vehicle group).

    Article Snippet: In short, the cerebellar sections were blocked with 20% normal goat serum (in 0.05 M PBS) and immunoreacted with primary rabbit anti-CBD-28k (diluted 1:1100; Cell Signaling Technology, Danvers, MA, USA), mouse anti-4HNE (diluted 1:450; Alexis Biochemicals, San Diego, CA, USA), sheep anti-SOD1 (1:1500; Calbiochem, Darmstadt, Germany) and sheep anti-SOD2 (1:1500; Calbiochem) at 4 °C for eight hours.

    Techniques: Immunohistochemistry