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horse anti mouse parv  (Vector Laboratories)


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    Vector Laboratories horse anti mouse parv
    FIGURE 4. Representative images of ChAT (top) and <t>Parv</t> (bottom) immunostainings in SHAM (A and E), SAP (B and F), OREX (C and G), and SAP/OREX (D and G) rats. For anti-Parv immunostaining, a slice showing nonspecific staining (no primary antibody used during incubation) is also shown. In the MS/vDBB regions (plate modified from Paxinos and Watson, 1998), the two squares on each side delimit the regions where ODs for anti-Parv immunostaning were measured. Cholinergic neurons were mark- edly depleted in SAP (C) and SAP/OREX (D) and relatively spared in OREX (B) rats. GABA neurons were markedly depleted in OREX (G) and SAP/OREX (H) and relatively preserved in SAP (F) rats. Both neuronal populations were unaltered in SHAM animals (A and E).
    Horse Anti Mouse Parv, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 96/100, based on 7554 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/horse+anti+mouse+parv/Biotinylated+Horse+Anti-Mouse+IgG+Antibody/pm20623740-100-37-44
    Average 96 stars, based on 7554 article reviews
    horse anti mouse parv - by Bioz Stars, 2026-09
    96/100 stars

    Images

    1) Product Images from "Septohippocampal pathways contribute to system consolidation of a spatial memory: sequential implication of GABAergic and cholinergic neurons."

    Article Title: Septohippocampal pathways contribute to system consolidation of a spatial memory: sequential implication of GABAergic and cholinergic neurons.

    Journal: Hippocampus

    doi: 10.1002/hipo.20837

    FIGURE 4. Representative images of ChAT (top) and Parv (bottom) immunostainings in SHAM (A and E), SAP (B and F), OREX (C and G), and SAP/OREX (D and G) rats. For anti-Parv immunostaining, a slice showing nonspecific staining (no primary antibody used during incubation) is also shown. In the MS/vDBB regions (plate modified from Paxinos and Watson, 1998), the two squares on each side delimit the regions where ODs for anti-Parv immunostaning were measured. Cholinergic neurons were mark- edly depleted in SAP (C) and SAP/OREX (D) and relatively spared in OREX (B) rats. GABA neurons were markedly depleted in OREX (G) and SAP/OREX (H) and relatively preserved in SAP (F) rats. Both neuronal populations were unaltered in SHAM animals (A and E).
    Figure Legend Snippet: FIGURE 4. Representative images of ChAT (top) and Parv (bottom) immunostainings in SHAM (A and E), SAP (B and F), OREX (C and G), and SAP/OREX (D and G) rats. For anti-Parv immunostaining, a slice showing nonspecific staining (no primary antibody used during incubation) is also shown. In the MS/vDBB regions (plate modified from Paxinos and Watson, 1998), the two squares on each side delimit the regions where ODs for anti-Parv immunostaning were measured. Cholinergic neurons were mark- edly depleted in SAP (C) and SAP/OREX (D) and relatively spared in OREX (B) rats. GABA neurons were markedly depleted in OREX (G) and SAP/OREX (H) and relatively preserved in SAP (F) rats. Both neuronal populations were unaltered in SHAM animals (A and E).

    Techniques Used: Immunostaining, Staining, Incubation

    Related Articles

    Immunostaining:

    Article Title: Septohippocampal pathways contribute to system consolidation of a spatial memory: sequential implication of GABAergic and cholinergic neurons.
    Article Snippet: Hippocampus MS/vDBB anti-ChAT and anti-Parv Immunostainning and Hippocampal AChE Staining Protocols of both immunostainings have been detailed in the study of Traissard et al. (2007).Hippocampus MS/vDBB anti-ChAT and anti-Parv Immunostainning and Hippocampal AChE Staining Protocols of both immunostainings have been detailed in the study of Traissard et al. (2007).. As primary antibodies, we used a goat polyclonal antibody directed against ChAT (1:500; Chemicon International, Temecula, CA) and a mouse monoclonal antibody directed against Parv (1:4000; Sigma-Aldrich, P 3088, St. Louis, MO), whereas donkey anti-goat (ChAT) and horse anti-mouse (Parv) biotinylated secondary antibody (1:500, Vector Laboratories International, Burlingame, CA) were used.. AChE histochemistry was performed according to Koelle (1954) with minor modifications: ethopropazine (0.3 mM; Sigma, St. Louis, MO) was used to block nonspecific cholinesterases and acetylcholine iodide (4 mM; Sigma, St Louis, MO) was used as the substrate.AChE histochemistry was performed according to Koelle (1954) with minor modifications: ethopropazine (0.3 mM; Sigma, St. Louis, MO) was used to block nonspecific cholinesterases and acetylcholine iodide (4 mM; Sigma, St Louis, MO) was used as the substrate.

    Staining:

    Article Title: Septohippocampal pathways contribute to system consolidation of a spatial memory: sequential implication of GABAergic and cholinergic neurons.
    Article Snippet: Hippocampus MS/vDBB anti-ChAT and anti-Parv Immunostainning and Hippocampal AChE Staining Protocols of both immunostainings have been detailed in the study of Traissard et al. (2007).Hippocampus MS/vDBB anti-ChAT and anti-Parv Immunostainning and Hippocampal AChE Staining Protocols of both immunostainings have been detailed in the study of Traissard et al. (2007).. As primary antibodies, we used a goat polyclonal antibody directed against ChAT (1:500; Chemicon International, Temecula, CA) and a mouse monoclonal antibody directed against Parv (1:4000; Sigma-Aldrich, P 3088, St. Louis, MO), whereas donkey anti-goat (ChAT) and horse anti-mouse (Parv) biotinylated secondary antibody (1:500, Vector Laboratories International, Burlingame, CA) were used.. AChE histochemistry was performed according to Koelle (1954) with minor modifications: ethopropazine (0.3 mM; Sigma, St. Louis, MO) was used to block nonspecific cholinesterases and acetylcholine iodide (4 mM; Sigma, St Louis, MO) was used as the substrate.AChE histochemistry was performed according to Koelle (1954) with minor modifications: ethopropazine (0.3 mM; Sigma, St. Louis, MO) was used to block nonspecific cholinesterases and acetylcholine iodide (4 mM; Sigma, St Louis, MO) was used as the substrate.

    Incubation:

    Article Title: Septohippocampal pathways contribute to system consolidation of a spatial memory: sequential implication of GABAergic and cholinergic neurons.
    Article Snippet: Hippocampus MS/vDBB anti-ChAT and anti-Parv Immunostainning and Hippocampal AChE Staining Protocols of both immunostainings have been detailed in the study of Traissard et al. (2007).Hippocampus MS/vDBB anti-ChAT and anti-Parv Immunostainning and Hippocampal AChE Staining Protocols of both immunostainings have been detailed in the study of Traissard et al. (2007).. As primary antibodies, we used a goat polyclonal antibody directed against ChAT (1:500; Chemicon International, Temecula, CA) and a mouse monoclonal antibody directed against Parv (1:4000; Sigma-Aldrich, P 3088, St. Louis, MO), whereas donkey anti-goat (ChAT) and horse anti-mouse (Parv) biotinylated secondary antibody (1:500, Vector Laboratories International, Burlingame, CA) were used.. AChE histochemistry was performed according to Koelle (1954) with minor modifications: ethopropazine (0.3 mM; Sigma, St. Louis, MO) was used to block nonspecific cholinesterases and acetylcholine iodide (4 mM; Sigma, St Louis, MO) was used as the substrate.AChE histochemistry was performed according to Koelle (1954) with minor modifications: ethopropazine (0.3 mM; Sigma, St. Louis, MO) was used to block nonspecific cholinesterases and acetylcholine iodide (4 mM; Sigma, St Louis, MO) was used as the substrate.



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    horse anti mouse parv  (Vector Laboratories)
    96
    Vector Laboratories horse anti mouse parv
    FIGURE 4. Representative images of ChAT (top) and <t>Parv</t> (bottom) immunostainings in SHAM (A and E), SAP (B and F), OREX (C and G), and SAP/OREX (D and G) rats. For anti-Parv immunostaining, a slice showing nonspecific staining (no primary antibody used during incubation) is also shown. In the MS/vDBB regions (plate modified from Paxinos and Watson, 1998), the two squares on each side delimit the regions where ODs for anti-Parv immunostaning were measured. Cholinergic neurons were mark- edly depleted in SAP (C) and SAP/OREX (D) and relatively spared in OREX (B) rats. GABA neurons were markedly depleted in OREX (G) and SAP/OREX (H) and relatively preserved in SAP (F) rats. Both neuronal populations were unaltered in SHAM animals (A and E).
    Horse Anti Mouse Parv, supplied by Vector Laboratories, 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/horse+anti+mouse+parv/Biotinylated+Horse+Anti-Mouse+IgG+Antibody/pm20623740-100-37-44
    Average 96 stars, based on 1 article reviews
    horse anti mouse parv - by Bioz Stars, 2026-09
    96/100 stars
    		  Buy from Supplier

    Image Search Results


    FIGURE 4. Representative images of ChAT (top) and Parv (bottom) immunostainings in SHAM (A and E), SAP (B and F), OREX (C and G), and SAP/OREX (D and G) rats. For anti-Parv immunostaining, a slice showing nonspecific staining (no primary antibody used during incubation) is also shown. In the MS/vDBB regions (plate modified from Paxinos and Watson, 1998), the two squares on each side delimit the regions where ODs for anti-Parv immunostaning were measured. Cholinergic neurons were mark- edly depleted in SAP (C) and SAP/OREX (D) and relatively spared in OREX (B) rats. GABA neurons were markedly depleted in OREX (G) and SAP/OREX (H) and relatively preserved in SAP (F) rats. Both neuronal populations were unaltered in SHAM animals (A and E).

    Journal: Hippocampus

    Article Title: Septohippocampal pathways contribute to system consolidation of a spatial memory: sequential implication of GABAergic and cholinergic neurons.

    doi: 10.1002/hipo.20837

    Figure Lengend Snippet: FIGURE 4. Representative images of ChAT (top) and Parv (bottom) immunostainings in SHAM (A and E), SAP (B and F), OREX (C and G), and SAP/OREX (D and G) rats. For anti-Parv immunostaining, a slice showing nonspecific staining (no primary antibody used during incubation) is also shown. In the MS/vDBB regions (plate modified from Paxinos and Watson, 1998), the two squares on each side delimit the regions where ODs for anti-Parv immunostaning were measured. Cholinergic neurons were mark- edly depleted in SAP (C) and SAP/OREX (D) and relatively spared in OREX (B) rats. GABA neurons were markedly depleted in OREX (G) and SAP/OREX (H) and relatively preserved in SAP (F) rats. Both neuronal populations were unaltered in SHAM animals (A and E).

    Article Snippet: As primary antibodies, we used a goat polyclonal antibody directed against ChAT (1:500; Chemicon International, Temecula, CA) and a mouse monoclonal antibody directed against Parv (1:4000; Sigma-Aldrich, P 3088, St. Louis, MO), whereas donkey anti-goat (ChAT) and horse anti-mouse (Parv) biotinylated secondary antibody (1:500, Vector Laboratories International, Burlingame, CA) were used.

    Techniques: Immunostaining, Staining, Incubation