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goat anti gad67  (Proteintech)


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    Structured Review

    Proteintech goat anti gad67
    Percentage of co-staining cells
    Goat Anti Gad67, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 167 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/goat anti gad67/product/Proteintech
    Average 96 stars, based on 167 article reviews
    goat anti gad67 - by Bioz Stars, 2026-02
    96/100 stars

    Images

    1) Product Images from "Innately activated TLR4 signal in the nucleus accumbens is sustained by CRF amplification loop and regulates impulsivity"

    Article Title: Innately activated TLR4 signal in the nucleus accumbens is sustained by CRF amplification loop and regulates impulsivity

    Journal: Brain, behavior, and immunity

    doi: 10.1016/j.bbi.2017.11.008

    Percentage of co-staining cells
    Figure Legend Snippet: Percentage of co-staining cells

    Techniques Used: Expressing



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    Depdc5 expression in the HA‐tagged Depdc5 mouse. (A–C) Quantified representative Western blots show HA‐Depdc5 expression in (A) various mouse organ lysates, (B) mouse brain lysates at developmental stages from embryonic day 10 (E10) to postnatal day 90 (P90), and (C) different brain regions of adult mouse (n = 1–3). Actin was used as the loading control. (D–H) Depdc5 expression in the somatosensory cortex. (D) Immunofluorescent colabeling of HA‐Depdc5 (red) with NeuN (green) showing specific expression of Depdc5 (compared to wild‐type untagged cortex, bottom) in neuronal soma (see insets , corresponding to the yellow squares). (E) Immunofluorescent colabeling of HA‐Depdc5 (red) with Lamp1 (green) showing specific enriched expression in lysosomes (compared to wild‐type untagged cortex, bottom). On the right of insets (corresponding to the yellow square) are the colocalization (Coloc.) between HA and Lamp1 (Pearson correlation coefficient for HA‐Depdc5 mouse = 0.49). (F) Immunofluorescent colabeling of HA‐Depdc5 (red) with Map2 (green) showing expression of Depdc5 in neurites. Bottom images are the insets (corresponding to the yellow square) showing HA (red) distribution along the MAP2‐positive (green) neurite. Arrows show aggregation of HA‐Depdc5 staining. (G) Immunofluorescent colabeling of HA‐Depdc5 (red) and CaMKII (excitatory neurons), <t>Gad67</t> (inhibitory neurons) or parvalbumin (PV; PV interneurons) shows Depdc5 is expressed in excitatory and inhibitory neurons. (H) Colabeling of HA‐Depdc5 (red) and Gfap, Olig2, Plp, and Iba1, shows no coexpression in glial and microglial cells. Three sections were done in duplicate. Scale bars represent 50μm (D, G, H), 25μm (E), or 20μm (F).
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    Depdc5 expression in the HA‐tagged Depdc5 mouse. (A–C) Quantified representative Western blots show HA‐Depdc5 expression in (A) various mouse organ lysates, (B) mouse brain lysates at developmental stages from embryonic day 10 (E10) to postnatal day 90 (P90), and (C) different brain regions of adult mouse (n = 1–3). Actin was used as the loading control. (D–H) Depdc5 expression in the somatosensory cortex. (D) Immunofluorescent colabeling of HA‐Depdc5 (red) with NeuN (green) showing specific expression of Depdc5 (compared to wild‐type untagged cortex, bottom) in neuronal soma (see insets , corresponding to the yellow squares). (E) Immunofluorescent colabeling of HA‐Depdc5 (red) with Lamp1 (green) showing specific enriched expression in lysosomes (compared to wild‐type untagged cortex, bottom). On the right of insets (corresponding to the yellow square) are the colocalization (Coloc.) between HA and Lamp1 (Pearson correlation coefficient for HA‐Depdc5 mouse = 0.49). (F) Immunofluorescent colabeling of HA‐Depdc5 (red) with Map2 (green) showing expression of Depdc5 in neurites. Bottom images are the insets (corresponding to the yellow square) showing HA (red) distribution along the MAP2‐positive (green) neurite. Arrows show aggregation of HA‐Depdc5 staining. (G) Immunofluorescent colabeling of HA‐Depdc5 (red) and CaMKII (excitatory neurons), <t>Gad67</t> (inhibitory neurons) or parvalbumin (PV; PV interneurons) shows Depdc5 is expressed in excitatory and inhibitory neurons. (H) Colabeling of HA‐Depdc5 (red) and Gfap, Olig2, Plp, and Iba1, shows no coexpression in glial and microglial cells. Three sections were done in duplicate. Scale bars represent 50μm (D, G, H), 25μm (E), or 20μm (F).
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    Depdc5 expression in the HA‐tagged Depdc5 mouse. (A–C) Quantified representative Western blots show HA‐Depdc5 expression in (A) various mouse organ lysates, (B) mouse brain lysates at developmental stages from embryonic day 10 (E10) to postnatal day 90 (P90), and (C) different brain regions of adult mouse (n = 1–3). Actin was used as the loading control. (D–H) Depdc5 expression in the somatosensory cortex. (D) Immunofluorescent colabeling of HA‐Depdc5 (red) with NeuN (green) showing specific expression of Depdc5 (compared to wild‐type untagged cortex, bottom) in neuronal soma (see insets , corresponding to the yellow squares). (E) Immunofluorescent colabeling of HA‐Depdc5 (red) with Lamp1 (green) showing specific enriched expression in lysosomes (compared to wild‐type untagged cortex, bottom). On the right of insets (corresponding to the yellow square) are the colocalization (Coloc.) between HA and Lamp1 (Pearson correlation coefficient for HA‐Depdc5 mouse = 0.49). (F) Immunofluorescent colabeling of HA‐Depdc5 (red) with Map2 (green) showing expression of Depdc5 in neurites. Bottom images are the insets (corresponding to the yellow square) showing HA (red) distribution along the MAP2‐positive (green) neurite. Arrows show aggregation of HA‐Depdc5 staining. (G) Immunofluorescent colabeling of HA‐Depdc5 (red) and CaMKII (excitatory neurons), <t>Gad67</t> (inhibitory neurons) or parvalbumin (PV; PV interneurons) shows Depdc5 is expressed in excitatory and inhibitory neurons. (H) Colabeling of HA‐Depdc5 (red) and Gfap, Olig2, Plp, and Iba1, shows no coexpression in glial and microglial cells. Three sections were done in duplicate. Scale bars represent 50μm (D, G, H), 25μm (E), or 20μm (F).
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    Percentage of co-staining cells
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    Percentage of co-staining cells
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    Image Search Results


    Depdc5 expression in the HA‐tagged Depdc5 mouse. (A–C) Quantified representative Western blots show HA‐Depdc5 expression in (A) various mouse organ lysates, (B) mouse brain lysates at developmental stages from embryonic day 10 (E10) to postnatal day 90 (P90), and (C) different brain regions of adult mouse (n = 1–3). Actin was used as the loading control. (D–H) Depdc5 expression in the somatosensory cortex. (D) Immunofluorescent colabeling of HA‐Depdc5 (red) with NeuN (green) showing specific expression of Depdc5 (compared to wild‐type untagged cortex, bottom) in neuronal soma (see insets , corresponding to the yellow squares). (E) Immunofluorescent colabeling of HA‐Depdc5 (red) with Lamp1 (green) showing specific enriched expression in lysosomes (compared to wild‐type untagged cortex, bottom). On the right of insets (corresponding to the yellow square) are the colocalization (Coloc.) between HA and Lamp1 (Pearson correlation coefficient for HA‐Depdc5 mouse = 0.49). (F) Immunofluorescent colabeling of HA‐Depdc5 (red) with Map2 (green) showing expression of Depdc5 in neurites. Bottom images are the insets (corresponding to the yellow square) showing HA (red) distribution along the MAP2‐positive (green) neurite. Arrows show aggregation of HA‐Depdc5 staining. (G) Immunofluorescent colabeling of HA‐Depdc5 (red) and CaMKII (excitatory neurons), Gad67 (inhibitory neurons) or parvalbumin (PV; PV interneurons) shows Depdc5 is expressed in excitatory and inhibitory neurons. (H) Colabeling of HA‐Depdc5 (red) and Gfap, Olig2, Plp, and Iba1, shows no coexpression in glial and microglial cells. Three sections were done in duplicate. Scale bars represent 50μm (D, G, H), 25μm (E), or 20μm (F).

    Journal: Annals of Neurology

    Article Title: Cardiac Investigations in Sudden Unexpected Death in DEPDC5 ‐Related Epilepsy

    doi: 10.1002/ana.26256

    Figure Lengend Snippet: Depdc5 expression in the HA‐tagged Depdc5 mouse. (A–C) Quantified representative Western blots show HA‐Depdc5 expression in (A) various mouse organ lysates, (B) mouse brain lysates at developmental stages from embryonic day 10 (E10) to postnatal day 90 (P90), and (C) different brain regions of adult mouse (n = 1–3). Actin was used as the loading control. (D–H) Depdc5 expression in the somatosensory cortex. (D) Immunofluorescent colabeling of HA‐Depdc5 (red) with NeuN (green) showing specific expression of Depdc5 (compared to wild‐type untagged cortex, bottom) in neuronal soma (see insets , corresponding to the yellow squares). (E) Immunofluorescent colabeling of HA‐Depdc5 (red) with Lamp1 (green) showing specific enriched expression in lysosomes (compared to wild‐type untagged cortex, bottom). On the right of insets (corresponding to the yellow square) are the colocalization (Coloc.) between HA and Lamp1 (Pearson correlation coefficient for HA‐Depdc5 mouse = 0.49). (F) Immunofluorescent colabeling of HA‐Depdc5 (red) with Map2 (green) showing expression of Depdc5 in neurites. Bottom images are the insets (corresponding to the yellow square) showing HA (red) distribution along the MAP2‐positive (green) neurite. Arrows show aggregation of HA‐Depdc5 staining. (G) Immunofluorescent colabeling of HA‐Depdc5 (red) and CaMKII (excitatory neurons), Gad67 (inhibitory neurons) or parvalbumin (PV; PV interneurons) shows Depdc5 is expressed in excitatory and inhibitory neurons. (H) Colabeling of HA‐Depdc5 (red) and Gfap, Olig2, Plp, and Iba1, shows no coexpression in glial and microglial cells. Three sections were done in duplicate. Scale bars represent 50μm (D, G, H), 25μm (E), or 20μm (F).

    Article Snippet: Primary antibodies used were rabbit anti‐HA (1/1,500, C29F4, Cell Signaling Technology), mouse anti‐NeuN (1/200, MAB377; Millipore, Billerica, MA), mouse anti‐Map2 (1/500, ab11267, Abcam), mouse anti‐CamkII (1/500, ab22609, Abcam), rat anti‐LAMP1 (1/500, 1D4B; DSHB, Iowa City, IA), goat anti‐Gad67 (1/400, MAB5406, Millipore), mouse antiparvalbumin (anti‐PV; 1/1,000, P3088, Sigma), mouse anti‐Gfap (1/300, MA5‐15086; Thermo Fisher Scientific, Waltham, MA), rat anti‐Plp (1/10, DSHB), mouse anti‐Olig2 (1/400, ab236540, Abcam), and goat anti‐Iba1 (1/500, 011‐27991; Wako, Osaka, Japan).

    Techniques: Expressing, Western Blot, Staining

    Percentage of co-staining cells

    Journal: Brain, behavior, and immunity

    Article Title: Innately activated TLR4 signal in the nucleus accumbens is sustained by CRF amplification loop and regulates impulsivity

    doi: 10.1016/j.bbi.2017.11.008

    Figure Lengend Snippet: Percentage of co-staining cells

    Article Snippet: Other antibodies were goat anti-GAD67 (glutamic acid decarboxylase 1 (GAD1)) (LifeSpan BioSciences, Seattle, WA, USA, Cat. # LS-B3027-50, RRID: AB_1965223), rabbit anti-CRFR1 (Thermo Fisher Scientific, Waltham, MA, USA, Cat. # 720290, RRID: AB_2633242), rabbit anti-NF-kB p65 (Abcam, Cambridge, MA, USA, Cat. # ab32536, RRID: AB_776751), mouse beta Actin (β-Actin; Proteintech Group, Rosemont, IL, USA, Cat. # 66009-1-Ig, RRID: AB_2687938), Alexa Fluor 488 goat anti-rabbit or donkey anti-goat IgG (H+L; Cat. # {"type":"entrez-nucleotide","attrs":{"text":"A11034","term_id":"489250","term_text":"A11034"}} A11034 , RRID: AB_2576217 or Cat. # {"type":"entrez-nucleotide","attrs":{"text":"A11055","term_id":"490909","term_text":"A11055"}} A11055 , RRID: AB_142672, respectively, Thermo Fisher Scientific), and Alexa Fluor 546 goat anti-mouse or goat anti-rabbit IgG (H+L; Cat.# {"type":"entrez-nucleotide","attrs":{"text":"A11030","term_id":"489248","term_text":"A11030"}} A11030 , RRID: AB_2534089, or Cat. # A11035, RRID: AB_2534093, respectively, Thermo Fisher Scientific).

    Techniques: Expressing