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rabbit anti-pitx3  (Thermo Fisher)


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    Structured Review

    Thermo Fisher rabbit anti-pitx3
    Effects of miR-124-3p in the expression of dopaminergic neuronal markers in the SN and striatum of a rat PQ model in vivo. (a) Design and timeline of the experimental animal procedure. Male Wistar rats were subjected to intranigral injection with 250 nM miR-124-3p, or saline, followed by four i.p injections of saline or PQ (10 mg/kg), separated by one day. Five days after the last PQ injection, the brains were collected for western blot analysis. Expression levels of TH in the (b) SN and (c) striatum, and (d) <t>PITX3</t> in the SN of adult Wistar rats treated with saline, PQ or 250 nM miR-124-3p + PQ. (e) Representative western blot protein bands of PITX3 (32 kDa) and actin (42 kDa). TH and PITX3 protein levels were normalized against actin. Data are expressed as a percentage of the controls (saline) ± SEM. Protein expression in the control condition (saline) was set to 100%. N = 3 or 4 rats. * p < 0.05 compared to the saline group and ## p < 0.01 compared to the PQ-treated group using the one-way ANOVA followed by Sidak’s multiple comparison test. Abbreviations: i.p, intraperitoneal; TH, tyrosine hydroxylase; PITX3, pituitary homeobox 3; PQ, paraquat; SN, substantia nigra
    Rabbit Anti Pitx3, supplied by Thermo Fisher, 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+pitx3/pmc11144150-57-58-61
    Average 90 stars, based on 1 article reviews
    rabbit anti-pitx3 - by Bioz Stars, 2026-09
    90/100 stars

    Images

    1) Product Images from "MicroRNA-124-3p Modulates Alpha-Synuclein Expression Levels in a Paraquat-Induced in vivo Model for Parkinson’s Disease"

    Article Title: MicroRNA-124-3p Modulates Alpha-Synuclein Expression Levels in a Paraquat-Induced in vivo Model for Parkinson’s Disease

    Journal: Neurochemical Research

    doi: 10.1007/s11064-024-04130-y

    Effects of miR-124-3p in the expression of dopaminergic neuronal markers in the SN and striatum of a rat PQ model in vivo. (a) Design and timeline of the experimental animal procedure. Male Wistar rats were subjected to intranigral injection with 250 nM miR-124-3p, or saline, followed by four i.p injections of saline or PQ (10 mg/kg), separated by one day. Five days after the last PQ injection, the brains were collected for western blot analysis. Expression levels of TH in the (b) SN and (c) striatum, and (d) PITX3 in the SN of adult Wistar rats treated with saline, PQ or 250 nM miR-124-3p + PQ. (e) Representative western blot protein bands of PITX3 (32 kDa) and actin (42 kDa). TH and PITX3 protein levels were normalized against actin. Data are expressed as a percentage of the controls (saline) ± SEM. Protein expression in the control condition (saline) was set to 100%. N = 3 or 4 rats. * p < 0.05 compared to the saline group and ## p < 0.01 compared to the PQ-treated group using the one-way ANOVA followed by Sidak’s multiple comparison test. Abbreviations: i.p, intraperitoneal; TH, tyrosine hydroxylase; PITX3, pituitary homeobox 3; PQ, paraquat; SN, substantia nigra
    Figure Legend Snippet: Effects of miR-124-3p in the expression of dopaminergic neuronal markers in the SN and striatum of a rat PQ model in vivo. (a) Design and timeline of the experimental animal procedure. Male Wistar rats were subjected to intranigral injection with 250 nM miR-124-3p, or saline, followed by four i.p injections of saline or PQ (10 mg/kg), separated by one day. Five days after the last PQ injection, the brains were collected for western blot analysis. Expression levels of TH in the (b) SN and (c) striatum, and (d) PITX3 in the SN of adult Wistar rats treated with saline, PQ or 250 nM miR-124-3p + PQ. (e) Representative western blot protein bands of PITX3 (32 kDa) and actin (42 kDa). TH and PITX3 protein levels were normalized against actin. Data are expressed as a percentage of the controls (saline) ± SEM. Protein expression in the control condition (saline) was set to 100%. N = 3 or 4 rats. * p < 0.05 compared to the saline group and ## p < 0.01 compared to the PQ-treated group using the one-way ANOVA followed by Sidak’s multiple comparison test. Abbreviations: i.p, intraperitoneal; TH, tyrosine hydroxylase; PITX3, pituitary homeobox 3; PQ, paraquat; SN, substantia nigra

    Techniques Used: Expressing, In Vivo, Injection, Saline, Western Blot, Comparison

    Related Articles

    Incubation:

    Article Title: Efficient induction of dopaminergic neuron differentiation from induced pluripotent stem cells reveals impaired mitophagy in PARK2 neurons.
    Article Snippet: Patient-specific induced pluripotent stem cells (iPSCs) show promise for use as tools for in vitro modeling of Parkinson's disease.. We sought to improve the efficiency of dopaminergic (DA) neuron induction from iPSCs by the using surface markers expressed in DA progenitors to increase the significance of the phenotypic analysis.. By sorting for a CD184high/CD44fraction during neural differentiation, we obtained a population of cells that were enriched in DA neuron precursor cells and achieved higher differentiation efficiencies than those obtained through the same protocol without sorting.

    other:

    Article Title: BMP/SMAD Pathway Promotes Neurogenesis of Midbrain Dopaminergic Neurons In Vivo and in Human Induced Pluripotent and Neural Stem Cells
    Article Snippet: 194 195 Primary antibodies 196 Primary antibodies used for the in vivo study were as follows: mouse anti- 197 SHH (1:10), mouse anti-NKX6.1 (1:10), mouse anti-ISLET1/2 (1:10), mouse anti- 198 MSX1/2 (1:10), mouse anti-FOXA2 (1:10), mouse anti NESTIN (1:10), mouse 199 anti EN1 (1:50) - all from DSHB, rabbit anti-LMX1A (1:400, Cat. #AB10533 200 Millipore), rabbit anti LMX1B (1:1000, gift from Dr. C. Birchmeier, MDC, Berlin), 201 rabbit anti-NURR1 (1:100, Cat. #SC991 Santa Cruz Biotech.), mouse anti 202 NURR1 (1:100, Cat.# 376984, Santa Cruz ) mouse anti NEUROGENIN-2 (1:800, 203 Cat. #MAB3314 R&D Systems), rabbit anti-TH (1:200, Cat. #AB152 Millipore), 204 mouse anti-TH (1:200, Cat. #MAB318 Millipore), rabbit anti PHOSPHO- 205 SMAD1/5/8 (1:200, #9511S Cell Signaling), sheep anti-BMP5 (1:10, Cat. 206 10 #AF6176 R&D Systems), rabbit anti PHOSPHO-HISTONE-H3 (1:1000, Cat. #06- 207 570 Millipore), rabbit anti PHOSPHO-P38 (1:1000, Cat. #4511 Cell Signaling), 208 rabbit anti GIRK2 (1:200, Cat. #APC-006, Alomone Labs), rabbit anti SOX6 209 (1:500, Cat. #ab30455 Abcam), mouse anti POU4F1 (1:300, Cat. #sc8429, 210 SantaCruz), mouse anti N-CADHERIN (1:200; Cat. #610920, BD), rabbit anti 211 ZO1 (1:100; Cat. #40-2200, Invitrogen), rabbit anti KI67 (1:100; Cat. # ab16667, 212 Abcam), rabbit anti cleaved-CASPASE3 (1:100; Cat. #3661, Cell Signaling), 213 rabbit anti MAP-2 (1:200; Cat. #sc20172 Santa Cruz Biotech.), rabbit anti β- 214 CATENIN (1:400; Cat. #9587s, Cell Signaling), rabbit anti SHH (1:50, Cat. 215 #sc9024 Santa Cruz Biotech.), rabbit anti BMPR1B (1:100, Cat. #10537 216 Orbigen), rabbit anti PITX3 (Cat. #38-2850; Thermo Fischer Scientific), mouse 217 anti BrdU (Cat. #B2531 Sigma Aldrich), rabbit anti CCND1(1:150, Cat. #sc-450 218 SantaCruz ), rabbit anti phospho- β-CATENIN (1:200, Cat.#9561s Cell 219 Signaling), rabbit anti CALBINDIN (1:500, Cat# d-28k Swant), rabbit anti beta III 220 tubulin/TUJ1 (1:500, Cat# 302 302 Synaptic Systems).

    Article Title: Pitx3 Is a Critical Mediator of GDNF-Induced BDNF Expression in Nigrostriatal Dopaminergic Neurons
    Article Snippet: Antibodies used were rabbit anti-Pitx3 (1:500, Zymed), anti-BDNF (1:500, catalog no. sc-546, Santa Cruz Biotechnology), and anti- -actin (1:2000, Sigma).

    In Vivo:

    Article Title: BMP/SMAD Pathway Promotes Neurogenesis of Midbrain Dopaminergic Neurons In Vivo and in Human Induced Pluripotent and Neural Stem Cells
    Article Snippet: .. Primary antibodies used for the in vivo study were as follows: mouse anti-SHH (1:10), mouse anti-NKX6.1 (1:10), mouse anti-ISLET1/2 (1:10), mouse anti-MSX1/2 (1:10), mouse anti-FOXA2 (1:10), mouse anti-NESTIN (1:10), mouse anti-EN1 (1:50) - all from DSHB, rabbit anti-LMX1A (1:400, catalog #AB10533; Millipore), rabbit anti-LMX1B (1:1000, gift from Dr. C. Birchmeier, MDC, Berlin), rabbit anti-NURR1 (1:100, catalog #SC991; Santa Cruz Biotechnology), mouse anti-NURR1 (1:100, catalog #376984; Santa Cruz Biotechnology) mouse anti-neurogenin-2 (1:800, catalog #MAB3314; R&D Systems), rabbit anti-TH (1:200, catalog #AB152; Millipore), mouse anti-TH (1:200, catalog #MAB318; Millipore), rabbit anti-phospho-SMAD1/5/8 (1:200, #9511S Cell Signaling), sheep anti-BMP5 (1:10, catalog #AF6176; R&D Systems), rabbit anti-phospho-histone-H3 (1:1000, catalog #06-570; Millipore), rabbit anti-phospho-P38 (1:1000, catalog #4511 Cell Signaling), rabbit anti-GIRK2 (1:200, catalog #APC-006; Alomone Laboratories), rabbit anti-SOX6 (1:500, catalog #ab30455; Abcam), mouse anti-POU4F1 (1:300, catalog #sc8429; Santa Cruz Biotechnology), mouse anti-N-cadherin (1:200, catalog #610920; BD Biosciences), rabbit anti-ZO1 (1:100, catalog #40-2200; Invitrogen), rabbit anti-KI67 (1:100, catalog # ab16667; Abcam), rabbit anti-cleaved-caspase 3 (1:100, catalog #3661; Cell Signaling Technology), rabbit anti-MAP-2 (1:200, catalog #sc20172; Santa Cruz Biotechnology), rabbit anti-β-catenin (1:400, catalog #9587s; Cell Signaling Technology), rabbit anti-SHH (1:50, catalog #sc9024; Santa Cruz Biotechnology), rabbit anti-BMPR1B (1:100, catalog #10537; Orbigen), rabbit anti-PITX3 (catalog #38-2850; Thermo Fisher Scientific), mouse anti-BrdU (catalog #B2531; Sigma-Aldrich), rabbit anti-CCND1(1:150, catalog #sc-450; Santa Cruz Biotechnology), rabbit anti-phospho-β-catenin (1:200, catalog #9561s; Cell Signaling Technology), rabbit anti-calbindin (1:500, catalog # d -28k; Swant), and rabbit anti-β III tubulin/TUJ1 (1:500, catalog #302 302; Synaptic Systems). .. For the in vitro study, the following primary antibodies were used: mouse anti-TH (1:1000, catalog #MAB318; Millipore), rabbit anti-TH (1:1000, catalog #ab112; Abcam), rat anti-DAT (1:50, catalog #sc-32259; SCBT), rabbit anti-LMX1A (1:1000, catalog # ab10533; Millipore), goat anti-GIRK2 (1:200, catalog #ab65096; Abcam), and rabbit anti-calbindin (1:1000, catalog #CB38; Swant).



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    Effects of miR-124-3p in the expression of dopaminergic neuronal markers in the SN and striatum of a rat PQ model in vivo. (a) Design and timeline of the experimental animal procedure. Male Wistar rats were subjected to intranigral injection with 250 nM miR-124-3p, or saline, followed by four i.p injections of saline or PQ (10 mg/kg), separated by one day. Five days after the last PQ injection, the brains were collected for western blot analysis. Expression levels of TH in the (b) SN and (c) striatum, and (d) <t>PITX3</t> in the SN of adult Wistar rats treated with saline, PQ or 250 nM miR-124-3p + PQ. (e) Representative western blot protein bands of PITX3 (32 kDa) and actin (42 kDa). TH and PITX3 protein levels were normalized against actin. Data are expressed as a percentage of the controls (saline) ± SEM. Protein expression in the control condition (saline) was set to 100%. N = 3 or 4 rats. * p < 0.05 compared to the saline group and ## p < 0.01 compared to the PQ-treated group using the one-way ANOVA followed by Sidak’s multiple comparison test. Abbreviations: i.p, intraperitoneal; TH, tyrosine hydroxylase; PITX3, pituitary homeobox 3; PQ, paraquat; SN, substantia nigra
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    Effects of miR-124-3p in the expression of dopaminergic neuronal markers in the SN and striatum of a rat PQ model in vivo. (a) Design and timeline of the experimental animal procedure. Male Wistar rats were subjected to intranigral injection with 250 nM miR-124-3p, or saline, followed by four i.p injections of saline or PQ (10 mg/kg), separated by one day. Five days after the last PQ injection, the brains were collected for western blot analysis. Expression levels of TH in the (b) SN and (c) striatum, and (d) <t>PITX3</t> in the SN of adult Wistar rats treated with saline, PQ or 250 nM miR-124-3p + PQ. (e) Representative western blot protein bands of PITX3 (32 kDa) and actin (42 kDa). TH and PITX3 protein levels were normalized against actin. Data are expressed as a percentage of the controls (saline) ± SEM. Protein expression in the control condition (saline) was set to 100%. N = 3 or 4 rats. * p < 0.05 compared to the saline group and ## p < 0.01 compared to the PQ-treated group using the one-way ANOVA followed by Sidak’s multiple comparison test. Abbreviations: i.p, intraperitoneal; TH, tyrosine hydroxylase; PITX3, pituitary homeobox 3; PQ, paraquat; SN, substantia nigra
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    HA injection decreases dopaminergic neurons without affecting β-III Tubulin. (A) Coronal sections of the ventral midbrain from E14 vehicle- and HA-injected rat embryos stained to detect neurons (β-III Tubulin+) and dopaminergic phenotype (TH+); a representative section of a vehicle-injected embryo showing many TH-positive neurons while in a similar midbrain section from a representative HA-injected embryo less TH-positive cells are present. Nuclei were detected with Hoechst. Inner white squares in the merge images represent the higher magnifications shown at the bottom. Scale bars: 150 μm and 50 μm for the low-power and high-power pictures, respectively. (B) β-III Tubulin and TH expression by qRT-PCR from E14 vehicle- and HA-injected embryos, with β-III Tubulin presenting no change, and a significant decrease in TH caused by HA. **p < 0.01. (C) Densitometric analyses of the effect of HA administration on protein levels of β-III Tubulin and diverse factors involved in dopaminergic specification and phenotype. HA injection decreased the protein level of TH, Lmx1a, Lmx1b and <t>Pitx3</t> in midbrain tissue from E14 HA-injected embryos without affecting the generation of neurons, compared to the vehicle-injected condition. Values were normalized to GAPDH signal. *p < 0.05.
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    HA injection decreases dopaminergic neurons without affecting β-III Tubulin. (A) Coronal sections of the ventral midbrain from E14 vehicle- and HA-injected rat embryos stained to detect neurons (β-III Tubulin+) and dopaminergic phenotype (TH+); a representative section of a vehicle-injected embryo showing many TH-positive neurons while in a similar midbrain section from a representative HA-injected embryo less TH-positive cells are present. Nuclei were detected with Hoechst. Inner white squares in the merge images represent the higher magnifications shown at the bottom. Scale bars: 150 μm and 50 μm for the low-power and high-power pictures, respectively. (B) β-III Tubulin and TH expression by qRT-PCR from E14 vehicle- and HA-injected embryos, with β-III Tubulin presenting no change, and a significant decrease in TH caused by HA. **p < 0.01. (C) Densitometric analyses of the effect of HA administration on protein levels of β-III Tubulin and diverse factors involved in dopaminergic specification and phenotype. HA injection decreased the protein level of TH, Lmx1a, Lmx1b and <t>Pitx3</t> in midbrain tissue from E14 HA-injected embryos without affecting the generation of neurons, compared to the vehicle-injected condition. Values were normalized to GAPDH signal. *p < 0.05.
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    Image Search Results


    Effects of miR-124-3p in the expression of dopaminergic neuronal markers in the SN and striatum of a rat PQ model in vivo. (a) Design and timeline of the experimental animal procedure. Male Wistar rats were subjected to intranigral injection with 250 nM miR-124-3p, or saline, followed by four i.p injections of saline or PQ (10 mg/kg), separated by one day. Five days after the last PQ injection, the brains were collected for western blot analysis. Expression levels of TH in the (b) SN and (c) striatum, and (d) PITX3 in the SN of adult Wistar rats treated with saline, PQ or 250 nM miR-124-3p + PQ. (e) Representative western blot protein bands of PITX3 (32 kDa) and actin (42 kDa). TH and PITX3 protein levels were normalized against actin. Data are expressed as a percentage of the controls (saline) ± SEM. Protein expression in the control condition (saline) was set to 100%. N = 3 or 4 rats. * p < 0.05 compared to the saline group and ## p < 0.01 compared to the PQ-treated group using the one-way ANOVA followed by Sidak’s multiple comparison test. Abbreviations: i.p, intraperitoneal; TH, tyrosine hydroxylase; PITX3, pituitary homeobox 3; PQ, paraquat; SN, substantia nigra

    Journal: Neurochemical Research

    Article Title: MicroRNA-124-3p Modulates Alpha-Synuclein Expression Levels in a Paraquat-Induced in vivo Model for Parkinson’s Disease

    doi: 10.1007/s11064-024-04130-y

    Figure Lengend Snippet: Effects of miR-124-3p in the expression of dopaminergic neuronal markers in the SN and striatum of a rat PQ model in vivo. (a) Design and timeline of the experimental animal procedure. Male Wistar rats were subjected to intranigral injection with 250 nM miR-124-3p, or saline, followed by four i.p injections of saline or PQ (10 mg/kg), separated by one day. Five days after the last PQ injection, the brains were collected for western blot analysis. Expression levels of TH in the (b) SN and (c) striatum, and (d) PITX3 in the SN of adult Wistar rats treated with saline, PQ or 250 nM miR-124-3p + PQ. (e) Representative western blot protein bands of PITX3 (32 kDa) and actin (42 kDa). TH and PITX3 protein levels were normalized against actin. Data are expressed as a percentage of the controls (saline) ± SEM. Protein expression in the control condition (saline) was set to 100%. N = 3 or 4 rats. * p < 0.05 compared to the saline group and ## p < 0.01 compared to the PQ-treated group using the one-way ANOVA followed by Sidak’s multiple comparison test. Abbreviations: i.p, intraperitoneal; TH, tyrosine hydroxylase; PITX3, pituitary homeobox 3; PQ, paraquat; SN, substantia nigra

    Article Snippet: Then, 30 µg of total protein was loaded in a 12.5% or 15% polyacrylamide gel, followed by electrophoresis and transfer onto a polyvinylidene difluoride (PVDF) membrane (GE Healthcare, Little Chalfont, UK) for 90 min. Membranes were blocked using 5% milk or 5% bovine serum albumin and then incubated with the following primary antibodies: mouse anti-TH (1:5000; BD Biosciences), rabbit anti-PITX3 (1:1000; Invitrogen), mouse anti-α-synuclein (1:500; BD Biosciences); rabbit anti-pS129-α-synuclein (1:200; Santa Cruz Biotechnology), goat anti-NOX1 (1:200; Santa Cruz Biotechnology), mouse anti-Rac1 (1:750; Millipore), rabbit anti-p47 phox (1:1000; Santa Cruz Biotechnology), mouse anti-actin (1:5000; BD Biosciences) and mouse anti-beta-tubulin (1:5000; BD Biosciences); and the secondary antibodies conjugated to horseradish peroxidase—HRP (chicken anti-goat, goat anti-rabbit or goat anti-mouse; 1:5000; all from Santa Cruz Biotechnology).

    Techniques: Expressing, In Vivo, Injection, Saline, Western Blot, Comparison

    HA injection decreases dopaminergic neurons without affecting β-III Tubulin. (A) Coronal sections of the ventral midbrain from E14 vehicle- and HA-injected rat embryos stained to detect neurons (β-III Tubulin+) and dopaminergic phenotype (TH+); a representative section of a vehicle-injected embryo showing many TH-positive neurons while in a similar midbrain section from a representative HA-injected embryo less TH-positive cells are present. Nuclei were detected with Hoechst. Inner white squares in the merge images represent the higher magnifications shown at the bottom. Scale bars: 150 μm and 50 μm for the low-power and high-power pictures, respectively. (B) β-III Tubulin and TH expression by qRT-PCR from E14 vehicle- and HA-injected embryos, with β-III Tubulin presenting no change, and a significant decrease in TH caused by HA. **p < 0.01. (C) Densitometric analyses of the effect of HA administration on protein levels of β-III Tubulin and diverse factors involved in dopaminergic specification and phenotype. HA injection decreased the protein level of TH, Lmx1a, Lmx1b and Pitx3 in midbrain tissue from E14 HA-injected embryos without affecting the generation of neurons, compared to the vehicle-injected condition. Values were normalized to GAPDH signal. *p < 0.05.

    Journal: Molecular Brain

    Article Title: Histamine impairs midbrain dopaminergic development in vivo by activating histamine type 1 receptors

    doi: 10.1186/s13041-014-0058-x

    Figure Lengend Snippet: HA injection decreases dopaminergic neurons without affecting β-III Tubulin. (A) Coronal sections of the ventral midbrain from E14 vehicle- and HA-injected rat embryos stained to detect neurons (β-III Tubulin+) and dopaminergic phenotype (TH+); a representative section of a vehicle-injected embryo showing many TH-positive neurons while in a similar midbrain section from a representative HA-injected embryo less TH-positive cells are present. Nuclei were detected with Hoechst. Inner white squares in the merge images represent the higher magnifications shown at the bottom. Scale bars: 150 μm and 50 μm for the low-power and high-power pictures, respectively. (B) β-III Tubulin and TH expression by qRT-PCR from E14 vehicle- and HA-injected embryos, with β-III Tubulin presenting no change, and a significant decrease in TH caused by HA. **p < 0.01. (C) Densitometric analyses of the effect of HA administration on protein levels of β-III Tubulin and diverse factors involved in dopaminergic specification and phenotype. HA injection decreased the protein level of TH, Lmx1a, Lmx1b and Pitx3 in midbrain tissue from E14 HA-injected embryos without affecting the generation of neurons, compared to the vehicle-injected condition. Values were normalized to GAPDH signal. *p < 0.05.

    Article Snippet: The following antibodies were used: rabbit anti-rat H 1 R polyclonal antibody (1:1500, Santa Cruz Biotechnology); goat anti-rat H 2 R polyclonal antibody (1:1500, Santa Cruz Biotechnology); rabbit anti-Lmx1a polyclonal antibody (1:100, Abcam); rabbit anti-Lmx1b polyclonal antibody (1:100, Abcam); rabbit polyclonal anti-tyrosine hydroxylase (TH, 1:1000; Pel-freez) and rabbit anti-Pitx3 polyclonal antibody (1:500, Zymed).

    Techniques: Injection, Staining, Expressing, Quantitative RT-PCR