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rabbit anti synaptopodin antibody  (Proteintech)


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    Structured Review

    Proteintech rabbit anti synaptopodin antibody
    Rabbit Anti Synaptopodin Antibody, supplied by Proteintech, used in various techniques. Bioz Stars score: 94/100, based on 94 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rabbit+anti+synaptopodin+antibody/Synaptopodin+Antibody/pm41904323-285-17-20
    Average 94 stars, based on 94 article reviews
    rabbit anti synaptopodin antibody - by Bioz Stars, 2026-10
    94/100 stars

    Images

    Related Articles

    Marker:

    Article Title: Overproduction of Mitochondrial Fission Proteins and Mitochondrial Fission in Podocytes of Lupus Nephritis Patients
    Article Snippet: The mouse anti-Drp1 and Fis1 antibody (Proteintech Group, Inc., Chicago, IL, USA) were used. .. While rabbit anti-synaptopodin antibody (Proteintech Group, Inc. Chicago, IL, USA) was used as a podocyte marker for double immunofluorescence staining. .. Images were taken with a fluorescence microscope (Nikon Eclipse C1, Japan).

    Double Immunofluorescence Staining:

    Article Title: Overproduction of Mitochondrial Fission Proteins and Mitochondrial Fission in Podocytes of Lupus Nephritis Patients
    Article Snippet: The mouse anti-Drp1 and Fis1 antibody (Proteintech Group, Inc., Chicago, IL, USA) were used. .. While rabbit anti-synaptopodin antibody (Proteintech Group, Inc. Chicago, IL, USA) was used as a podocyte marker for double immunofluorescence staining. .. Images were taken with a fluorescence microscope (Nikon Eclipse C1, Japan).

    Incubation:

    Article Title: CDKAL1 dysfunction impairs lysine codon translation in podocytes and accelerates chronic kidney disease.
    Article Snippet: Samples were then electrophoresed in 10% polyacrylamide-SDS gels and transferred to polyvinylidene fluoride membranes (Merck Millipore). .. The membranes were incubated with rabbit anti-CDKAL1 antibody (Invitrogen), rabbit anti-CD2AP antibody (Gene Tex) at 1:500 dilutions, rabbit anti-Synaptopodin antibody (Proteintech) at a 1:1000 dilution and rabbit anti-GAPDH antibody (Gene Tex) at a 1:20,000 dilution. .. Cultured cells and sieved mouse glomeruli were pelleted by centrifugation and lysed in chilled lysis buffer (150 mM NaCl, 50 mM Tris-HCl pH 8.0, and 1% NP-40) containing protease inhibitor cocktail (Roche).



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    PLCXD2 hinders SA formation (see also Supplementary figure S5). (A) DIV16 mouse cultured hippocampal neuron co-expressing PLCXD2-FLAG and GFP immunostained for FLAG (red), GFP (gray) and F-actin (cyan). Scale bar 10 µm, inset 5 µm. (B) Representative images of dendritic spines from cultured hippocampal neurons lacking or containing PLCXD2-FLAG, immunostained for F-actin (cyan). Scale bar 1 µm. (C) Quantification of F-actin fluorescence intensity in spines. Each pair of dot plots represents the average F-actin fluorescence intensity in PLCXD2- and PLCXD2+ spines from the same neuron ( n = 3 cultures, 13 neurons). *** P <0.001, Wilcoxon matched-pairs signed rank test. (D) DIV16 mouse cultured hippocampal neuron co-expressing PLCXD2-FLAG and GFP were immunostained for FLAG (red), GFP (gray) and <t>SYNPO</t> (cyan). Scale bar 10 µm, inset 5 µm. (E) Percentage of PLCXD2+ spines containing SYNPO and vice versa. (F) Quantification of SYNPO fluorescence intensity. Each pair of dot plots represents the average SYNPO fluorescence intensity in PLCXD2- and PLCXD2+ spines from the same neuron ( n = 3 cultures, 14 neurons). **** P <0.0001, two-tailed paired t -test.
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    Image Search Results


    Antigen targets and corresponding antibodies

    Journal: NPJ Parkinson's Disease

    Article Title: Advancing age and the rs6265 BDNF SNP are permissive to graft-induced dyskinesias in parkinsonian rats

    doi: 10.1038/s41531-024-00771-6

    Figure Lengend Snippet: Antigen targets and corresponding antibodies

    Article Snippet: TH-Synaptopodin , Synaptopodin , rabbit anti-synaptopodin , 1:4000 , Synaptic Systems , 163002 , A21207.

    Techniques:

    PLCXD2 hinders SA formation (see also Supplementary figure S5). (A) DIV16 mouse cultured hippocampal neuron co-expressing PLCXD2-FLAG and GFP immunostained for FLAG (red), GFP (gray) and F-actin (cyan). Scale bar 10 µm, inset 5 µm. (B) Representative images of dendritic spines from cultured hippocampal neurons lacking or containing PLCXD2-FLAG, immunostained for F-actin (cyan). Scale bar 1 µm. (C) Quantification of F-actin fluorescence intensity in spines. Each pair of dot plots represents the average F-actin fluorescence intensity in PLCXD2- and PLCXD2+ spines from the same neuron ( n = 3 cultures, 13 neurons). *** P <0.001, Wilcoxon matched-pairs signed rank test. (D) DIV16 mouse cultured hippocampal neuron co-expressing PLCXD2-FLAG and GFP were immunostained for FLAG (red), GFP (gray) and SYNPO (cyan). Scale bar 10 µm, inset 5 µm. (E) Percentage of PLCXD2+ spines containing SYNPO and vice versa. (F) Quantification of SYNPO fluorescence intensity. Each pair of dot plots represents the average SYNPO fluorescence intensity in PLCXD2- and PLCXD2+ spines from the same neuron ( n = 3 cultures, 14 neurons). **** P <0.0001, two-tailed paired t -test.

    Journal: bioRxiv

    Article Title: Cell-surface receptor-mediated regulation of synaptic organelle distribution controls dendritic spine maturation

    doi: 10.1101/2024.05.08.592949

    Figure Lengend Snippet: PLCXD2 hinders SA formation (see also Supplementary figure S5). (A) DIV16 mouse cultured hippocampal neuron co-expressing PLCXD2-FLAG and GFP immunostained for FLAG (red), GFP (gray) and F-actin (cyan). Scale bar 10 µm, inset 5 µm. (B) Representative images of dendritic spines from cultured hippocampal neurons lacking or containing PLCXD2-FLAG, immunostained for F-actin (cyan). Scale bar 1 µm. (C) Quantification of F-actin fluorescence intensity in spines. Each pair of dot plots represents the average F-actin fluorescence intensity in PLCXD2- and PLCXD2+ spines from the same neuron ( n = 3 cultures, 13 neurons). *** P <0.001, Wilcoxon matched-pairs signed rank test. (D) DIV16 mouse cultured hippocampal neuron co-expressing PLCXD2-FLAG and GFP were immunostained for FLAG (red), GFP (gray) and SYNPO (cyan). Scale bar 10 µm, inset 5 µm. (E) Percentage of PLCXD2+ spines containing SYNPO and vice versa. (F) Quantification of SYNPO fluorescence intensity. Each pair of dot plots represents the average SYNPO fluorescence intensity in PLCXD2- and PLCXD2+ spines from the same neuron ( n = 3 cultures, 14 neurons). **** P <0.0001, two-tailed paired t -test.

    Article Snippet: Primary antibodies were the following: chicken anti-GFP (1:1000, Aves Labs), rat anti-HA (1:250, Roche), mouse anti-β-galactosidase (1:1000, Roche), rabbit anti- GPR158 (1:200, Sigma-Aldrich), rabbit anti-synaptopodin SE19 (1:500, Sigma- Aldrich), camelid PSD95-FluoTag-X2 (1:500, Synaptic Systems), guinea-pig anti- VGluT1 (1:000, Synaptic Systems), and guinea-pig anti-VGluT2 (1:1000, Synaptic Systems).

    Techniques: Cell Culture, Expressing, Fluorescence, Two Tailed Test

    A GPR158-PLCXD2 complex regulates SA content and maturation of dendritic spines (see also Supplementary figure S7). (A) Experimental strategy to achieve simultaneous sparse gene cKO and cell labeling. Leakage of the TRE promoter drives weak expression of Cre and, subsequently, tTA in a very small population of neurons that carry both vectors. Next, tTA enhances Cre expression by binding to TRE. This positive feedback of successive tTA-TRE cycles facilitates expression of Cre and GFP in the scarce population of transduced neurons. (B-D) Representative images of dendritic segments from WT (B) , Gpr158 cKO (C) and Gpr158 : Plcxd2 dcKO (D) neurons in L4 of the barrel cortex, immunostained for GFP and SYNPO at P14. Scale bar 5 µm. ( E) Quantification of dendritic spine morphology in WT (N = 3 mice, n = 9 neurons), Gpr158 cKO ( N = 3 mice, n = 9 neurons) and Gpr158 : Plcxd2 dcKO neurons ( N = 3 mice, n = 9 neurons). ** P <0.001, *** P <0.001, nested 1-way ANOVA, Tukey’s multiple comparisons. (F) Quantification of SYNPO-containing spines in WT (N = 3 mice, n = 9 neurons), Gpr158 cKO ( N = 3 mice, n = 9 neurons) and Gpr158 : Plcxd2 dcKO neurons ( N = 3 mice, n = 9 neurons). **** P <0.0001, nested 1-way ANOVA, Tukey’s multiple comparisons. (G) Quantification of SYNPO-containing mushroom-type spines in WT ( N = 3 mice, n = 9 neurons), Gpr158 cKO ( N = 3 mice, n = 9 neurons) and Gpr158 : Plcxd2 dcKO neurons ( N = 3 mice, n = 9 neurons). * P <0.05, nested 1-way ANOVA, Tukey’s multiple comparisons. (H) Quantification of dendritic spine density in WT ( N = 3 mice, n = 9 neurons), Gpr158 cKO ( N = 3 mice, n = 9 neurons) and Gpr158 : Plcxd2 dcKO neurons ( N = 3 mice, n = 9 neurons).

    Journal: bioRxiv

    Article Title: Cell-surface receptor-mediated regulation of synaptic organelle distribution controls dendritic spine maturation

    doi: 10.1101/2024.05.08.592949

    Figure Lengend Snippet: A GPR158-PLCXD2 complex regulates SA content and maturation of dendritic spines (see also Supplementary figure S7). (A) Experimental strategy to achieve simultaneous sparse gene cKO and cell labeling. Leakage of the TRE promoter drives weak expression of Cre and, subsequently, tTA in a very small population of neurons that carry both vectors. Next, tTA enhances Cre expression by binding to TRE. This positive feedback of successive tTA-TRE cycles facilitates expression of Cre and GFP in the scarce population of transduced neurons. (B-D) Representative images of dendritic segments from WT (B) , Gpr158 cKO (C) and Gpr158 : Plcxd2 dcKO (D) neurons in L4 of the barrel cortex, immunostained for GFP and SYNPO at P14. Scale bar 5 µm. ( E) Quantification of dendritic spine morphology in WT (N = 3 mice, n = 9 neurons), Gpr158 cKO ( N = 3 mice, n = 9 neurons) and Gpr158 : Plcxd2 dcKO neurons ( N = 3 mice, n = 9 neurons). ** P <0.001, *** P <0.001, nested 1-way ANOVA, Tukey’s multiple comparisons. (F) Quantification of SYNPO-containing spines in WT (N = 3 mice, n = 9 neurons), Gpr158 cKO ( N = 3 mice, n = 9 neurons) and Gpr158 : Plcxd2 dcKO neurons ( N = 3 mice, n = 9 neurons). **** P <0.0001, nested 1-way ANOVA, Tukey’s multiple comparisons. (G) Quantification of SYNPO-containing mushroom-type spines in WT ( N = 3 mice, n = 9 neurons), Gpr158 cKO ( N = 3 mice, n = 9 neurons) and Gpr158 : Plcxd2 dcKO neurons ( N = 3 mice, n = 9 neurons). * P <0.05, nested 1-way ANOVA, Tukey’s multiple comparisons. (H) Quantification of dendritic spine density in WT ( N = 3 mice, n = 9 neurons), Gpr158 cKO ( N = 3 mice, n = 9 neurons) and Gpr158 : Plcxd2 dcKO neurons ( N = 3 mice, n = 9 neurons).

    Article Snippet: Primary antibodies were the following: chicken anti-GFP (1:1000, Aves Labs), rat anti-HA (1:250, Roche), mouse anti-β-galactosidase (1:1000, Roche), rabbit anti- GPR158 (1:200, Sigma-Aldrich), rabbit anti-synaptopodin SE19 (1:500, Sigma- Aldrich), camelid PSD95-FluoTag-X2 (1:500, Synaptic Systems), guinea-pig anti- VGluT1 (1:000, Synaptic Systems), and guinea-pig anti-VGluT2 (1:1000, Synaptic Systems).

    Techniques: Labeling, Expressing, Binding Assay