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probdnf antibody  (Alomone Labs)


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    Structured Review

    Alomone Labs probdnf antibody
    SINEUP strategy, specificity and efficacy in targeting BDNF protein upregulation. A-B . Rat BDNF gene structure with schematic representation of BDNF transcripts characterised by multiple alternative splicing of 5’ and 3’UTRs (grey boxes), a coding sequence (CDS, white boxes) and two poly-adenylation sites (polyA). B. SINEUP-PAN and SINEUP-Ex1 annealing sites on BDNF transcripts used in this study. <t>C-H.</t> <t>HEK293T</t> cells are co-transfected with different plasmids to demonstrate the efficacy of SINEUP-PAN or SINEUP-Ex1 on the indicated BDNF transcripts with respect to control (GFP). Plasmids were transfected in 1:3 ratio. Tubulin (55 kDa) is indicative of gel loading and is used for normalization in the Western blot analysis. Histograms quantify average data from n = 4 experiments. The molecular weight for the BDNF-GFP band of 64–65 KDa correspond to the predicted size for a chimeric protein made of the <t>proBDNF</t> form (32–34 KDa) and the GFP (27–30 KDa). C . Effect of SINEUP-PAN on protein levels encoded by the transfected chimeric Ex1-BDNF-GFP transcript with respect to control represented by the plasmid encoding the reporter protein GFP alone. p = 0.0005. D . Effect of SINEUP-Ex1 on protein levels encoded by the transfected chimeric Ex1-BDNF-GFP transcript. p = 0.0299. E-F . Effect of SINEUP-PAN on protein levels encoded by the transfected chimeric Ex2B-BDNF-GFP (E) and chimeric Ex2C-BDNF-GFP (F) transcripts. n = 3. G-H . Effect of SINEUP-Ex1 on chimeric Ex2B-BDNF-GFP (G) and chimeric Ex2C-BDNF-GFP (H) transcripts with respect to control (GFP). All the quantitative results shown are produced from a repetition of n = 3 experiments and the Western blot images show the greatest effect obtained and therefore, are not representative of the average results
    Probdnf Antibody, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 94/100, based on 42 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Images

    1) Product Images from "Long non-coding SINEUP RNA enhancing BDNF translation prevents dendritic atrophy following an Aβ-peptide challenge"

    Article Title: Long non-coding SINEUP RNA enhancing BDNF translation prevents dendritic atrophy following an Aβ-peptide challenge

    Journal: Cellular and Molecular Life Sciences: CMLS

    doi: 10.1007/s00018-026-06175-4

    SINEUP strategy, specificity and efficacy in targeting BDNF protein upregulation. A-B . Rat BDNF gene structure with schematic representation of BDNF transcripts characterised by multiple alternative splicing of 5’ and 3’UTRs (grey boxes), a coding sequence (CDS, white boxes) and two poly-adenylation sites (polyA). B. SINEUP-PAN and SINEUP-Ex1 annealing sites on BDNF transcripts used in this study. C-H. HEK293T cells are co-transfected with different plasmids to demonstrate the efficacy of SINEUP-PAN or SINEUP-Ex1 on the indicated BDNF transcripts with respect to control (GFP). Plasmids were transfected in 1:3 ratio. Tubulin (55 kDa) is indicative of gel loading and is used for normalization in the Western blot analysis. Histograms quantify average data from n = 4 experiments. The molecular weight for the BDNF-GFP band of 64–65 KDa correspond to the predicted size for a chimeric protein made of the proBDNF form (32–34 KDa) and the GFP (27–30 KDa). C . Effect of SINEUP-PAN on protein levels encoded by the transfected chimeric Ex1-BDNF-GFP transcript with respect to control represented by the plasmid encoding the reporter protein GFP alone. p = 0.0005. D . Effect of SINEUP-Ex1 on protein levels encoded by the transfected chimeric Ex1-BDNF-GFP transcript. p = 0.0299. E-F . Effect of SINEUP-PAN on protein levels encoded by the transfected chimeric Ex2B-BDNF-GFP (E) and chimeric Ex2C-BDNF-GFP (F) transcripts. n = 3. G-H . Effect of SINEUP-Ex1 on chimeric Ex2B-BDNF-GFP (G) and chimeric Ex2C-BDNF-GFP (H) transcripts with respect to control (GFP). All the quantitative results shown are produced from a repetition of n = 3 experiments and the Western blot images show the greatest effect obtained and therefore, are not representative of the average results
    Figure Legend Snippet: SINEUP strategy, specificity and efficacy in targeting BDNF protein upregulation. A-B . Rat BDNF gene structure with schematic representation of BDNF transcripts characterised by multiple alternative splicing of 5’ and 3’UTRs (grey boxes), a coding sequence (CDS, white boxes) and two poly-adenylation sites (polyA). B. SINEUP-PAN and SINEUP-Ex1 annealing sites on BDNF transcripts used in this study. C-H. HEK293T cells are co-transfected with different plasmids to demonstrate the efficacy of SINEUP-PAN or SINEUP-Ex1 on the indicated BDNF transcripts with respect to control (GFP). Plasmids were transfected in 1:3 ratio. Tubulin (55 kDa) is indicative of gel loading and is used for normalization in the Western blot analysis. Histograms quantify average data from n = 4 experiments. The molecular weight for the BDNF-GFP band of 64–65 KDa correspond to the predicted size for a chimeric protein made of the proBDNF form (32–34 KDa) and the GFP (27–30 KDa). C . Effect of SINEUP-PAN on protein levels encoded by the transfected chimeric Ex1-BDNF-GFP transcript with respect to control represented by the plasmid encoding the reporter protein GFP alone. p = 0.0005. D . Effect of SINEUP-Ex1 on protein levels encoded by the transfected chimeric Ex1-BDNF-GFP transcript. p = 0.0299. E-F . Effect of SINEUP-PAN on protein levels encoded by the transfected chimeric Ex2B-BDNF-GFP (E) and chimeric Ex2C-BDNF-GFP (F) transcripts. n = 3. G-H . Effect of SINEUP-Ex1 on chimeric Ex2B-BDNF-GFP (G) and chimeric Ex2C-BDNF-GFP (H) transcripts with respect to control (GFP). All the quantitative results shown are produced from a repetition of n = 3 experiments and the Western blot images show the greatest effect obtained and therefore, are not representative of the average results

    Techniques Used: Alternative Splicing, Sequencing, Transfection, Control, Western Blot, Molecular Weight, Plasmid Preparation, Produced



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    SINEUP strategy, specificity and efficacy in targeting BDNF protein upregulation. A-B . Rat BDNF gene structure with schematic representation of BDNF transcripts characterised by multiple alternative splicing of 5’ and 3’UTRs (grey boxes), a coding sequence (CDS, white boxes) and two poly-adenylation sites (polyA). B. SINEUP-PAN and SINEUP-Ex1 annealing sites on BDNF transcripts used in this study. <t>C-H.</t> <t>HEK293T</t> cells are co-transfected with different plasmids to demonstrate the efficacy of SINEUP-PAN or SINEUP-Ex1 on the indicated BDNF transcripts with respect to control (GFP). Plasmids were transfected in 1:3 ratio. Tubulin (55 kDa) is indicative of gel loading and is used for normalization in the Western blot analysis. Histograms quantify average data from n = 4 experiments. The molecular weight for the BDNF-GFP band of 64–65 KDa correspond to the predicted size for a chimeric protein made of the <t>proBDNF</t> form (32–34 KDa) and the GFP (27–30 KDa). C . Effect of SINEUP-PAN on protein levels encoded by the transfected chimeric Ex1-BDNF-GFP transcript with respect to control represented by the plasmid encoding the reporter protein GFP alone. p = 0.0005. D . Effect of SINEUP-Ex1 on protein levels encoded by the transfected chimeric Ex1-BDNF-GFP transcript. p = 0.0299. E-F . Effect of SINEUP-PAN on protein levels encoded by the transfected chimeric Ex2B-BDNF-GFP (E) and chimeric Ex2C-BDNF-GFP (F) transcripts. n = 3. G-H . Effect of SINEUP-Ex1 on chimeric Ex2B-BDNF-GFP (G) and chimeric Ex2C-BDNF-GFP (H) transcripts with respect to control (GFP). All the quantitative results shown are produced from a repetition of n = 3 experiments and the Western blot images show the greatest effect obtained and therefore, are not representative of the average results
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    Image Search Results


    SINEUP strategy, specificity and efficacy in targeting BDNF protein upregulation. A-B . Rat BDNF gene structure with schematic representation of BDNF transcripts characterised by multiple alternative splicing of 5’ and 3’UTRs (grey boxes), a coding sequence (CDS, white boxes) and two poly-adenylation sites (polyA). B. SINEUP-PAN and SINEUP-Ex1 annealing sites on BDNF transcripts used in this study. C-H. HEK293T cells are co-transfected with different plasmids to demonstrate the efficacy of SINEUP-PAN or SINEUP-Ex1 on the indicated BDNF transcripts with respect to control (GFP). Plasmids were transfected in 1:3 ratio. Tubulin (55 kDa) is indicative of gel loading and is used for normalization in the Western blot analysis. Histograms quantify average data from n = 4 experiments. The molecular weight for the BDNF-GFP band of 64–65 KDa correspond to the predicted size for a chimeric protein made of the proBDNF form (32–34 KDa) and the GFP (27–30 KDa). C . Effect of SINEUP-PAN on protein levels encoded by the transfected chimeric Ex1-BDNF-GFP transcript with respect to control represented by the plasmid encoding the reporter protein GFP alone. p = 0.0005. D . Effect of SINEUP-Ex1 on protein levels encoded by the transfected chimeric Ex1-BDNF-GFP transcript. p = 0.0299. E-F . Effect of SINEUP-PAN on protein levels encoded by the transfected chimeric Ex2B-BDNF-GFP (E) and chimeric Ex2C-BDNF-GFP (F) transcripts. n = 3. G-H . Effect of SINEUP-Ex1 on chimeric Ex2B-BDNF-GFP (G) and chimeric Ex2C-BDNF-GFP (H) transcripts with respect to control (GFP). All the quantitative results shown are produced from a repetition of n = 3 experiments and the Western blot images show the greatest effect obtained and therefore, are not representative of the average results

    Journal: Cellular and Molecular Life Sciences: CMLS

    Article Title: Long non-coding SINEUP RNA enhancing BDNF translation prevents dendritic atrophy following an Aβ-peptide challenge

    doi: 10.1007/s00018-026-06175-4

    Figure Lengend Snippet: SINEUP strategy, specificity and efficacy in targeting BDNF protein upregulation. A-B . Rat BDNF gene structure with schematic representation of BDNF transcripts characterised by multiple alternative splicing of 5’ and 3’UTRs (grey boxes), a coding sequence (CDS, white boxes) and two poly-adenylation sites (polyA). B. SINEUP-PAN and SINEUP-Ex1 annealing sites on BDNF transcripts used in this study. C-H. HEK293T cells are co-transfected with different plasmids to demonstrate the efficacy of SINEUP-PAN or SINEUP-Ex1 on the indicated BDNF transcripts with respect to control (GFP). Plasmids were transfected in 1:3 ratio. Tubulin (55 kDa) is indicative of gel loading and is used for normalization in the Western blot analysis. Histograms quantify average data from n = 4 experiments. The molecular weight for the BDNF-GFP band of 64–65 KDa correspond to the predicted size for a chimeric protein made of the proBDNF form (32–34 KDa) and the GFP (27–30 KDa). C . Effect of SINEUP-PAN on protein levels encoded by the transfected chimeric Ex1-BDNF-GFP transcript with respect to control represented by the plasmid encoding the reporter protein GFP alone. p = 0.0005. D . Effect of SINEUP-Ex1 on protein levels encoded by the transfected chimeric Ex1-BDNF-GFP transcript. p = 0.0299. E-F . Effect of SINEUP-PAN on protein levels encoded by the transfected chimeric Ex2B-BDNF-GFP (E) and chimeric Ex2C-BDNF-GFP (F) transcripts. n = 3. G-H . Effect of SINEUP-Ex1 on chimeric Ex2B-BDNF-GFP (G) and chimeric Ex2C-BDNF-GFP (H) transcripts with respect to control (GFP). All the quantitative results shown are produced from a repetition of n = 3 experiments and the Western blot images show the greatest effect obtained and therefore, are not representative of the average results

    Article Snippet: The membrane was blocked by 5% non-fat milk in TBST- solution (1 h, RT) and then, the HEK293T cells were incubated with the rabbit polyclonal anti proBDNF antibody (Alomone, Cat. # ANT-006, dilution 1:1000, over-night at 4 °C) while the SH-SY5Y cells were incubated also with the mouse monoclonal anti-BDNF recognizing both BDNF forms (Sigma Cat. #B5050, dilution 1:1000, over-night at 4 °C). and mouse anti alpha tubulin (Sigma, Cat. # T6074, dilution 1:3000) over-night at 4 °C.

    Techniques: Alternative Splicing, Sequencing, Transfection, Control, Western Blot, Molecular Weight, Plasmid Preparation, Produced