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recombinant pro bdnf  (Alomone Labs)


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    Structured Review

    Alomone Labs recombinant pro bdnf
    (A) Role of endogenous <t>BDNF</t> and its receptor TrkB on CRC cell proliferation: effects of exogenous BDNF and suppressing endogenous TrkB receptor on cell proliferation. The four cell lines were cultured for 24 h in FCS-free medium (FCS 10%, −) in the presence of exogenous BDNF <t>(+),</t> <t>K252a</t> (+) alone or in combination. Cell proliferation was determined by flow cytometry analysis using EdU Alexa Fluor 488. The data are presented as histograms of proliferating cells in relative units ± SEM of five independent experiments. *, p <0.05; **, p <0.01; ***, p <0.001, when compared with serum-free medium. (B, C) Effects of exogenous BDNF and suppressing endogenous TrkB receptor on cell survival. Apoptotic ratios of soluble nucleosomes were detected by ELISA Cell for WiDr, SW480, SW620, and COLO 205 induced by serum deprivation alone (FCS 10%, −) or in association either with exogenous BDNF (+), or with K252a (+), during 24–72 h of serum deprivation. Histograms, mean ratio of apoptotic cells ± SEM of at least three independent experiments. *, p <0.05; **, p <0.01; ***, p <0.001, when compared with serum-free condition alone. (D, E) apoptotic ratio after 24 h serum deprivation alone (0% FCS) or with combination with a neutralizing anti-BDNF mAb (0% anti-BDNF). Histograms, mean ratio of apoptotic cells ± SEM of three independent experiments. *, p <0.05; **, p <0.01; ***, p <0.001, when compared with serum-free condition alone.
    Recombinant Pro Bdnf, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 93/100, based on 133 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Images

    1) Product Images from "Fine-Tuning Roles of Endogenous Brain-Derived Neurotrophic Factor, TrkB and Sortilin in Colorectal Cancer Cell Survival"

    Article Title: Fine-Tuning Roles of Endogenous Brain-Derived Neurotrophic Factor, TrkB and Sortilin in Colorectal Cancer Cell Survival

    Journal: PLoS ONE

    doi: 10.1371/journal.pone.0025097

    (A) Role of endogenous BDNF and its receptor TrkB on CRC cell proliferation: effects of exogenous BDNF and suppressing endogenous TrkB receptor on cell proliferation. The four cell lines were cultured for 24 h in FCS-free medium (FCS 10%, −) in the presence of exogenous BDNF (+), K252a (+) alone or in combination. Cell proliferation was determined by flow cytometry analysis using EdU Alexa Fluor 488. The data are presented as histograms of proliferating cells in relative units ± SEM of five independent experiments. *, p <0.05; **, p <0.01; ***, p <0.001, when compared with serum-free medium. (B, C) Effects of exogenous BDNF and suppressing endogenous TrkB receptor on cell survival. Apoptotic ratios of soluble nucleosomes were detected by ELISA Cell for WiDr, SW480, SW620, and COLO 205 induced by serum deprivation alone (FCS 10%, −) or in association either with exogenous BDNF (+), or with K252a (+), during 24–72 h of serum deprivation. Histograms, mean ratio of apoptotic cells ± SEM of at least three independent experiments. *, p <0.05; **, p <0.01; ***, p <0.001, when compared with serum-free condition alone. (D, E) apoptotic ratio after 24 h serum deprivation alone (0% FCS) or with combination with a neutralizing anti-BDNF mAb (0% anti-BDNF). Histograms, mean ratio of apoptotic cells ± SEM of three independent experiments. *, p <0.05; **, p <0.01; ***, p <0.001, when compared with serum-free condition alone.
    Figure Legend Snippet: (A) Role of endogenous BDNF and its receptor TrkB on CRC cell proliferation: effects of exogenous BDNF and suppressing endogenous TrkB receptor on cell proliferation. The four cell lines were cultured for 24 h in FCS-free medium (FCS 10%, −) in the presence of exogenous BDNF (+), K252a (+) alone or in combination. Cell proliferation was determined by flow cytometry analysis using EdU Alexa Fluor 488. The data are presented as histograms of proliferating cells in relative units ± SEM of five independent experiments. *, p <0.05; **, p <0.01; ***, p <0.001, when compared with serum-free medium. (B, C) Effects of exogenous BDNF and suppressing endogenous TrkB receptor on cell survival. Apoptotic ratios of soluble nucleosomes were detected by ELISA Cell for WiDr, SW480, SW620, and COLO 205 induced by serum deprivation alone (FCS 10%, −) or in association either with exogenous BDNF (+), or with K252a (+), during 24–72 h of serum deprivation. Histograms, mean ratio of apoptotic cells ± SEM of at least three independent experiments. *, p <0.05; **, p <0.01; ***, p <0.001, when compared with serum-free condition alone. (D, E) apoptotic ratio after 24 h serum deprivation alone (0% FCS) or with combination with a neutralizing anti-BDNF mAb (0% anti-BDNF). Histograms, mean ratio of apoptotic cells ± SEM of three independent experiments. *, p <0.05; **, p <0.01; ***, p <0.001, when compared with serum-free condition alone.

    Techniques Used: Cell Culture, Flow Cytometry, Enzyme-linked Immunosorbent Assay

    (A, B) Sortilin as a coreceptor of p75 NTR . Double staining (yellow) of sortilin (red) and p75 NTR (green) in SW480 cells (A) and SW620 (B) after 24 h of serum deprivation. (C) Colocalization of pro-BDNF and sortilin. Confocal microscopy study of a WiDr cells stained with an anti-pro-BDNF Ab (green) and an anti-sortilin Ab (red), and double staining (yellow) after 24 h of serum deprivation. (D, E) apoptotic ratios after 24 h serum deprivation alone (0% FCS) or combined with recombinant Pro-BDNF (0% Pro-BDNF). Histograms, mean ratio of apoptotic cells ± SEM of three independent experiments. *, p <0.05; **, p <0.01; ***, p <0.001, when compared with serum-free condition alone (0% FCS).
    Figure Legend Snippet: (A, B) Sortilin as a coreceptor of p75 NTR . Double staining (yellow) of sortilin (red) and p75 NTR (green) in SW480 cells (A) and SW620 (B) after 24 h of serum deprivation. (C) Colocalization of pro-BDNF and sortilin. Confocal microscopy study of a WiDr cells stained with an anti-pro-BDNF Ab (green) and an anti-sortilin Ab (red), and double staining (yellow) after 24 h of serum deprivation. (D, E) apoptotic ratios after 24 h serum deprivation alone (0% FCS) or combined with recombinant Pro-BDNF (0% Pro-BDNF). Histograms, mean ratio of apoptotic cells ± SEM of three independent experiments. *, p <0.05; **, p <0.01; ***, p <0.001, when compared with serum-free condition alone (0% FCS).

    Techniques Used: Double Staining, Confocal Microscopy, Staining, Recombinant



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    (A) Role of endogenous <t>BDNF</t> and its receptor TrkB on CRC cell proliferation: effects of exogenous BDNF and suppressing endogenous TrkB receptor on cell proliferation. The four cell lines were cultured for 24 h in FCS-free medium (FCS 10%, −) in the presence of exogenous BDNF <t>(+),</t> <t>K252a</t> (+) alone or in combination. Cell proliferation was determined by flow cytometry analysis using EdU Alexa Fluor 488. The data are presented as histograms of proliferating cells in relative units ± SEM of five independent experiments. *, p <0.05; **, p <0.01; ***, p <0.001, when compared with serum-free medium. (B, C) Effects of exogenous BDNF and suppressing endogenous TrkB receptor on cell survival. Apoptotic ratios of soluble nucleosomes were detected by ELISA Cell for WiDr, SW480, SW620, and COLO 205 induced by serum deprivation alone (FCS 10%, −) or in association either with exogenous BDNF (+), or with K252a (+), during 24–72 h of serum deprivation. Histograms, mean ratio of apoptotic cells ± SEM of at least three independent experiments. *, p <0.05; **, p <0.01; ***, p <0.001, when compared with serum-free condition alone. (D, E) apoptotic ratio after 24 h serum deprivation alone (0% FCS) or with combination with a neutralizing anti-BDNF mAb (0% anti-BDNF). Histograms, mean ratio of apoptotic cells ± SEM of three independent experiments. *, p <0.05; **, p <0.01; ***, p <0.001, when compared with serum-free condition alone.
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    <t>BDNF</t> Signaling. (A) Prefrontal cortex <t>total</t> <t>TrkB,</t> pTrkB (AU) and pTrkB/total TrkB ratio. (B) Hippocampus total TrkB, pTrkB (AU) and pTrkB/total TrkB ratio. (C) Prefrontal cortex total CREB, pCREB (AU) and pCREB/total CREB ratio. (D) Hippocampus total CREB, pCREB (AU) and pCREB/total CREB ratio. All graphs are accompanied by representative blots. All data analyzed using a two-way ANOVA, TrkB, tropomyosin receptor kinase B; CREB, cAMP response element-binding protein; AU, arbitrary units; SED, sedentary; VWR, voluntary wheel running; OVX, ovariectomized; SHAM, sham operated. Significance is set to *P ≤ 0.05; **P ≤ 0.005; P ≤ 0.05; n=10 per group.
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    <t>BDNF</t> Signaling. (A) Prefrontal cortex <t>total</t> <t>TrkB,</t> pTrkB (AU) and pTrkB/total TrkB ratio. (B) Hippocampus total TrkB, pTrkB (AU) and pTrkB/total TrkB ratio. (C) Prefrontal cortex total CREB, pCREB (AU) and pCREB/total CREB ratio. (D) Hippocampus total CREB, pCREB (AU) and pCREB/total CREB ratio. All graphs are accompanied by representative blots. All data analyzed using a two-way ANOVA, TrkB, tropomyosin receptor kinase B; CREB, cAMP response element-binding protein; AU, arbitrary units; SED, sedentary; VWR, voluntary wheel running; OVX, ovariectomized; SHAM, sham operated. Significance is set to *P ≤ 0.05; **P ≤ 0.005; P ≤ 0.05; n=10 per group.
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    <t>BDNF</t> Signaling. (A) Prefrontal cortex <t>total</t> <t>TrkB,</t> pTrkB (AU) and pTrkB/total TrkB ratio. (B) Hippocampus total TrkB, pTrkB (AU) and pTrkB/total TrkB ratio. (C) Prefrontal cortex total CREB, pCREB (AU) and pCREB/total CREB ratio. (D) Hippocampus total CREB, pCREB (AU) and pCREB/total CREB ratio. All graphs are accompanied by representative blots. All data analyzed using a two-way ANOVA, TrkB, tropomyosin receptor kinase B; CREB, cAMP response element-binding protein; AU, arbitrary units; SED, sedentary; VWR, voluntary wheel running; OVX, ovariectomized; SHAM, sham operated. Significance is set to *P ≤ 0.05; **P ≤ 0.005; P ≤ 0.05; n=10 per group.
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    Image Search Results


    Journal: iScience

    Article Title: Induced neural stem cells suppressed neuroinflammation by inhibiting the microglial pyroptotic pathway in intracerebral hemorrhage rats

    doi: 10.1016/j.isci.2023.107022

    Figure Lengend Snippet:

    Article Snippet: Rabbit monoclonal anti-BDNF/pro-BDNF , abcam , Cat#: ab108319; RRID: AB_10862052.

    Techniques: Recombinant, Bicinchoninic Acid Protein Assay, Staining, Enzyme-linked Immunosorbent Assay, Software, Microscopy

    (A) Role of endogenous BDNF and its receptor TrkB on CRC cell proliferation: effects of exogenous BDNF and suppressing endogenous TrkB receptor on cell proliferation. The four cell lines were cultured for 24 h in FCS-free medium (FCS 10%, −) in the presence of exogenous BDNF (+), K252a (+) alone or in combination. Cell proliferation was determined by flow cytometry analysis using EdU Alexa Fluor 488. The data are presented as histograms of proliferating cells in relative units ± SEM of five independent experiments. *, p <0.05; **, p <0.01; ***, p <0.001, when compared with serum-free medium. (B, C) Effects of exogenous BDNF and suppressing endogenous TrkB receptor on cell survival. Apoptotic ratios of soluble nucleosomes were detected by ELISA Cell for WiDr, SW480, SW620, and COLO 205 induced by serum deprivation alone (FCS 10%, −) or in association either with exogenous BDNF (+), or with K252a (+), during 24–72 h of serum deprivation. Histograms, mean ratio of apoptotic cells ± SEM of at least three independent experiments. *, p <0.05; **, p <0.01; ***, p <0.001, when compared with serum-free condition alone. (D, E) apoptotic ratio after 24 h serum deprivation alone (0% FCS) or with combination with a neutralizing anti-BDNF mAb (0% anti-BDNF). Histograms, mean ratio of apoptotic cells ± SEM of three independent experiments. *, p <0.05; **, p <0.01; ***, p <0.001, when compared with serum-free condition alone.

    Journal: PLoS ONE

    Article Title: Fine-Tuning Roles of Endogenous Brain-Derived Neurotrophic Factor, TrkB and Sortilin in Colorectal Cancer Cell Survival

    doi: 10.1371/journal.pone.0025097

    Figure Lengend Snippet: (A) Role of endogenous BDNF and its receptor TrkB on CRC cell proliferation: effects of exogenous BDNF and suppressing endogenous TrkB receptor on cell proliferation. The four cell lines were cultured for 24 h in FCS-free medium (FCS 10%, −) in the presence of exogenous BDNF (+), K252a (+) alone or in combination. Cell proliferation was determined by flow cytometry analysis using EdU Alexa Fluor 488. The data are presented as histograms of proliferating cells in relative units ± SEM of five independent experiments. *, p <0.05; **, p <0.01; ***, p <0.001, when compared with serum-free medium. (B, C) Effects of exogenous BDNF and suppressing endogenous TrkB receptor on cell survival. Apoptotic ratios of soluble nucleosomes were detected by ELISA Cell for WiDr, SW480, SW620, and COLO 205 induced by serum deprivation alone (FCS 10%, −) or in association either with exogenous BDNF (+), or with K252a (+), during 24–72 h of serum deprivation. Histograms, mean ratio of apoptotic cells ± SEM of at least three independent experiments. *, p <0.05; **, p <0.01; ***, p <0.001, when compared with serum-free condition alone. (D, E) apoptotic ratio after 24 h serum deprivation alone (0% FCS) or with combination with a neutralizing anti-BDNF mAb (0% anti-BDNF). Histograms, mean ratio of apoptotic cells ± SEM of three independent experiments. *, p <0.05; **, p <0.01; ***, p <0.001, when compared with serum-free condition alone.

    Article Snippet: Recombinant human BDNF (100 ng/ml), recombinant pro-BDNF (4 ng/ml), and K252a (200 nM) were purchased from Alomone labs.

    Techniques: Cell Culture, Flow Cytometry, Enzyme-linked Immunosorbent Assay

    (A, B) Sortilin as a coreceptor of p75 NTR . Double staining (yellow) of sortilin (red) and p75 NTR (green) in SW480 cells (A) and SW620 (B) after 24 h of serum deprivation. (C) Colocalization of pro-BDNF and sortilin. Confocal microscopy study of a WiDr cells stained with an anti-pro-BDNF Ab (green) and an anti-sortilin Ab (red), and double staining (yellow) after 24 h of serum deprivation. (D, E) apoptotic ratios after 24 h serum deprivation alone (0% FCS) or combined with recombinant Pro-BDNF (0% Pro-BDNF). Histograms, mean ratio of apoptotic cells ± SEM of three independent experiments. *, p <0.05; **, p <0.01; ***, p <0.001, when compared with serum-free condition alone (0% FCS).

    Journal: PLoS ONE

    Article Title: Fine-Tuning Roles of Endogenous Brain-Derived Neurotrophic Factor, TrkB and Sortilin in Colorectal Cancer Cell Survival

    doi: 10.1371/journal.pone.0025097

    Figure Lengend Snippet: (A, B) Sortilin as a coreceptor of p75 NTR . Double staining (yellow) of sortilin (red) and p75 NTR (green) in SW480 cells (A) and SW620 (B) after 24 h of serum deprivation. (C) Colocalization of pro-BDNF and sortilin. Confocal microscopy study of a WiDr cells stained with an anti-pro-BDNF Ab (green) and an anti-sortilin Ab (red), and double staining (yellow) after 24 h of serum deprivation. (D, E) apoptotic ratios after 24 h serum deprivation alone (0% FCS) or combined with recombinant Pro-BDNF (0% Pro-BDNF). Histograms, mean ratio of apoptotic cells ± SEM of three independent experiments. *, p <0.05; **, p <0.01; ***, p <0.001, when compared with serum-free condition alone (0% FCS).

    Article Snippet: Recombinant human BDNF (100 ng/ml), recombinant pro-BDNF (4 ng/ml), and K252a (200 nM) were purchased from Alomone labs.

    Techniques: Double Staining, Confocal Microscopy, Staining, Recombinant

    BDNF Signaling. (A) Prefrontal cortex total TrkB, pTrkB (AU) and pTrkB/total TrkB ratio. (B) Hippocampus total TrkB, pTrkB (AU) and pTrkB/total TrkB ratio. (C) Prefrontal cortex total CREB, pCREB (AU) and pCREB/total CREB ratio. (D) Hippocampus total CREB, pCREB (AU) and pCREB/total CREB ratio. All graphs are accompanied by representative blots. All data analyzed using a two-way ANOVA, TrkB, tropomyosin receptor kinase B; CREB, cAMP response element-binding protein; AU, arbitrary units; SED, sedentary; VWR, voluntary wheel running; OVX, ovariectomized; SHAM, sham operated. Significance is set to *P ≤ 0.05; **P ≤ 0.005; P ≤ 0.05; n=10 per group.

    Journal: Frontiers in Endocrinology

    Article Title: Voluntary wheel running alters markers of amyloid-beta precursor protein processing in an ovarian hormone depleted model

    doi: 10.3389/fendo.2022.1069404

    Figure Lengend Snippet: BDNF Signaling. (A) Prefrontal cortex total TrkB, pTrkB (AU) and pTrkB/total TrkB ratio. (B) Hippocampus total TrkB, pTrkB (AU) and pTrkB/total TrkB ratio. (C) Prefrontal cortex total CREB, pCREB (AU) and pCREB/total CREB ratio. (D) Hippocampus total CREB, pCREB (AU) and pCREB/total CREB ratio. All graphs are accompanied by representative blots. All data analyzed using a two-way ANOVA, TrkB, tropomyosin receptor kinase B; CREB, cAMP response element-binding protein; AU, arbitrary units; SED, sedentary; VWR, voluntary wheel running; OVX, ovariectomized; SHAM, sham operated. Significance is set to *P ≤ 0.05; **P ≤ 0.005; P ≤ 0.05; n=10 per group.

    Article Snippet: Western blotting was used to determine protein marker content of the amyloidogenic proteins BACE1 (Cat. No. 5606S, Cell Signaling), ADAM10 (Cat. No. ab1997, abcam), ABPP (Cat. No. 825001, BioLegend), sABPPα (Cat. No. 11088, IBL) and sABPPB (Cat. No. 813401, BioLegend) as well as markers of BDNF signaling such as pro/mature BDNF (Cat. No. ab108319, abcam), TrkB (Cat. No. 80E3, Cell Signalling), pTrkB (Cat. No. ab109684, abcam), CREB (Cat. No. 48H2, Cell Signaling), Erα (Cat. No. sc-528195, Santa Cruz Biotechnology), ErB (Cat. No. sc-530103, Santa Cruz Biotechnology) and pCREB (Cat. No. S133, Cell Signaling).

    Techniques: Binding Assay