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human recombinant gdnf  (Miltenyi Biotec)


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    Structured Review

    Miltenyi Biotec human recombinant gdnf
    Human Recombinant Gdnf, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 93/100, based on 9 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/gdnf/Human+GDNF%2C+premium+grade/pm42410656-98-61-64
    Average 93 stars, based on 9 article reviews
    human recombinant gdnf - by Bioz Stars, 2026-10
    93/100 stars

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    Related Articles

    other:

    Article Title: Generation of human appetite-regulating neurons and tanycytes from stem cells
    Article Snippet: All differentiations received 10 μM SB413542 (Miltenyi, #130-106-543), and 100 ng/mL Noggin (Miltenyi, #130-103-456) in N2 basal medium from day 0 to 9, 0.2 mM ascorbic acid (Sigma-Merck, #A4403-100MG) and 20 μg/mL BDNF (Miltenyi, #130-096-286) from d11 and 500 μM dibutyryl-cAMP (Sigma-Merck, #D0627-1G), 1 μM DAPT (Miltenyi, #130-110-489), 10 ng/mL GDNF (Miltenyi, #130-098-449) from d16 onwards.

    Article Title: Inkjet-Printed 3D Sensor Arrays with FIB-Induced Electrode Refinement for Low-Noise Amperometric Recordings in hiPSC-Derived Brain Organoids.
    Article Snippet: StemMACS iPS-Brew XF (human), dorsomorphin, SHH, SB 431542, BDNF, and GDNF were purchased from Miltenyi Biotec (Germany).

    Article Title: Inkjet-Printed 3D Sensor Arrays with FIB-Induced Electrode Refinement for Low-Noise Amperometric Recordings in hiPSC-Derived Brain Organoids
    Article Snippet: StemMACS iPS-Brew XF (human), dorsomorphin, SHH, SB 431542, BDNF, and GDNF were purchased from Miltenyi Biotec (Germany).

    Article Title: TDP43 aggregation at ER-exit sites impairs ER-to-Golgi transport
    Article Snippet: Then MN maturation media, i.e. NM + 10 ng/mL GDNF (Miltenyi Biotec 130-129-547) + 10 ng/mL BDNF (Miltenyi Biotec 130-093-811) + 200 μM L-ascorbic acid (Sigma A5960), was added and changed every other day until MNs were ready on D28.

    Article Title: REST and RCOR genes display distinct expression profiles in neurons and astrocytes using 2D and 3D human pluripotent stem cell models
    Article Snippet: Spheroids where then transferred to 24 well plates to accommodate the larger media volume needs, maintained in normoxic conditions (20 % O 2 , 5 % CO 2 , 37 °C), and matured through the addition of 5 ng/mL BDNF (Miltenyi Biotec, #130-096-286) and 10 ng/mL GDNF (Miltenyi Biotec, #130-098-449) from day 26, and 10 ng/mL NRG1 (Peprotech, #AF-100-03) and 20 ng/mL NT-3 (Miltenyi Biotec, #130-093-973) from day 34, after which partial media changes were performed every 3–4 days until the end of the 9 months (∼270 days).

    Cell Culture:

    Article Title: Unveiling sequence-agnostic mixed-chemical modification patterns for splice-switching oligonucleotides using the NATURA platform.
    Article Snippet: Received 13 June 2024; accepted 10 December 2024; https://doi.org/10.1016/j.omtn.2024.102422.. These authors contributed equally Correspondence: Tommaso Tabaglio, Institute of Molecular and Cell Biology (IMCB), Agency for Science, Technology and Research (A*STAR), Singapore, Singapore.. E-mail: ttabaglio@imcb.a-star.edu.sg Correspondence: Guccione Ernesto, Center for OncoGenomics and Innovative Therapeutics (COGIT), Center for Therapeutics Discovery, Department of Oncological Sciences and Pharmacological Sciences, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

    Article Title: Unveiling sequence-agnostic mixed-chemical modification patterns for splice-switching oligonucleotides using the NATURA platform
    Article Snippet: Motor neuron progenitor cells were expanded from Day 10 onward in motor neuron progenitor expansion medium, which included basal medium supplemented with 1 μM RA and 1 μM purmorphamine (#130-104-465; Miltenyi Biotec). .. Beginning on day 17, the cells were cultured in motor neuron maturation medium, which contained basal medium supplemented with 10 ng/mL GDNF (#130-129-546; Miltenyi Biotec), 10 ng/mL BDNF (#130-103-435; Miltenyi Biotec), and 200 μM ascorbic acid (#A4544; Sigma). ..

    Magnetic Cell Separation:

    Article Title: Method and kit for characterizing dopaminergic progenitor cells obtained by differentiating pluripotent stem cells
    Article Snippet: From d2-d9 Purmorphamine (0.5 μM, Miltenyi Biotec 130-104-465) was added to the medium. .. On day 11 of differentiation, the cells were dissociated into single cells with TrypLE and replated on dry PO/LN/FN coated plates in droplets of 10,000 cells/μl in MACS Neuro medium, NeuroBrew-21 w/o vitamin A (1:50), BDNF (20 ng/ml; Miltenyi Biotec 130-096-285), GDNF (10 ng/ml; Miltenyi Biotec 130-096-290) and ascorbic acid (200 μM; Sigma A5960). ..



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    Image Search Results


    YFP+ axon regeneration through nerve repair constructs. (A) Representative fluorescence images of YFP+ axons regenerating through either nerve grafts or PCL or PCL + GDNF conduits ( n = 6 per group). (B) Box and whisker plots show median, interquartile range (box), and the minimum and maximum values (whiskers) of total axon counts. (C) Axon counts were normalised to the proximal stump and expressed as a percentage (mean ± SD). Data were analysed with two-way ANOVA with Tukey's post hoc test p < 0.05 (*), p < 0.01 (**) (Scale bars = 200 µm).

    Journal: RSC Advances

    Article Title: Evaluation of a GDNF-eluting nanofibrous PCL conduit in a mouse model of peripheral nerve injury

    doi: 10.1039/d6ra03291e

    Figure Lengend Snippet: YFP+ axon regeneration through nerve repair constructs. (A) Representative fluorescence images of YFP+ axons regenerating through either nerve grafts or PCL or PCL + GDNF conduits ( n = 6 per group). (B) Box and whisker plots show median, interquartile range (box), and the minimum and maximum values (whiskers) of total axon counts. (C) Axon counts were normalised to the proximal stump and expressed as a percentage (mean ± SD). Data were analysed with two-way ANOVA with Tukey's post hoc test p < 0.05 (*), p < 0.01 (**) (Scale bars = 200 µm).

    Article Snippet: The endings were trimmed to create a gap of 3 mm between the proximal and distal stumps, and either a PCL or PCL + GDNF conduit was sutured end-to-end to the stumps using four 9–0 monofilament polyamide sutures (Ethilon®; Ethicon Ltd, England).

    Techniques: Construct, Fluorescence, Whisker Assay

    β-III tubulin+ axon regeneration through nerve repair constructs. (A) Representative fluorescence images of TUBB3+ axons regenerating through either nerve grafts or PCL or PCL + GDNF conduits ( n = 6 per group). (B) Box and whisker plots show median, interquartile range (box), and the minimum and maximum values (whiskers) of total axon counts. (C) Axon counts were normalised to the proximal stump and expressed as a percentage (mean ± SD). Data were analysed with two-way ANOVA with Tukey's post hoc test. p < 0.01 (**) (Scale bars = 200 µm).

    Journal: RSC Advances

    Article Title: Evaluation of a GDNF-eluting nanofibrous PCL conduit in a mouse model of peripheral nerve injury

    doi: 10.1039/d6ra03291e

    Figure Lengend Snippet: β-III tubulin+ axon regeneration through nerve repair constructs. (A) Representative fluorescence images of TUBB3+ axons regenerating through either nerve grafts or PCL or PCL + GDNF conduits ( n = 6 per group). (B) Box and whisker plots show median, interquartile range (box), and the minimum and maximum values (whiskers) of total axon counts. (C) Axon counts were normalised to the proximal stump and expressed as a percentage (mean ± SD). Data were analysed with two-way ANOVA with Tukey's post hoc test. p < 0.01 (**) (Scale bars = 200 µm).

    Article Snippet: The endings were trimmed to create a gap of 3 mm between the proximal and distal stumps, and either a PCL or PCL + GDNF conduit was sutured end-to-end to the stumps using four 9–0 monofilament polyamide sutures (Ethilon®; Ethicon Ltd, England).

    Techniques: Construct, Fluorescence, Whisker Assay

    Schwann cell presence within nerve repair constructs. (A) Representative fluorescence images of S100B+ Schwann cells within nerve grafts or PCL or PCL + GDNF conduits. Cells migrated into fibrin hydrogel-filled spaces between nanofibrous mat folds. (B) S100B+ fluorescent area (µm 2 ) for Schwann cell quantification. (C) Fluorescent area was normalised to the entire measured area and expressed as a percentage (mean ± SD). Data were analysed by two-way ANOVA with Tukey's multiple comparisons test. Asterisks indicate significant differences between groups within the same segment ( p < 0.05 (*)), and all such comparisons are shown. Hash symbols ( p < 0.05 (#)) indicate significant differences between segments within the same group, and all such comparisons are shown, except that comparisons involving proximal segments are omitted. (Scale bars = 200 µm).

    Journal: RSC Advances

    Article Title: Evaluation of a GDNF-eluting nanofibrous PCL conduit in a mouse model of peripheral nerve injury

    doi: 10.1039/d6ra03291e

    Figure Lengend Snippet: Schwann cell presence within nerve repair constructs. (A) Representative fluorescence images of S100B+ Schwann cells within nerve grafts or PCL or PCL + GDNF conduits. Cells migrated into fibrin hydrogel-filled spaces between nanofibrous mat folds. (B) S100B+ fluorescent area (µm 2 ) for Schwann cell quantification. (C) Fluorescent area was normalised to the entire measured area and expressed as a percentage (mean ± SD). Data were analysed by two-way ANOVA with Tukey's multiple comparisons test. Asterisks indicate significant differences between groups within the same segment ( p < 0.05 (*)), and all such comparisons are shown. Hash symbols ( p < 0.05 (#)) indicate significant differences between segments within the same group, and all such comparisons are shown, except that comparisons involving proximal segments are omitted. (Scale bars = 200 µm).

    Article Snippet: The endings were trimmed to create a gap of 3 mm between the proximal and distal stumps, and either a PCL or PCL + GDNF conduit was sutured end-to-end to the stumps using four 9–0 monofilament polyamide sutures (Ethilon®; Ethicon Ltd, England).

    Techniques: Construct, Fluorescence