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ebss  (Worthington Biochemical)


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    Structured Review

    Worthington Biochemical ebss
    Ebss, supplied by Worthington Biochemical, used in various techniques. Bioz Stars score: 99/100, based on 29 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/ebss/PDS+Kit%2C+EBSS+Vial/pmc13134484-1357-0-2
    Average 99 stars, based on 29 article reviews
    ebss - by Bioz Stars, 2026-10
    99/100 stars

    Images

    Related Articles

    other:

    Article Title: A spatial code governs olfactory receptor choice and aligns sensory maps in the nose and brain
    Article Snippet: EBSS , Worthington , Cat# LK003188.

    Article Title: A transcriptional rheostat couples past activity to future sensory responses
    Article Snippet: EBSS , Worthington , Cat# {"type":"entrez-nucleotide","attrs":{"text":"LK003188","term_id":"635211105","term_text":"LK003188"}} LK003188.

    Protease Inhibitor:

    Article Title: ASXL3 controls cortical neuron fate specification through extrinsic self-renewal pathways
    Article Snippet: .. Cells were resuspended with ovomucoid protease inhibitor (Worthington Biochemical Corporation) and 50 mg/ml DNase I in O 2 :CO 2 equilibrated EBSS and passed through a 70 micron cell strainer. ..

    Transferring:

    Article Title: C9orf72 in myeloid cells prevents an inflammatory response to microbial glycogen.
    Article Snippet: Spleen samples were then subjected to RBC lysis buffer (eBioscience 00-4300-54) for 10 minutes. .. Spinal cords were transferred into papain and DNase diluted in EBSS (Worthington LK003150) and manually broken apart using a pipette. .. Spinal cord cells were then strained through a 40uM filter, centrifuged at 300xG, and then resuspended in isotonic Percoll Plus (Cytiva 17544501) diluted to 30% using autoMACS running buffer and centrifuged for 15 minutes with no brake applied.



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    Image Search Results


    RyR3 deficiency induces autophagy defects A. Quantification of control and patients primary myoblasts cell death under basal culture conditions and 4h starvation (EBSS). *p < 0.05, ***p < 0.001, ****p < 0.0001, ns , non-significant from 2-way ANOVA and Sidak’s post hoc test. B-C. Representative images ( B ) and quantification ( C ) of LC3 positive vesicles in control and patients’ primary myoblasts cultured in basal or 2h starvation conditions. ****p < 0.0001, ns , non-significan from two-way ANOVA followed by Sidak’s post hoc test. D-E. Representative western blotting ( D ) and quantification ( E ) of LC3-II in control and RYR3 patients’ primary myoblasts starved (EBSS) or incubated with the autophagosome-lysosome fusion inhibitor bafilomycin A1 (Baf) for indicated time points. Data are represented as mean + SD, *p < 0.05, **p < 0.01, ****p < 0.0001 from two-way ANOVA and Bonferonni post-hoc test. F-G. Representative western blotting ( F ) and quantification ( G ) of LC3-II in control and RYR1 patients primary myoblasts starved (EBSS) or incubated with bafilomycin A1 (Baf) for indicated time points. Data are represented as mean + SD *p < 0.05, **p < 0.01, ****p < 0.0001 from two-way ANOVA and Bonferonni post-hoc test. H-I. Confocal imaging of skeletal muscle ( H ) and autophagy index quantification of the normalized RFP to GFP signal ( I ) of larvae co-injected with the autophagic GFP-LC3-RFP-LC3ΔG probe and control-MO or ryr3-MO. *p < 0.05 from Student’s t-test.

    Journal: medRxiv

    Article Title: Novel variants in ryanodine receptor type 3 predispose to acute rhabdomyolysis due to impaired autophagy

    doi: 10.64898/2026.02.27.26345848

    Figure Lengend Snippet: RyR3 deficiency induces autophagy defects A. Quantification of control and patients primary myoblasts cell death under basal culture conditions and 4h starvation (EBSS). *p < 0.05, ***p < 0.001, ****p < 0.0001, ns , non-significant from 2-way ANOVA and Sidak’s post hoc test. B-C. Representative images ( B ) and quantification ( C ) of LC3 positive vesicles in control and patients’ primary myoblasts cultured in basal or 2h starvation conditions. ****p < 0.0001, ns , non-significan from two-way ANOVA followed by Sidak’s post hoc test. D-E. Representative western blotting ( D ) and quantification ( E ) of LC3-II in control and RYR3 patients’ primary myoblasts starved (EBSS) or incubated with the autophagosome-lysosome fusion inhibitor bafilomycin A1 (Baf) for indicated time points. Data are represented as mean + SD, *p < 0.05, **p < 0.01, ****p < 0.0001 from two-way ANOVA and Bonferonni post-hoc test. F-G. Representative western blotting ( F ) and quantification ( G ) of LC3-II in control and RYR1 patients primary myoblasts starved (EBSS) or incubated with bafilomycin A1 (Baf) for indicated time points. Data are represented as mean + SD *p < 0.05, **p < 0.01, ****p < 0.0001 from two-way ANOVA and Bonferonni post-hoc test. H-I. Confocal imaging of skeletal muscle ( H ) and autophagy index quantification of the normalized RFP to GFP signal ( I ) of larvae co-injected with the autophagic GFP-LC3-RFP-LC3ΔG probe and control-MO or ryr3-MO. *p < 0.05 from Student’s t-test.

    Article Snippet: To mimic environmental stress, the GM was replaced with EBSS medium with or without 100 nM bafilomycin A1 (ref: tlrl-bafA1, InvivoGen) for 1h and 3h.

    Techniques: Control, Cell Culture, Western Blot, Incubation, Imaging, Injection

    A. Representative immunoblot of LC3 lipidation upon starvation (EBSS: Earle’s Balanced Salt Solution) and Bafilomycin A1 treatment (Baf) in primary myoblasts from RYR3 P1 and RYR3 P2 patients. Due to limited proliferative capacity of primary cells, the experiment could only be repeated twice. GM: Growth Medium. β-actin was used as a loading control. n.r. (non relevant) indicates lanes that were included on the blot but are not relevant for the present study. B. Representative immunoblot of LC3 lipidation upon starvation in siRNA-mediated RYR3 depleted primary myoblasts. β-actin was used as a loading control.

    Journal: medRxiv

    Article Title: Novel variants in ryanodine receptor type 3 predispose to acute rhabdomyolysis due to impaired autophagy

    doi: 10.64898/2026.02.27.26345848

    Figure Lengend Snippet: A. Representative immunoblot of LC3 lipidation upon starvation (EBSS: Earle’s Balanced Salt Solution) and Bafilomycin A1 treatment (Baf) in primary myoblasts from RYR3 P1 and RYR3 P2 patients. Due to limited proliferative capacity of primary cells, the experiment could only be repeated twice. GM: Growth Medium. β-actin was used as a loading control. n.r. (non relevant) indicates lanes that were included on the blot but are not relevant for the present study. B. Representative immunoblot of LC3 lipidation upon starvation in siRNA-mediated RYR3 depleted primary myoblasts. β-actin was used as a loading control.

    Article Snippet: To mimic environmental stress, the GM was replaced with EBSS medium with or without 100 nM bafilomycin A1 (ref: tlrl-bafA1, InvivoGen) for 1h and 3h.

    Techniques: Western Blot, Control