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Sangon Biotech l plantarum
L Plantarum, supplied by Sangon Biotech, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/l+plantarum/l+plantarum/pm42029031-264-3-8
Average 86 stars, based on 1 article reviews
l plantarum - by Bioz Stars, 2026-09
86/100 stars

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Clone Assay:

Article Title: Oral administration of Lactiplantibacillus plantarum displaying multiple ASFV antigen proteins on the surface induces systemic immune responses in mice.
Article Snippet: .. Codon optimization for L. plantarum was performed by Sangon Biotech (China), and the optimized sequences were subsequently cloned into the pSIP409-pgsA’ vector, generating five recombinant plasmids, each designed to express a specific ASFV antigen. ..

Plasmid Preparation:

Article Title: Oral administration of Lactiplantibacillus plantarum displaying multiple ASFV antigen proteins on the surface induces systemic immune responses in mice.
Article Snippet: .. Codon optimization for L. plantarum was performed by Sangon Biotech (China), and the optimized sequences were subsequently cloned into the pSIP409-pgsA’ vector, generating five recombinant plasmids, each designed to express a specific ASFV antigen. ..

Recombinant:

Article Title: Oral administration of Lactiplantibacillus plantarum displaying multiple ASFV antigen proteins on the surface induces systemic immune responses in mice.
Article Snippet: .. Codon optimization for L. plantarum was performed by Sangon Biotech (China), and the optimized sequences were subsequently cloned into the pSIP409-pgsA’ vector, generating five recombinant plasmids, each designed to express a specific ASFV antigen. ..



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Strain‐specific immune activation and enhanced activity of the combined formulation in RAW 264.7 macrophages. (A) Heat‐killed L. plantarum <t>IDCC</t> <t>3501</t> and L. salivarius IDCC 3551 significantly increased NO production compared with the commercial strain L. rhamnosus GG. (B, C) IDCC 3501 and IDCC 3551 exhibited the highest NO‐inducing activity among their respective species, indicating strain‐specific immune potency. (D, E) The combined formulation (IBP35) further enhanced NO production across all tested concentrations, indicating enhanced activity relative to the individual strains under the tested conditions. Data are presented as the mean ± SD (three independent experiments). Statistical analysis was performed using one‐way ANOVA with Dunnett's post hoc test. Statistical significance was set at p < 0.05. # p < 0.05, ## p < 0.01, ### p < 0.001.
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Strain‐specific immune activation and enhanced activity of the combined formulation in RAW 264.7 macrophages. (A) Heat‐killed L. plantarum <t>IDCC</t> <t>3501</t> and L. salivarius IDCC 3551 significantly increased NO production compared with the commercial strain L. rhamnosus GG. (B, C) IDCC 3501 and IDCC 3551 exhibited the highest NO‐inducing activity among their respective species, indicating strain‐specific immune potency. (D, E) The combined formulation (IBP35) further enhanced NO production across all tested concentrations, indicating enhanced activity relative to the individual strains under the tested conditions. Data are presented as the mean ± SD (three independent experiments). Statistical analysis was performed using one‐way ANOVA with Dunnett's post hoc test. Statistical significance was set at p < 0.05. # p < 0.05, ## p < 0.01, ### p < 0.001.
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Strain‐specific immune activation and enhanced activity of the combined formulation in RAW 264.7 macrophages. (A) Heat‐killed L. plantarum <t>IDCC</t> <t>3501</t> and L. salivarius IDCC 3551 significantly increased NO production compared with the commercial strain L. rhamnosus GG. (B, C) IDCC 3501 and IDCC 3551 exhibited the highest NO‐inducing activity among their respective species, indicating strain‐specific immune potency. (D, E) The combined formulation (IBP35) further enhanced NO production across all tested concentrations, indicating enhanced activity relative to the individual strains under the tested conditions. Data are presented as the mean ± SD (three independent experiments). Statistical analysis was performed using one‐way ANOVA with Dunnett's post hoc test. Statistical significance was set at p < 0.05. # p < 0.05, ## p < 0.01, ### p < 0.001.
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Strain‐specific immune activation and enhanced activity of the combined formulation in RAW 264.7 macrophages. (A) Heat‐killed L. plantarum IDCC 3501 and L. salivarius IDCC 3551 significantly increased NO production compared with the commercial strain L. rhamnosus GG. (B, C) IDCC 3501 and IDCC 3551 exhibited the highest NO‐inducing activity among their respective species, indicating strain‐specific immune potency. (D, E) The combined formulation (IBP35) further enhanced NO production across all tested concentrations, indicating enhanced activity relative to the individual strains under the tested conditions. Data are presented as the mean ± SD (three independent experiments). Statistical analysis was performed using one‐way ANOVA with Dunnett's post hoc test. Statistical significance was set at p < 0.05. # p < 0.05, ## p < 0.01, ### p < 0.001.

Journal: Food Science & Nutrition

Article Title: Immune‐Enhancing Effects of IBP35 , a Combination of Lactiplantibacillus plantarum and Ligilactobacillus salivarius , in Macrophages and Cyclophosphamide‐Induced Immunosuppressed Mice

doi: 10.1002/fsn3.71831

Figure Lengend Snippet: Strain‐specific immune activation and enhanced activity of the combined formulation in RAW 264.7 macrophages. (A) Heat‐killed L. plantarum IDCC 3501 and L. salivarius IDCC 3551 significantly increased NO production compared with the commercial strain L. rhamnosus GG. (B, C) IDCC 3501 and IDCC 3551 exhibited the highest NO‐inducing activity among their respective species, indicating strain‐specific immune potency. (D, E) The combined formulation (IBP35) further enhanced NO production across all tested concentrations, indicating enhanced activity relative to the individual strains under the tested conditions. Data are presented as the mean ± SD (three independent experiments). Statistical analysis was performed using one‐way ANOVA with Dunnett's post hoc test. Statistical significance was set at p < 0.05. # p < 0.05, ## p < 0.01, ### p < 0.001.

Article Snippet: L. plantarum IDCC 3501 and L. salivarius IDCC 3551 were obtained from the culture collection of Ildong Bioscience Co. Ltd. (Republic of Korea).

Techniques: Activation Assay, Activity Assay, Formulation