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vaginal lactobacilli l crispatus atcc  (ATCC)


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    ATCC vaginal lactobacilli l crispatus atcc
    Vaginal Lactobacilli L Crispatus Atcc, supplied by ATCC, used in various techniques. Bioz Stars score: 95/100, based on 140 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/vaginal+lactobacilli/Lactobacillus+crispatus+(Brygoo+and+Aladame)+Moore+and+Holdeman/pm39696572-216-6-10
    Average 95 stars, based on 140 article reviews
    vaginal lactobacilli l crispatus atcc - by Bioz Stars, 2026-09
    95/100 stars

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    Proximity Ligation Assay:

    Article Title: Electrospinning technologies for the delivery of Biopharmaceuticals: Current status and future trends.
    Article Snippet: .. - 30 - IGF-1 (Mw: 7.65kDa) HAMA/P CL Dural substitutes [238] IGF-2 (Mw: 7.5kDa) Chitosan/ PCL Wound healing [239] VEGF-A (Mw: 45kDa) PCL Neuroprotective Effects [240] TGF-β (Mw: 25kDa) PCL/PLA Tissue engineering (cardiac repair) [241] IGF-1,VEGF (Mw: 45kDa) Silk Fibroin Bone defect repair and angiogenesis [242] TGFβ3 (Mw: 25.5kDa) PCL Tissue engineering (cartilage) [243] VEGF PCL/Gela tin Tissue engineering (Patellar Ligament Regeneration) [244] SDF-1α (Mw: 8.0kDa) PLGA Trap the residual GBM cells in the brain [245] - 31 - SDF-1α/CXCL12 (Mw: 10kDa) PLA Neural Regeneration Therapy [246] TGF-β3 and SDF-1α Hyaluroni c acid Tissue engineering (articular cartilage repair) [247] Thyroid hormone triiodothyronine (Mw: 0,65kDa) (with ibuprofen) PLGA/PL LA Treatment of Acute Injuries of the Central Nervous System [248] Melatonin (Mw: 0.23kDa) PCL Tissue engineering (tendon) [249] Melatonin Chitosan/ PCL/PVA Wound healing [250] Insulin (Mw: 5.81kDa) PCL/PEO Wound healing [251] F(ab) (Mw: 50kDa) PVP Inflammatory oral mucosal disease [252] Bevacizumab (Mw: 149kDa) PCL Age-related macular degeneration [253] - 32 - Bevacizumab PCL/Gela tin Age-related macular degeneration [254] Infliximab (Mw: 144 kDa) HP-β-CD Treatment of Crohn’s disease [171] plasmid DNA (Mw: around 2000kDa) GelatinCollagenPEG Gene therapy [255] plasmid DNA Gelatin Gene therapy [256] miR‐132/miR‐222/miR‐431 (Mw: 7.14-8.5kDa) Collagen Promote Axon Regeneration [257] miR‐132/miR‐31 (Mw: 7.14-8.5kDa) PVA Wound healing [258] Nucleic acids miR‐181a/b‐1 (Mw: 7.14-8.5kDa) PEG/PLG A Tissue engineering (osteogenesis of human mesenchymal stem cells) [259] - 33 - Antisense oligonucleotide HP-β-CD Gene suppression [260 ] Escherichia coli strain Nissle 1917 PVA/CA Probiotics delivery (gut) [261] Vaginal lactobacilli (Lactobacillus crispatus ATCC 33820, Lactobacillus gasseri ATCC 33323, and Lactobacillus jensenii ATCC 25258) PEO Probiotics delivery (Vaginal) [262] L. rhamnosus CRL1332 PVA Probiotics delivery (Vaginal) [263] E. coli. ..

    Plasmid Preparation:

    Article Title: Electrospinning technologies for the delivery of Biopharmaceuticals: Current status and future trends.
    Article Snippet: .. - 30 - IGF-1 (Mw: 7.65kDa) HAMA/P CL Dural substitutes [238] IGF-2 (Mw: 7.5kDa) Chitosan/ PCL Wound healing [239] VEGF-A (Mw: 45kDa) PCL Neuroprotective Effects [240] TGF-β (Mw: 25kDa) PCL/PLA Tissue engineering (cardiac repair) [241] IGF-1,VEGF (Mw: 45kDa) Silk Fibroin Bone defect repair and angiogenesis [242] TGFβ3 (Mw: 25.5kDa) PCL Tissue engineering (cartilage) [243] VEGF PCL/Gela tin Tissue engineering (Patellar Ligament Regeneration) [244] SDF-1α (Mw: 8.0kDa) PLGA Trap the residual GBM cells in the brain [245] - 31 - SDF-1α/CXCL12 (Mw: 10kDa) PLA Neural Regeneration Therapy [246] TGF-β3 and SDF-1α Hyaluroni c acid Tissue engineering (articular cartilage repair) [247] Thyroid hormone triiodothyronine (Mw: 0,65kDa) (with ibuprofen) PLGA/PL LA Treatment of Acute Injuries of the Central Nervous System [248] Melatonin (Mw: 0.23kDa) PCL Tissue engineering (tendon) [249] Melatonin Chitosan/ PCL/PVA Wound healing [250] Insulin (Mw: 5.81kDa) PCL/PEO Wound healing [251] F(ab) (Mw: 50kDa) PVP Inflammatory oral mucosal disease [252] Bevacizumab (Mw: 149kDa) PCL Age-related macular degeneration [253] - 32 - Bevacizumab PCL/Gela tin Age-related macular degeneration [254] Infliximab (Mw: 144 kDa) HP-β-CD Treatment of Crohn’s disease [171] plasmid DNA (Mw: around 2000kDa) GelatinCollagenPEG Gene therapy [255] plasmid DNA Gelatin Gene therapy [256] miR‐132/miR‐222/miR‐431 (Mw: 7.14-8.5kDa) Collagen Promote Axon Regeneration [257] miR‐132/miR‐31 (Mw: 7.14-8.5kDa) PVA Wound healing [258] Nucleic acids miR‐181a/b‐1 (Mw: 7.14-8.5kDa) PEG/PLG A Tissue engineering (osteogenesis of human mesenchymal stem cells) [259] - 33 - Antisense oligonucleotide HP-β-CD Gene suppression [260 ] Escherichia coli strain Nissle 1917 PVA/CA Probiotics delivery (gut) [261] Vaginal lactobacilli (Lactobacillus crispatus ATCC 33820, Lactobacillus gasseri ATCC 33323, and Lactobacillus jensenii ATCC 25258) PEO Probiotics delivery (Vaginal) [262] L. rhamnosus CRL1332 PVA Probiotics delivery (Vaginal) [263] E. coli. ..

    Probiotics:

    Article Title: Electrospinning technologies for the delivery of Biopharmaceuticals: Current status and future trends.
    Article Snippet: .. - 30 - IGF-1 (Mw: 7.65kDa) HAMA/P CL Dural substitutes [238] IGF-2 (Mw: 7.5kDa) Chitosan/ PCL Wound healing [239] VEGF-A (Mw: 45kDa) PCL Neuroprotective Effects [240] TGF-β (Mw: 25kDa) PCL/PLA Tissue engineering (cardiac repair) [241] IGF-1,VEGF (Mw: 45kDa) Silk Fibroin Bone defect repair and angiogenesis [242] TGFβ3 (Mw: 25.5kDa) PCL Tissue engineering (cartilage) [243] VEGF PCL/Gela tin Tissue engineering (Patellar Ligament Regeneration) [244] SDF-1α (Mw: 8.0kDa) PLGA Trap the residual GBM cells in the brain [245] - 31 - SDF-1α/CXCL12 (Mw: 10kDa) PLA Neural Regeneration Therapy [246] TGF-β3 and SDF-1α Hyaluroni c acid Tissue engineering (articular cartilage repair) [247] Thyroid hormone triiodothyronine (Mw: 0,65kDa) (with ibuprofen) PLGA/PL LA Treatment of Acute Injuries of the Central Nervous System [248] Melatonin (Mw: 0.23kDa) PCL Tissue engineering (tendon) [249] Melatonin Chitosan/ PCL/PVA Wound healing [250] Insulin (Mw: 5.81kDa) PCL/PEO Wound healing [251] F(ab) (Mw: 50kDa) PVP Inflammatory oral mucosal disease [252] Bevacizumab (Mw: 149kDa) PCL Age-related macular degeneration [253] - 32 - Bevacizumab PCL/Gela tin Age-related macular degeneration [254] Infliximab (Mw: 144 kDa) HP-β-CD Treatment of Crohn’s disease [171] plasmid DNA (Mw: around 2000kDa) GelatinCollagenPEG Gene therapy [255] plasmid DNA Gelatin Gene therapy [256] miR‐132/miR‐222/miR‐431 (Mw: 7.14-8.5kDa) Collagen Promote Axon Regeneration [257] miR‐132/miR‐31 (Mw: 7.14-8.5kDa) PVA Wound healing [258] Nucleic acids miR‐181a/b‐1 (Mw: 7.14-8.5kDa) PEG/PLG A Tissue engineering (osteogenesis of human mesenchymal stem cells) [259] - 33 - Antisense oligonucleotide HP-β-CD Gene suppression [260 ] Escherichia coli strain Nissle 1917 PVA/CA Probiotics delivery (gut) [261] Vaginal lactobacilli (Lactobacillus crispatus ATCC 33820, Lactobacillus gasseri ATCC 33323, and Lactobacillus jensenii ATCC 25258) PEO Probiotics delivery (Vaginal) [262] L. rhamnosus CRL1332 PVA Probiotics delivery (Vaginal) [263] E. coli. ..



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    Image Search Results


    Concentration-dependent fluorescence of lactobacilli expressing different fluorescent proteins. Linear regression analyses of fluorescence and OD 600 of lactobacilli grown at 37 °C without and with shaking (aeration) are shown. Nontransformed (NT) bacteria were used as controls. FU—fluorescence unit.

    Journal: International Journal of Molecular Sciences

    Article Title: Engineering of Vaginal Lactobacilli to Express Fluorescent Proteins Enables the Analysis of Their Mixture in Nanofibers

    doi: 10.3390/ijms222413631

    Figure Lengend Snippet: Concentration-dependent fluorescence of lactobacilli expressing different fluorescent proteins. Linear regression analyses of fluorescence and OD 600 of lactobacilli grown at 37 °C without and with shaking (aeration) are shown. Nontransformed (NT) bacteria were used as controls. FU—fluorescence unit.

    Article Snippet: Here, we engineered three model vaginal lactobacilli ( Lactobacillus crispatus ATCC 33820, Lactobacillus gasseri ATCC 33323, and Lactobacillus jensenii ATCC 25258) and a control Lactobacillus plantarum ATCC 8014 to express fluorescent proteins with different spectral properties, including infrared fluorescent protein (IRFP), green fluorescent protein (GFP), red fluorescent protein (mCherry), and blue fluorescent protein (mTagBFP2).

    Techniques: Concentration Assay, Fluorescence, Expressing, Bacteria

    Representative confocal microscopy images of the lactobacilli expressing the different fluorescent proteins, as L. plantarum expressing IRFP, L. gasseri expressing mCherry, L. crispatus expressing GFP, and L. jensenii expressing mTagBFP2, in comparison to the nontransformed bacteria.

    Journal: International Journal of Molecular Sciences

    Article Title: Engineering of Vaginal Lactobacilli to Express Fluorescent Proteins Enables the Analysis of Their Mixture in Nanofibers

    doi: 10.3390/ijms222413631

    Figure Lengend Snippet: Representative confocal microscopy images of the lactobacilli expressing the different fluorescent proteins, as L. plantarum expressing IRFP, L. gasseri expressing mCherry, L. crispatus expressing GFP, and L. jensenii expressing mTagBFP2, in comparison to the nontransformed bacteria.

    Article Snippet: Here, we engineered three model vaginal lactobacilli ( Lactobacillus crispatus ATCC 33820, Lactobacillus gasseri ATCC 33323, and Lactobacillus jensenii ATCC 25258) and a control Lactobacillus plantarum ATCC 8014 to express fluorescent proteins with different spectral properties, including infrared fluorescent protein (IRFP), green fluorescent protein (GFP), red fluorescent protein (mCherry), and blue fluorescent protein (mTagBFP2).

    Techniques: Confocal Microscopy, Expressing, Comparison, Bacteria

    Distinction between the same species of Lactobacillus expressing different fluorescent proteins. Fluorescence was measured for the individual fluorescent strains and their mixtures, using settings corresponding to all four of the fluorescent proteins. The ratios indicate the proportions of the species expressing the fluorescent proteins in the following order: IRFP:GFP:mCherry:mTagBFP2. The encircled graphs represent the combination of fluorescent proteins and lactobacilli that were selected for further studies. * p < 0.05 (Student’s t tests) relative to nontransformed strain (NT, high-lighted with # for clarity). FU—fluorescence units; PBS—phosphate-buffered saline.

    Journal: International Journal of Molecular Sciences

    Article Title: Engineering of Vaginal Lactobacilli to Express Fluorescent Proteins Enables the Analysis of Their Mixture in Nanofibers

    doi: 10.3390/ijms222413631

    Figure Lengend Snippet: Distinction between the same species of Lactobacillus expressing different fluorescent proteins. Fluorescence was measured for the individual fluorescent strains and their mixtures, using settings corresponding to all four of the fluorescent proteins. The ratios indicate the proportions of the species expressing the fluorescent proteins in the following order: IRFP:GFP:mCherry:mTagBFP2. The encircled graphs represent the combination of fluorescent proteins and lactobacilli that were selected for further studies. * p < 0.05 (Student’s t tests) relative to nontransformed strain (NT, high-lighted with # for clarity). FU—fluorescence units; PBS—phosphate-buffered saline.

    Article Snippet: Here, we engineered three model vaginal lactobacilli ( Lactobacillus crispatus ATCC 33820, Lactobacillus gasseri ATCC 33323, and Lactobacillus jensenii ATCC 25258) and a control Lactobacillus plantarum ATCC 8014 to express fluorescent proteins with different spectral properties, including infrared fluorescent protein (IRFP), green fluorescent protein (GFP), red fluorescent protein (mCherry), and blue fluorescent protein (mTagBFP2).

    Techniques: Expressing, Fluorescence, Saline

    Fluorescence-based distinction of the different fluorescent lactobacilli and the nontransformed (NT) lactobacilli. Fluorescence was measured for the individual fluorescent species or their mixtures using the settings for all four of the fluorescent proteins. The ratios indicate the proportions of species in the mixtures in the following order: L. plantarum expressing IRFP; L. crispatus expressing GFP; L. gasseri expressing mCherry; and L. jensenii expressing mTagBFP2. * p < 0.05 (Student’s t tests), obtained by comparing fluorescent strain (F) to its nontransformed counterpart (NT). Lpl— L. plantarum ; Lga— L. gasseri ; Lcr— L. crispatus ; Lje— L. jensenii ; PBS—phosphate-buffered saline.

    Journal: International Journal of Molecular Sciences

    Article Title: Engineering of Vaginal Lactobacilli to Express Fluorescent Proteins Enables the Analysis of Their Mixture in Nanofibers

    doi: 10.3390/ijms222413631

    Figure Lengend Snippet: Fluorescence-based distinction of the different fluorescent lactobacilli and the nontransformed (NT) lactobacilli. Fluorescence was measured for the individual fluorescent species or their mixtures using the settings for all four of the fluorescent proteins. The ratios indicate the proportions of species in the mixtures in the following order: L. plantarum expressing IRFP; L. crispatus expressing GFP; L. gasseri expressing mCherry; and L. jensenii expressing mTagBFP2. * p < 0.05 (Student’s t tests), obtained by comparing fluorescent strain (F) to its nontransformed counterpart (NT). Lpl— L. plantarum ; Lga— L. gasseri ; Lcr— L. crispatus ; Lje— L. jensenii ; PBS—phosphate-buffered saline.

    Article Snippet: Here, we engineered three model vaginal lactobacilli ( Lactobacillus crispatus ATCC 33820, Lactobacillus gasseri ATCC 33323, and Lactobacillus jensenii ATCC 25258) and a control Lactobacillus plantarum ATCC 8014 to express fluorescent proteins with different spectral properties, including infrared fluorescent protein (IRFP), green fluorescent protein (GFP), red fluorescent protein (mCherry), and blue fluorescent protein (mTagBFP2).

    Techniques: Fluorescence, Expressing, Saline

    Representative confocal microscopy images of the mixtures of the lactobacilli expressing the different fluorescent proteins (F). Lpl— L. plantarum ; Lga— L. gasseri ; Lcr— L. crispatus ; Lje— L. jensenii ; NT—nontransformed species. Fluorescence images were obtained by using settings for denoted fluorescent proteins and merging thus obtained images, whereby settings for all four fluorescent proteins were used for the mixture.

    Journal: International Journal of Molecular Sciences

    Article Title: Engineering of Vaginal Lactobacilli to Express Fluorescent Proteins Enables the Analysis of Their Mixture in Nanofibers

    doi: 10.3390/ijms222413631

    Figure Lengend Snippet: Representative confocal microscopy images of the mixtures of the lactobacilli expressing the different fluorescent proteins (F). Lpl— L. plantarum ; Lga— L. gasseri ; Lcr— L. crispatus ; Lje— L. jensenii ; NT—nontransformed species. Fluorescence images were obtained by using settings for denoted fluorescent proteins and merging thus obtained images, whereby settings for all four fluorescent proteins were used for the mixture.

    Article Snippet: Here, we engineered three model vaginal lactobacilli ( Lactobacillus crispatus ATCC 33820, Lactobacillus gasseri ATCC 33323, and Lactobacillus jensenii ATCC 25258) and a control Lactobacillus plantarum ATCC 8014 to express fluorescent proteins with different spectral properties, including infrared fluorescent protein (IRFP), green fluorescent protein (GFP), red fluorescent protein (mCherry), and blue fluorescent protein (mTagBFP2).

    Techniques: Confocal Microscopy, Expressing, Fluorescence

    Scanning electron microscopy images of individual lactobacilli and as mixtures under high and low magnification. Columns 1 and 3, air-dried bacteria from water suspensions; Columns 2 and 4, bacteria incorporated into nanofibers. Average nanofiber diameters are specified in the last column.

    Journal: International Journal of Molecular Sciences

    Article Title: Engineering of Vaginal Lactobacilli to Express Fluorescent Proteins Enables the Analysis of Their Mixture in Nanofibers

    doi: 10.3390/ijms222413631

    Figure Lengend Snippet: Scanning electron microscopy images of individual lactobacilli and as mixtures under high and low magnification. Columns 1 and 3, air-dried bacteria from water suspensions; Columns 2 and 4, bacteria incorporated into nanofibers. Average nanofiber diameters are specified in the last column.

    Article Snippet: Here, we engineered three model vaginal lactobacilli ( Lactobacillus crispatus ATCC 33820, Lactobacillus gasseri ATCC 33323, and Lactobacillus jensenii ATCC 25258) and a control Lactobacillus plantarum ATCC 8014 to express fluorescent proteins with different spectral properties, including infrared fluorescent protein (IRFP), green fluorescent protein (GFP), red fluorescent protein (mCherry), and blue fluorescent protein (mTagBFP2).

    Techniques: Electron Microscopy, Bacteria

    Representative confocal microscopy images of the fluorescent lactobacilli and the nontransformed lactobacilli when incorporated in PEO electrospun nanofibers individually or as mixture of all 4 fluorescent lactobacilli.

    Journal: International Journal of Molecular Sciences

    Article Title: Engineering of Vaginal Lactobacilli to Express Fluorescent Proteins Enables the Analysis of Their Mixture in Nanofibers

    doi: 10.3390/ijms222413631

    Figure Lengend Snippet: Representative confocal microscopy images of the fluorescent lactobacilli and the nontransformed lactobacilli when incorporated in PEO electrospun nanofibers individually or as mixture of all 4 fluorescent lactobacilli.

    Article Snippet: Here, we engineered three model vaginal lactobacilli ( Lactobacillus crispatus ATCC 33820, Lactobacillus gasseri ATCC 33323, and Lactobacillus jensenii ATCC 25258) and a control Lactobacillus plantarum ATCC 8014 to express fluorescent proteins with different spectral properties, including infrared fluorescent protein (IRFP), green fluorescent protein (GFP), red fluorescent protein (mCherry), and blue fluorescent protein (mTagBFP2).

    Techniques: Confocal Microscopy