antibiotics against k pneumoniae atcc 13883 Search Results


weak antibacterial effects against k pneumoniae atcc 13883  (ATCC)
99
ATCC weak antibacterial effects against k pneumoniae atcc 13883
Weak Antibacterial Effects Against K Pneumoniae Atcc 13883, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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cux1  (Novus Biologicals)
94
Novus Biologicals cux1
(a) Immunofluorescence staining of <t>Cux1</t> (green) and Ctip2 (red) in coronal sections of Mboat7 heterozygous and KO mice at E18.5. (b) Immunofluorescence staining of Tbr1 (green) and Ctip2 (red) in coronal sections of Mboat7 heterozygous and KO mice at E18.5. (c) Quantitative analysis of layer VI (Tbr1 + ), V (Tbr1 - ; Ctip2 + ), and II-IV (Cux1 + ) neurons per area within 300 µm wide bins (n=3 mice for each genotype). (d) Double staining at E13.5 for BrdU (injected at E12.5) and Tbr1. Arrows show neurons (BrdU + ; Tbr1 + ). (e) The rate of neuronal differentiation (ratio of BrdU + ; Tbr1 + /BrdU + cells) (n=4 mice for each genotype). (f) The rate of differentiation into IPCs (ratio of BrdU + ; Tbr2 + /BrdU + cells) (n=3 mice for each genotype). (g) The rate of RGCs (ratio of BrdU + ; Pax6 + /BrdU + cells) (n=3 mice for each genotype). (h) Immunofluorescence staining of Sox2 (green) and Tbr2 (magenta) in coronal sections of Mboat7 heterozygous and KO mice at E13.5. (i,j) Quantitative analysis of cells positive for Tbr2 (i) and Sox2 (j) per area within 200 µm wide bins (n=3 mice for each genotype). (k) Total BrdU + cells in 200 µm cortex at E13.5 (BrdU injected at E12.5) (n=4 mice for each genotype). (l) Immunofluorescence staining for phospho-histone H3 (p-H3) in the cortices of Mboat7 heterozygous and KO mice from E10.5 to E14.5. (m) Quantitative analysis of cells positive for p-H3 per area within 200 µm wide bins (n=3-5 mice for each genotype). Data are shown as mean ± SEM. Unpaired two-tailed Student’s t-test; *p<0.05, **p<0.01 and ***p<0.001. Scale bars, 100 µm.
Cux1, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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critical pathogens  (ATCC)
99
ATCC critical pathogens
(a) Immunofluorescence staining of <t>Cux1</t> (green) and Ctip2 (red) in coronal sections of Mboat7 heterozygous and KO mice at E18.5. (b) Immunofluorescence staining of Tbr1 (green) and Ctip2 (red) in coronal sections of Mboat7 heterozygous and KO mice at E18.5. (c) Quantitative analysis of layer VI (Tbr1 + ), V (Tbr1 - ; Ctip2 + ), and II-IV (Cux1 + ) neurons per area within 300 µm wide bins (n=3 mice for each genotype). (d) Double staining at E13.5 for BrdU (injected at E12.5) and Tbr1. Arrows show neurons (BrdU + ; Tbr1 + ). (e) The rate of neuronal differentiation (ratio of BrdU + ; Tbr1 + /BrdU + cells) (n=4 mice for each genotype). (f) The rate of differentiation into IPCs (ratio of BrdU + ; Tbr2 + /BrdU + cells) (n=3 mice for each genotype). (g) The rate of RGCs (ratio of BrdU + ; Pax6 + /BrdU + cells) (n=3 mice for each genotype). (h) Immunofluorescence staining of Sox2 (green) and Tbr2 (magenta) in coronal sections of Mboat7 heterozygous and KO mice at E13.5. (i,j) Quantitative analysis of cells positive for Tbr2 (i) and Sox2 (j) per area within 200 µm wide bins (n=3 mice for each genotype). (k) Total BrdU + cells in 200 µm cortex at E13.5 (BrdU injected at E12.5) (n=4 mice for each genotype). (l) Immunofluorescence staining for phospho-histone H3 (p-H3) in the cortices of Mboat7 heterozygous and KO mice from E10.5 to E14.5. (m) Quantitative analysis of cells positive for p-H3 per area within 200 µm wide bins (n=3-5 mice for each genotype). Data are shown as mean ± SEM. Unpaired two-tailed Student’s t-test; *p<0.05, **p<0.01 and ***p<0.001. Scale bars, 100 µm.
Critical Pathogens, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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gram negative  (ATCC)
99
ATCC gram negative
(a) Immunofluorescence staining of <t>Cux1</t> (green) and Ctip2 (red) in coronal sections of Mboat7 heterozygous and KO mice at E18.5. (b) Immunofluorescence staining of Tbr1 (green) and Ctip2 (red) in coronal sections of Mboat7 heterozygous and KO mice at E18.5. (c) Quantitative analysis of layer VI (Tbr1 + ), V (Tbr1 - ; Ctip2 + ), and II-IV (Cux1 + ) neurons per area within 300 µm wide bins (n=3 mice for each genotype). (d) Double staining at E13.5 for BrdU (injected at E12.5) and Tbr1. Arrows show neurons (BrdU + ; Tbr1 + ). (e) The rate of neuronal differentiation (ratio of BrdU + ; Tbr1 + /BrdU + cells) (n=4 mice for each genotype). (f) The rate of differentiation into IPCs (ratio of BrdU + ; Tbr2 + /BrdU + cells) (n=3 mice for each genotype). (g) The rate of RGCs (ratio of BrdU + ; Pax6 + /BrdU + cells) (n=3 mice for each genotype). (h) Immunofluorescence staining of Sox2 (green) and Tbr2 (magenta) in coronal sections of Mboat7 heterozygous and KO mice at E13.5. (i,j) Quantitative analysis of cells positive for Tbr2 (i) and Sox2 (j) per area within 200 µm wide bins (n=3 mice for each genotype). (k) Total BrdU + cells in 200 µm cortex at E13.5 (BrdU injected at E12.5) (n=4 mice for each genotype). (l) Immunofluorescence staining for phospho-histone H3 (p-H3) in the cortices of Mboat7 heterozygous and KO mice from E10.5 to E14.5. (m) Quantitative analysis of cells positive for p-H3 per area within 200 µm wide bins (n=3-5 mice for each genotype). Data are shown as mean ± SEM. Unpaired two-tailed Student’s t-test; *p<0.05, **p<0.01 and ***p<0.001. Scale bars, 100 µm.
Gram Negative, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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b subtilis atcc 6633 b cereus atcc 6629 k pneumoniae atcc 13883 p aeruginosa atcc 27953 c albicans atcc 10231 k pneumoniae  (ATCC)
94
ATCC b subtilis atcc 6633 b cereus atcc 6629 k pneumoniae atcc 13883 p aeruginosa atcc 27953 c albicans atcc 10231 k pneumoniae
(a) Immunofluorescence staining of <t>Cux1</t> (green) and Ctip2 (red) in coronal sections of Mboat7 heterozygous and KO mice at E18.5. (b) Immunofluorescence staining of Tbr1 (green) and Ctip2 (red) in coronal sections of Mboat7 heterozygous and KO mice at E18.5. (c) Quantitative analysis of layer VI (Tbr1 + ), V (Tbr1 - ; Ctip2 + ), and II-IV (Cux1 + ) neurons per area within 300 µm wide bins (n=3 mice for each genotype). (d) Double staining at E13.5 for BrdU (injected at E12.5) and Tbr1. Arrows show neurons (BrdU + ; Tbr1 + ). (e) The rate of neuronal differentiation (ratio of BrdU + ; Tbr1 + /BrdU + cells) (n=4 mice for each genotype). (f) The rate of differentiation into IPCs (ratio of BrdU + ; Tbr2 + /BrdU + cells) (n=3 mice for each genotype). (g) The rate of RGCs (ratio of BrdU + ; Pax6 + /BrdU + cells) (n=3 mice for each genotype). (h) Immunofluorescence staining of Sox2 (green) and Tbr2 (magenta) in coronal sections of Mboat7 heterozygous and KO mice at E13.5. (i,j) Quantitative analysis of cells positive for Tbr2 (i) and Sox2 (j) per area within 200 µm wide bins (n=3 mice for each genotype). (k) Total BrdU + cells in 200 µm cortex at E13.5 (BrdU injected at E12.5) (n=4 mice for each genotype). (l) Immunofluorescence staining for phospho-histone H3 (p-H3) in the cortices of Mboat7 heterozygous and KO mice from E10.5 to E14.5. (m) Quantitative analysis of cells positive for p-H3 per area within 200 µm wide bins (n=3-5 mice for each genotype). Data are shown as mean ± SEM. Unpaired two-tailed Student’s t-test; *p<0.05, **p<0.01 and ***p<0.001. Scale bars, 100 µm.
B Subtilis Atcc 6633 B Cereus Atcc 6629 K Pneumoniae Atcc 13883 P Aeruginosa Atcc 27953 C Albicans Atcc 10231 K Pneumoniae, supplied by ATCC, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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pantothenamides against other strains  (ATCC)
99
ATCC pantothenamides against other strains
Structure of pantothenic acid and N-substituted <t>pantothenamides</t>
Pantothenamides Against Other Strains, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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s aureus atcc 6538p k pneumoniae atcc 13883  (ATCC)
99
ATCC s aureus atcc 6538p k pneumoniae atcc 13883
Structure of pantothenic acid and N-substituted <t>pantothenamides</t>
S Aureus Atcc 6538p K Pneumoniae Atcc 13883, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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eskape pathogens  (ATCC)
98
ATCC eskape pathogens
Structure of pantothenic acid and N-substituted <t>pantothenamides</t>
Eskape Pathogens, supplied by ATCC, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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ethyl acetate fraction  (ATCC)
99
ATCC ethyl acetate fraction
Structure of pantothenic acid and N-substituted <t>pantothenamides</t>
Ethyl Acetate Fraction, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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pathogens  (ATCC)
99
ATCC pathogens
Structure of pantothenic acid and N-substituted <t>pantothenamides</t>
Pathogens, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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indicator pathogens  (ATCC)
99
ATCC indicator pathogens
Structure of pantothenic acid and N-substituted <t>pantothenamides</t>
Indicator Pathogens, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


(a) Immunofluorescence staining of Cux1 (green) and Ctip2 (red) in coronal sections of Mboat7 heterozygous and KO mice at E18.5. (b) Immunofluorescence staining of Tbr1 (green) and Ctip2 (red) in coronal sections of Mboat7 heterozygous and KO mice at E18.5. (c) Quantitative analysis of layer VI (Tbr1 + ), V (Tbr1 - ; Ctip2 + ), and II-IV (Cux1 + ) neurons per area within 300 µm wide bins (n=3 mice for each genotype). (d) Double staining at E13.5 for BrdU (injected at E12.5) and Tbr1. Arrows show neurons (BrdU + ; Tbr1 + ). (e) The rate of neuronal differentiation (ratio of BrdU + ; Tbr1 + /BrdU + cells) (n=4 mice for each genotype). (f) The rate of differentiation into IPCs (ratio of BrdU + ; Tbr2 + /BrdU + cells) (n=3 mice for each genotype). (g) The rate of RGCs (ratio of BrdU + ; Pax6 + /BrdU + cells) (n=3 mice for each genotype). (h) Immunofluorescence staining of Sox2 (green) and Tbr2 (magenta) in coronal sections of Mboat7 heterozygous and KO mice at E13.5. (i,j) Quantitative analysis of cells positive for Tbr2 (i) and Sox2 (j) per area within 200 µm wide bins (n=3 mice for each genotype). (k) Total BrdU + cells in 200 µm cortex at E13.5 (BrdU injected at E12.5) (n=4 mice for each genotype). (l) Immunofluorescence staining for phospho-histone H3 (p-H3) in the cortices of Mboat7 heterozygous and KO mice from E10.5 to E14.5. (m) Quantitative analysis of cells positive for p-H3 per area within 200 µm wide bins (n=3-5 mice for each genotype). Data are shown as mean ± SEM. Unpaired two-tailed Student’s t-test; *p<0.05, **p<0.01 and ***p<0.001. Scale bars, 100 µm.

Journal: bioRxiv

Article Title: Arachidonic acid incorporation into phosphatidylinositol by LPLAT11/MBOAT7 ensures radial glial cell integrity in developing neocortex

doi: 10.1101/2024.04.30.588048

Figure Lengend Snippet: (a) Immunofluorescence staining of Cux1 (green) and Ctip2 (red) in coronal sections of Mboat7 heterozygous and KO mice at E18.5. (b) Immunofluorescence staining of Tbr1 (green) and Ctip2 (red) in coronal sections of Mboat7 heterozygous and KO mice at E18.5. (c) Quantitative analysis of layer VI (Tbr1 + ), V (Tbr1 - ; Ctip2 + ), and II-IV (Cux1 + ) neurons per area within 300 µm wide bins (n=3 mice for each genotype). (d) Double staining at E13.5 for BrdU (injected at E12.5) and Tbr1. Arrows show neurons (BrdU + ; Tbr1 + ). (e) The rate of neuronal differentiation (ratio of BrdU + ; Tbr1 + /BrdU + cells) (n=4 mice for each genotype). (f) The rate of differentiation into IPCs (ratio of BrdU + ; Tbr2 + /BrdU + cells) (n=3 mice for each genotype). (g) The rate of RGCs (ratio of BrdU + ; Pax6 + /BrdU + cells) (n=3 mice for each genotype). (h) Immunofluorescence staining of Sox2 (green) and Tbr2 (magenta) in coronal sections of Mboat7 heterozygous and KO mice at E13.5. (i,j) Quantitative analysis of cells positive for Tbr2 (i) and Sox2 (j) per area within 200 µm wide bins (n=3 mice for each genotype). (k) Total BrdU + cells in 200 µm cortex at E13.5 (BrdU injected at E12.5) (n=4 mice for each genotype). (l) Immunofluorescence staining for phospho-histone H3 (p-H3) in the cortices of Mboat7 heterozygous and KO mice from E10.5 to E14.5. (m) Quantitative analysis of cells positive for p-H3 per area within 200 µm wide bins (n=3-5 mice for each genotype). Data are shown as mean ± SEM. Unpaired two-tailed Student’s t-test; *p<0.05, **p<0.01 and ***p<0.001. Scale bars, 100 µm.

Article Snippet: Antibody to Cux1 (NBP2-13883) was purchased from Novus Biologicals.

Techniques: Immunofluorescence, Staining, Double Staining, Injection, Two Tailed Test

Structure of pantothenic acid and N-substituted pantothenamides

Journal:

Article Title: Geminal dialkyl derivatives of N -substituted pantothenamides: Synthesis and antibacterial activity

doi: 10.1016/j.bmc.2011.02.053

Figure Lengend Snippet: Structure of pantothenic acid and N-substituted pantothenamides

Article Snippet: A preliminary screen of these pantothenamides against other strains ( Acinetobacter baumannii ATCC 19606, Klebsiella penumoniae ATCC 13883, Escherichia coli ATCC 25922 and 11775, and Bacillus subtilis ATCC 6051 and 6633) using the agar diffusion method suggests no antimicrobial activity (inhibition zone <1.1 cm for a 1 cm disc impregnated with the desired compound). table ft1 table-wrap mode="anchored" t5 caption a7 MIC (μM) a S. aureus b MRSA c Open in a separate window 9a 7 ± 6 7± 3 Open in a separate window 9b 13 ± 7 13± 2 Open in a separate window 9c 101 ± 45 51 ± 15 Open in a separate window 9d 374 ± 187 374 ± 153 Open in a separate window 9e >715 >715 Open in a separate window 9f 3.2 ± 0.8 3.2 ± 0.9 Open in a separate window 9g >703 >703 Open in a separate window 9h >744 >744 Open in a separate window 9i 376 ± 217 376 ± 109 Open in a separate window 9j 1 ± 0.9 1 ± 0.7 Open in a separate window 9k(N5-pan) 7 ± 2 7 ± 2 Open in a separate window 9l (N9-pan) 0.4 ± 0.2 0.4 ± 0.2 Open in a separate window 9m 24 ± 14 24 ± 14 Open in a separate window a Minimum inhibitory concentrations (MICs) were determined using the following concentrations: 0.5, 1, 2, 4, 8, 16, 32, 64, 128, and 256 μg/mL.

Techniques:

Synthetic route to new N-substituted pantothenamides

Journal:

Article Title: Geminal dialkyl derivatives of N -substituted pantothenamides: Synthesis and antibacterial activity

doi: 10.1016/j.bmc.2011.02.053

Figure Lengend Snippet: Synthetic route to new N-substituted pantothenamides

Article Snippet: A preliminary screen of these pantothenamides against other strains ( Acinetobacter baumannii ATCC 19606, Klebsiella penumoniae ATCC 13883, Escherichia coli ATCC 25922 and 11775, and Bacillus subtilis ATCC 6051 and 6633) using the agar diffusion method suggests no antimicrobial activity (inhibition zone <1.1 cm for a 1 cm disc impregnated with the desired compound). table ft1 table-wrap mode="anchored" t5 caption a7 MIC (μM) a S. aureus b MRSA c Open in a separate window 9a 7 ± 6 7± 3 Open in a separate window 9b 13 ± 7 13± 2 Open in a separate window 9c 101 ± 45 51 ± 15 Open in a separate window 9d 374 ± 187 374 ± 153 Open in a separate window 9e >715 >715 Open in a separate window 9f 3.2 ± 0.8 3.2 ± 0.9 Open in a separate window 9g >703 >703 Open in a separate window 9h >744 >744 Open in a separate window 9i 376 ± 217 376 ± 109 Open in a separate window 9j 1 ± 0.9 1 ± 0.7 Open in a separate window 9k(N5-pan) 7 ± 2 7 ± 2 Open in a separate window 9l (N9-pan) 0.4 ± 0.2 0.4 ± 0.2 Open in a separate window 9m 24 ± 14 24 ± 14 Open in a separate window a Minimum inhibitory concentrations (MICs) were determined using the following concentrations: 0.5, 1, 2, 4, 8, 16, 32, 64, 128, and 256 μg/mL.

Techniques:

Antibacterial activity of N -substituted pantothenamides 9a–9m

Journal:

Article Title: Geminal dialkyl derivatives of N -substituted pantothenamides: Synthesis and antibacterial activity

doi: 10.1016/j.bmc.2011.02.053

Figure Lengend Snippet: Antibacterial activity of N -substituted pantothenamides 9a–9m

Article Snippet: A preliminary screen of these pantothenamides against other strains ( Acinetobacter baumannii ATCC 19606, Klebsiella penumoniae ATCC 13883, Escherichia coli ATCC 25922 and 11775, and Bacillus subtilis ATCC 6051 and 6633) using the agar diffusion method suggests no antimicrobial activity (inhibition zone <1.1 cm for a 1 cm disc impregnated with the desired compound). table ft1 table-wrap mode="anchored" t5 caption a7 MIC (μM) a S. aureus b MRSA c Open in a separate window 9a 7 ± 6 7± 3 Open in a separate window 9b 13 ± 7 13± 2 Open in a separate window 9c 101 ± 45 51 ± 15 Open in a separate window 9d 374 ± 187 374 ± 153 Open in a separate window 9e >715 >715 Open in a separate window 9f 3.2 ± 0.8 3.2 ± 0.9 Open in a separate window 9g >703 >703 Open in a separate window 9h >744 >744 Open in a separate window 9i 376 ± 217 376 ± 109 Open in a separate window 9j 1 ± 0.9 1 ± 0.7 Open in a separate window 9k(N5-pan) 7 ± 2 7 ± 2 Open in a separate window 9l (N9-pan) 0.4 ± 0.2 0.4 ± 0.2 Open in a separate window 9m 24 ± 14 24 ± 14 Open in a separate window a Minimum inhibitory concentrations (MICs) were determined using the following concentrations: 0.5, 1, 2, 4, 8, 16, 32, 64, 128, and 256 μg/mL.

Techniques: Activity Assay