lactobacillus casei lmg 6904  (ATCC)


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    ATCC lactobacillus casei lmg 6904
    Lactobacillus Casei Lmg 6904, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    lactobacillus casei lmg 6904  (ATCC)


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    ATCC lactobacillus casei lmg 6904
    Lactobacillus Casei Lmg 6904, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    yersinia pseudotuberculosis atcc 6904  (ATCC)


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    ATCC yersinia pseudotuberculosis atcc 6904
    Yersinia Pseudotuberculosis Atcc 6904, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    glc 15  (ATCC)


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    ATCC glc 15
    The effects of combined HDACi and Dasatinib on SCLC cells. A, Flow cytometry-based analyses of apoptosis (Annexin V positive cells; left) and lipid reactive oxygen species (ROS; right) assayed on SCLC cells <t>(GLC-15)</t> treated for 48h with Dasatinib (0.5 μM) and Vorinostat (HDACi; 1 μM), alone or in combination. The corresponding quantifications (n=3) were shown on the right. *p < 0.05, **p < 0.01, ****p < 0.0001 by ANOVA test. NS, non-significance. B, Small–cell lung cancer (SCLC) cells (GLC-15) were treated for 72h with combined Vorinostat (HDACi; 1 μM) and Dasatinib (0.5 μM) with or without 2.5 mM N-acetyl-L-cysteine (NAC). Cells were seeded 1,000 cells per well in 96-well plates. ****p < 0.0001 (n=3) by ANOVA test. NS, non-significance. C, Flow cytometry-based analyses of apoptosis (Annexin V positive cells; left) and lipid reactive oxygen species (ROS; right) assayed on SCLC cells (GLC-15) treated for 24h with Dasatinib (0.5 μM) and Vorinostat (HDACi; 1 μM), alone or in combination. The assay was repeated twice.
    Glc 15, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    1) Product Images from "Pharmaco-transcriptomic correlation analysis reveals novel responsive signatures to HDAC inhibitors and identifies Dasatinib as a synergistic interactor in small-cell lung cancer"

    Article Title: Pharmaco-transcriptomic correlation analysis reveals novel responsive signatures to HDAC inhibitors and identifies Dasatinib as a synergistic interactor in small-cell lung cancer

    Journal: EBioMedicine

    doi: 10.1016/j.ebiom.2021.103457

    The effects of combined HDACi and Dasatinib on SCLC cells. A, Flow cytometry-based analyses of apoptosis (Annexin V positive cells; left) and lipid reactive oxygen species (ROS; right) assayed on SCLC cells (GLC-15) treated for 48h with Dasatinib (0.5 μM) and Vorinostat (HDACi; 1 μM), alone or in combination. The corresponding quantifications (n=3) were shown on the right. *p < 0.05, **p < 0.01, ****p < 0.0001 by ANOVA test. NS, non-significance. B, Small–cell lung cancer (SCLC) cells (GLC-15) were treated for 72h with combined Vorinostat (HDACi; 1 μM) and Dasatinib (0.5 μM) with or without 2.5 mM N-acetyl-L-cysteine (NAC). Cells were seeded 1,000 cells per well in 96-well plates. ****p < 0.0001 (n=3) by ANOVA test. NS, non-significance. C, Flow cytometry-based analyses of apoptosis (Annexin V positive cells; left) and lipid reactive oxygen species (ROS; right) assayed on SCLC cells (GLC-15) treated for 24h with Dasatinib (0.5 μM) and Vorinostat (HDACi; 1 μM), alone or in combination. The assay was repeated twice.
    Figure Legend Snippet: The effects of combined HDACi and Dasatinib on SCLC cells. A, Flow cytometry-based analyses of apoptosis (Annexin V positive cells; left) and lipid reactive oxygen species (ROS; right) assayed on SCLC cells (GLC-15) treated for 48h with Dasatinib (0.5 μM) and Vorinostat (HDACi; 1 μM), alone or in combination. The corresponding quantifications (n=3) were shown on the right. *p < 0.05, **p < 0.01, ****p < 0.0001 by ANOVA test. NS, non-significance. B, Small–cell lung cancer (SCLC) cells (GLC-15) were treated for 72h with combined Vorinostat (HDACi; 1 μM) and Dasatinib (0.5 μM) with or without 2.5 mM N-acetyl-L-cysteine (NAC). Cells were seeded 1,000 cells per well in 96-well plates. ****p < 0.0001 (n=3) by ANOVA test. NS, non-significance. C, Flow cytometry-based analyses of apoptosis (Annexin V positive cells; left) and lipid reactive oxygen species (ROS; right) assayed on SCLC cells (GLC-15) treated for 24h with Dasatinib (0.5 μM) and Vorinostat (HDACi; 1 μM), alone or in combination. The assay was repeated twice.

    Techniques Used: Flow Cytometry

    yersinia pseudotuberculosis strain atcc 6904  (ATCC)


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    ATCC yersinia pseudotuberculosis strain atcc 6904
    Yersinia Pseudotuberculosis Strain Atcc 6904, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    lactobacillus fermentum lmg 6902  (ATCC)


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    ATCC lactobacillus fermentum lmg 6902
    Lactobacillus Fermentum Lmg 6902, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    lactobacillus casei lmg 6904  (ATCC)


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    ATCC lactobacillus casei lmg 6904
    Lactobacillus Casei Lmg 6904, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    amc tb4  (ATCC)


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    ATCC amc tb4
    Microarray-detected AMR genes in Yersinia spp. strains.
    Amc Tb4, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    1) Product Images from "A Survey of Antimicrobial Resistance Determinants in Category A Select Agents, Exempt Strains, and Near-Neighbor Species"

    Article Title: A Survey of Antimicrobial Resistance Determinants in Category A Select Agents, Exempt Strains, and Near-Neighbor Species

    Journal: International Journal of Molecular Sciences

    doi: 10.3390/ijms21051669

    Microarray-detected AMR genes in Yersinia spp. strains.
    Figure Legend Snippet: Microarray-detected AMR genes in Yersinia spp. strains.

    Techniques Used: Microarray

    GyrA melt temperatures and clusters for Yersinia spp. strains analyzed by HRMA.
    Figure Legend Snippet: GyrA melt temperatures and clusters for Yersinia spp. strains analyzed by HRMA.

    Techniques Used:

    Other Yersinia spp. strains used in this study.
    Figure Legend Snippet: Other Yersinia spp. strains used in this study.

    Techniques Used:

    yersinia pseudotuberculosis  (ATCC)


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    ATCC yersinia pseudotuberculosis
    Yersinia Pseudotuberculosis, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    trichosporon asahii  (ATCC)


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    ATCC trichosporon asahii
    Reference set of melting temperatures (Tm°C) generated using the four molecular beacons following amplification of DNA from standard fungal strains. Beacon PFC11 gave a TM with all strains tested while PFA21 and PYCT41 gave adequate difference in Tm to enable speciation. Beacon PFM3 gave Tm with only zygomycetes.
    Trichosporon Asahii, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    1) Product Images from "Speciation of fungi using real time PCR with molecular beacons: Can we solve the enigma of diagnosis of invasive fungal disease?"

    Article Title: Speciation of fungi using real time PCR with molecular beacons: Can we solve the enigma of diagnosis of invasive fungal disease?

    Journal: Medical Journal, Armed Forces India

    doi: 10.1016/j.mjafi.2017.12.003

    Reference set of melting temperatures (Tm°C) generated using the four molecular beacons following amplification of DNA from standard fungal strains. Beacon PFC11 gave a TM with all strains tested while PFA21 and PYCT41 gave adequate difference in Tm to enable speciation. Beacon PFM3 gave Tm with only zygomycetes.
    Figure Legend Snippet: Reference set of melting temperatures (Tm°C) generated using the four molecular beacons following amplification of DNA from standard fungal strains. Beacon PFC11 gave a TM with all strains tested while PFA21 and PYCT41 gave adequate difference in Tm to enable speciation. Beacon PFM3 gave Tm with only zygomycetes.

    Techniques Used: Generated, Amplification

    Melting temperatures (Tm°C) of the beacons generated after PCR on clinical samples. The fungus was identified by matching these with the reference set of Tm in .
    Figure Legend Snippet: Melting temperatures (Tm°C) of the beacons generated after PCR on clinical samples. The fungus was identified by matching these with the reference set of Tm in .

    Techniques Used: Generated

    trichosporon asahii  (ATCC)


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    ATCC trichosporon asahii
    Reference set of melting temperatures (Tm°C) generated using the four molecular beacons following amplification of DNA from standard fungal strains. Beacon PFC11 gave a TM with all strains tested while PFA21 and PYCT41 gave adequate difference in Tm to enable speciation. Beacon PFM3 gave Tm with only zygomycetes.
    Trichosporon Asahii, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    1) Product Images from "Speciation of fungi using real time PCR with molecular beacons: Can we solve the enigma of diagnosis of invasive fungal disease?"

    Article Title: Speciation of fungi using real time PCR with molecular beacons: Can we solve the enigma of diagnosis of invasive fungal disease?

    Journal: Medical Journal, Armed Forces India

    doi: 10.1016/j.mjafi.2017.12.003

    Reference set of melting temperatures (Tm°C) generated using the four molecular beacons following amplification of DNA from standard fungal strains. Beacon PFC11 gave a TM with all strains tested while PFA21 and PYCT41 gave adequate difference in Tm to enable speciation. Beacon PFM3 gave Tm with only zygomycetes.
    Figure Legend Snippet: Reference set of melting temperatures (Tm°C) generated using the four molecular beacons following amplification of DNA from standard fungal strains. Beacon PFC11 gave a TM with all strains tested while PFA21 and PYCT41 gave adequate difference in Tm to enable speciation. Beacon PFM3 gave Tm with only zygomycetes.

    Techniques Used: Generated, Amplification

    Melting temperatures (Tm°C) of the beacons generated after PCR on clinical samples. The fungus was identified by matching these with the reference set of Tm in .
    Figure Legend Snippet: Melting temperatures (Tm°C) of the beacons generated after PCR on clinical samples. The fungus was identified by matching these with the reference set of Tm in .

    Techniques Used: Generated

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    ATCC lactobacillus casei lmg 6904
    Lactobacillus Casei Lmg 6904, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ATCC yersinia pseudotuberculosis atcc 6904
    Yersinia Pseudotuberculosis Atcc 6904, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    glc 15  (ATCC)
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    ATCC glc 15
    The effects of combined HDACi and Dasatinib on SCLC cells. A, Flow cytometry-based analyses of apoptosis (Annexin V positive cells; left) and lipid reactive oxygen species (ROS; right) assayed on SCLC cells <t>(GLC-15)</t> treated for 48h with Dasatinib (0.5 μM) and Vorinostat (HDACi; 1 μM), alone or in combination. The corresponding quantifications (n=3) were shown on the right. *p < 0.05, **p < 0.01, ****p < 0.0001 by ANOVA test. NS, non-significance. B, Small–cell lung cancer (SCLC) cells (GLC-15) were treated for 72h with combined Vorinostat (HDACi; 1 μM) and Dasatinib (0.5 μM) with or without 2.5 mM N-acetyl-L-cysteine (NAC). Cells were seeded 1,000 cells per well in 96-well plates. ****p < 0.0001 (n=3) by ANOVA test. NS, non-significance. C, Flow cytometry-based analyses of apoptosis (Annexin V positive cells; left) and lipid reactive oxygen species (ROS; right) assayed on SCLC cells (GLC-15) treated for 24h with Dasatinib (0.5 μM) and Vorinostat (HDACi; 1 μM), alone or in combination. The assay was repeated twice.
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    ATCC yersinia pseudotuberculosis strain atcc 6904
    The effects of combined HDACi and Dasatinib on SCLC cells. A, Flow cytometry-based analyses of apoptosis (Annexin V positive cells; left) and lipid reactive oxygen species (ROS; right) assayed on SCLC cells <t>(GLC-15)</t> treated for 48h with Dasatinib (0.5 μM) and Vorinostat (HDACi; 1 μM), alone or in combination. The corresponding quantifications (n=3) were shown on the right. *p < 0.05, **p < 0.01, ****p < 0.0001 by ANOVA test. NS, non-significance. B, Small–cell lung cancer (SCLC) cells (GLC-15) were treated for 72h with combined Vorinostat (HDACi; 1 μM) and Dasatinib (0.5 μM) with or without 2.5 mM N-acetyl-L-cysteine (NAC). Cells were seeded 1,000 cells per well in 96-well plates. ****p < 0.0001 (n=3) by ANOVA test. NS, non-significance. C, Flow cytometry-based analyses of apoptosis (Annexin V positive cells; left) and lipid reactive oxygen species (ROS; right) assayed on SCLC cells (GLC-15) treated for 24h with Dasatinib (0.5 μM) and Vorinostat (HDACi; 1 μM), alone or in combination. The assay was repeated twice.
    Yersinia Pseudotuberculosis Strain Atcc 6904, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ATCC lactobacillus fermentum lmg 6902
    The effects of combined HDACi and Dasatinib on SCLC cells. A, Flow cytometry-based analyses of apoptosis (Annexin V positive cells; left) and lipid reactive oxygen species (ROS; right) assayed on SCLC cells <t>(GLC-15)</t> treated for 48h with Dasatinib (0.5 μM) and Vorinostat (HDACi; 1 μM), alone or in combination. The corresponding quantifications (n=3) were shown on the right. *p < 0.05, **p < 0.01, ****p < 0.0001 by ANOVA test. NS, non-significance. B, Small–cell lung cancer (SCLC) cells (GLC-15) were treated for 72h with combined Vorinostat (HDACi; 1 μM) and Dasatinib (0.5 μM) with or without 2.5 mM N-acetyl-L-cysteine (NAC). Cells were seeded 1,000 cells per well in 96-well plates. ****p < 0.0001 (n=3) by ANOVA test. NS, non-significance. C, Flow cytometry-based analyses of apoptosis (Annexin V positive cells; left) and lipid reactive oxygen species (ROS; right) assayed on SCLC cells (GLC-15) treated for 24h with Dasatinib (0.5 μM) and Vorinostat (HDACi; 1 μM), alone or in combination. The assay was repeated twice.
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    ATCC amc tb4
    Microarray-detected AMR genes in Yersinia spp. strains.
    Amc Tb4, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ATCC yersinia pseudotuberculosis
    Microarray-detected AMR genes in Yersinia spp. strains.
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    ATCC trichosporon asahii
    Reference set of melting temperatures (Tm°C) generated using the four molecular beacons following amplification of DNA from standard fungal strains. Beacon PFC11 gave a TM with all strains tested while PFA21 and PYCT41 gave adequate difference in Tm to enable speciation. Beacon PFM3 gave Tm with only zygomycetes.
    Trichosporon Asahii, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    The effects of combined HDACi and Dasatinib on SCLC cells. A, Flow cytometry-based analyses of apoptosis (Annexin V positive cells; left) and lipid reactive oxygen species (ROS; right) assayed on SCLC cells (GLC-15) treated for 48h with Dasatinib (0.5 μM) and Vorinostat (HDACi; 1 μM), alone or in combination. The corresponding quantifications (n=3) were shown on the right. *p < 0.05, **p < 0.01, ****p < 0.0001 by ANOVA test. NS, non-significance. B, Small–cell lung cancer (SCLC) cells (GLC-15) were treated for 72h with combined Vorinostat (HDACi; 1 μM) and Dasatinib (0.5 μM) with or without 2.5 mM N-acetyl-L-cysteine (NAC). Cells were seeded 1,000 cells per well in 96-well plates. ****p < 0.0001 (n=3) by ANOVA test. NS, non-significance. C, Flow cytometry-based analyses of apoptosis (Annexin V positive cells; left) and lipid reactive oxygen species (ROS; right) assayed on SCLC cells (GLC-15) treated for 24h with Dasatinib (0.5 μM) and Vorinostat (HDACi; 1 μM), alone or in combination. The assay was repeated twice.

    Journal: EBioMedicine

    Article Title: Pharmaco-transcriptomic correlation analysis reveals novel responsive signatures to HDAC inhibitors and identifies Dasatinib as a synergistic interactor in small-cell lung cancer

    doi: 10.1016/j.ebiom.2021.103457

    Figure Lengend Snippet: The effects of combined HDACi and Dasatinib on SCLC cells. A, Flow cytometry-based analyses of apoptosis (Annexin V positive cells; left) and lipid reactive oxygen species (ROS; right) assayed on SCLC cells (GLC-15) treated for 48h with Dasatinib (0.5 μM) and Vorinostat (HDACi; 1 μM), alone or in combination. The corresponding quantifications (n=3) were shown on the right. *p < 0.05, **p < 0.01, ****p < 0.0001 by ANOVA test. NS, non-significance. B, Small–cell lung cancer (SCLC) cells (GLC-15) were treated for 72h with combined Vorinostat (HDACi; 1 μM) and Dasatinib (0.5 μM) with or without 2.5 mM N-acetyl-L-cysteine (NAC). Cells were seeded 1,000 cells per well in 96-well plates. ****p < 0.0001 (n=3) by ANOVA test. NS, non-significance. C, Flow cytometry-based analyses of apoptosis (Annexin V positive cells; left) and lipid reactive oxygen species (ROS; right) assayed on SCLC cells (GLC-15) treated for 24h with Dasatinib (0.5 μM) and Vorinostat (HDACi; 1 μM), alone or in combination. The assay was repeated twice.

    Article Snippet: SCLC (DMS-114 [ATCC Cat# CRL-2066, RRID:CVCL_1174], DMS-53 [ATCC Cat# CRL-2062, RRID:CVCL_1177], GLC-15 [KCB Cat# KCB 90028YJ, RRID:CVCL_6904]) and NSCLC cell lines (H1650 [KCLB Cat# 91650, RRID:CVCL_1483], H4006 [ATCC Cat# CRL-2871, RRID:CVCL_1269], H1792 [ATCC Cat# CRL-5895, RRID:CVCL_1495], H1944 [ATCC Cat# CRL-5907, RRID:CVCL_1508]) were cultured in RPMI-1640 (Sigma-Aldrich, R8758), supplemented with 10% fetal bovine serum (FBS) (Gibco) and 1% penicillin/streptomycin (Sigma-Aldrich) at 37 °C in a humid incubator with 5% CO2.

    Techniques: Flow Cytometry

    Microarray-detected AMR genes in Yersinia spp. strains.

    Journal: International Journal of Molecular Sciences

    Article Title: A Survey of Antimicrobial Resistance Determinants in Category A Select Agents, Exempt Strains, and Near-Neighbor Species

    doi: 10.3390/ijms21051669

    Figure Lengend Snippet: Microarray-detected AMR genes in Yersinia spp. strains.

    Article Snippet: AMC TB4 , ATCC 6904; YE1022 , YERS008 , , .

    Techniques: Microarray

    GyrA melt temperatures and clusters for Yersinia spp. strains analyzed by HRMA.

    Journal: International Journal of Molecular Sciences

    Article Title: A Survey of Antimicrobial Resistance Determinants in Category A Select Agents, Exempt Strains, and Near-Neighbor Species

    doi: 10.3390/ijms21051669

    Figure Lengend Snippet: GyrA melt temperatures and clusters for Yersinia spp. strains analyzed by HRMA.

    Article Snippet: AMC TB4 , ATCC 6904; YE1022 , YERS008 , , .

    Techniques:

    Other Yersinia spp. strains used in this study.

    Journal: International Journal of Molecular Sciences

    Article Title: A Survey of Antimicrobial Resistance Determinants in Category A Select Agents, Exempt Strains, and Near-Neighbor Species

    doi: 10.3390/ijms21051669

    Figure Lengend Snippet: Other Yersinia spp. strains used in this study.

    Article Snippet: AMC TB4 , ATCC 6904; YE1022 , YERS008 , , .

    Techniques:

    Reference set of melting temperatures (Tm°C) generated using the four molecular beacons following amplification of DNA from standard fungal strains. Beacon PFC11 gave a TM with all strains tested while PFA21 and PYCT41 gave adequate difference in Tm to enable speciation. Beacon PFM3 gave Tm with only zygomycetes.

    Journal: Medical Journal, Armed Forces India

    Article Title: Speciation of fungi using real time PCR with molecular beacons: Can we solve the enigma of diagnosis of invasive fungal disease?

    doi: 10.1016/j.mjafi.2017.12.003

    Figure Lengend Snippet: Reference set of melting temperatures (Tm°C) generated using the four molecular beacons following amplification of DNA from standard fungal strains. Beacon PFC11 gave a TM with all strains tested while PFA21 and PYCT41 gave adequate difference in Tm to enable speciation. Beacon PFM3 gave Tm with only zygomycetes.

    Article Snippet: The top of each panel shows the meting curves while the bottom half shows the melting peaks. panel a: beacon PFC11, panel b: beacon PFA21, panel c: beacon PFM3 (zygomycetes), panel d: PYCT41 (yeast). table ft1 table-wrap mode="anchored" t5 caption a7 ATCC no. Fungal strains Molecular beacon PFC11 PFA21 PFM3 PYCT41 ATCC 204304 Aspergillus flavus 64.26 70.38 – 82.23 ATCC 293 Aspergillus fumigatus 69.59 74 – 64.93 ATCC 9508 Aspergillus niger 64.17 69.92 – 64.93 Clinical isolate Aspergillus terreus 64.12 70.47 – 82.8 Clinical isolate Aspergillus nidulans 64.21 70.34 – 81.96 Clinical isolate Aspergillus glaucus 63.75 70.2 – 46 Clinical isolate Mucor 49.66 46.44 59.03 61.72 Clinical isolate Rhizopus 63.9 46.61 58.59 61.49 ATCC 90028 Candida albicans 65.19 70.34 – 45.63 ATCC 750 Candida tropicalis 65.19 70.31 – 62.47 ATCC 6258 Candida krusei 65.33 70.38 – – ATCC 22019 Candida parapsilosis 65.23 70.31 – 41.19 ATCC 6258 Candida guillermondii 64.75 70.25 – – ATCC 208821 Cryptococcus neoformans 62 68.91 – 61 Clinical isolate Trichosporon asahii 61.09 69.04 – 61.72 Clinical isolate Penicillium spp.

    Techniques: Generated, Amplification

    Melting temperatures (Tm°C) of the beacons generated after PCR on clinical samples. The fungus was identified by matching these with the reference set of Tm in .

    Journal: Medical Journal, Armed Forces India

    Article Title: Speciation of fungi using real time PCR with molecular beacons: Can we solve the enigma of diagnosis of invasive fungal disease?

    doi: 10.1016/j.mjafi.2017.12.003

    Figure Lengend Snippet: Melting temperatures (Tm°C) of the beacons generated after PCR on clinical samples. The fungus was identified by matching these with the reference set of Tm in .

    Article Snippet: The top of each panel shows the meting curves while the bottom half shows the melting peaks. panel a: beacon PFC11, panel b: beacon PFA21, panel c: beacon PFM3 (zygomycetes), panel d: PYCT41 (yeast). table ft1 table-wrap mode="anchored" t5 caption a7 ATCC no. Fungal strains Molecular beacon PFC11 PFA21 PFM3 PYCT41 ATCC 204304 Aspergillus flavus 64.26 70.38 – 82.23 ATCC 293 Aspergillus fumigatus 69.59 74 – 64.93 ATCC 9508 Aspergillus niger 64.17 69.92 – 64.93 Clinical isolate Aspergillus terreus 64.12 70.47 – 82.8 Clinical isolate Aspergillus nidulans 64.21 70.34 – 81.96 Clinical isolate Aspergillus glaucus 63.75 70.2 – 46 Clinical isolate Mucor 49.66 46.44 59.03 61.72 Clinical isolate Rhizopus 63.9 46.61 58.59 61.49 ATCC 90028 Candida albicans 65.19 70.34 – 45.63 ATCC 750 Candida tropicalis 65.19 70.31 – 62.47 ATCC 6258 Candida krusei 65.33 70.38 – – ATCC 22019 Candida parapsilosis 65.23 70.31 – 41.19 ATCC 6258 Candida guillermondii 64.75 70.25 – – ATCC 208821 Cryptococcus neoformans 62 68.91 – 61 Clinical isolate Trichosporon asahii 61.09 69.04 – 61.72 Clinical isolate Penicillium spp.

    Techniques: Generated