m tuberculosis h37rv Search Results


mtb h37rv cell fractions and proteins  (BEI Resources)
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BEI Resources mtb h37rv cell fractions and proteins
Mtb H37rv Cell Fractions And Proteins, supplied by BEI Resources, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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luminescent m. tuberculosis h37rv reporter strain  (MiddleBrook Pharmaceuticals)
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MiddleBrook Pharmaceuticals luminescent m. tuberculosis h37rv reporter strain
Luminescent M. Tuberculosis H37rv Reporter Strain, supplied by MiddleBrook Pharmaceuticals, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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h37rv bacterial qdna pcr control  (Advanced Biotechnologies Inc)
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H37rv Bacterial Qdna Pcr Control, supplied by Advanced Biotechnologies Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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mycobacterium tuberculosis h37rv  (Johns Hopkins HealthCare)
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Johns Hopkins HealthCare mycobacterium tuberculosis h37rv
Mycobacterium Tuberculosis H37rv, supplied by Johns Hopkins HealthCare, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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extract from the virulent m. tuberculosis strain h37rv  (Mycobacteria Research Laboratories)
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Mycobacteria Research Laboratories extract from the virulent m. tuberculosis strain h37rv
Extract From The Virulent M. Tuberculosis Strain H37rv, supplied by Mycobacteria Research Laboratories, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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extract from the virulent m. tuberculosis strain h37rv - by Bioz Stars, 2026-10
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h37rv reference strain  (National Reference Center for Legionella)
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National Reference Center for Legionella h37rv reference strain
H37rv Reference Strain, supplied by National Reference Center for Legionella, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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purified protein derivative of m. tuberculosis h37rv protein (cat# dag2684)  (Abace Biotechnology Co Ltd)
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Abace Biotechnology Co Ltd purified protein derivative of m. tuberculosis h37rv protein (cat# dag2684)
The evaluation of <t>PPD-specific</t> immune response. Peritoneal macrophages were added to ELISPOT plates to enhance antigen presentation. ( a , d ) Representative images of spots formed after being stimulated with APC only, APC+PPD, or PMA+ionomycin. Numbers of PPD-specific IFN-γ secreting cell were compared between Il12rb1 −/− and C57BL/6 mice after being inoculated with BCG, either subcutaneously ( b ) or intranasally ( c ). The comparisons of the average optical intensities of spots stimulated by PPD between Il12rb1 −/− and C57BL/6 mice after being inoculated with BCG, either subcutaneously ( e ) or intranasally ( f ). ( g , h ) showed the comparisons of IFN-γ secreting cell numbers and the average optical intensities of spots between Il12rb1 −/− and C57BL/6 mice after PMA+ionomycin stimulation. ( i ) The cell culture supernatant in the wells of ELISPOT plates was collected for CBA assay. Levels of TNF-a were compared between Il12rb1 −/− and C57BL/6 mice inoculated with BCG, either subcutaneously or intranasally. All the above data were shown as mean ± SD. Statistical analysis were performed by the method two-tailed t -test (*, p < 0.05, **, p < 0.01, ***, p < 0.001). PPD-specific binding antibodies were detected <t>by</t> <t>ELISA.</t> Optical density (OD) values were compared between Il12rb1 −/− and C57BL/6 mice ( j ). Data are shown as mean ± SD. Statistical analyses were performed by the two-way ANOVA method (*, p < 0.05, **, p < 0.01).
Purified Protein Derivative Of M. Tuberculosis H37rv Protein (Cat# Dag2684), supplied by Abace Biotechnology Co Ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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custom m. tuberculosis h37rv array  (Genotypic Technology Pvt Ltd)
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Genotypic Technology Pvt Ltd custom m. tuberculosis h37rv array
The evaluation of <t>PPD-specific</t> immune response. Peritoneal macrophages were added to ELISPOT plates to enhance antigen presentation. ( a , d ) Representative images of spots formed after being stimulated with APC only, APC+PPD, or PMA+ionomycin. Numbers of PPD-specific IFN-γ secreting cell were compared between Il12rb1 −/− and C57BL/6 mice after being inoculated with BCG, either subcutaneously ( b ) or intranasally ( c ). The comparisons of the average optical intensities of spots stimulated by PPD between Il12rb1 −/− and C57BL/6 mice after being inoculated with BCG, either subcutaneously ( e ) or intranasally ( f ). ( g , h ) showed the comparisons of IFN-γ secreting cell numbers and the average optical intensities of spots between Il12rb1 −/− and C57BL/6 mice after PMA+ionomycin stimulation. ( i ) The cell culture supernatant in the wells of ELISPOT plates was collected for CBA assay. Levels of TNF-a were compared between Il12rb1 −/− and C57BL/6 mice inoculated with BCG, either subcutaneously or intranasally. All the above data were shown as mean ± SD. Statistical analysis were performed by the method two-tailed t -test (*, p < 0.05, **, p < 0.01, ***, p < 0.001). PPD-specific binding antibodies were detected <t>by</t> <t>ELISA.</t> Optical density (OD) values were compared between Il12rb1 −/− and C57BL/6 mice ( j ). Data are shown as mean ± SD. Statistical analyses were performed by the two-way ANOVA method (*, p < 0.05, **, p < 0.01).
Custom M. Tuberculosis H37rv Array, supplied by Genotypic Technology Pvt Ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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dna from reference strains m. tuberculosis h37rv and mycobacterium bovis (m. bovis) bcg p3  (Ocimum Biosolutions)
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Ocimum Biosolutions dna from reference strains m. tuberculosis h37rv and mycobacterium bovis (m. bovis) bcg p3
The evaluation of <t>PPD-specific</t> immune response. Peritoneal macrophages were added to ELISPOT plates to enhance antigen presentation. ( a , d ) Representative images of spots formed after being stimulated with APC only, APC+PPD, or PMA+ionomycin. Numbers of PPD-specific IFN-γ secreting cell were compared between Il12rb1 −/− and C57BL/6 mice after being inoculated with BCG, either subcutaneously ( b ) or intranasally ( c ). The comparisons of the average optical intensities of spots stimulated by PPD between Il12rb1 −/− and C57BL/6 mice after being inoculated with BCG, either subcutaneously ( e ) or intranasally ( f ). ( g , h ) showed the comparisons of IFN-γ secreting cell numbers and the average optical intensities of spots between Il12rb1 −/− and C57BL/6 mice after PMA+ionomycin stimulation. ( i ) The cell culture supernatant in the wells of ELISPOT plates was collected for CBA assay. Levels of TNF-a were compared between Il12rb1 −/− and C57BL/6 mice inoculated with BCG, either subcutaneously or intranasally. All the above data were shown as mean ± SD. Statistical analysis were performed by the method two-tailed t -test (*, p < 0.05, **, p < 0.01, ***, p < 0.001). PPD-specific binding antibodies were detected <t>by</t> <t>ELISA.</t> Optical density (OD) values were compared between Il12rb1 −/− and C57BL/6 mice ( j ). Data are shown as mean ± SD. Statistical analyses were performed by the two-way ANOVA method (*, p < 0.05, **, p < 0.01).
Dna From Reference Strains M. Tuberculosis H37rv And Mycobacterium Bovis (M. Bovis) Bcg P3, supplied by Ocimum Biosolutions, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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dna from reference strains m. tuberculosis h37rv and mycobacterium bovis (m. bovis) bcg p3 - by Bioz Stars, 2026-10
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virulent mtb h37rv strain harboring psmt1-plasmid for luciferase-expression  (HUYGEN)
90
HUYGEN virulent mtb h37rv strain harboring psmt1-plasmid for luciferase-expression
The evaluation of <t>PPD-specific</t> immune response. Peritoneal macrophages were added to ELISPOT plates to enhance antigen presentation. ( a , d ) Representative images of spots formed after being stimulated with APC only, APC+PPD, or PMA+ionomycin. Numbers of PPD-specific IFN-γ secreting cell were compared between Il12rb1 −/− and C57BL/6 mice after being inoculated with BCG, either subcutaneously ( b ) or intranasally ( c ). The comparisons of the average optical intensities of spots stimulated by PPD between Il12rb1 −/− and C57BL/6 mice after being inoculated with BCG, either subcutaneously ( e ) or intranasally ( f ). ( g , h ) showed the comparisons of IFN-γ secreting cell numbers and the average optical intensities of spots between Il12rb1 −/− and C57BL/6 mice after PMA+ionomycin stimulation. ( i ) The cell culture supernatant in the wells of ELISPOT plates was collected for CBA assay. Levels of TNF-a were compared between Il12rb1 −/− and C57BL/6 mice inoculated with BCG, either subcutaneously or intranasally. All the above data were shown as mean ± SD. Statistical analysis were performed by the method two-tailed t -test (*, p < 0.05, **, p < 0.01, ***, p < 0.001). PPD-specific binding antibodies were detected <t>by</t> <t>ELISA.</t> Optical density (OD) values were compared between Il12rb1 −/− and C57BL/6 mice ( j ). Data are shown as mean ± SD. Statistical analyses were performed by the two-way ANOVA method (*, p < 0.05, **, p < 0.01).
Virulent Mtb H37rv Strain Harboring Psmt1 Plasmid For Luciferase Expression, supplied by HUYGEN, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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dna sequence of the mycobacterium tuberculosis h37rv tres gene  (GenScript corporation)
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GenScript corporation dna sequence of the mycobacterium tuberculosis h37rv tres gene
The evaluation of <t>PPD-specific</t> immune response. Peritoneal macrophages were added to ELISPOT plates to enhance antigen presentation. ( a , d ) Representative images of spots formed after being stimulated with APC only, APC+PPD, or PMA+ionomycin. Numbers of PPD-specific IFN-γ secreting cell were compared between Il12rb1 −/− and C57BL/6 mice after being inoculated with BCG, either subcutaneously ( b ) or intranasally ( c ). The comparisons of the average optical intensities of spots stimulated by PPD between Il12rb1 −/− and C57BL/6 mice after being inoculated with BCG, either subcutaneously ( e ) or intranasally ( f ). ( g , h ) showed the comparisons of IFN-γ secreting cell numbers and the average optical intensities of spots between Il12rb1 −/− and C57BL/6 mice after PMA+ionomycin stimulation. ( i ) The cell culture supernatant in the wells of ELISPOT plates was collected for CBA assay. Levels of TNF-a were compared between Il12rb1 −/− and C57BL/6 mice inoculated with BCG, either subcutaneously or intranasally. All the above data were shown as mean ± SD. Statistical analysis were performed by the method two-tailed t -test (*, p < 0.05, **, p < 0.01, ***, p < 0.001). PPD-specific binding antibodies were detected <t>by</t> <t>ELISA.</t> Optical density (OD) values were compared between Il12rb1 −/− and C57BL/6 mice ( j ). Data are shown as mean ± SD. Statistical analyses were performed by the two-way ANOVA method (*, p < 0.05, **, p < 0.01).
Dna Sequence Of The Mycobacterium Tuberculosis H37rv Tres Gene, supplied by GenScript corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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m. tuberculosis h37rv  (Robinson Services Inc)
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Robinson Services Inc m. tuberculosis h37rv
The evaluation of <t>PPD-specific</t> immune response. Peritoneal macrophages were added to ELISPOT plates to enhance antigen presentation. ( a , d ) Representative images of spots formed after being stimulated with APC only, APC+PPD, or PMA+ionomycin. Numbers of PPD-specific IFN-γ secreting cell were compared between Il12rb1 −/− and C57BL/6 mice after being inoculated with BCG, either subcutaneously ( b ) or intranasally ( c ). The comparisons of the average optical intensities of spots stimulated by PPD between Il12rb1 −/− and C57BL/6 mice after being inoculated with BCG, either subcutaneously ( e ) or intranasally ( f ). ( g , h ) showed the comparisons of IFN-γ secreting cell numbers and the average optical intensities of spots between Il12rb1 −/− and C57BL/6 mice after PMA+ionomycin stimulation. ( i ) The cell culture supernatant in the wells of ELISPOT plates was collected for CBA assay. Levels of TNF-a were compared between Il12rb1 −/− and C57BL/6 mice inoculated with BCG, either subcutaneously or intranasally. All the above data were shown as mean ± SD. Statistical analysis were performed by the method two-tailed t -test (*, p < 0.05, **, p < 0.01, ***, p < 0.001). PPD-specific binding antibodies were detected <t>by</t> <t>ELISA.</t> Optical density (OD) values were compared between Il12rb1 −/− and C57BL/6 mice ( j ). Data are shown as mean ± SD. Statistical analyses were performed by the two-way ANOVA method (*, p < 0.05, **, p < 0.01).
M. Tuberculosis H37rv, supplied by Robinson Services Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


The evaluation of PPD-specific immune response. Peritoneal macrophages were added to ELISPOT plates to enhance antigen presentation. ( a , d ) Representative images of spots formed after being stimulated with APC only, APC+PPD, or PMA+ionomycin. Numbers of PPD-specific IFN-γ secreting cell were compared between Il12rb1 −/− and C57BL/6 mice after being inoculated with BCG, either subcutaneously ( b ) or intranasally ( c ). The comparisons of the average optical intensities of spots stimulated by PPD between Il12rb1 −/− and C57BL/6 mice after being inoculated with BCG, either subcutaneously ( e ) or intranasally ( f ). ( g , h ) showed the comparisons of IFN-γ secreting cell numbers and the average optical intensities of spots between Il12rb1 −/− and C57BL/6 mice after PMA+ionomycin stimulation. ( i ) The cell culture supernatant in the wells of ELISPOT plates was collected for CBA assay. Levels of TNF-a were compared between Il12rb1 −/− and C57BL/6 mice inoculated with BCG, either subcutaneously or intranasally. All the above data were shown as mean ± SD. Statistical analysis were performed by the method two-tailed t -test (*, p < 0.05, **, p < 0.01, ***, p < 0.001). PPD-specific binding antibodies were detected by ELISA. Optical density (OD) values were compared between Il12rb1 −/− and C57BL/6 mice ( j ). Data are shown as mean ± SD. Statistical analyses were performed by the two-way ANOVA method (*, p < 0.05, **, p < 0.01).

Journal: Vaccines

Article Title: Immune Correlates of Disseminated BCG Infection in IL12RB1-Deficient Mice

doi: 10.3390/vaccines10071147

Figure Lengend Snippet: The evaluation of PPD-specific immune response. Peritoneal macrophages were added to ELISPOT plates to enhance antigen presentation. ( a , d ) Representative images of spots formed after being stimulated with APC only, APC+PPD, or PMA+ionomycin. Numbers of PPD-specific IFN-γ secreting cell were compared between Il12rb1 −/− and C57BL/6 mice after being inoculated with BCG, either subcutaneously ( b ) or intranasally ( c ). The comparisons of the average optical intensities of spots stimulated by PPD between Il12rb1 −/− and C57BL/6 mice after being inoculated with BCG, either subcutaneously ( e ) or intranasally ( f ). ( g , h ) showed the comparisons of IFN-γ secreting cell numbers and the average optical intensities of spots between Il12rb1 −/− and C57BL/6 mice after PMA+ionomycin stimulation. ( i ) The cell culture supernatant in the wells of ELISPOT plates was collected for CBA assay. Levels of TNF-a were compared between Il12rb1 −/− and C57BL/6 mice inoculated with BCG, either subcutaneously or intranasally. All the above data were shown as mean ± SD. Statistical analysis were performed by the method two-tailed t -test (*, p < 0.05, **, p < 0.01, ***, p < 0.001). PPD-specific binding antibodies were detected by ELISA. Optical density (OD) values were compared between Il12rb1 −/− and C57BL/6 mice ( j ). Data are shown as mean ± SD. Statistical analyses were performed by the two-way ANOVA method (*, p < 0.05, **, p < 0.01).

Article Snippet: An in-house ELISA protocol was developed using purified PPD (purified protein derivative of M. tuberculosis H37Rv) protein (Cat# DAG2684, ABACE-BIOLOGY, Beijing, China) as coating antigen.

Techniques: Enzyme-linked Immunospot, Immunopeptidomics, Cell Culture, Two Tailed Test, Binding Assay, Enzyme-linked Immunosorbent Assay