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MiddleBrook Pharmaceuticals 7h9 liquid culture medium
7h9 Liquid Culture Medium, 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
https://www.bioz.com/product/7h9+liquid+culture+medium/7h9+liquid+medium/pm40301886-80-6-10
Average 90 stars, based on 1 article reviews
7h9 liquid culture medium - by Bioz Stars, 2026-09
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Related Articles

Bacteria:

Article Title: ClpB is an essential stress regulator of Mycobacterium tuberculosis and endows survival advantage to dormant bacilli.
Article Snippet: .. Bacteria were cultured in a BSL-3 facility in Middlebrook 7H9 liquid culture medium supplemented with 0.5 % glycerol, 0.05 % Tween 80 and 10 % ADC (Albumin, Dextrose, Catalase) and grown to mid-log phase (A600 ∼ 0.6–0.8) at 37 °C with shaking at 100 rpm. ..

Cell Culture:

Article Title: ClpB is an essential stress regulator of Mycobacterium tuberculosis and endows survival advantage to dormant bacilli.
Article Snippet: .. Bacteria were cultured in a BSL-3 facility in Middlebrook 7H9 liquid culture medium supplemented with 0.5 % glycerol, 0.05 % Tween 80 and 10 % ADC (Albumin, Dextrose, Catalase) and grown to mid-log phase (A600 ∼ 0.6–0.8) at 37 °C with shaking at 100 rpm. ..

Incubation:

Article Title: Nontuberculous mycobacterial infections in a Brazilian pediatric population: a seven-year survey
Article Snippet: .. Mycobacterial growth was performed in Middlebrook 7H9 liquid culture medium with a maximum incubation period of 42 days, and the automated MGIT® System (Becton Dickinson, New Jersey, NY, United States) was used for primary isolation. ..

Isolation:

Article Title: Nontuberculous mycobacterial infections in a Brazilian pediatric population: a seven-year survey
Article Snippet: .. Mycobacterial growth was performed in Middlebrook 7H9 liquid culture medium with a maximum incubation period of 42 days, and the automated MGIT® System (Becton Dickinson, New Jersey, NY, United States) was used for primary isolation. ..

other:

Article Title: Mechanisms, Detection, and Relevance of Protein Acetylation in Prokaryotes
Article Snippet: , Mycobacterium tuberculosis H37Ra , None , EP and SP , Middlebrook 7H9 liquid culture medium , 226 , 137.



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7h9 Liquid Culture Medium, 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
https://www.bioz.com/product/7h9+liquid+culture+medium/7h9+liquid+medium/pm40301886-80-6-10
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Tn-seq and RNAtag-seq reveal that omamC is critical for survival during carbon starvation. ( A ) Carbon starvation-resuscitation growth scheme. A pooled M. tuberculosis H37Rv transposon library was grown in rich media <t>[7H9,</t> 10% oleic acid-albumin-dextrose-catalase (OADC), 0.5% glycerol, 0.05% tyloxapol] for 5 days, diluted into starvation media (7H9 salts, 0.05% tyloxapol), and cultured for 5 weeks, followed by resuscitation in rich media for 5 days. Transposon mutants present in the pool prior to carbon starvation and resuscitation cycling (input pool) and after three cycles of growth, starvation, and resuscitation performed over 4.5 months (output pool) were determined using Tn-seq. ( B ) Gene set enrichment analysis of genes (102) that were significantly [ P < 0.03 (Mann-Whitney U test); log 2 (FC) <−3.5] underrepresented in the output pool after three cycles of starvation and resuscitation. Genes are color coded based on the pathway with which they are associated with the positive control genes sigB and relA , known to be involved in carbon starvation, indicated in purple (compare Fig. S4; Table S3). ( C ) Of seven mce genes defined as hits by Tn-seq ( B ), only omamC is expressed during carbon starvation. Depicted are relative transcript levels during starvation of 298 genes whose corresponding transposon mutants were significantly changed in the starvation-resuscitation Tn-seq screen (with a threshold of P < 0.03, Mann-Whitney U test (MWU)). Differences in gene expression during carbon starvation compared to logarithmic growth were determined using RNAtag-seq and DESeq2 (R). The results of the Tn-seq screen are shown as fitness, i.e. , a function of the transposon input/output pool. The log 2 (FC) is shown in both cases. Depicted in gray are all genes that had a P -value <0.03 ( P (-log 10 ) >1.52) in the Tn-seq analysis. Carbon starvation controls sigB and relA ( , ) are shown in purple. All values are listed in Tables S4 to S6.
Middlebrook 7h9 Liquid Culture Medium, supplied by Difco, 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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Tn-seq and RNAtag-seq reveal that omamC is critical for survival during carbon starvation. ( A ) Carbon starvation-resuscitation growth scheme. A pooled M. tuberculosis H37Rv transposon library was grown in rich media <t>[7H9,</t> 10% oleic acid-albumin-dextrose-catalase (OADC), 0.5% glycerol, 0.05% tyloxapol] for 5 days, diluted into starvation media (7H9 salts, 0.05% tyloxapol), and cultured for 5 weeks, followed by resuscitation in rich media for 5 days. Transposon mutants present in the pool prior to carbon starvation and resuscitation cycling (input pool) and after three cycles of growth, starvation, and resuscitation performed over 4.5 months (output pool) were determined using Tn-seq. ( B ) Gene set enrichment analysis of genes (102) that were significantly [ P < 0.03 (Mann-Whitney U test); log 2 (FC) <−3.5] underrepresented in the output pool after three cycles of starvation and resuscitation. Genes are color coded based on the pathway with which they are associated with the positive control genes sigB and relA , known to be involved in carbon starvation, indicated in purple (compare Fig. S4; Table S3). ( C ) Of seven mce genes defined as hits by Tn-seq ( B ), only omamC is expressed during carbon starvation. Depicted are relative transcript levels during starvation of 298 genes whose corresponding transposon mutants were significantly changed in the starvation-resuscitation Tn-seq screen (with a threshold of P < 0.03, Mann-Whitney U test (MWU)). Differences in gene expression during carbon starvation compared to logarithmic growth were determined using RNAtag-seq and DESeq2 (R). The results of the Tn-seq screen are shown as fitness, i.e. , a function of the transposon input/output pool. The log 2 (FC) is shown in both cases. Depicted in gray are all genes that had a P -value <0.03 ( P (-log 10 ) >1.52) in the Tn-seq analysis. Carbon starvation controls sigB and relA ( , ) are shown in purple. All values are listed in Tables S4 to S6.
Liquid Culture Medium Middlebrook 7h9 Broth Supplemented With 10% Oleic Acid Albumin Catalase–Dextrose (Oadc), 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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Tn-seq and RNAtag-seq reveal that omamC is critical for survival during carbon starvation. ( A ) Carbon starvation-resuscitation growth scheme. A pooled M. tuberculosis H37Rv transposon library was grown in rich media <t>[7H9,</t> 10% oleic acid-albumin-dextrose-catalase (OADC), 0.5% glycerol, 0.05% tyloxapol] for 5 days, diluted into starvation media (7H9 salts, 0.05% tyloxapol), and cultured for 5 weeks, followed by resuscitation in rich media for 5 days. Transposon mutants present in the pool prior to carbon starvation and resuscitation cycling (input pool) and after three cycles of growth, starvation, and resuscitation performed over 4.5 months (output pool) were determined using Tn-seq. ( B ) Gene set enrichment analysis of genes (102) that were significantly [ P < 0.03 (Mann-Whitney U test); log 2 (FC) <−3.5] underrepresented in the output pool after three cycles of starvation and resuscitation. Genes are color coded based on the pathway with which they are associated with the positive control genes sigB and relA , known to be involved in carbon starvation, indicated in purple (compare Fig. S4; Table S3). ( C ) Of seven mce genes defined as hits by Tn-seq ( B ), only omamC is expressed during carbon starvation. Depicted are relative transcript levels during starvation of 298 genes whose corresponding transposon mutants were significantly changed in the starvation-resuscitation Tn-seq screen (with a threshold of P < 0.03, Mann-Whitney U test (MWU)). Differences in gene expression during carbon starvation compared to logarithmic growth were determined using RNAtag-seq and DESeq2 (R). The results of the Tn-seq screen are shown as fitness, i.e. , a function of the transposon input/output pool. The log 2 (FC) is shown in both cases. Depicted in gray are all genes that had a P -value <0.03 ( P (-log 10 ) >1.52) in the Tn-seq analysis. Carbon starvation controls sigB and relA ( , ) are shown in purple. All values are listed in Tables S4 to S6.
Middlebrook® 7h9 Liquid Culture Medium, 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
https://www.bioz.com/product/7h9+liquid+culture+medium/middlebrook+7h10+medium/pm35758621-371-1-0
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Tn-seq and RNAtag-seq reveal that omamC is critical for survival during carbon starvation. ( A ) Carbon starvation-resuscitation growth scheme. A pooled M. tuberculosis H37Rv transposon library was grown in rich media <t>[7H9,</t> 10% oleic acid-albumin-dextrose-catalase (OADC), 0.5% glycerol, 0.05% tyloxapol] for 5 days, diluted into starvation media (7H9 salts, 0.05% tyloxapol), and cultured for 5 weeks, followed by resuscitation in rich media for 5 days. Transposon mutants present in the pool prior to carbon starvation and resuscitation cycling (input pool) and after three cycles of growth, starvation, and resuscitation performed over 4.5 months (output pool) were determined using Tn-seq. ( B ) Gene set enrichment analysis of genes (102) that were significantly [ P < 0.03 (Mann-Whitney U test); log 2 (FC) <−3.5] underrepresented in the output pool after three cycles of starvation and resuscitation. Genes are color coded based on the pathway with which they are associated with the positive control genes sigB and relA , known to be involved in carbon starvation, indicated in purple (compare Fig. S4; Table S3). ( C ) Of seven mce genes defined as hits by Tn-seq ( B ), only omamC is expressed during carbon starvation. Depicted are relative transcript levels during starvation of 298 genes whose corresponding transposon mutants were significantly changed in the starvation-resuscitation Tn-seq screen (with a threshold of P < 0.03, Mann-Whitney U test (MWU)). Differences in gene expression during carbon starvation compared to logarithmic growth were determined using RNAtag-seq and DESeq2 (R). The results of the Tn-seq screen are shown as fitness, i.e. , a function of the transposon input/output pool. The log 2 (FC) is shown in both cases. Depicted in gray are all genes that had a P -value <0.03 ( P (-log 10 ) >1.52) in the Tn-seq analysis. Carbon starvation controls sigB and relA ( , ) are shown in purple. All values are listed in Tables S4 to S6.
Liquid Culture Medium Middlebrook 7h9 Broth With Oadc, 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
https://www.bioz.com/product/7h9+liquid+culture+medium/liquid+culture+medium+middlebrook+7h9+broth+with+oadc/pmc08931439-273-13-17
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Tn-seq and RNAtag-seq reveal that omamC is critical for survival during carbon starvation. ( A ) Carbon starvation-resuscitation growth scheme. A pooled M. tuberculosis H37Rv transposon library was grown in rich media [7H9, 10% oleic acid-albumin-dextrose-catalase (OADC), 0.5% glycerol, 0.05% tyloxapol] for 5 days, diluted into starvation media (7H9 salts, 0.05% tyloxapol), and cultured for 5 weeks, followed by resuscitation in rich media for 5 days. Transposon mutants present in the pool prior to carbon starvation and resuscitation cycling (input pool) and after three cycles of growth, starvation, and resuscitation performed over 4.5 months (output pool) were determined using Tn-seq. ( B ) Gene set enrichment analysis of genes (102) that were significantly [ P < 0.03 (Mann-Whitney U test); log 2 (FC) <−3.5] underrepresented in the output pool after three cycles of starvation and resuscitation. Genes are color coded based on the pathway with which they are associated with the positive control genes sigB and relA , known to be involved in carbon starvation, indicated in purple (compare Fig. S4; Table S3). ( C ) Of seven mce genes defined as hits by Tn-seq ( B ), only omamC is expressed during carbon starvation. Depicted are relative transcript levels during starvation of 298 genes whose corresponding transposon mutants were significantly changed in the starvation-resuscitation Tn-seq screen (with a threshold of P < 0.03, Mann-Whitney U test (MWU)). Differences in gene expression during carbon starvation compared to logarithmic growth were determined using RNAtag-seq and DESeq2 (R). The results of the Tn-seq screen are shown as fitness, i.e. , a function of the transposon input/output pool. The log 2 (FC) is shown in both cases. Depicted in gray are all genes that had a P -value <0.03 ( P (-log 10 ) >1.52) in the Tn-seq analysis. Carbon starvation controls sigB and relA ( , ) are shown in purple. All values are listed in Tables S4 to S6.

Journal: mBio

Article Title: Genetic factors affecting storage and utilization of lipids during dormancy in Mycobacterium tuberculosis

doi: 10.1128/mbio.03208-23

Figure Lengend Snippet: Tn-seq and RNAtag-seq reveal that omamC is critical for survival during carbon starvation. ( A ) Carbon starvation-resuscitation growth scheme. A pooled M. tuberculosis H37Rv transposon library was grown in rich media [7H9, 10% oleic acid-albumin-dextrose-catalase (OADC), 0.5% glycerol, 0.05% tyloxapol] for 5 days, diluted into starvation media (7H9 salts, 0.05% tyloxapol), and cultured for 5 weeks, followed by resuscitation in rich media for 5 days. Transposon mutants present in the pool prior to carbon starvation and resuscitation cycling (input pool) and after three cycles of growth, starvation, and resuscitation performed over 4.5 months (output pool) were determined using Tn-seq. ( B ) Gene set enrichment analysis of genes (102) that were significantly [ P < 0.03 (Mann-Whitney U test); log 2 (FC) <−3.5] underrepresented in the output pool after three cycles of starvation and resuscitation. Genes are color coded based on the pathway with which they are associated with the positive control genes sigB and relA , known to be involved in carbon starvation, indicated in purple (compare Fig. S4; Table S3). ( C ) Of seven mce genes defined as hits by Tn-seq ( B ), only omamC is expressed during carbon starvation. Depicted are relative transcript levels during starvation of 298 genes whose corresponding transposon mutants were significantly changed in the starvation-resuscitation Tn-seq screen (with a threshold of P < 0.03, Mann-Whitney U test (MWU)). Differences in gene expression during carbon starvation compared to logarithmic growth were determined using RNAtag-seq and DESeq2 (R). The results of the Tn-seq screen are shown as fitness, i.e. , a function of the transposon input/output pool. The log 2 (FC) is shown in both cases. Depicted in gray are all genes that had a P -value <0.03 ( P (-log 10 ) >1.52) in the Tn-seq analysis. Carbon starvation controls sigB and relA ( , ) are shown in purple. All values are listed in Tables S4 to S6.

Article Snippet: Mtb H37Rv and derivative strains were grown at 37°C in Middlebrook 7H9 (Difco) liquid culture medium supplemented with 10% oleic acid-albumin-dextrose-catalase (OADC), 0.5% glycerol, and 0.05% tyloxapol (referred to as growth in rich media in the text) or on Middlebrook 7H10 (Difco) solid culture medium supplemented with 10% OADC (BD Biosciences) and 0.5% glycerol.

Techniques: Cell Culture, MANN-WHITNEY, Positive Control, Expressing