casitone Search Results


macrocystis pyrifera kelp casein enzymatic digest  (Thermo Fisher)
93
Thermo Fisher macrocystis pyrifera kelp casein enzymatic digest
Macrocystis Pyrifera Kelp Casein Enzymatic Digest, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/casitone/Enzymatic+Digest+Casein+Hydrolysate/us07439034-187-23-30
Average 93 stars, based on 1 article reviews
macrocystis pyrifera kelp casein enzymatic digest - by Bioz Stars, 2026-09
93/100 stars
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csm ura medium  (Valiant Co Ltd)
94
Valiant Co Ltd csm ura medium
Csm Ura Medium, supplied by Valiant Co Ltd, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/casitone/Casein+hydrolysate/pm25089527-80-29-31
Average 94 stars, based on 1 article reviews
csm ura medium - by Bioz Stars, 2026-09
94/100 stars
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casein hydrolysate usb cspd appliedbiosystems nitro block  (Thermo Fisher)
95
Thermo Fisher casein hydrolysate usb cspd appliedbiosystems nitro block
Casein Hydrolysate Usb Cspd Appliedbiosystems Nitro Block, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/casitone/CASEIN+HYDROLYSATE/pmc03535447-58-0-6
Average 95 stars, based on 1 article reviews
casein hydrolysate usb cspd appliedbiosystems nitro block - by Bioz Stars, 2026-09
95/100 stars
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casitone medium  (Eiken Chemical)
90
Eiken Chemical casitone medium
Casitone Medium, supplied by Eiken Chemical, 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/casitone/casitone+medium/pmc11635101-119-46-48
Average 90 stars, based on 1 article reviews
casitone medium - by Bioz Stars, 2026-09
90/100 stars
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casitone agar  (Becton Dickinson)
90
Becton Dickinson casitone agar
Casitone Agar, supplied by Becton Dickinson, 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/casitone/casitone+agar/pmc06505865-63-20-22
Average 90 stars, based on 1 article reviews
casitone agar - by Bioz Stars, 2026-09
90/100 stars
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mtb mic middlebrook 7h9/glucose/bsa/tx  (MiddleBrook Pharmaceuticals)
90
MiddleBrook Pharmaceuticals mtb mic middlebrook 7h9/glucose/bsa/tx
Chemoproteomic profiling of 1 and 2 identified HadA, HadB, and BCG_0547c (HadD) as targets. (A) Compounds 2 (blue) or 1 (red) were analyzed in a Mycobacterium bovis BCG protein extract with compound 3 and 4 attached to a bead matrix. Only three proteins showed competition by both compounds, HadA, HadB, and BCG_0547c (HadD). (B) Compound 1 (red) showed stronger inhibition of all three proteins from bead-binding in comparison to compound 2 (blue), indicating higher potency ( n = 3). (C) Correlation of target binding and antimycobacterial activity of compounds from the 1,3-diarylpyrazolyl-acylsulfonamide series. Active compounds ( 1 - 5 ) showed inhibition of proteins HadA, HadB, and BCG_0547c (HadD) from 4 -bead-binding, whereas inactive compounds ( 6 – 8 ) did not (results on 3 -beads are comparable, Figure S1 ). Numbers indicate compounds. r , Pearson correlation coefficient; p , p -value (calculated probability); pMIC99 defined as <t>−log10(</t> <t>Mtb</t> <t>MIC</t> 99 in M).
Mtb Mic Middlebrook 7h9/Glucose/Bsa/Tx, 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/casitone/mtb+mic+middlebrook+7h9+casitone+tx/pmc09673142-1-0-2
Average 90 stars, based on 1 article reviews
mtb mic middlebrook 7h9/glucose/bsa/tx - by Bioz Stars, 2026-09
90/100 stars
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casitone  (BioLife Solutions)
90
BioLife Solutions casitone
Chemoproteomic profiling of 1 and 2 identified HadA, HadB, and BCG_0547c (HadD) as targets. (A) Compounds 2 (blue) or 1 (red) were analyzed in a Mycobacterium bovis BCG protein extract with compound 3 and 4 attached to a bead matrix. Only three proteins showed competition by both compounds, HadA, HadB, and BCG_0547c (HadD). (B) Compound 1 (red) showed stronger inhibition of all three proteins from bead-binding in comparison to compound 2 (blue), indicating higher potency ( n = 3). (C) Correlation of target binding and antimycobacterial activity of compounds from the 1,3-diarylpyrazolyl-acylsulfonamide series. Active compounds ( 1 - 5 ) showed inhibition of proteins HadA, HadB, and BCG_0547c (HadD) from 4 -bead-binding, whereas inactive compounds ( 6 – 8 ) did not (results on 3 -beads are comparable, Figure S1 ). Numbers indicate compounds. r , Pearson correlation coefficient; p , p -value (calculated probability); pMIC99 defined as <t>−log10(</t> <t>Mtb</t> <t>MIC</t> 99 in M).
Casitone, supplied by BioLife Solutions, 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/casitone/casitone/pm25554388-71-6-7
Average 90 stars, based on 1 article reviews
casitone - by Bioz Stars, 2026-09
90/100 stars
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bactotm casitone medium  (Becton Dickinson)
90
Becton Dickinson bactotm casitone medium
Chemoproteomic profiling of 1 and 2 identified HadA, HadB, and BCG_0547c (HadD) as targets. (A) Compounds 2 (blue) or 1 (red) were analyzed in a Mycobacterium bovis BCG protein extract with compound 3 and 4 attached to a bead matrix. Only three proteins showed competition by both compounds, HadA, HadB, and BCG_0547c (HadD). (B) Compound 1 (red) showed stronger inhibition of all three proteins from bead-binding in comparison to compound 2 (blue), indicating higher potency ( n = 3). (C) Correlation of target binding and antimycobacterial activity of compounds from the 1,3-diarylpyrazolyl-acylsulfonamide series. Active compounds ( 1 - 5 ) showed inhibition of proteins HadA, HadB, and BCG_0547c (HadD) from 4 -bead-binding, whereas inactive compounds ( 6 – 8 ) did not (results on 3 -beads are comparable, Figure S1 ). Numbers indicate compounds. r , Pearson correlation coefficient; p , p -value (calculated probability); pMIC99 defined as <t>−log10(</t> <t>Mtb</t> <t>MIC</t> 99 in M).
Bactotm Casitone Medium, supplied by Becton Dickinson, 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/casitone/bactotm+casitone+medium/pm25014111-58-5-20
Average 90 stars, based on 1 article reviews
bactotm casitone medium - by Bioz Stars, 2026-09
90/100 stars
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casitone  (Becton Dickinson)
90
Becton Dickinson casitone
Chemoproteomic profiling of 1 and 2 identified HadA, HadB, and BCG_0547c (HadD) as targets. (A) Compounds 2 (blue) or 1 (red) were analyzed in a Mycobacterium bovis BCG protein extract with compound 3 and 4 attached to a bead matrix. Only three proteins showed competition by both compounds, HadA, HadB, and BCG_0547c (HadD). (B) Compound 1 (red) showed stronger inhibition of all three proteins from bead-binding in comparison to compound 2 (blue), indicating higher potency ( n = 3). (C) Correlation of target binding and antimycobacterial activity of compounds from the 1,3-diarylpyrazolyl-acylsulfonamide series. Active compounds ( 1 - 5 ) showed inhibition of proteins HadA, HadB, and BCG_0547c (HadD) from 4 -bead-binding, whereas inactive compounds ( 6 – 8 ) did not (results on 3 -beads are comparable, Figure S1 ). Numbers indicate compounds. r , Pearson correlation coefficient; p , p -value (calculated probability); pMIC99 defined as <t>−log10(</t> <t>Mtb</t> <t>MIC</t> 99 in M).
Casitone, supplied by Becton Dickinson, 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/casitone/casitone/pmc03961388-267-5-7
Average 90 stars, based on 1 article reviews
casitone - by Bioz Stars, 2026-09
90/100 stars
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casitone  (HiMedia Laboratories)
90
HiMedia Laboratories casitone
Chemoproteomic profiling of 1 and 2 identified HadA, HadB, and BCG_0547c (HadD) as targets. (A) Compounds 2 (blue) or 1 (red) were analyzed in a Mycobacterium bovis BCG protein extract with compound 3 and 4 attached to a bead matrix. Only three proteins showed competition by both compounds, HadA, HadB, and BCG_0547c (HadD). (B) Compound 1 (red) showed stronger inhibition of all three proteins from bead-binding in comparison to compound 2 (blue), indicating higher potency ( n = 3). (C) Correlation of target binding and antimycobacterial activity of compounds from the 1,3-diarylpyrazolyl-acylsulfonamide series. Active compounds ( 1 - 5 ) showed inhibition of proteins HadA, HadB, and BCG_0547c (HadD) from 4 -bead-binding, whereas inactive compounds ( 6 – 8 ) did not (results on 3 -beads are comparable, Figure S1 ). Numbers indicate compounds. r , Pearson correlation coefficient; p , p -value (calculated probability); pMIC99 defined as <t>−log10(</t> <t>Mtb</t> <t>MIC</t> 99 in M).
Casitone, supplied by HiMedia Laboratories, 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/casitone/casitone/pmc06367689-66-0-7
Average 90 stars, based on 1 article reviews
casitone - by Bioz Stars, 2026-09
90/100 stars
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bacto-casitone  (Becton Dickinson)
90
Becton Dickinson bacto-casitone
Chemoproteomic profiling of 1 and 2 identified HadA, HadB, and BCG_0547c (HadD) as targets. (A) Compounds 2 (blue) or 1 (red) were analyzed in a Mycobacterium bovis BCG protein extract with compound 3 and 4 attached to a bead matrix. Only three proteins showed competition by both compounds, HadA, HadB, and BCG_0547c (HadD). (B) Compound 1 (red) showed stronger inhibition of all three proteins from bead-binding in comparison to compound 2 (blue), indicating higher potency ( n = 3). (C) Correlation of target binding and antimycobacterial activity of compounds from the 1,3-diarylpyrazolyl-acylsulfonamide series. Active compounds ( 1 - 5 ) showed inhibition of proteins HadA, HadB, and BCG_0547c (HadD) from 4 -bead-binding, whereas inactive compounds ( 6 – 8 ) did not (results on 3 -beads are comparable, Figure S1 ). Numbers indicate compounds. r , Pearson correlation coefficient; p , p -value (calculated probability); pMIC99 defined as <t>−log10(</t> <t>Mtb</t> <t>MIC</t> 99 in M).
Bacto Casitone, supplied by Becton Dickinson, 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/casitone/bacto+casitone/10__1128_slash_jb__02081___12-32-15-17
Average 90 stars, based on 1 article reviews
bacto-casitone - by Bioz Stars, 2026-09
90/100 stars
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yeast casitone fatty acid (ycfa, anaerobe system inc., morgan hill, ca, usa)  (Anaerobe Systems Inc)
90
Anaerobe Systems Inc yeast casitone fatty acid (ycfa, anaerobe system inc., morgan hill, ca, usa)
Chemoproteomic profiling of 1 and 2 identified HadA, HadB, and BCG_0547c (HadD) as targets. (A) Compounds 2 (blue) or 1 (red) were analyzed in a Mycobacterium bovis BCG protein extract with compound 3 and 4 attached to a bead matrix. Only three proteins showed competition by both compounds, HadA, HadB, and BCG_0547c (HadD). (B) Compound 1 (red) showed stronger inhibition of all three proteins from bead-binding in comparison to compound 2 (blue), indicating higher potency ( n = 3). (C) Correlation of target binding and antimycobacterial activity of compounds from the 1,3-diarylpyrazolyl-acylsulfonamide series. Active compounds ( 1 - 5 ) showed inhibition of proteins HadA, HadB, and BCG_0547c (HadD) from 4 -bead-binding, whereas inactive compounds ( 6 – 8 ) did not (results on 3 -beads are comparable, Figure S1 ). Numbers indicate compounds. r , Pearson correlation coefficient; p , p -value (calculated probability); pMIC99 defined as <t>−log10(</t> <t>Mtb</t> <t>MIC</t> 99 in M).
Yeast Casitone Fatty Acid (Ycfa, Anaerobe System Inc., Morgan Hill, Ca, Usa), supplied by Anaerobe Systems Inc, 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/casitone/yeast+casitone+fatty+acid++ycfa++anaerobe+system+inc+++morgan+hill++ca++usa+/pm35805168-75-18-23
Average 90 stars, based on 1 article reviews
yeast casitone fatty acid (ycfa, anaerobe system inc., morgan hill, ca, usa) - by Bioz Stars, 2026-09
90/100 stars
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Image Search Results


Chemoproteomic profiling of 1 and 2 identified HadA, HadB, and BCG_0547c (HadD) as targets. (A) Compounds 2 (blue) or 1 (red) were analyzed in a Mycobacterium bovis BCG protein extract with compound 3 and 4 attached to a bead matrix. Only three proteins showed competition by both compounds, HadA, HadB, and BCG_0547c (HadD). (B) Compound 1 (red) showed stronger inhibition of all three proteins from bead-binding in comparison to compound 2 (blue), indicating higher potency ( n = 3). (C) Correlation of target binding and antimycobacterial activity of compounds from the 1,3-diarylpyrazolyl-acylsulfonamide series. Active compounds ( 1 - 5 ) showed inhibition of proteins HadA, HadB, and BCG_0547c (HadD) from 4 -bead-binding, whereas inactive compounds ( 6 – 8 ) did not (results on 3 -beads are comparable, Figure S1 ). Numbers indicate compounds. r , Pearson correlation coefficient; p , p -value (calculated probability); pMIC99 defined as −log10( Mtb MIC 99 in M).

Journal: ACS Infectious Diseases

Article Title: 1,3-Diarylpyrazolyl-acylsulfonamides Target HadAB/BC Complex in Mycobacterium tuberculosis

doi: 10.1021/acsinfecdis.2c00392

Figure Lengend Snippet: Chemoproteomic profiling of 1 and 2 identified HadA, HadB, and BCG_0547c (HadD) as targets. (A) Compounds 2 (blue) or 1 (red) were analyzed in a Mycobacterium bovis BCG protein extract with compound 3 and 4 attached to a bead matrix. Only three proteins showed competition by both compounds, HadA, HadB, and BCG_0547c (HadD). (B) Compound 1 (red) showed stronger inhibition of all three proteins from bead-binding in comparison to compound 2 (blue), indicating higher potency ( n = 3). (C) Correlation of target binding and antimycobacterial activity of compounds from the 1,3-diarylpyrazolyl-acylsulfonamide series. Active compounds ( 1 - 5 ) showed inhibition of proteins HadA, HadB, and BCG_0547c (HadD) from 4 -bead-binding, whereas inactive compounds ( 6 – 8 ) did not (results on 3 -beads are comparable, Figure S1 ). Numbers indicate compounds. r , Pearson correlation coefficient; p , p -value (calculated probability); pMIC99 defined as −log10( Mtb MIC 99 in M).

Article Snippet: Mtb MIC (Middlebrook 7H9/glucose/BSA/Tx) , 1.2 , 4.7.

Techniques: Inhibition, Binding Assay, Comparison, Activity Assay

Effect of 1,3-diarylpyrazolyl-acylsulfonamides on mycolic acid biosynthesis in Mycobacterium tuberculosis . Mtb H37Rv mc 2 6206 grown in Middlebrook 7H9-OADC-tyloxapol supplemented with casamino acids, pantothenate, and l -leucine at 37 °C was treated with no drug or 2 or 13 (1 to 6× MIC) and metabolically labeled with [1,2- 14 C]-acetate for 24 h. The same volume of [ 14 C]-acetate-labeled fatty acid and mycolic acid methyl esters (FAMEs and MAMEs) from treated and untreated cells were analyzed by TLC in the solvent system [ n -hexanes/ethyl acetate 95:5; by vol.; three developments] and revealed by PhosphorImaging. Compound 2 , a potent HadAB inhibitor, inhibited biosynthesis of mycolic acids up to 86% at 3× MIC in 24 h, whereas only 0–49% inhibition was observed with a weaker HadAB inhibitor 13 at 3× MIC.

Journal: ACS Infectious Diseases

Article Title: 1,3-Diarylpyrazolyl-acylsulfonamides Target HadAB/BC Complex in Mycobacterium tuberculosis

doi: 10.1021/acsinfecdis.2c00392

Figure Lengend Snippet: Effect of 1,3-diarylpyrazolyl-acylsulfonamides on mycolic acid biosynthesis in Mycobacterium tuberculosis . Mtb H37Rv mc 2 6206 grown in Middlebrook 7H9-OADC-tyloxapol supplemented with casamino acids, pantothenate, and l -leucine at 37 °C was treated with no drug or 2 or 13 (1 to 6× MIC) and metabolically labeled with [1,2- 14 C]-acetate for 24 h. The same volume of [ 14 C]-acetate-labeled fatty acid and mycolic acid methyl esters (FAMEs and MAMEs) from treated and untreated cells were analyzed by TLC in the solvent system [ n -hexanes/ethyl acetate 95:5; by vol.; three developments] and revealed by PhosphorImaging. Compound 2 , a potent HadAB inhibitor, inhibited biosynthesis of mycolic acids up to 86% at 3× MIC in 24 h, whereas only 0–49% inhibition was observed with a weaker HadAB inhibitor 13 at 3× MIC.

Article Snippet: Mtb MIC (Middlebrook 7H9/glucose/BSA/Tx) , 1.2 , 4.7.

Techniques: Metabolic Labelling, Labeling, Solvent, Inhibition

Mtb Whole-Cell Activities of 1 and 2

Journal: ACS Infectious Diseases

Article Title: 1,3-Diarylpyrazolyl-acylsulfonamides Target HadAB/BC Complex in Mycobacterium tuberculosis

doi: 10.1021/acsinfecdis.2c00392

Figure Lengend Snippet: Mtb Whole-Cell Activities of 1 and 2

Article Snippet: Mtb MIC (Middlebrook 7H9/glucose/BSA/Tx) , 1.2 , 4.7.

Techniques: Solubility