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nzycolour protein marker ii  (NZYTech Inc)

 
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    Structured Review

    NZYTech Inc nzycolour protein marker ii
    (A) Growth kinetic parameters of B. subtilis WT and mutants Δ msmX (IQB495), Δ msmX ΔS1254 (ISN51), Δ msmX frlPstop (ISN72) and P spank(hy) frlP (ISN15) were measured in CSK minimal medium supplemented with 0.1 % (wt/vol) arabinotriose as sole carbon and energy source and are shown as doubling time (min). Values above 500 min were considered no growth ( , ). The results represent at least three independent experiments and error bars represent standard deviation of the mean. (B) Representation of relative expression of frlP in the respective strains compared to the WT in CSK minimal medium supplemented with 0.1 % (wt/vol) arabinose. Primers ARA925 and ARA926 were used for frlP and fold-change was normalized using primers ARA583 and ARA584 for the 16S gene. Error bars represent standard deviation of the mean from C t values of at least three independent assays. (C) Western blot analysis of FrlP (c.a. 41.4 kDa) accumulation in total cell extracts of different B. subtilis strains. P spank(hy) - frlP (ISN15) and Δ frlP (IQB618) were used as positive and negative controls, respectively. <t>NZYColour</t> Protein Marker II (NZYTech) was applied as standard, and it is partially represented (MWM). The uncropped image of this bolt is presented in Fig. S3. Statistical significance of doubling time and fold-change of different strains compared to the respective controls is indicated (*p<0.05; **p<0.01; ***p<0.001).
    Nzycolour Protein Marker Ii, supplied by NZYTech 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/nzycolour+protein+marker+ii/bio_rxiv__2025__07__11__664333-214-27-31?v=NZYTech+Inc
    Average 90 stars, based on 1 article reviews
    nzycolour protein marker ii - by Bioz Stars, 2026-08
    90/100 stars

    Images

    1) Product Images from "FrlP, an ABC type I importer component of Bacillus subtilis : regulation and impact in bacterial fitness"

    Article Title: FrlP, an ABC type I importer component of Bacillus subtilis : regulation and impact in bacterial fitness

    Journal: bioRxiv

    doi: 10.1101/2025.07.11.664333

    (A) Growth kinetic parameters of B. subtilis WT and mutants Δ msmX (IQB495), Δ msmX ΔS1254 (ISN51), Δ msmX frlPstop (ISN72) and P spank(hy) frlP (ISN15) were measured in CSK minimal medium supplemented with 0.1 % (wt/vol) arabinotriose as sole carbon and energy source and are shown as doubling time (min). Values above 500 min were considered no growth ( , ). The results represent at least three independent experiments and error bars represent standard deviation of the mean. (B) Representation of relative expression of frlP in the respective strains compared to the WT in CSK minimal medium supplemented with 0.1 % (wt/vol) arabinose. Primers ARA925 and ARA926 were used for frlP and fold-change was normalized using primers ARA583 and ARA584 for the 16S gene. Error bars represent standard deviation of the mean from C t values of at least three independent assays. (C) Western blot analysis of FrlP (c.a. 41.4 kDa) accumulation in total cell extracts of different B. subtilis strains. P spank(hy) - frlP (ISN15) and Δ frlP (IQB618) were used as positive and negative controls, respectively. NZYColour Protein Marker II (NZYTech) was applied as standard, and it is partially represented (MWM). The uncropped image of this bolt is presented in Fig. S3. Statistical significance of doubling time and fold-change of different strains compared to the respective controls is indicated (*p<0.05; **p<0.01; ***p<0.001).
    Figure Legend Snippet: (A) Growth kinetic parameters of B. subtilis WT and mutants Δ msmX (IQB495), Δ msmX ΔS1254 (ISN51), Δ msmX frlPstop (ISN72) and P spank(hy) frlP (ISN15) were measured in CSK minimal medium supplemented with 0.1 % (wt/vol) arabinotriose as sole carbon and energy source and are shown as doubling time (min). Values above 500 min were considered no growth ( , ). The results represent at least three independent experiments and error bars represent standard deviation of the mean. (B) Representation of relative expression of frlP in the respective strains compared to the WT in CSK minimal medium supplemented with 0.1 % (wt/vol) arabinose. Primers ARA925 and ARA926 were used for frlP and fold-change was normalized using primers ARA583 and ARA584 for the 16S gene. Error bars represent standard deviation of the mean from C t values of at least three independent assays. (C) Western blot analysis of FrlP (c.a. 41.4 kDa) accumulation in total cell extracts of different B. subtilis strains. P spank(hy) - frlP (ISN15) and Δ frlP (IQB618) were used as positive and negative controls, respectively. NZYColour Protein Marker II (NZYTech) was applied as standard, and it is partially represented (MWM). The uncropped image of this bolt is presented in Fig. S3. Statistical significance of doubling time and fold-change of different strains compared to the respective controls is indicated (*p<0.05; **p<0.01; ***p<0.001).

    Techniques Used: Standard Deviation, Expressing, Western Blot, Marker



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    (A) Growth kinetic parameters of B. subtilis WT and mutants Δ msmX (IQB495), Δ msmX ΔS1254 (ISN51), Δ msmX frlPstop (ISN72) and P spank(hy) frlP (ISN15) were measured in CSK minimal medium supplemented with 0.1 % (wt/vol) arabinotriose as sole carbon and energy source and are shown as doubling time (min). Values above 500 min were considered no growth ( , ). The results represent at least three independent experiments and error bars represent standard deviation of the mean. (B) Representation of relative expression of frlP in the respective strains compared to the WT in CSK minimal medium supplemented with 0.1 % (wt/vol) arabinose. Primers ARA925 and ARA926 were used for frlP and fold-change was normalized using primers ARA583 and ARA584 for the 16S gene. Error bars represent standard deviation of the mean from C t values of at least three independent assays. (C) Western blot analysis of FrlP (c.a. 41.4 kDa) accumulation in total cell extracts of different B. subtilis strains. P spank(hy) - frlP (ISN15) and Δ frlP (IQB618) were used as positive and negative controls, respectively. <t>NZYColour</t> Protein Marker II (NZYTech) was applied as standard, and it is partially represented (MWM). The uncropped image of this bolt is presented in Fig. S3. Statistical significance of doubling time and fold-change of different strains compared to the respective controls is indicated (*p<0.05; **p<0.01; ***p<0.001).
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    (A) Growth kinetic parameters of B. subtilis WT and mutants Δ msmX (IQB495), Δ msmX ΔS1254 (ISN51), Δ msmX frlPstop (ISN72) and P spank(hy) frlP (ISN15) were measured in CSK minimal medium supplemented with 0.1 % (wt/vol) arabinotriose as sole carbon and energy source and are shown as doubling time (min). Values above 500 min were considered no growth ( , ). The results represent at least three independent experiments and error bars represent standard deviation of the mean. (B) Representation of relative expression of frlP in the respective strains compared to the WT in CSK minimal medium supplemented with 0.1 % (wt/vol) arabinose. Primers ARA925 and ARA926 were used for frlP and fold-change was normalized using primers ARA583 and ARA584 for the 16S gene. Error bars represent standard deviation of the mean from C t values of at least three independent assays. (C) Western blot analysis of FrlP (c.a. 41.4 kDa) accumulation in total cell extracts of different B. subtilis strains. P spank(hy) - frlP (ISN15) and Δ frlP (IQB618) were used as positive and negative controls, respectively. <t>NZYColour</t> Protein Marker II (NZYTech) was applied as standard, and it is partially represented (MWM). The uncropped image of this bolt is presented in Fig. S3. Statistical significance of doubling time and fold-change of different strains compared to the respective controls is indicated (*p<0.05; **p<0.01; ***p<0.001).
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    Image Search Results


    (A) Growth kinetic parameters of B. subtilis WT and mutants Δ msmX (IQB495), Δ msmX ΔS1254 (ISN51), Δ msmX frlPstop (ISN72) and P spank(hy) frlP (ISN15) were measured in CSK minimal medium supplemented with 0.1 % (wt/vol) arabinotriose as sole carbon and energy source and are shown as doubling time (min). Values above 500 min were considered no growth ( , ). The results represent at least three independent experiments and error bars represent standard deviation of the mean. (B) Representation of relative expression of frlP in the respective strains compared to the WT in CSK minimal medium supplemented with 0.1 % (wt/vol) arabinose. Primers ARA925 and ARA926 were used for frlP and fold-change was normalized using primers ARA583 and ARA584 for the 16S gene. Error bars represent standard deviation of the mean from C t values of at least three independent assays. (C) Western blot analysis of FrlP (c.a. 41.4 kDa) accumulation in total cell extracts of different B. subtilis strains. P spank(hy) - frlP (ISN15) and Δ frlP (IQB618) were used as positive and negative controls, respectively. NZYColour Protein Marker II (NZYTech) was applied as standard, and it is partially represented (MWM). The uncropped image of this bolt is presented in Fig. S3. Statistical significance of doubling time and fold-change of different strains compared to the respective controls is indicated (*p<0.05; **p<0.01; ***p<0.001).

    Journal: bioRxiv

    Article Title: FrlP, an ABC type I importer component of Bacillus subtilis : regulation and impact in bacterial fitness

    doi: 10.1101/2025.07.11.664333

    Figure Lengend Snippet: (A) Growth kinetic parameters of B. subtilis WT and mutants Δ msmX (IQB495), Δ msmX ΔS1254 (ISN51), Δ msmX frlPstop (ISN72) and P spank(hy) frlP (ISN15) were measured in CSK minimal medium supplemented with 0.1 % (wt/vol) arabinotriose as sole carbon and energy source and are shown as doubling time (min). Values above 500 min were considered no growth ( , ). The results represent at least three independent experiments and error bars represent standard deviation of the mean. (B) Representation of relative expression of frlP in the respective strains compared to the WT in CSK minimal medium supplemented with 0.1 % (wt/vol) arabinose. Primers ARA925 and ARA926 were used for frlP and fold-change was normalized using primers ARA583 and ARA584 for the 16S gene. Error bars represent standard deviation of the mean from C t values of at least three independent assays. (C) Western blot analysis of FrlP (c.a. 41.4 kDa) accumulation in total cell extracts of different B. subtilis strains. P spank(hy) - frlP (ISN15) and Δ frlP (IQB618) were used as positive and negative controls, respectively. NZYColour Protein Marker II (NZYTech) was applied as standard, and it is partially represented (MWM). The uncropped image of this bolt is presented in Fig. S3. Statistical significance of doubling time and fold-change of different strains compared to the respective controls is indicated (*p<0.05; **p<0.01; ***p<0.001).

    Article Snippet: 20 μg of total protein from each extract were loaded in a 12.5 % SDS-PAGE and run at constant electrical current (80 mA) for 50 min using NZYColour Protein Marker II (NZYTech) as standard.

    Techniques: Standard Deviation, Expressing, Western Blot, Marker