type strain m4  (ATCC)


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    ATCC type strain m4
    Cross reaction values of different strains of N2-fixing bacteria against Gluconacetobacter diazotrophicus antiserum.
    Type Strain M4, supplied by ATCC, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    type strain m4 - by Bioz Stars, 2023-01
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    Images

    1) Product Images from "Quantification of natural populations of Gluconacetobacter diazotrophicus and Herbaspirillum spp. In sugar cane ( Saccharum spp.) Using differente polyclonal antibodies"

    Article Title: Quantification of natural populations of Gluconacetobacter diazotrophicus and Herbaspirillum spp. In sugar cane ( Saccharum spp.) Using differente polyclonal antibodies

    Journal: Brazilian Journal of Microbiology

    doi: 10.1590/S1517-838220090004000018

    Cross reaction values of different strains of N2-fixing bacteria against Gluconacetobacter diazotrophicus antiserum.
    Figure Legend Snippet: Cross reaction values of different strains of N2-fixing bacteria against Gluconacetobacter diazotrophicus antiserum.

    Techniques Used: Purification

    Cross reaction values of different strains of N 2 -fixing bacteria against Herbaspirillum seropedicae antiserum
    Figure Legend Snippet: Cross reaction values of different strains of N 2 -fixing bacteria against Herbaspirillum seropedicae antiserum

    Techniques Used: Purification

    Cross reaction values of different strains of N2-fixing bacteria against Herbaspirillum  rubrisubalbicans  antiserum.
    Figure Legend Snippet: Cross reaction values of different strains of N2-fixing bacteria against Herbaspirillum rubrisubalbicans antiserum.

    Techniques Used: Purification

    Titre of the polyclonal antibodies produced against the species G. diazotrophicus, H. seropedicae and H. rubrisubalbicans . Primary antibodies (PA) used: anti-PR2 [GB-pH 3.0 (ptn 0.640 mg mL -1 ) and GB-pH 4.0 (ptn 0.205 mg mL- 1 )]; anti-PAL3 [GB-pH 3.0 (ptn 0.255 mg mL -1 ) and GB-pH 4.0 (ptn 0.342 mg mL -1 )]; anti-Z 67 [GB-pH 3.0 (ptn 0.473 mg mL -1 ) and GB-pH 4.0 (ptn 0.362 mg mL -1 )]; anti-HRC54 [GB-pH 3.0 (ptn 0.115 mg mL -1 ) and GB-pH 4.0 (ptn 0.285 mg mL- 1 )]; anti-M4 [GB-pH 3.0 (ptn 0.609 mg mL -1 ) and GB-pH 4.0 (ptn– 0.382 mg mL -1 )]; anti-HCC103 [GB-pH 3 .0 (ptn 0.117 mg mL -1 ) and GB-pH 4.0 (ptn 0. 330 mg mL -1 )]. The concentrations of antigens used were 10 8 cell mL -1 . Secondary antibody (SA) dilution was 1:300. The incubations with the antibodies were processed at 37 ºC for 30 min to PA and for 45 min to SA, after rotation at 300 rpm for 3 min. Reaction time with the ABTS substrate were inferior for 9 min at 100 rpm. Means of 4 replicates. The absorbance of the pre-immune serum was subtracted from the absorbance of the samples. Absorbance read at λ= 405 nm.
    Figure Legend Snippet: Titre of the polyclonal antibodies produced against the species G. diazotrophicus, H. seropedicae and H. rubrisubalbicans . Primary antibodies (PA) used: anti-PR2 [GB-pH 3.0 (ptn 0.640 mg mL -1 ) and GB-pH 4.0 (ptn 0.205 mg mL- 1 )]; anti-PAL3 [GB-pH 3.0 (ptn 0.255 mg mL -1 ) and GB-pH 4.0 (ptn 0.342 mg mL -1 )]; anti-Z 67 [GB-pH 3.0 (ptn 0.473 mg mL -1 ) and GB-pH 4.0 (ptn 0.362 mg mL -1 )]; anti-HRC54 [GB-pH 3.0 (ptn 0.115 mg mL -1 ) and GB-pH 4.0 (ptn 0.285 mg mL- 1 )]; anti-M4 [GB-pH 3.0 (ptn 0.609 mg mL -1 ) and GB-pH 4.0 (ptn– 0.382 mg mL -1 )]; anti-HCC103 [GB-pH 3 .0 (ptn 0.117 mg mL -1 ) and GB-pH 4.0 (ptn 0. 330 mg mL -1 )]. The concentrations of antigens used were 10 8 cell mL -1 . Secondary antibody (SA) dilution was 1:300. The incubations with the antibodies were processed at 37 ºC for 30 min to PA and for 45 min to SA, after rotation at 300 rpm for 3 min. Reaction time with the ABTS substrate were inferior for 9 min at 100 rpm. Means of 4 replicates. The absorbance of the pre-immune serum was subtracted from the absorbance of the samples. Absorbance read at λ= 405 nm.

    Techniques Used: Produced

    rubrisubalbicans  (ATCC)


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    ATCC rubrisubalbicans
    Cross reaction values of different strains of N2-fixing bacteria against Gluconacetobacter diazotrophicus antiserum.
    Rubrisubalbicans, supplied by ATCC, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    rubrisubalbicans - by Bioz Stars, 2023-01
    86/100 stars

    Images

    1) Product Images from "Quantification of natural populations of Gluconacetobacter diazotrophicus and Herbaspirillum spp. In sugar cane ( Saccharum spp.) Using differente polyclonal antibodies"

    Article Title: Quantification of natural populations of Gluconacetobacter diazotrophicus and Herbaspirillum spp. In sugar cane ( Saccharum spp.) Using differente polyclonal antibodies

    Journal: Brazilian Journal of Microbiology

    doi: 10.1590/S1517-838220090004000018

    Cross reaction values of different strains of N2-fixing bacteria against Gluconacetobacter diazotrophicus antiserum.
    Figure Legend Snippet: Cross reaction values of different strains of N2-fixing bacteria against Gluconacetobacter diazotrophicus antiserum.

    Techniques Used: Purification

    Cross reaction values of different strains of N 2 -fixing bacteria against Herbaspirillum seropedicae antiserum
    Figure Legend Snippet: Cross reaction values of different strains of N 2 -fixing bacteria against Herbaspirillum seropedicae antiserum

    Techniques Used: Purification

    Cross reaction values of different strains of N2-fixing bacteria against Herbaspirillum  rubrisubalbicans  antiserum.
    Figure Legend Snippet: Cross reaction values of different strains of N2-fixing bacteria against Herbaspirillum rubrisubalbicans antiserum.

    Techniques Used: Purification

    Titre of the polyclonal antibodies produced against the species G. diazotrophicus, H. seropedicae and H. rubrisubalbicans . Primary antibodies (PA) used: anti-PR2 [GB-pH 3.0 (ptn 0.640 mg mL -1 ) and GB-pH 4.0 (ptn 0.205 mg mL- 1 )]; anti-PAL3 [GB-pH 3.0 (ptn 0.255 mg mL -1 ) and GB-pH 4.0 (ptn 0.342 mg mL -1 )]; anti-Z 67 [GB-pH 3.0 (ptn 0.473 mg mL -1 ) and GB-pH 4.0 (ptn 0.362 mg mL -1 )]; anti-HRC54 [GB-pH 3.0 (ptn 0.115 mg mL -1 ) and GB-pH 4.0 (ptn 0.285 mg mL- 1 )]; anti-M4 [GB-pH 3.0 (ptn 0.609 mg mL -1 ) and GB-pH 4.0 (ptn– 0.382 mg mL -1 )]; anti-HCC103 [GB-pH 3 .0 (ptn 0.117 mg mL -1 ) and GB-pH 4.0 (ptn 0. 330 mg mL -1 )]. The concentrations of antigens used were 10 8 cell mL -1 . Secondary antibody (SA) dilution was 1:300. The incubations with the antibodies were processed at 37 ºC for 30 min to PA and for 45 min to SA, after rotation at 300 rpm for 3 min. Reaction time with the ABTS substrate were inferior for 9 min at 100 rpm. Means of 4 replicates. The absorbance of the pre-immune serum was subtracted from the absorbance of the samples. Absorbance read at λ= 405 nm.
    Figure Legend Snippet: Titre of the polyclonal antibodies produced against the species G. diazotrophicus, H. seropedicae and H. rubrisubalbicans . Primary antibodies (PA) used: anti-PR2 [GB-pH 3.0 (ptn 0.640 mg mL -1 ) and GB-pH 4.0 (ptn 0.205 mg mL- 1 )]; anti-PAL3 [GB-pH 3.0 (ptn 0.255 mg mL -1 ) and GB-pH 4.0 (ptn 0.342 mg mL -1 )]; anti-Z 67 [GB-pH 3.0 (ptn 0.473 mg mL -1 ) and GB-pH 4.0 (ptn 0.362 mg mL -1 )]; anti-HRC54 [GB-pH 3.0 (ptn 0.115 mg mL -1 ) and GB-pH 4.0 (ptn 0.285 mg mL- 1 )]; anti-M4 [GB-pH 3.0 (ptn 0.609 mg mL -1 ) and GB-pH 4.0 (ptn– 0.382 mg mL -1 )]; anti-HCC103 [GB-pH 3 .0 (ptn 0.117 mg mL -1 ) and GB-pH 4.0 (ptn 0. 330 mg mL -1 )]. The concentrations of antigens used were 10 8 cell mL -1 . Secondary antibody (SA) dilution was 1:300. The incubations with the antibodies were processed at 37 ºC for 30 min to PA and for 45 min to SA, after rotation at 300 rpm for 3 min. Reaction time with the ABTS substrate were inferior for 9 min at 100 rpm. Means of 4 replicates. The absorbance of the pre-immune serum was subtracted from the absorbance of the samples. Absorbance read at λ= 405 nm.

    Techniques Used: Produced

    type strain m4  (ATCC)


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    Structured Review

    ATCC type strain m4
    Cross reaction values of different strains of N2-fixing bacteria against Gluconacetobacter diazotrophicus antiserum.
    Type Strain M4, supplied by ATCC, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Average 94 stars, based on 1 article reviews
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    type strain m4 - by Bioz Stars, 2023-01
    94/100 stars

    Images

    1) Product Images from "Quantification of natural populations of Gluconacetobacter diazotrophicus and Herbaspirillum spp. In sugar cane ( Saccharum spp.) Using differente polyclonal antibodies"

    Article Title: Quantification of natural populations of Gluconacetobacter diazotrophicus and Herbaspirillum spp. In sugar cane ( Saccharum spp.) Using differente polyclonal antibodies

    Journal: Brazilian Journal of Microbiology

    doi: 10.1590/S1517-838220090004000018

    Cross reaction values of different strains of N2-fixing bacteria against Gluconacetobacter diazotrophicus antiserum.
    Figure Legend Snippet: Cross reaction values of different strains of N2-fixing bacteria against Gluconacetobacter diazotrophicus antiserum.

    Techniques Used: Purification

    Cross reaction values of different strains of N 2 -fixing bacteria against Herbaspirillum seropedicae antiserum
    Figure Legend Snippet: Cross reaction values of different strains of N 2 -fixing bacteria against Herbaspirillum seropedicae antiserum

    Techniques Used: Purification

    Cross reaction values of different strains of N2-fixing bacteria against Herbaspirillum  rubrisubalbicans  antiserum.
    Figure Legend Snippet: Cross reaction values of different strains of N2-fixing bacteria against Herbaspirillum rubrisubalbicans antiserum.

    Techniques Used: Purification

    Titre of the polyclonal antibodies produced against the species G. diazotrophicus, H. seropedicae and H. rubrisubalbicans . Primary antibodies (PA) used: anti-PR2 [GB-pH 3.0 (ptn 0.640 mg mL -1 ) and GB-pH 4.0 (ptn 0.205 mg mL- 1 )]; anti-PAL3 [GB-pH 3.0 (ptn 0.255 mg mL -1 ) and GB-pH 4.0 (ptn 0.342 mg mL -1 )]; anti-Z 67 [GB-pH 3.0 (ptn 0.473 mg mL -1 ) and GB-pH 4.0 (ptn 0.362 mg mL -1 )]; anti-HRC54 [GB-pH 3.0 (ptn 0.115 mg mL -1 ) and GB-pH 4.0 (ptn 0.285 mg mL- 1 )]; anti-M4 [GB-pH 3.0 (ptn 0.609 mg mL -1 ) and GB-pH 4.0 (ptn– 0.382 mg mL -1 )]; anti-HCC103 [GB-pH 3 .0 (ptn 0.117 mg mL -1 ) and GB-pH 4.0 (ptn 0. 330 mg mL -1 )]. The concentrations of antigens used were 10 8 cell mL -1 . Secondary antibody (SA) dilution was 1:300. The incubations with the antibodies were processed at 37 ºC for 30 min to PA and for 45 min to SA, after rotation at 300 rpm for 3 min. Reaction time with the ABTS substrate were inferior for 9 min at 100 rpm. Means of 4 replicates. The absorbance of the pre-immune serum was subtracted from the absorbance of the samples. Absorbance read at λ= 405 nm.
    Figure Legend Snippet: Titre of the polyclonal antibodies produced against the species G. diazotrophicus, H. seropedicae and H. rubrisubalbicans . Primary antibodies (PA) used: anti-PR2 [GB-pH 3.0 (ptn 0.640 mg mL -1 ) and GB-pH 4.0 (ptn 0.205 mg mL- 1 )]; anti-PAL3 [GB-pH 3.0 (ptn 0.255 mg mL -1 ) and GB-pH 4.0 (ptn 0.342 mg mL -1 )]; anti-Z 67 [GB-pH 3.0 (ptn 0.473 mg mL -1 ) and GB-pH 4.0 (ptn 0.362 mg mL -1 )]; anti-HRC54 [GB-pH 3.0 (ptn 0.115 mg mL -1 ) and GB-pH 4.0 (ptn 0.285 mg mL- 1 )]; anti-M4 [GB-pH 3.0 (ptn 0.609 mg mL -1 ) and GB-pH 4.0 (ptn– 0.382 mg mL -1 )]; anti-HCC103 [GB-pH 3 .0 (ptn 0.117 mg mL -1 ) and GB-pH 4.0 (ptn 0. 330 mg mL -1 )]. The concentrations of antigens used were 10 8 cell mL -1 . Secondary antibody (SA) dilution was 1:300. The incubations with the antibodies were processed at 37 ºC for 30 min to PA and for 45 min to SA, after rotation at 300 rpm for 3 min. Reaction time with the ABTS substrate were inferior for 9 min at 100 rpm. Means of 4 replicates. The absorbance of the pre-immune serum was subtracted from the absorbance of the samples. Absorbance read at λ= 405 nm.

    Techniques Used: Produced

    rubrisubalbicans os34  (ATCC)


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    ATCC rubrisubalbicans os34
    Plate assay of tannase activities. a Bacterial cells. WT00C: H. camelliae WT00C; WT00F: H. camelliae WT00F; Z67: H. seropedica e Z67; <t>Os34:</t> H. <t>rubrisubalbicans</t> Os34. b The purified enzymes. Tan1-4: four enzymes expressed respectively by 4 putative genes of H. camelliae WT00C in E.coli
    Rubrisubalbicans Os34, supplied by ATCC, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    rubrisubalbicans os34 - by Bioz Stars, 2023-01
    86/100 stars

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    1) Product Images from "Degradation of epigallocatechin and epicatechin gallates by a novel tannase Tan Hcw from Herbaspirillum camelliae"

    Article Title: Degradation of epigallocatechin and epicatechin gallates by a novel tannase Tan Hcw from Herbaspirillum camelliae

    Journal: Microbial Cell Factories

    doi: 10.1186/s12934-021-01685-1

    Plate assay of tannase activities. a Bacterial cells. WT00C: H. camelliae WT00C; WT00F: H. camelliae WT00F; Z67: H. seropedica e Z67; Os34: H. rubrisubalbicans Os34. b The purified enzymes. Tan1-4: four enzymes expressed respectively by 4 putative genes of H. camelliae WT00C in E.coli
    Figure Legend Snippet: Plate assay of tannase activities. a Bacterial cells. WT00C: H. camelliae WT00C; WT00F: H. camelliae WT00F; Z67: H. seropedica e Z67; Os34: H. rubrisubalbicans Os34. b The purified enzymes. Tan1-4: four enzymes expressed respectively by 4 putative genes of H. camelliae WT00C in E.coli

    Techniques Used: Purification

    herbaspirillum rubrisubalbicans nr112081 atcc 19308 unknown japan hu  (ATCC)


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    ATCC herbaspirillum rubrisubalbicans nr112081 atcc 19308 unknown japan hu
    Herbaspirillum Rubrisubalbicans Nr112081 Atcc 19308 Unknown Japan Hu, supplied by ATCC, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    rubrisubalbicans os34  (ATCC)


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    ATCC rubrisubalbicans os34
    Rubrisubalbicans Os34, supplied by ATCC, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    rubrisubalbicans os34  (ATCC)


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    ATCC rubrisubalbicans os34
    Rubrisubalbicans Os34, supplied by ATCC, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    herbaspirillum rubrisubalbicans atcc 19308  (ATCC)


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    ATCC herbaspirillum rubrisubalbicans atcc 19308
    Herbaspirillum Rubrisubalbicans Atcc 19308, supplied by ATCC, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    eudoraea adriatica dsm 19308t am745437 eudoraea chungangensis kctc 42048t  (ATCC)


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    ATCC eudoraea adriatica dsm 19308t am745437 eudoraea chungangensis kctc 42048t
    Eudoraea Adriatica Dsm 19308t Am745437 Eudoraea Chungangensis Kctc 42048t, supplied by ATCC, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    herbaspirillum rubrisubalbicans icmp 5777t af137508 herbaspirillum aquaticum ieh 4430t  (ATCC)


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    ATCC herbaspirillum rubrisubalbicans icmp 5777t af137508 herbaspirillum aquaticum ieh 4430t
    Herbaspirillum Rubrisubalbicans Icmp 5777t Af137508 Herbaspirillum Aquaticum Ieh 4430t, supplied by ATCC, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    herbaspirillum rubrisubalbicans atcc 19308t  (ATCC)


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    ATCC herbaspirillum rubrisubalbicans atcc 19308t
    Herbaspirillum Rubrisubalbicans Atcc 19308t, supplied by ATCC, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ATCC type strain m4
    Cross reaction values of different strains of N2-fixing bacteria against Gluconacetobacter diazotrophicus antiserum.
    Type Strain M4, supplied by ATCC, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ATCC rubrisubalbicans
    Cross reaction values of different strains of N2-fixing bacteria against Gluconacetobacter diazotrophicus antiserum.
    Rubrisubalbicans, supplied by ATCC, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ATCC rubrisubalbicans os34
    Plate assay of tannase activities. a Bacterial cells. WT00C: H. camelliae WT00C; WT00F: H. camelliae WT00F; Z67: H. seropedica e Z67; <t>Os34:</t> H. <t>rubrisubalbicans</t> Os34. b The purified enzymes. Tan1-4: four enzymes expressed respectively by 4 putative genes of H. camelliae WT00C in E.coli
    Rubrisubalbicans Os34, supplied by ATCC, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ATCC herbaspirillum rubrisubalbicans nr112081 atcc 19308 unknown japan hu
    Plate assay of tannase activities. a Bacterial cells. WT00C: H. camelliae WT00C; WT00F: H. camelliae WT00F; Z67: H. seropedica e Z67; <t>Os34:</t> H. <t>rubrisubalbicans</t> Os34. b The purified enzymes. Tan1-4: four enzymes expressed respectively by 4 putative genes of H. camelliae WT00C in E.coli
    Herbaspirillum Rubrisubalbicans Nr112081 Atcc 19308 Unknown Japan Hu, supplied by ATCC, 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/result/herbaspirillum rubrisubalbicans nr112081 atcc 19308 unknown japan hu/product/ATCC
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    94
    ATCC herbaspirillum rubrisubalbicans atcc 19308
    Plate assay of tannase activities. a Bacterial cells. WT00C: H. camelliae WT00C; WT00F: H. camelliae WT00F; Z67: H. seropedica e Z67; <t>Os34:</t> H. <t>rubrisubalbicans</t> Os34. b The purified enzymes. Tan1-4: four enzymes expressed respectively by 4 putative genes of H. camelliae WT00C in E.coli
    Herbaspirillum Rubrisubalbicans Atcc 19308, supplied by ATCC, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Average 94 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
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    94
    ATCC eudoraea adriatica dsm 19308t am745437 eudoraea chungangensis kctc 42048t
    Plate assay of tannase activities. a Bacterial cells. WT00C: H. camelliae WT00C; WT00F: H. camelliae WT00F; Z67: H. seropedica e Z67; <t>Os34:</t> H. <t>rubrisubalbicans</t> Os34. b The purified enzymes. Tan1-4: four enzymes expressed respectively by 4 putative genes of H. camelliae WT00C in E.coli
    Eudoraea Adriatica Dsm 19308t Am745437 Eudoraea Chungangensis Kctc 42048t, supplied by ATCC, 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/result/eudoraea adriatica dsm 19308t am745437 eudoraea chungangensis kctc 42048t/product/ATCC
    Average 94 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    eudoraea adriatica dsm 19308t am745437 eudoraea chungangensis kctc 42048t - by Bioz Stars, 2023-01
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    86
    ATCC herbaspirillum rubrisubalbicans icmp 5777t af137508 herbaspirillum aquaticum ieh 4430t
    Plate assay of tannase activities. a Bacterial cells. WT00C: H. camelliae WT00C; WT00F: H. camelliae WT00F; Z67: H. seropedica e Z67; <t>Os34:</t> H. <t>rubrisubalbicans</t> Os34. b The purified enzymes. Tan1-4: four enzymes expressed respectively by 4 putative genes of H. camelliae WT00C in E.coli
    Herbaspirillum Rubrisubalbicans Icmp 5777t Af137508 Herbaspirillum Aquaticum Ieh 4430t, supplied by ATCC, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/herbaspirillum rubrisubalbicans icmp 5777t af137508 herbaspirillum aquaticum ieh 4430t/product/ATCC
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    herbaspirillum rubrisubalbicans icmp 5777t af137508 herbaspirillum aquaticum ieh 4430t - by Bioz Stars, 2023-01
    86/100 stars
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    94
    ATCC herbaspirillum rubrisubalbicans atcc 19308t
    Plate assay of tannase activities. a Bacterial cells. WT00C: H. camelliae WT00C; WT00F: H. camelliae WT00F; Z67: H. seropedica e Z67; <t>Os34:</t> H. <t>rubrisubalbicans</t> Os34. b The purified enzymes. Tan1-4: four enzymes expressed respectively by 4 putative genes of H. camelliae WT00C in E.coli
    Herbaspirillum Rubrisubalbicans Atcc 19308t, supplied by ATCC, 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/result/herbaspirillum rubrisubalbicans atcc 19308t/product/ATCC
    Average 94 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    herbaspirillum rubrisubalbicans atcc 19308t - by Bioz Stars, 2023-01
    94/100 stars
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    Image Search Results


    Cross reaction values of different strains of N2-fixing bacteria against Gluconacetobacter diazotrophicus antiserum.

    Journal: Brazilian Journal of Microbiology

    Article Title: Quantification of natural populations of Gluconacetobacter diazotrophicus and Herbaspirillum spp. In sugar cane ( Saccharum spp.) Using differente polyclonal antibodies

    doi: 10.1590/S1517-838220090004000018

    Figure Lengend Snippet: Cross reaction values of different strains of N2-fixing bacteria against Gluconacetobacter diazotrophicus antiserum.

    Article Snippet: For H. rubrisubalbicans , type strain M4 (BR 11192, ATCC 19308, DSM 9440, LMG 2286) isolated from sugar cane in the USA was used, along with HCC103 (BR 11504) isolated from roots of sugar cane in Brazil.

    Techniques: Purification

    Cross reaction values of different strains of N 2 -fixing bacteria against Herbaspirillum seropedicae antiserum

    Journal: Brazilian Journal of Microbiology

    Article Title: Quantification of natural populations of Gluconacetobacter diazotrophicus and Herbaspirillum spp. In sugar cane ( Saccharum spp.) Using differente polyclonal antibodies

    doi: 10.1590/S1517-838220090004000018

    Figure Lengend Snippet: Cross reaction values of different strains of N 2 -fixing bacteria against Herbaspirillum seropedicae antiserum

    Article Snippet: For H. rubrisubalbicans , type strain M4 (BR 11192, ATCC 19308, DSM 9440, LMG 2286) isolated from sugar cane in the USA was used, along with HCC103 (BR 11504) isolated from roots of sugar cane in Brazil.

    Techniques: Purification

    Cross reaction values of different strains of N2-fixing bacteria against Herbaspirillum  rubrisubalbicans  antiserum.

    Journal: Brazilian Journal of Microbiology

    Article Title: Quantification of natural populations of Gluconacetobacter diazotrophicus and Herbaspirillum spp. In sugar cane ( Saccharum spp.) Using differente polyclonal antibodies

    doi: 10.1590/S1517-838220090004000018

    Figure Lengend Snippet: Cross reaction values of different strains of N2-fixing bacteria against Herbaspirillum rubrisubalbicans antiserum.

    Article Snippet: For H. rubrisubalbicans , type strain M4 (BR 11192, ATCC 19308, DSM 9440, LMG 2286) isolated from sugar cane in the USA was used, along with HCC103 (BR 11504) isolated from roots of sugar cane in Brazil.

    Techniques: Purification

    Titre of the polyclonal antibodies produced against the species G. diazotrophicus, H. seropedicae and H. rubrisubalbicans . Primary antibodies (PA) used: anti-PR2 [GB-pH 3.0 (ptn 0.640 mg mL -1 ) and GB-pH 4.0 (ptn 0.205 mg mL- 1 )]; anti-PAL3 [GB-pH 3.0 (ptn 0.255 mg mL -1 ) and GB-pH 4.0 (ptn 0.342 mg mL -1 )]; anti-Z 67 [GB-pH 3.0 (ptn 0.473 mg mL -1 ) and GB-pH 4.0 (ptn 0.362 mg mL -1 )]; anti-HRC54 [GB-pH 3.0 (ptn 0.115 mg mL -1 ) and GB-pH 4.0 (ptn 0.285 mg mL- 1 )]; anti-M4 [GB-pH 3.0 (ptn 0.609 mg mL -1 ) and GB-pH 4.0 (ptn– 0.382 mg mL -1 )]; anti-HCC103 [GB-pH 3 .0 (ptn 0.117 mg mL -1 ) and GB-pH 4.0 (ptn 0. 330 mg mL -1 )]. The concentrations of antigens used were 10 8 cell mL -1 . Secondary antibody (SA) dilution was 1:300. The incubations with the antibodies were processed at 37 ºC for 30 min to PA and for 45 min to SA, after rotation at 300 rpm for 3 min. Reaction time with the ABTS substrate were inferior for 9 min at 100 rpm. Means of 4 replicates. The absorbance of the pre-immune serum was subtracted from the absorbance of the samples. Absorbance read at λ= 405 nm.

    Journal: Brazilian Journal of Microbiology

    Article Title: Quantification of natural populations of Gluconacetobacter diazotrophicus and Herbaspirillum spp. In sugar cane ( Saccharum spp.) Using differente polyclonal antibodies

    doi: 10.1590/S1517-838220090004000018

    Figure Lengend Snippet: Titre of the polyclonal antibodies produced against the species G. diazotrophicus, H. seropedicae and H. rubrisubalbicans . Primary antibodies (PA) used: anti-PR2 [GB-pH 3.0 (ptn 0.640 mg mL -1 ) and GB-pH 4.0 (ptn 0.205 mg mL- 1 )]; anti-PAL3 [GB-pH 3.0 (ptn 0.255 mg mL -1 ) and GB-pH 4.0 (ptn 0.342 mg mL -1 )]; anti-Z 67 [GB-pH 3.0 (ptn 0.473 mg mL -1 ) and GB-pH 4.0 (ptn 0.362 mg mL -1 )]; anti-HRC54 [GB-pH 3.0 (ptn 0.115 mg mL -1 ) and GB-pH 4.0 (ptn 0.285 mg mL- 1 )]; anti-M4 [GB-pH 3.0 (ptn 0.609 mg mL -1 ) and GB-pH 4.0 (ptn– 0.382 mg mL -1 )]; anti-HCC103 [GB-pH 3 .0 (ptn 0.117 mg mL -1 ) and GB-pH 4.0 (ptn 0. 330 mg mL -1 )]. The concentrations of antigens used were 10 8 cell mL -1 . Secondary antibody (SA) dilution was 1:300. The incubations with the antibodies were processed at 37 ºC for 30 min to PA and for 45 min to SA, after rotation at 300 rpm for 3 min. Reaction time with the ABTS substrate were inferior for 9 min at 100 rpm. Means of 4 replicates. The absorbance of the pre-immune serum was subtracted from the absorbance of the samples. Absorbance read at λ= 405 nm.

    Article Snippet: For H. rubrisubalbicans , type strain M4 (BR 11192, ATCC 19308, DSM 9440, LMG 2286) isolated from sugar cane in the USA was used, along with HCC103 (BR 11504) isolated from roots of sugar cane in Brazil.

    Techniques: Produced

    Cross reaction values of different strains of N2-fixing bacteria against Gluconacetobacter diazotrophicus antiserum.

    Journal: Brazilian Journal of Microbiology

    Article Title: Quantification of natural populations of Gluconacetobacter diazotrophicus and Herbaspirillum spp. In sugar cane ( Saccharum spp.) Using differente polyclonal antibodies

    doi: 10.1590/S1517-838220090004000018

    Figure Lengend Snippet: Cross reaction values of different strains of N2-fixing bacteria against Gluconacetobacter diazotrophicus antiserum.

    Article Snippet: For H. rubrisubalbicans , type strain M4 (BR 11192, ATCC 19308, DSM 9440, LMG 2286) isolated from sugar cane in the USA was used, along with HCC103 (BR 11504) isolated from roots of sugar cane in Brazil.

    Techniques: Purification

    Cross reaction values of different strains of N 2 -fixing bacteria against Herbaspirillum seropedicae antiserum

    Journal: Brazilian Journal of Microbiology

    Article Title: Quantification of natural populations of Gluconacetobacter diazotrophicus and Herbaspirillum spp. In sugar cane ( Saccharum spp.) Using differente polyclonal antibodies

    doi: 10.1590/S1517-838220090004000018

    Figure Lengend Snippet: Cross reaction values of different strains of N 2 -fixing bacteria against Herbaspirillum seropedicae antiserum

    Article Snippet: For H. rubrisubalbicans , type strain M4 (BR 11192, ATCC 19308, DSM 9440, LMG 2286) isolated from sugar cane in the USA was used, along with HCC103 (BR 11504) isolated from roots of sugar cane in Brazil.

    Techniques: Purification

    Cross reaction values of different strains of N2-fixing bacteria against Herbaspirillum  rubrisubalbicans  antiserum.

    Journal: Brazilian Journal of Microbiology

    Article Title: Quantification of natural populations of Gluconacetobacter diazotrophicus and Herbaspirillum spp. In sugar cane ( Saccharum spp.) Using differente polyclonal antibodies

    doi: 10.1590/S1517-838220090004000018

    Figure Lengend Snippet: Cross reaction values of different strains of N2-fixing bacteria against Herbaspirillum rubrisubalbicans antiserum.

    Article Snippet: For H. rubrisubalbicans , type strain M4 (BR 11192, ATCC 19308, DSM 9440, LMG 2286) isolated from sugar cane in the USA was used, along with HCC103 (BR 11504) isolated from roots of sugar cane in Brazil.

    Techniques: Purification

    Titre of the polyclonal antibodies produced against the species G. diazotrophicus, H. seropedicae and H. rubrisubalbicans . Primary antibodies (PA) used: anti-PR2 [GB-pH 3.0 (ptn 0.640 mg mL -1 ) and GB-pH 4.0 (ptn 0.205 mg mL- 1 )]; anti-PAL3 [GB-pH 3.0 (ptn 0.255 mg mL -1 ) and GB-pH 4.0 (ptn 0.342 mg mL -1 )]; anti-Z 67 [GB-pH 3.0 (ptn 0.473 mg mL -1 ) and GB-pH 4.0 (ptn 0.362 mg mL -1 )]; anti-HRC54 [GB-pH 3.0 (ptn 0.115 mg mL -1 ) and GB-pH 4.0 (ptn 0.285 mg mL- 1 )]; anti-M4 [GB-pH 3.0 (ptn 0.609 mg mL -1 ) and GB-pH 4.0 (ptn– 0.382 mg mL -1 )]; anti-HCC103 [GB-pH 3 .0 (ptn 0.117 mg mL -1 ) and GB-pH 4.0 (ptn 0. 330 mg mL -1 )]. The concentrations of antigens used were 10 8 cell mL -1 . Secondary antibody (SA) dilution was 1:300. The incubations with the antibodies were processed at 37 ºC for 30 min to PA and for 45 min to SA, after rotation at 300 rpm for 3 min. Reaction time with the ABTS substrate were inferior for 9 min at 100 rpm. Means of 4 replicates. The absorbance of the pre-immune serum was subtracted from the absorbance of the samples. Absorbance read at λ= 405 nm.

    Journal: Brazilian Journal of Microbiology

    Article Title: Quantification of natural populations of Gluconacetobacter diazotrophicus and Herbaspirillum spp. In sugar cane ( Saccharum spp.) Using differente polyclonal antibodies

    doi: 10.1590/S1517-838220090004000018

    Figure Lengend Snippet: Titre of the polyclonal antibodies produced against the species G. diazotrophicus, H. seropedicae and H. rubrisubalbicans . Primary antibodies (PA) used: anti-PR2 [GB-pH 3.0 (ptn 0.640 mg mL -1 ) and GB-pH 4.0 (ptn 0.205 mg mL- 1 )]; anti-PAL3 [GB-pH 3.0 (ptn 0.255 mg mL -1 ) and GB-pH 4.0 (ptn 0.342 mg mL -1 )]; anti-Z 67 [GB-pH 3.0 (ptn 0.473 mg mL -1 ) and GB-pH 4.0 (ptn 0.362 mg mL -1 )]; anti-HRC54 [GB-pH 3.0 (ptn 0.115 mg mL -1 ) and GB-pH 4.0 (ptn 0.285 mg mL- 1 )]; anti-M4 [GB-pH 3.0 (ptn 0.609 mg mL -1 ) and GB-pH 4.0 (ptn– 0.382 mg mL -1 )]; anti-HCC103 [GB-pH 3 .0 (ptn 0.117 mg mL -1 ) and GB-pH 4.0 (ptn 0. 330 mg mL -1 )]. The concentrations of antigens used were 10 8 cell mL -1 . Secondary antibody (SA) dilution was 1:300. The incubations with the antibodies were processed at 37 ºC for 30 min to PA and for 45 min to SA, after rotation at 300 rpm for 3 min. Reaction time with the ABTS substrate were inferior for 9 min at 100 rpm. Means of 4 replicates. The absorbance of the pre-immune serum was subtracted from the absorbance of the samples. Absorbance read at λ= 405 nm.

    Article Snippet: For H. rubrisubalbicans , type strain M4 (BR 11192, ATCC 19308, DSM 9440, LMG 2286) isolated from sugar cane in the USA was used, along with HCC103 (BR 11504) isolated from roots of sugar cane in Brazil.

    Techniques: Produced

    Plate assay of tannase activities. a Bacterial cells. WT00C: H. camelliae WT00C; WT00F: H. camelliae WT00F; Z67: H. seropedica e Z67; Os34: H. rubrisubalbicans Os34. b The purified enzymes. Tan1-4: four enzymes expressed respectively by 4 putative genes of H. camelliae WT00C in E.coli

    Journal: Microbial Cell Factories

    Article Title: Degradation of epigallocatechin and epicatechin gallates by a novel tannase Tan Hcw from Herbaspirillum camelliae

    doi: 10.1186/s12934-021-01685-1

    Figure Lengend Snippet: Plate assay of tannase activities. a Bacterial cells. WT00C: H. camelliae WT00C; WT00F: H. camelliae WT00F; Z67: H. seropedica e Z67; Os34: H. rubrisubalbicans Os34. b The purified enzymes. Tan1-4: four enzymes expressed respectively by 4 putative genes of H. camelliae WT00C in E.coli

    Article Snippet: H. rubrisubalbicans Os34 [ ] was given by Zhejiang University as a gift, and H. seropedica e Z67 [ ] (#ATCC35892) was purchased from ATCC (American Type Culture and Collection).

    Techniques: Purification