restriction enzyme noti Search Results


restriction enzyme noti  (Promega)
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Promega restriction enzyme noti
Restriction Enzyme Noti, supplied by Promega, 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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restriction enzyme noti  (Enzynomics co Ltd)
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Enzynomics co Ltd restriction enzyme noti
Restriction Enzyme Noti, supplied by Enzynomics 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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restriction enzymes kpni, xhoi, noti  (Promega)
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Promega restriction enzymes kpni, xhoi, noti
Restriction Enzymes Kpni, Xhoi, Noti, supplied by Promega, 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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restriction enzymes noti and bglii  (Promega)
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Promega restriction enzymes noti and bglii
Restriction Enzymes Noti And Bglii, supplied by Promega, 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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restriction enzymes ncoi, bamhi, noti, scai, xbai, bstxi  (GeneSearch Inc)
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GeneSearch Inc restriction enzymes ncoi, bamhi, noti, scai, xbai, bstxi
Restriction Enzymes Ncoi, Bamhi, Noti, Scai, Xbai, Bstxi, supplied by GeneSearch 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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restriction enzymes noti and spei  (Promega)
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Promega restriction enzymes noti and spei
Restriction Enzymes Noti And Spei, supplied by Promega, 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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restriction enzymes asci and noti  (Promega)
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Promega restriction enzymes asci and noti
Restriction Enzymes Asci And Noti, supplied by Promega, 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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noti -hf™ restriction enzyme  (Vilber Lourmat)
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Vilber Lourmat noti -hf™ restriction enzyme
Dendrogram, Showing the Genetic Relationships Between <t>the</t> <t>Bioluminescent</t> V. harveyi Strains Based on the Pulsed-Field Gel Electrophoresis Analysis of the Genomic Restriction Fragments Formed With the <t>NotI</t> -HF™
Noti Hf™ Restriction Enzyme, supplied by Vilber Lourmat, 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/restriction+enzyme+noti/pmc04584076-116-9-18?v=Vilber+Lourmat
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restriction enzymes noti and bg1ii  (Promega)
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Promega restriction enzymes noti and bg1ii
Dendrogram, Showing the Genetic Relationships Between <t>the</t> <t>Bioluminescent</t> V. harveyi Strains Based on the Pulsed-Field Gel Electrophoresis Analysis of the Genomic Restriction Fragments Formed With the <t>NotI</t> -HF™
Restriction Enzymes Noti And Bg1ii, supplied by Promega, 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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noti restriction enzyme  (SinaClon BioScience)
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SinaClon BioScience noti restriction enzyme
Dendrogram, Showing the Genetic Relationships Between <t>the</t> <t>Bioluminescent</t> V. harveyi Strains Based on the Pulsed-Field Gel Electrophoresis Analysis of the Genomic Restriction Fragments Formed With the <t>NotI</t> -HF™
Noti Restriction Enzyme, supplied by SinaClon BioScience, 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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restriction enzymes apai and noti  (Biomatik)
90
Biomatik restriction enzymes apai and noti
S1653R and E2124G human in muscle-specific A-kinase anchoring protein (mAKAP) single-nucleotide polymorphisms (SNPs) were successfully created by site-directed mutagenesis, and both mutants did not alter mAKAP expression along with β1- and β2-adrenergic receptors (β1- and β2-ARs). A: double digestion of <t>mutated</t> <t>plasmids</t> by the restriction enzymes ApaI and <t>NotI</t> with only two expected bands and no other contaminating bands on 1% Tris-acetate-EDTA gels, as provided by Biomatik. The DNA marker shows the corresponding molecular weight of DNA (in bp). B: representative Western blots showing mAKAP and GAPDH bands and quantification of the same using one-way ANOVA with Tukey’s multiple-comparison test. Three independent experiments (n = 3) of human embryonic kidney (HEK)-293T cell lysates were analyzed, and data are expressed as means ± SE. **P < 0.01 vs. control untransfected cells [control: 0.2409 ± 0.06368; wild type (WT): 1.417 ± 0.1330; S1653R: 1.261 ± 0.2145; E2124G: 1.375 ± 0.1905]. C: representative Western blots for β1- and β2-ARs along with GAPDH and quantification by one-way ANOVA with Tukey’s multiple-comparison test. Four independent experiments (n = 4) were performed, and data are expressed as means ± SE: β1-AR (control: 0.8779 ± 0.1198; WT: 1.005 ± 0.09496; S1653R: 1.015 ± 0.1226; E2124G: 0.9573 ± 0.05715) and β2-AR (control: 2.166 ± 0.08062; WT: 1.903 ± 0.1221; S1653R: 1.927 ± 0.2458; E2124G: 1.894 ± 0.1986).
Restriction Enzymes Apai And Noti, supplied by Biomatik, 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/restriction+enzyme+noti/pmc06087776-291-13-31?v=Biomatik
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restriction enzymes apai and noti - by Bioz Stars, 2026-08
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restriction enzyme noti  (Becton Dickinson)
90
Becton Dickinson restriction enzyme noti
S1653R and E2124G human in muscle-specific A-kinase anchoring protein (mAKAP) single-nucleotide polymorphisms (SNPs) were successfully created by site-directed mutagenesis, and both mutants did not alter mAKAP expression along with β1- and β2-adrenergic receptors (β1- and β2-ARs). A: double digestion of <t>mutated</t> <t>plasmids</t> by the restriction enzymes ApaI and <t>NotI</t> with only two expected bands and no other contaminating bands on 1% Tris-acetate-EDTA gels, as provided by Biomatik. The DNA marker shows the corresponding molecular weight of DNA (in bp). B: representative Western blots showing mAKAP and GAPDH bands and quantification of the same using one-way ANOVA with Tukey’s multiple-comparison test. Three independent experiments (n = 3) of human embryonic kidney (HEK)-293T cell lysates were analyzed, and data are expressed as means ± SE. **P < 0.01 vs. control untransfected cells [control: 0.2409 ± 0.06368; wild type (WT): 1.417 ± 0.1330; S1653R: 1.261 ± 0.2145; E2124G: 1.375 ± 0.1905]. C: representative Western blots for β1- and β2-ARs along with GAPDH and quantification by one-way ANOVA with Tukey’s multiple-comparison test. Four independent experiments (n = 4) were performed, and data are expressed as means ± SE: β1-AR (control: 0.8779 ± 0.1198; WT: 1.005 ± 0.09496; S1653R: 1.015 ± 0.1226; E2124G: 0.9573 ± 0.05715) and β2-AR (control: 2.166 ± 0.08062; WT: 1.903 ± 0.1221; S1653R: 1.927 ± 0.2458; E2124G: 1.894 ± 0.1986).
Restriction Enzyme Noti, 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/restriction+enzyme+noti/pm10337466-32-7-26?v=Becton+Dickinson
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Image Search Results


Dendrogram, Showing the Genetic Relationships Between the Bioluminescent V. harveyi Strains Based on the Pulsed-Field Gel Electrophoresis Analysis of the Genomic Restriction Fragments Formed With the NotI -HF™

Journal: Jundishapur Journal of Microbiology

Article Title: Determination of the Genetic Diversity of Different Bioluminescent Bacteria by Pulsed-Field Gel Electrophoresis (PFGE)

doi: 10.5812/jjm.28378v2

Figure Lengend Snippet: Dendrogram, Showing the Genetic Relationships Between the Bioluminescent V. harveyi Strains Based on the Pulsed-Field Gel Electrophoresis Analysis of the Genomic Restriction Fragments Formed With the NotI -HF™

Article Snippet: The band profile of the bioluminescent strains for the NotI -HF™ restriction enzyme was analyzed using Bio-Profil-1D++ software (Vilber Lourmat, Deutschland) at 10% homology coefficient.

Techniques: Pulsed-Field Gel, Electrophoresis

Dendrogram, Showing the Genetic Relationships Between the Bioluminescent V. gigantis Strains Based on the Pulsed-Field Gel Electrophoresis Analysis of the Genomic Restriction Fragments Formed With the NotI -HF™

Journal: Jundishapur Journal of Microbiology

Article Title: Determination of the Genetic Diversity of Different Bioluminescent Bacteria by Pulsed-Field Gel Electrophoresis (PFGE)

doi: 10.5812/jjm.28378v2

Figure Lengend Snippet: Dendrogram, Showing the Genetic Relationships Between the Bioluminescent V. gigantis Strains Based on the Pulsed-Field Gel Electrophoresis Analysis of the Genomic Restriction Fragments Formed With the NotI -HF™

Article Snippet: The band profile of the bioluminescent strains for the NotI -HF™ restriction enzyme was analyzed using Bio-Profil-1D++ software (Vilber Lourmat, Deutschland) at 10% homology coefficient.

Techniques: Pulsed-Field Gel, Electrophoresis

Dendrogram, Showing the Genetic Relationships Between the Bioluminescent V. lentus , V. azureus , V. orientalis , S. woodyi , V. crassostreae , A. fischeri , A. logei, and P. kishitanii Strains Based on the Pulsed-Field Gel Electrophoresis Analysis of the Genomic Restriction Fragments Formed with the NotI -HF™

Journal: Jundishapur Journal of Microbiology

Article Title: Determination of the Genetic Diversity of Different Bioluminescent Bacteria by Pulsed-Field Gel Electrophoresis (PFGE)

doi: 10.5812/jjm.28378v2

Figure Lengend Snippet: Dendrogram, Showing the Genetic Relationships Between the Bioluminescent V. lentus , V. azureus , V. orientalis , S. woodyi , V. crassostreae , A. fischeri , A. logei, and P. kishitanii Strains Based on the Pulsed-Field Gel Electrophoresis Analysis of the Genomic Restriction Fragments Formed with the NotI -HF™

Article Snippet: The band profile of the bioluminescent strains for the NotI -HF™ restriction enzyme was analyzed using Bio-Profil-1D++ software (Vilber Lourmat, Deutschland) at 10% homology coefficient.

Techniques: Pulsed-Field Gel, Electrophoresis

S1653R and E2124G human in muscle-specific A-kinase anchoring protein (mAKAP) single-nucleotide polymorphisms (SNPs) were successfully created by site-directed mutagenesis, and both mutants did not alter mAKAP expression along with β1- and β2-adrenergic receptors (β1- and β2-ARs). A: double digestion of mutated plasmids by the restriction enzymes ApaI and NotI with only two expected bands and no other contaminating bands on 1% Tris-acetate-EDTA gels, as provided by Biomatik. The DNA marker shows the corresponding molecular weight of DNA (in bp). B: representative Western blots showing mAKAP and GAPDH bands and quantification of the same using one-way ANOVA with Tukey’s multiple-comparison test. Three independent experiments (n = 3) of human embryonic kidney (HEK)-293T cell lysates were analyzed, and data are expressed as means ± SE. **P < 0.01 vs. control untransfected cells [control: 0.2409 ± 0.06368; wild type (WT): 1.417 ± 0.1330; S1653R: 1.261 ± 0.2145; E2124G: 1.375 ± 0.1905]. C: representative Western blots for β1- and β2-ARs along with GAPDH and quantification by one-way ANOVA with Tukey’s multiple-comparison test. Four independent experiments (n = 4) were performed, and data are expressed as means ± SE: β1-AR (control: 0.8779 ± 0.1198; WT: 1.005 ± 0.09496; S1653R: 1.015 ± 0.1226; E2124G: 0.9573 ± 0.05715) and β2-AR (control: 2.166 ± 0.08062; WT: 1.903 ± 0.1221; S1653R: 1.927 ± 0.2458; E2124G: 1.894 ± 0.1986).

Journal: American Journal of Physiology - Heart and Circulatory Physiology

Article Title: Human muscle-specific A-kinase anchoring protein polymorphisms modulate the susceptibility to cardiovascular diseases by altering cAMP/PKA signaling

doi: 10.1152/ajpheart.00034.2018

Figure Lengend Snippet: S1653R and E2124G human in muscle-specific A-kinase anchoring protein (mAKAP) single-nucleotide polymorphisms (SNPs) were successfully created by site-directed mutagenesis, and both mutants did not alter mAKAP expression along with β1- and β2-adrenergic receptors (β1- and β2-ARs). A: double digestion of mutated plasmids by the restriction enzymes ApaI and NotI with only two expected bands and no other contaminating bands on 1% Tris-acetate-EDTA gels, as provided by Biomatik. The DNA marker shows the corresponding molecular weight of DNA (in bp). B: representative Western blots showing mAKAP and GAPDH bands and quantification of the same using one-way ANOVA with Tukey’s multiple-comparison test. Three independent experiments (n = 3) of human embryonic kidney (HEK)-293T cell lysates were analyzed, and data are expressed as means ± SE. **P < 0.01 vs. control untransfected cells [control: 0.2409 ± 0.06368; wild type (WT): 1.417 ± 0.1330; S1653R: 1.261 ± 0.2145; E2124G: 1.375 ± 0.1905]. C: representative Western blots for β1- and β2-ARs along with GAPDH and quantification by one-way ANOVA with Tukey’s multiple-comparison test. Four independent experiments (n = 4) were performed, and data are expressed as means ± SE: β1-AR (control: 0.8779 ± 0.1198; WT: 1.005 ± 0.09496; S1653R: 1.015 ± 0.1226; E2124G: 0.9573 ± 0.05715) and β2-AR (control: 2.166 ± 0.08062; WT: 1.903 ± 0.1221; S1653R: 1.927 ± 0.2458; E2124G: 1.894 ± 0.1986).

Article Snippet: A : double digestion of mutated plasmids by the restriction enzymes ApaI and NotI with only two expected bands and no other contaminating bands on 1% Tris-acetate-EDTA gels, as provided by Biomatik.

Techniques: Mutagenesis, Expressing, Marker, Molecular Weight, Western Blot, Comparison, Control