restriction enzyme apai Search Results


restriction enzyme apai  (Promega)
90
Promega restriction enzyme apai
Restriction Enzyme Apai, 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
https://www.bioz.com/result/restriction enzyme apai/product/Promega
Average 90 stars, based on 1 article reviews
restriction enzyme apai - by Bioz Stars, 2026-03
90/100 stars
  Buy from Supplier
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/result/restriction enzymes apai and noti/product/Biomatik
Average 90 stars, based on 1 article reviews
restriction enzymes apai and noti - by Bioz Stars, 2026-03
90/100 stars
  Buy from Supplier
restriction enzymes apai, avai, ecori, bsshii, xbai and hindiii  (Boehringer Mannheim)
90
Boehringer Mannheim restriction enzymes apai, avai, ecori, bsshii, xbai and hindiii
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, Avai, Ecori, Bsshii, Xbai And Hindiii, supplied by Boehringer Mannheim, 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/result/restriction enzymes apai, avai, ecori, bsshii, xbai and hindiii/product/Boehringer Mannheim
Average 90 stars, based on 1 article reviews
restriction enzymes apai, avai, ecori, bsshii, xbai and hindiii - by Bioz Stars, 2026-03
90/100 stars
  Buy from Supplier
restriction enzyme kpni  (Boehringer Mannheim)
90
Boehringer Mannheim restriction enzyme kpni
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 Kpni, supplied by Boehringer Mannheim, 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/result/restriction enzyme kpni/product/Boehringer Mannheim
Average 90 stars, based on 1 article reviews
restriction enzyme kpni - by Bioz Stars, 2026-03
90/100 stars
  Buy from Supplier
restriction enzyme apai r6361  (Promega)
90
Promega restriction enzyme apai r6361
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 Apai R6361, 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
https://www.bioz.com/result/restriction enzyme apai r6361/product/Promega
Average 90 stars, based on 1 article reviews
restriction enzyme apai r6361 - by Bioz Stars, 2026-03
90/100 stars
  Buy from Supplier
restriction enzymes apai, hpai, bglii, or ncoi  (NZYTech Inc)
90
NZYTech Inc restriction enzymes apai, hpai, bglii, or ncoi
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, Hpai, Bglii, Or Ncoi, 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/result/restriction enzymes apai, hpai, bglii, or ncoi/product/NZYTech Inc
Average 90 stars, based on 1 article reviews
restriction enzymes apai, hpai, bglii, or ncoi - by Bioz Stars, 2026-03
90/100 stars
  Buy from Supplier
restriction enzyme apai fastdigest  (Fisher Scientific)
90
Fisher Scientific restriction enzyme apai fastdigest
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 Apai Fastdigest, supplied by Fisher Scientific, 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/result/restriction enzyme apai fastdigest/product/Fisher Scientific
Average 90 stars, based on 1 article reviews
restriction enzyme apai fastdigest - by Bioz Stars, 2026-03
90/100 stars
  Buy from Supplier
restriction enzyme apai  (Amersham Life Sciences Inc)
90
Amersham Life Sciences Inc restriction enzyme apai
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 Apai, supplied by Amersham Life Sciences 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/result/restriction enzyme apai/product/Amersham Life Sciences Inc
Average 90 stars, based on 1 article reviews
restriction enzyme apai - by Bioz Stars, 2026-03
90/100 stars
  Buy from Supplier
0.5 ll of apai or taqi restriction enzyme (10 u ⁄ ll each)  (Promega)
90
Promega 0.5 ll of apai or taqi restriction enzyme (10 u ⁄ ll each)
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).
0.5 Ll Of Apai Or Taqi Restriction Enzyme (10 U ⁄ Ll Each), 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
https://www.bioz.com/result/0.5 ll of apai or taqi restriction enzyme (10 u ⁄ ll each)/product/Promega
Average 90 stars, based on 1 article reviews
0.5 ll of apai or taqi restriction enzyme (10 u ⁄ ll each) - by Bioz Stars, 2026-03
90/100 stars
  Buy from Supplier
restriction enzyme taxon apai  (Taxon Biosciences)
90
Taxon Biosciences restriction enzyme taxon apai
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 Taxon Apai, supplied by Taxon Biosciences, 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/result/restriction enzyme taxon apai/product/Taxon Biosciences
Average 90 stars, based on 1 article reviews
restriction enzyme taxon apai - by Bioz Stars, 2026-03
90/100 stars
  Buy from Supplier
restriction enzymes noti, kpni, saci, apai, ecori and bamhi  (Promega)
90
Promega restriction enzymes noti, kpni, saci, apai, ecori and bamhi
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 Noti, Kpni, Saci, Apai, Ecori And Bamhi, 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
https://www.bioz.com/result/restriction enzymes noti, kpni, saci, apai, ecori and bamhi/product/Promega
Average 90 stars, based on 1 article reviews
restriction enzymes noti, kpni, saci, apai, ecori and bamhi - by Bioz Stars, 2026-03
90/100 stars
  Buy from Supplier
restriction enzymes apai, bamhi, bglii, kpni, sali and xhoi  (Promega)
90
Promega restriction enzymes apai, bamhi, bglii, kpni, sali and xhoi
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, Bamhi, Bglii, Kpni, Sali And Xhoi, 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
https://www.bioz.com/result/restriction enzymes apai, bamhi, bglii, kpni, sali and xhoi/product/Promega
Average 90 stars, based on 1 article reviews
restriction enzymes apai, bamhi, bglii, kpni, sali and xhoi - by Bioz Stars, 2026-03
90/100 stars
  Buy from Supplier

Image Search Results


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