Long-Term Effect of Ultrathin-Strut Versus Thin-Strut Drug-Eluting Stents in Patients With Small Vessel Coronary Artery Disease Undergoing Percutaneous Coronary Intervention: A Subgroup Analysis of the BIOSCIENCE Randomized Trial.
Orsiro randomized trials evaluating the biodegradable polymer sirolimus-eluting stent (BP-SES; 60 and 80 pM stent strut thickness to diameter ≤3 and> 3 mm, respectively) did not stratify according to size of the ship and failed to determine the impact of ultrathin- strut thickness the long-term clinical outcomes compared with a durable polymer everolimus-eluting stent (DP-EES).
We are trying to assess the long-term effects of ultrathin-strut (60 m) BP-SES compared to thin-strut (81 m) DP-ees on long-term outcomes in patients undergoing percutaneous coronary revascularization for small boats disease.In subgroup analysis of a randomized, multicenter, noninferiority trial Bioscience, patients with stable coronary artery disease or acute coronary syndrome were randomly assigned to treatment with BP-SES or DP-EES grouped by the size of the vessel (≤3 mm vs> 3 mm) as a replacement for comparing patients treated with ultrathin-thin-strut strut vs. drug-eluting stent. The primary endpoint is target lesion failure, a composite of cardiac death, target vessel myocardial infarction and clinically indicated target lesion revascularization, within 5 years.
RESULTS Among the 2109 patients, 1234 (59%) treated for small vessel disease. At 5 years, the target lesion failure occurred in 124 patients (cumulative incidence, 22.3%) were treated with ultrathin-strut BP-SES and 109 patients (18.3%) were treated with a thin-strut DP-EES (rate ratio, 1 , 22; 95% CI, 0.94 to 1.58; P = 0.13).
The cumulative incidence of cardiac death, target vessel myocardial infarction and clinically indicated target lesion revascularization and definite stent thrombosis at 5 years was similar in patients treated with ultrathin-strut BP-SES and thin-strut DP-EES. After adjustment for potential confounders, there was no significant interaction between treatment effect size of the ship and BP-SES compared to DP-EES. We found no significant differences in clinical outcomes throughout the 5 years between patients with small vessel disease treated with ultrathin-strut BP-SES compared to thin-strut DP-EES.URL
Long-Term Effect of Ultrathin-Strut Versus Thin-Strut Drug-Eluting Stents in Patients With Small Vessel Coronary Artery Disease Undergoing Percutaneous Coronary Intervention: A Subgroup Analysis of the BIOSCIENCE Randomized Trial.
ALFA-tag is a very versatile tool for nanobody-based bioscience applications.
Special epitope tags are widely used to detect, manipulate or purify proteins, but often they have limited flexibility. Here, we introduce ALFA-tags, epitope tags are designed rationally serves a very broad spectrum of applications in life sciences while outperformed tag was established as ha-, FLAG®- or myc-tag. ALFA-forms of α-helix tag is small and stable despite its position in the target protein functional in prokaryotic and eukaryotic hosts.
We characterize nanobody (NbALFA) binding protein ALFA-tag of the original specimen or stick with low picomolar affinity. It is suitable for super-resolution microscopy, immunoprecipitations and Western blotting, and also allows the in vivo detection of protein. We were shown a complex crystal structure that allows us to design a mutant nanobody (NbALFAPE) which allows the efficient purification step original ALFA-tagged proteins, complexes and even whole living cells using a peptide elution under physiological conditions.
Recent developments in genotyping technology coupled with the growing desire to characterize genomic variation in populations of Anopheles an opportunity to develop more effective strategies for the genotypes of high-throughput screening. A major obstacle of this objective is the extraction of nucleic acids.
Description: A sandwich quantitative ELISA assay kit for detection of Rat Histone Deacetylase 1 (HDAC1) in samples from tissue homogenates, cell lysates or other biological fluids.
Description: A sandwich quantitative ELISA assay kit for detection of Rat Histone Deacetylase 1 (HDAC1) in samples from tissue homogenates, cell lysates or other biological fluids.
Description: A polyclonal antibody against HDAC1. Recognizes HDAC1 from Human, Mouse, Rat. This antibody is Unconjugated. Tested in the following application: ELISA, WB, IHC;WB:1:500-1:3000, IHC:1:50-1:100
Description: A polyclonal antibody against HDAC1. Recognizes HDAC1 from Human, Mouse, Rat. This antibody is Unconjugated. Tested in the following application: ELISA, WB, IHC;WB:1:500-1:3000, IHC:1:50-1:100
Description: A polyclonal antibody against HDAC1. Recognizes HDAC1 from Human. This antibody is Unconjugated. Tested in the following application: ELISA, IHC, IF, ChIP; Recommended dilution: IHC:1:20-1:200, IF:1:100-1:500
Description: A polyclonal antibody against HDAC1. Recognizes HDAC1 from Human, Mouse, Rat. This antibody is Unconjugated. Tested in the following application: ELISA, IHC;ELISA:1:2000-1:5000, IHC:1:25-1:100
Description: A polyclonal antibody against HDAC1. Recognizes HDAC1 from Human, Mouse, Rat. This antibody is Unconjugated. Tested in the following application: WB, IHC, ELISA;WB:1/500-1/2000.IHC:1/100-1/300.ELISA:1/5000
Description: A polyclonal antibody against HDAC1. Recognizes HDAC1 from Human, Mouse, Rat. This antibody is Unconjugated. Tested in the following application: WB, IHC, IF, ELISA;WB:1/500-1/2000.IHC:1/100-1/300.IF:1/200-1/1000.ELISA:1/10000
Description: A polyclonal antibody against HDAC1. Recognizes HDAC1 from Human, Mouse, Rat. This antibody is Unconjugated. Tested in the following application: ELISA, WB, IHC;ELISA:1:1000-1:5000, WB:1:200-1:1000, IHC:1:10-1:50
Description: A polyclonal antibody against HDAC1. Recognizes HDAC1 from Human, Mouse, Rat. This antibody is Unconjugated. Tested in the following application: ELISA, WB, IHC;ELISA:1:1000-1:5000, WB:1:200-1:1000, IHC:1:25-1:100
Description: A polyclonal antibody against HDAC1. Recognizes HDAC1 from Human, Mouse, Rat. This antibody is Unconjugated. Tested in the following application: ELISA, WB, IHC;ELISA:1:1000-1:5000, WB:1:500-1:2000, IHC:1:25-1:100
Description: A polyclonal antibody against HDAC1. Recognizes HDAC1 from Human, Mouse, Rat. This antibody is Unconjugated. Tested in the following application: ELISA, WB, IHC, IF
Description: A polyclonal antibody against HDAC1. Recognizes HDAC1 from Human, Mouse, Rat. This antibody is Unconjugated. Tested in the following application: WB, ELISA;WB:1/500-1/2000.ELISA:1/20000
Description: The histone deacetylase (HDAC) family contains multiple members which are divided into four classes. Class I of the HDAC family comprises four members, HDAC1, 2, 3, and 8, each of which contains a deacetylase domain and exhibits a different, individual substrate specificity and function in vivo (1). HDAC1 is responsible for the deacetylation of lysine residues on the N-terminal part of the core histones (H2A, H2B, H3 and H4) (1,2). HDAC1 gives a tag for epigenetic repression and plays an important role in transcriptional regulation, cell cycle progression and developmental events (3,4).
Description: The histone deacetylase (HDAC) family contains multiple members which are divided into four classes. Class I of the HDAC family comprises four members, HDAC1, 2, 3, and 8, each of which contains a deacetylase domain and exhibits a different, individual substrate specificity and function in vivo (1). HDAC1 is responsible for the deacetylation of lysine residues on the N-terminal part of the core histones (H2A, H2B, H3 and H4) (1,2). HDAC1 gives a tag for epigenetic repression and plays an important role in transcriptional regulation, cell cycle progression and developmental events (3,4).
Description: A polyclonal antibody for detection of HDAC1 from Human, Mouse, Rat. This HDAC1 antibody is for WB, IHC-P, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from the Internal region of human HDAC1
Description: A polyclonal antibody for detection of HDAC1 from Human, Mouse, Rat. This HDAC1 antibody is for WB, IHC-P, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from the Internal region of human HDAC1
Description: A polyclonal antibody for detection of HDAC1 from Human, Mouse, Rat. This HDAC1 antibody is for WB, IHC-P, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from the Internal region of human HDAC1
Description: A polyclonal antibody for detection of HDAC1 from Human, Mouse, Rat. This HDAC1 antibody is for WB, IHC-P, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from human HDAC1 around the non-phosphorylation site of S421
Description: A polyclonal antibody for detection of HDAC1 from Human, Mouse, Rat. This HDAC1 antibody is for WB, IHC-P, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from human HDAC1 around the non-phosphorylation site of S421
Description: A polyclonal antibody for detection of HDAC1 from Human, Mouse, Rat. This HDAC1 antibody is for WB, IHC-P, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from human HDAC1 around the non-phosphorylation site of S421
Here, we test the feasibility of using an integral part of the foot of mosquitoes as the source of template DNA for whole genome amplification (WGA) by primer-extension preamplification. We use Agena Biosciences MassARRAY (®) platform (formerly Sequenom) to genotype SNPs 78 to 265 feet WGA samples.
Beau
