Nucleotide sequence alignment of porA gene sequences from the examined English Neisseria gonorrhoeae porA mutants, compared to the porA sequences of previously.

Slides:



Advertisements
Similar presentations
Figure S1. Alignment of sequences from the 5′-end to the Sm binding site of reported genomic sequences (9-15) for HSUR 1. MicroRNA binding sites are.
Advertisements

DETECTION OF THE VIRUSES BY USING RT-PCR
Supplemental Fig. S1 A B AtMYBS aa AtMYBS
22 kDa a-coixin gene cluster
Fig. 1. (A) The nucleotide and deduced amino acid sequences of the vacuolar serine protease protein of F. proliferatum (Fus p , GenBank accession.
From: Computational analysis of bacterial RNA-Seq data
A Common Human β Globin Splicing Mutation Modeled in Mice
Measures of discordancy among stable sexual partnerships across 20 countries in sub-Saharan Africa. Measures of discordancy among stable sexual partnerships.
Cross sectional comparisons of GAPDH and β-actin gene expression.
Oligonucleotide sequences of polymerase chain reaction (PCR) primers and competitive templates. Oligonucleotide sequences of polymerase chain reaction.
A Fast Real-Time Polymerase Chain Reaction Method for Sensitive and Specific Detection of the Neisseria gonorrhoeae porA Pseudogene  Stig Ove Hjelmevoll,
Accelerated Partner Therapy (APT) index patient and sex partner flow diagram, clinics A and B. (1) Number of clinic attenders diagnosed with chlamydia,
Catherine E. Keegan, Anthony A. Killeen 
ATF5 transactivates Egr-1 via the ATF5CON sites in the Egr-1 promoter.
Trans-Splicing to Spliceosomal U2 snRNA Suggests Disruption of Branch Site-U2 Pairing during Pre-mRNA Splicing  Duncan J. Smith, Charles C. Query, Maria.
Molecular cloning of pms916 salt hypersensitive T-DNA mutant.
Characterization of an Avian Influenza A (H5N1) Virus Isolated from a Child with a Fatal Respiratory Illness by Kanta Subbarao, Alexander Klimov, Jacqueline.
Yit-Heng Chooi, Ralph Cacho, Yi Tang  Chemistry & Biology 
Comparative phylogenetic analysis of sapoviruses based on complete RdRp and VP1 nucleotide sequences. Comparative phylogenetic analysis of sapoviruses.
Categorization of the top 200 N
Products seen by gel electrophoresis following two rounds of the multiplex herpesvirus PCR. The material in lanes 1–15 was derived from genital swabs.
Expression of a microRNA-Resistant Target Transgene Misrepresents the Functional Significance of the Endogenous microRNA: Target Gene Relationship  Junyan.
A highly sensitive novel PCR assay for detection of Pneumocystis jirovecii DNA in bronchoalveloar lavage specimens from immunocompromised patients  T.
Volume 26, Issue 13, Pages (July 2016)
Adapted viruses replicate in mismatched miR-122-expressing cells.
Volume 2, Issue 1, Pages (January 2009)
Genetic and molecular characterization of DicF-ftsZ mRNA interactions.
Phylogenetic tree of 38 Pseudomonas type strains, based on the V3-V5 region sequence of the 16S rRNA gene (V3 primer, positions 442 to 492; and V5 primer,
iraL shares sequence identity with iraM from E
The parameters in the Reference Group model fit by EPP
Alignment of wild-type and mosaic Neisseria gonorrhoeae mtr promoters with N. lactamica and N. meningitidis references. Alignment of wild-type and mosaic.
Two way sensitivity analyses of the sensitivity and specificity of HSV-2 type specific ELISA. Each line represents a different estimate of ELISA specificity.
Illustration of the mutation and ADA2 activity.
(A) Venn diagrams comparing Chlamydia trachomatis Chlamydia trachomatis (CT) and (B) Neisseria Neisseria gonorrhoeae (NG) percent positive results across.
Gel electrophoresis of measles virus cDNA amplicons (HU2 control measles virus RNA) amplified under optimised reaction conditions. Gel electrophoresis.
Inactivation of the Dp1 locus.
Fig. 4. Mutations induced by TALENs are heritable through the germline
Fig. 1. Generation of WNK3 knockout mice
Elevated expression of vegfaa in hemangiosarcoma.
The Bov-A2 element is conserved in the NOS2 gene of bovid species.
Alignment of the deduced amino acid sequences of the myosin light chain 2 (MLC2) proteins. Alignment of the deduced amino acid sequences of the myosin.
Fig. 6. F1 trβ mutants accomplish natural metamorphosis.
Multiple sequence alignment of Twisted gastrulation (TSG) proteins.
Genotyping the intron 22 XbaI A restriction fragment length polymorphism (RFLP) using long distance PCR (LD-PCR). Genotyping the intron 22 XbaI A restriction.
(A) The result of a qPCR assay comparing fluorescence with cycle number. (A) The result of a qPCR assay comparing fluorescence with cycle number. The results.
Amplicon sequencing analysis of on-target sites in trβ crispants
Multiplexed Mutagenesis Using the Csy4 System in Tomato Protoplasts.
Sequence variation of 16S rRNA gene primer-binding sites.
Target versatility. Target versatility. (A) Δctl0063, Δctl0064, Δctl0065, ΔtrpA, and wild-type C. trachomatis were analyzed by PCR with primers immediately.
Schematic representation of Epstein-Barr virus (EBV) nuclear antigen 1 (EBNA1) transcripts derived from the four different promoters. Schematic representation.
Nucleotide sequences of the IS1016-bexAdeletion region of type b strain Hib and type a strains 1, 2, and 5. Nucleotide sequences of the IS1016-bexAdeletion.
Mutation of the Ca2+ Channel β Subunit Gene Cchb4 Is Associated with Ataxia and Seizures in the Lethargic (lh) Mouse  Daniel L Burgess, Julie M Jones,
Agarose gel electrophoresis of ribosomal RNA gene polymerase chain reaction (PCR) products using Borrelia afzelii (top) and B burgdorferi sensu stricto.
Reverse transcription (RT) in situ polymerase chain reaction (PCR) experiment using a single stranded biotinylated oligonucleotide probe for the detection.
Phylogenetic tree of Mycoplasmagenitalium-positive samples using dual locus sequence typing. Phylogenetic tree of Mycoplasmagenitalium-positive samples.
(A) Bayesian phylogenetic tree of the H gene nucleotide alignment from tigers Pt2004 and Pt and representative CDV sequences obtained from GenBank.
* Supplementary Fig. 1 (Yamanaka et al.) * * * ** ** ** * * **
Targeting DCLK1 by miRNA-137.
Forest plot of various sensitivity analyses of the risk for pelvic inflammatory disease (PID), ectopic pregnancy and tubal factor infertility (TFI) between.
CCA1 Binds the Promoter of GI in Vitro and in Vivo.
Chest CT scans obtained at the time of first onset of illness (A), at the time of the first visit to our hospital (B), on the day of bronchoscopic examination.
Coloured dotplot of mortality rate per population in Scotland by age for those aged 30 to 89 years, from 1974 to 2015, stratified by sex for IHD.
Relationship of partial rpoB gene sequences inferred by the neighbor-joining method for Canadian study strains of C. pyruviciproducens. Relationship of.
Mean number of contacts of selected populations in an individual’s network and subpopulation size. Mean number of contacts of selected populations in an.
Lack of pilE expression in NZCM238 is associated with lower TNF-α secretion by 16HBE cells during coculture. Lack of pilE expression in NZCM238 is associated.
Deterministic model simulations representing the impact of STD syndromic management and mass antibiotic administration with comparisons to their impact.
A line drawing showing the measurements made on the ultrasound images in figs 2-5 (A–D, respectively), with arrows indicating the correct caliper position.
Confirmation of spliced RNA in cells transfected with a wild-type or Pol(−) MR766 ZIKV plasmid. Confirmation of spliced RNA in cells transfected with a.
Variability in measures of discordancy with respect to HIV prevalence across 20 countries in sub-Saharan Africa. Variability in measures of discordancy.
Fig. 3 Genome editing of the MSTN gene.
Presentation transcript:

Nucleotide sequence alignment of porA gene sequences from the examined English Neisseria gonorrhoeae porA mutants, compared to the porA sequences of previously identified porA mutants in Sweden,15 Scotland,14 and Australia,13 as well as the wild-type porA pseudogene sequence of N gonorrhoeae reference strain FA1090 (GenBank accession no. Nucleotide sequence alignment of porA gene sequences from the examined English Neisseria gonorrhoeae porA mutants, compared to the porA sequences of previously identified porA mutants in Sweden,15 Scotland,14 and Australia,13 as well as the wild-type porA pseudogene sequence of N gonorrhoeae reference strain FA1090 (GenBank accession no. AJ223447) and the porA gene sequence of Neisseria meningitidis strain 278 (GenBank accession no. GQ173789). Sequences in full boxes and in dashed boxes indicate PCR primer and probe binding sites for the porA pseudogene PCR described by Whiley et al11 and Hjelmevoll et al12 respectively. Catherine A Ison et al. Sex Transm Infect 2013;89:197-201 ©2013 by BMJ Publishing Group Ltd