Reverse transcription (RT) in situ polymerase chain reaction (PCR) experiment using a single stranded biotinylated oligonucleotide probe for the detection.

Slides:



Advertisements
Similar presentations
Figure 2 depicts the positions of the primers and the probe in a multiple alignment of the 5´NTR of various enteroviruses. Moreover, the sensitivity of.
Advertisements

The Polymerase Chain Reaction Some milestones In molecular biology recognised by the award of the Nobel prize.
PCR Optimization To optimize PCR the following must be evaluated and fine tuned Target DNA Too small or too large Good or poor quality Complete or incomplete.
Takehiko Wada, Jeffrey W. Pippin, Yoshio Terada, Stuart J. Shankland 
Midterm Review Feb
Fig. 4. Determination of the optimal dose of compound 48/80 in studying biomarkers for cutaneous neurogenic inflammation (CNI). (A) Reverse transcriptase-
Fig. 1. Algorithm for diagnosis and treatment of hypereosinophilia
Stephen Lory, PhD, Jeffrey K. Ichikawa, PhD  CHEST 
PCR Polymerase Chain Reaction
RT-PCR and qRT-PCR analyses of the hasA upstream region.
Hypereosinophilic Syndrome and Clonal Eosinophilia: Point-of-Care Diagnostic Algorithm and Treatment Update  Ayalew Tefferi, MD, Jason Gotlib, MD, Animesh.
Fatal human rabies infection confirmed with skin biopsy specimen
Demonstration of Helicobacter pylori by the four staining methods: (A) modified Giemsa, (B) anti-H pylori antibody immunostain, (C) modified McMullen's.
 (A,B) mRNA in situ hybridisation (ISH) with Epstein–Barr virus-encoded small RNA-1 probe in a case of Hodgkin’s lymphoma focally affecting the bone marrow.
 Pilomatricoma: (A) a multilobulated mass in fibrous stroma reaching the subcutis; (B) basaloid and ghost cells; (C) mitoses in an early lesion; and (D)
 (A–F) Hairy-cell leukaemia, haematoxylin and eosin (H&E) staining (A) ×40; (B) ×200; (C) TRAP, ×200; (D) CD25, ×200; (E) DBA44, ×200; (F) CD20, ×200.
Oligonucleotide sequences of polymerase chain reaction (PCR) primers and competitive templates. Oligonucleotide sequences of polymerase chain reaction.
(A) Histiocytes of duct ectasia, where in the absence of an intact duct, the histiocytic population can resemble the tumour cells of histiocytoid breast.
Frozen sections of (A) fetal intestine, (B) tonsil, and (C) mantle cell lymphoma, stained using anti-CD3 (immunoperoxidase; brown) followed by anti-CD5.
DEPARTMENT OF ERROR The Lancet Volume 362, Issue 9385, (August 2003)
Mismatch repair immunohistochemistry (MMR IHC).
Polymerase Chain Reaction
(A–C) Electron microscopic images obtained from two different cases, (A) a cluster of large malignant cells with cytoplasmic mucin vacuoles consistent.
Schematic representation of hepatitis E virus (HEV) genotype 3 in developed countries. Schematic representation of hepatitis E virus (HEV) genotype 3 in.
(A) 7-Deaza-2`-deoxyguanosine (deaza-dGTP) allows PCR of the human p16INK4A promoter because the specific 140 bp product (black arrow, 140) is clearly.
qRT-PCR analysis of expression profile of GbNAC1.
(A) Excision specimen of monophasic synovial sarcoma, showing a cellular neoplasm composed of loose fascicles of uniform spindle cells without significant.
APOE Gene Targeting (A) Schematic representation of the endogenous APOE locus, the gene targeting vector and the targeted APOE locus. The exons of the.
Impact of RTEL1 variants on telomere maintenance.
TOLLIP expression in nasal and alveolar epithelium.
Published in Thyroid. January 2014, 24(1): DOI: /thy
Neuroimaging and macroscopic features.
IFN and neutrophil gene expression studies.
(A) Haematoxylin and eosin stained section of multicentric Castleman's disease in a human immunodeficiency virus (HIV) positive patient showing a high.
Gel electrophoresis of measles virus cDNA amplicons (HU2 control measles virus RNA) amplified under optimised reaction conditions. Gel electrophoresis.
(A) Non-isotopic in situ hybridisation of human papillomavirus type 16 (HPV-16). (A) Non-isotopic in situ hybridisation of human papillomavirus type 16.
Agarose gel electrophoresis of DNA extracted from EDTA and formic acid decalcified bone marrow trephine biopsies. Agarose gel electrophoresis of DNA extracted.
x Ray diffraction photograph taken at PX7
Histological and immunohistochemical evaluation of primary central nervous system lymphoma. Histological and immunohistochemical evaluation of primary.
Detection of Ebola virus infection in nonfatal versus fatal cases.
T2 weighted (T2W), FLAIR (fluid attenuated inversion recovery), and T1W images demonstrate severe head atrophy with ex vacuo dilatation of the frontal.
Comparative genomic expressive hybridisation detection and quantification. Comparative genomic expressive hybridisation detection and quantification. (A)
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.
Agarose gel electrophoresis illustrating randomly amplified polymorphic DNA (RAPD) fingerprints of the four reference strains and 12 tick isolates produced.
Expression of selected genes in the ΔSMcomS strain in response to increasing concentrations of XIP. RT-PCR analysis of gene expression was performed in.
BEZ235 induces MAPK signaling in a FOXO3A-dependent manner.
Reverse transcriptase polymerase chain reaction (RT-PCR) analysis of EBNA1 promoter usage in Epstein-Barr virus (EBV) associated disorders. Reverse transcriptase.
Sensitivity and specificity plots of human epididymis protein 4 (HE4) (A and B, respectively) and carbohydrate antigen 125 (CA-125) (C and D, respectively)
RNAi screening formats.
Fig. 1. DEL-1 is expressed by human and mouse osteoclasts.
The sesquiterpene lactone PN up-regulates MDM2 and p53 proteins.
Schematic representation of Epstein-Barr virus (EBV) nuclear antigen 1 (EBNA1) transcripts derived from the four different promoters. Schematic representation.
Agarose gel electrophoresis illustrating randomly amplified polymorphic DNA (RAPD) fingerprints of the four reference strains and 12 tick isolates produced.
Agarose gel electrophoresis of ribosomal RNA gene polymerase chain reaction (PCR) products using Borrelia afzelii (top) and B burgdorferi sensu stricto.
Amplification curve from the MeVA RT-qPCR on the Roche LightCycler 480 system. Amplification curve from the MeVA RT-qPCR on the Roche LightCycler 480 system.
Specificity of the MeVA RT-qPCR assay, using an Applied Biosystems 7500 platform. Specificity of the MeVA RT-qPCR assay, using an Applied Biosystems 7500.
Diagram of the relationship between the T4 transcriptional pattern and the different mechanisms of DNA replication and recombination. Diagram of the relationship.
Fig. 2. Notch1 and hairy and enhancer of split (HES) 1 expression in psoriasis. (A) Quantitative reverse transcription polymerase chain reaction results.
SAF-1 expression in clinical breast cancer tissues.
Characterization of the complex formed at the Fra-1 RCE1.
 (A) Parathyroid imprint cytology showing the typical evenly stained round nuclei (May-Grünwald-Giemsa stain).  (A) Parathyroid imprint cytology showing.
A, gel retardation assay in colon cancer cell line SW480.
Establishment of HeLa/rtTAA/TRE-N1-IC cell line.
Hcy decreases VEGFR1/2 and Angs (Ang1, Ang2) gene transcription
(Left panel) Incidence of non-traumatic cardiac arrest (NTCA) per 100 000 population by age group and sex (n=8557): age or sex data were not recorded in.
Dahliae-resistant analysis of GbNAC1-silencing (TRV: GbNAC1) and control (TRV: 00) in Xinhai15 (G. barbadense L.). dahliae-resistant analysis of GbNAC1-silencing.
Optimization of incubation time for visibly stained spot formation in Vero-E6 infected by four serotype DENVs and the efficiency of DENV-4 plaque formation.
Analysis of TNF-α gene transcription and mRNA accumulation in THP-1 cells. Analysis of TNF-α gene transcription and mRNA accumulation in THP-1 cells. (A)
A representative case of coexisting granulomatous inflammation (black arrowheads) and squamous cell carcinoma (white arrows) in a lobectomy specimen in.
Presentation transcript:

Reverse transcription (RT) in situ polymerase chain reaction (PCR) experiment using a single stranded biotinylated oligonucleotide probe for the detection of the measles virus Nucleocapsid (N) gene in infected Vero cells. Reverse transcription (RT) in situ polymerase chain reaction (PCR) experiment using a single stranded biotinylated oligonucleotide probe for the detection of the measles virus Nucleocapsid (N) gene in infected Vero cells. Optimal cytoplasmic staining is achieved in (A) (1 μg/ml), higher probe concentrations in panels (B) (1.5 μg/ml) and (C) (2 μg/ml) showed increasing non-specific nuclear staining. V Uhlmann et al. Mol Path 2002;55:84-90 ©2002 by BMJ Publishing Group Ltd and Association of Clinical Pathologists