Virus Pathogen Database and Analysis Resource (ViPR) – Herpesviridae – Protein Details for LORF2 –

Detection of anatid herpesvirus 1 gC gene by TaqMan fluorescent quantitative real-time PCR with specific primers and probe. Polyclonal antibody against the DPV UL46M protein can be a diagnostic candidate. Purification of anatid herpesvirus 1 particles by tangential-flow ultrafiltration and sucrose gradient ultracentrifugation. Polyclonal antibody against the DPV UL46M protein can be a diagnostic candidate. Polyclonal antibody against the DPV UL46M protein can be a diagnostic candidate. Polyclonal antibody against the DPV UL46M protein can be a diagnostic candidate. Detection of anatid herpesvirus 1 gC gene by TaqMan fluorescent quantitative real-time PCR with specific primers and probe.

Detection of anatid herpesvirus 1 gC gene by TaqMan fluorescent quantitative real-time PCR with specific primers and probe. R. Detection of anatid herpesvirus 1 gC gene by TaqMan fluorescent quantitative real-time PCR with specific primers and probe. Anatid herpesvirus 1 (AHV-1) infection causes substantial economic losses to the world-wide waterfowl production. Polyclonal antibody against the DPV UL46M protein can be a diagnostic candidate. Detection of anatid herpesvirus 1 gC gene by TaqMan fluorescent quantitative real-time PCR with specific primers and probe. Detection of anatid herpesvirus 1 gC gene by TaqMan fluorescent quantitative real-time PCR with specific primers and probe.

Purification of anatid herpesvirus 1 particles by tangential-flow ultrafiltration and sucrose gradient ultracentrifugation. Purification of anatid herpesvirus 1 particles by tangential-flow ultrafiltration and sucrose gradient ultracentrifugation. Purification of anatid herpesvirus 1 particles by tangential-flow ultrafiltration and sucrose gradient ultracentrifugation. Methods MDBK was used as a model to study the precise signaling pathways of apoptosis induced by BHV-1 infection. Detection of anatid herpesvirus 1 gC gene by TaqMan fluorescent quantitative real-time PCR with specific primers and probe. Polyclonal antibody against the DPV UL46M protein can be a diagnostic candidate. However, in all groups of inoculated calves, limiting dilution analysis showed marked individual variability in the number of BHV1 specific T lymphocytes that were stimulated.

Polyclonal antibody against the DPV UL46M protein can be a diagnostic candidate. Detection of anatid herpesvirus 1 gC gene by TaqMan fluorescent quantitative real-time PCR with specific primers and probe. Polyclonal antibody against the DPV UL46M protein can be a diagnostic candidate. Template DNA was extracted from the viral and bacterial stock solutions using the High Pure PCR Template Preparation kit (Roche Diagnostics GmbH, Mannheim, Germany) according to the manufacturer’s instructions. Here we describe a fluorescent quantitative real-time PCR (FQ-PCR) method developed for fast measurement of AHV-1 DNA based on TaqMan MGB technology. Since prevention and early detection are presently the most logical strategies for virus control, the most effective way of controlling the disease would be by conducting routine screening of this virus [19]. Detection of anatid herpesvirus 1 gC gene by TaqMan fluorescent quantitative real-time PCR with specific primers and probe.

Polyclonal antibody against the DPV UL46M protein can be a diagnostic candidate. Other herpesviruses can infect are pigeon (Columbid herpesvirus 1), parrots (Psittacid herpesvirus 1 – Pacheco’s disease) and other species of pet or wild birds. Polyclonal antibody against the DPV UL46M protein can be a diagnostic candidate. Detection of anatid herpesvirus 1 gC gene by TaqMan fluorescent quantitative real-time PCR with specific primers and probe. Complete genome sequence of virulent duck enteritis virus (DEV) strain 2085 and comparison with genome sequences of virulent and attenuated DEV strains. The gK is one of the major envelope glycoproteins of DEV. Polyclonal antibody against the DPV UL46M protein can be a diagnostic candidate.

Detection of anatid herpesvirus 1 gC gene by TaqMan fluorescent quantitative real-time PCR with specific primers and probe. To explore the function of the UL37 N terminus, we used the three-dimensional framework provided by the structure in combination with evolutionary trace analysis to pinpoint several surface-exposed regions of potential functional importance and test their importance using mutagenesis. Polyclonal antibody against the DPV UL46M protein can be a diagnostic candidate. Abstract BackgroundMicroRNAs (miRNAs) are a group of short (~22 nt) noncoding RNAs that specifically regulate gene expression at the post-transcriptional level. The apparent inhibition constants were 1 to 3 muM. Polyclonal antibody against the DPV UL46M protein can be a diagnostic candidate. Purification of anatid herpesvirus 1 particles by tangential-flow ultrafiltration and sucrose gradient ultracentrifugation.

The genome encodes approximately 130 putative protein-coding genes, of which 70 are orthologs of conserved alphaherpesvirus and Mardivirus proteins. Since titration of the virus load is labor-consuming and requires about 5 days for evaluation of virus-induced CPE, distinguishing between virus-induced CPE and non-specific cell alterations may be difficult, the established real-time PCR assay will be particularly suitable in these studies. The close antigenic relationship amongst the mardiviruses has been exploited since the 1970s through the use of MeHV-1 as a live vaccine to reduce production losses resulting from MD [3]. The infection did not spread to other species on the same premises. The genome encodes approximately 130 putative protein-coding genes, of which 70 are orthologs of conserved alphaherpesvirus and Mardivirus proteins.