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Probes for INS

ACD can configure probes for the various manual and automated assays for INS for RNAscope Assay, or for Basescope Assay compatible for your species of interest.

  • Probes for INS (0)
  • Kits & Accessories (0)
  • Support & Documents (0)
  • Publications (2)
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Refine Probe List

Content for comparison

Gene

  • TBD (3) Apply TBD filter
  • C. felis 18S (2) Apply C. felis 18S filter
  • (-) Remove ORF1ab FIPV filter ORF1ab FIPV (2)
  • GAPDH (1) Apply GAPDH filter
  • TNF-α (1) Apply TNF-α filter
  • Il-6 (1) Apply Il-6 filter
  • PCV3 (1) Apply PCV3 filter
  • MAPK8 (1) Apply MAPK8 filter
  • FcaGHV1 (1) Apply FcaGHV1 filter
  • C. felis GAPDH (1) Apply C. felis GAPDH filter
  • PRRSV (1) Apply PRRSV filter
  • EqPV-H VP1 (1) Apply EqPV-H VP1 filter
  • PaBV4 (1) Apply PaBV4 filter
  • SVA (1) Apply SVA filter
  • BPV-1 / 2 (1) Apply BPV-1 / 2 filter
  • RHDV2 VP60 (1) Apply RHDV2 VP60 filter
  • IALNCR (1) Apply IALNCR filter
  • RusV (1) Apply RusV filter
  • TFV1 (1) Apply TFV1 filter
  • MCP (1) Apply MCP filter

Product

  • RNAscope 2.5 HD Red assay (1) Apply RNAscope 2.5 HD Red assay filter
  • RNAscope 2.5 LS Assay (1) Apply RNAscope 2.5 LS Assay filter

Research area

  • (-) Remove Other: Zoological Disease filter Other: Zoological Disease (2)
  • Cat Virus (2) Apply Cat Virus filter
  • Feline Coronavirus (1) Apply Feline Coronavirus filter
  • Feline infectious peritonitis (1) Apply Feline infectious peritonitis filter
  • Feline infectious peritonitis (Covid) (1) Apply Feline infectious peritonitis (Covid) filter

Category

  • Publications (2) Apply Publications filter
Relationship between Uveal Inflammation and Viral Detection in 30 Cats with Feline Infectious Peritonitis

Pathogens (Basel, Switzerland)

2022 Aug 05

Carossino, M;Del Piero, F;Lee, J;Needle, DB;Levine, JM;Riis, RR;Maes, R;Wise, AG;Mullaney, K;Ferracone, J;Langohr, IM;
PMID: 36015004 | DOI: 10.3390/pathogens11080883

Feline infectious peritonitis (FIP) virus is the most common infectious cause of uveitis in cats. Confirmatory diagnosis is usually only reached at postmortem examination. The relationship between the histologic inflammatory pattern, which depends on the stage of the disease, and the likelihood of detection of the viral antigen and/or RNA has not been investigated. We hypothesized that viral detection rate by either immunohistochemistry, in situ hybridization or RT-qPCR is dependent upon the predominant type of uveal inflammatory response (i.e., pyogranulomatous vs. plasmacytic). Thus, the aims of this study were to evaluate cases of FIP-induced uveitis, localize the viral antigen and RNA, and assess the relationship between the inflammatory pattern (macrophage- vs. plasma cell-rich) and the likelihood of detecting the FIP antigen and/or RNA. We evaluated 30 cats with FIP-induced uveitis. The viral antigen and/or RNA were detected within uveal macrophages in 11/30 cases, of which 8 tested positive by RT-qPCR. Correlation analysis determined a weak to moderate but significant negative correlation between the degree of plasmacytic uveal inflammation and the likelihood of detecting the FIP antigen and RNA. This study suggests that predominance of plasmacytic inflammation in cases of FIP uveitis reduces the odds of a confirmatory diagnosis through the viral detection methods available.
RNA in-situ hybridization for pathology-based diagnosis of feline infectious peritonitis (FIP): current diagnostics for FIP and comparison to the current gold standard

Qeios

2022 Aug 02

Sweet, A; Andre, N; Licitra BN; Whittaker, B
| DOI: 10.32388/bv6713

The authors made a thorough study on the comparison of the gold standard method, IHC with a newly established RNAscope ISH method. The manuscript is clear, well-written, and uses appropriate English language. It starts with a clear introduction and review of current knowledge on FCoV/FIP, then goes into details on the key diagnostic methods we can use currently. The authors proved, that RNAscope ISH is sensitive and specific, more sensitive than the IHC method - therefore it can be used better in clinical and research settings as well. Images seem to be free of manipulation, and they explain clearly the difference between IHC and ISH.
X
Description
sense
Example: Hs-LAG3-sense
Standard probes for RNA detection are in antisense. Sense probe is reverse complent to the corresponding antisense probe.
Intron#
Example: Mm-Htt-intron2
Probe targets the indicated intron in the target gene, commonly used for pre-mRNA detection
Pool/Pan
Example: Hs-CD3-pool (Hs-CD3D, Hs-CD3E, Hs-CD3G)
A mixture of multiple probe sets targeting multiple genes or transcripts
No-XSp
Example: Hs-PDGFB-No-XMm
Does not cross detect with the species (Sp)
XSp
Example: Rn-Pde9a-XMm
designed to cross detect with the species (Sp)
O#
Example: Mm-Islr-O1
Alternative design targeting different regions of the same transcript or isoforms
CDS
Example: Hs-SLC31A-CDS
Probe targets the protein-coding sequence only
EnEmProbe targets exons n and m
En-EmProbe targets region from exon n to exon m
Retired Nomenclature
tvn
Example: Hs-LEPR-tv1
Designed to target transcript variant n
ORF
Example: Hs-ACVRL1-ORF
Probe targets open reading frame
UTR
Example: Hs-HTT-UTR-C3
Probe targets the untranslated region (non-protein-coding region) only
5UTR
Example: Hs-GNRHR-5UTR
Probe targets the 5' untranslated region only
3UTR
Example: Rn-Npy1r-3UTR
Probe targets the 3' untranslated region only
Pan
Example: Pool
A mixture of multiple probe sets targeting multiple genes or transcripts

Enabling research, drug development (CDx) and diagnostics

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