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.
Front Neuroanat.
2015 Sep 03
Liu Y, Huang Y, Lee S, Bookout AL, Castorena CM, Wu H, Gautron L.
PMID: 26388745 | DOI: 10.3389/fnana.2015.00120.
Peroxisome proliferator-activated receptor gamma (PPARγ) is a ligand-activated transcription factor that was originally identified as a regulator of peroxisome proliferation and adipocyte differentiation. Emerging evidence suggests that functional PPARγ signaling also occurs within the hypothalamus. However, the exact distribution and identities of PPARγ-expressing hypothalamic cells remains under debate. The present study systematically mapped PPARγ mRNA expression in the adult mouse brain using in situ hybridization histochemistry. PPARγ mRNA was found to be expressed at high levels outside the hypothalamus including the neocortex, the olfactory bulb, the organ of the vasculosum of the lamina terminalis (VOLT), and the subfornical organ. Within the hypothalamus, PPARγ was present at moderate levels in the suprachiasmatic nucleus (SCh) and the ependymal of the 3rd ventricle. In all examined feeding-related hypothalamic nuclei, PPARγ was expressed at very low levels that were close to the limit of detection. Using qPCR techniques, we demonstrated that PPARγ mRNA expression was upregulated in the SCh in response to fasting. Double in situ hybridization further demonstrated that PPARγ was primarily expressed in neurons rather than glia. Collectively, our observations provide a comprehensive map of PPARγ distribution in the intact adult mouse hypothalamus.
Nature communications
2022 Sep 20
Geldhof, V;de Rooij, LPMH;Sokol, L;Amersfoort, J;De Schepper, M;Rohlenova, K;Hoste, G;Vanderstichele, A;Delsupehe, AM;Isnaldi, E;Dai, N;Taverna, F;Khan, S;Truong, AK;Teuwen, LA;Richard, F;Treps, L;Smeets, A;Nevelsteen, I;Weynand, B;Vinckier, S;Schoonjans, L;Kalucka, J;Desmedt, C;Neven, P;Mazzone, M;Floris, G;Punie, K;Dewerchin, M;Eelen, G;Wildiers, H;Li, X;Luo, Y;Carmeliet, P;
PMID: 36127427 | DOI: 10.1038/s41467-022-33052-y
EMBO Rep
2020 Feb 13
Pereira B, Amaral AL, Dias A, Mendes N, Muncan V, Silva AR, Thibert C, Radu AG, David L, M�ximo V, van den Brink GR, Billaud M, Almeida R
PMID: 32052574 | DOI: 10.15252/embr.201948938
Nature metabolism
2023 Jun 01
Palani, NP;Horvath, C;Timshel, PN;Folkertsma, P;Grønning, AGB;Henriksen, TI;Peijs, L;Jensen, VH;Sun, W;Jespersen, NZ;Wolfrum, C;Pers, TH;Nielsen, S;Scheele, C;
PMID: 37337126 | DOI: 10.1038/s42255-023-00820-z
Description | ||
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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 | |
EnEm | Probe targets exons n and m | |
En-Em | Probe 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 |
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