glial cell nuclei (Developmental Studies Hybridoma Bank)
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Developmental Studies Hybridoma Bank
glial cell nuclei
Glial Cell Nuclei, supplied by Developmental Studies Hybridoma Bank, used in various techniques. Bioz Stars score: 94/100, based on 24 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/glial+nuclei/anti-Nuclei/pm35990742-55-13-19
Average 94 stars, based on 24 article reviews
Glial Cell Nuclei, supplied by Developmental Studies Hybridoma Bank, used in various techniques. Bioz Stars score: 94/100, based on 24 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/glial+nuclei/anti-Nuclei/pm35990742-55-13-19
Average 94 stars, based on 24 article reviews
glial cell nuclei - by Bioz Stars,
2026-09
94/100 stars
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Staining:Article Title: Alignment between glioblastoma internal clock and environmental cues ameliorates survival in Drosophila. Article Snippet: Adult brains were dissected and fixed with 4% formaldehyde in phosphate-buffered saline for 20 min whereas adult NMJ were fixed for 10 min; in both cases, samples were washed 3 × 15min with 10 COMMUNICATIONS BIOLOGY | (2022) 5:644 | https://doi.org/10.1038/s42003-022-03600-9 | www.nature.com/commsbio PBS+ 0.4% triton, blocked for 1 h with PBS+ 0.4% triton+BSA 5%, incubated overnight with primary antibodies, washed 3 × 15min, incubated with secondary antibodies for 2 h and mounted in Vectashield mounting medium, with DAPI in the case of the brains.0.4% triton, blocked for 1 h with PBS+ 0.4% triton+BSA 5%, incubated overnight with primary antibodies, washed 3 × 15min, incubated with secondary antibodies for 2 h and mounted in Vectashield mounting medium, with DAPI in the case of the brains. ... The primary antibodies used were mouse anti-repo (1:200, DSHB) to recognize Article Title: Alignment between glioblastoma internal clock and environmental cues ameliorates survival in Drosophila Article Snippet: Adult brains were dissected and fixed with 4% formaldehyde in phosphate-buffered saline for 20 min whereas adult NMJ were fixed for 10 min; in both cases, samples were washed 3 × 15 min with PBS + 0.4% triton, blocked for 1 h with PBS + 0.4% triton+BSA 5%, incubated overnight with primary antibodies, washed 3 × 15 min, incubated with secondary antibodies for 2 h and mounted in Vectashield mounting medium, with DAPI in the case of the brains.blocked for 1 h with PBS + 0.4% triton+BSA 5%, incubated overnight with primary antibodies, washed 3 × 15 min, incubated with secondary antibodies for 2 h and mounted in Vectashield mounting medium, with DAPI in the case of the brains. ... The primary antibodies used were mouse anti-repo (1:200, DSHB) to recognize Article Title: Circadian Gene cry Controls Tumorigenesis through Modulation of Myc Accumulation in Glioblastoma Cells Article Snippet: Adult brains were dissected and fixed with 4% formaldehyde in phosphate-buffered saline for 20 min, whereas adult NMJ were fixed for 10 min; in both cases, samples were washed 3 × 15 min with PBS + 0.4% triton, blocked for 1 h with PBS + 0.4% triton + BSA 5%, incubated overnight with primary antibodies, washed 3 × 15 min, incubated with secondary antibodies for 2 h and mounted in Vectashield mounting medium with DAPI in the case of the brains.triton + BSA 5%, incubated overnight with primary antibodies, washed 3 × 15 min, incubated with secondary antibodies for 2 h and mounted in Vectashield mounting medium with DAPI in the case of the brains. ... The primary antibodies used were anti-Repo mouse (1/200; DSHB, Iowa City, IA, USA) to recognize Article Title: Circadian Gene <em>cry</em> Controls Glioblastoma Tumorigenesis through Modulation of <em>myc</em> Expression Article Snippet: Adult brains were dissected and fixed with 4% formaldehyde in phosphatebuffered saline for 20 min whereas adult NMJ were fixed 10 min; in both cases, samples were washed 3 × 15 min with PBS+0.4% triton, blocked for 1 h with PBS+0.4% triton+ BSA 5%, incubated overnight with primary antibodies, washed 3 × 15 min, incubated with secondary antibodies for 2 h, and mounted in Vectashield mounting medium, with DAPI in the case of the brains.PBS+0.4% triton, blocked for 1 h with PBS+0.4% triton+ BSA 5%, incubated overnight with primary antibodies, washed 3 × 15 min, incubated with secondary antibodies for 2 h, and mounted in Vectashield mounting medium, with DAPI in the case of the brains. ... The primary antibodies used were anti-repo mouse (1/200; DSHB) to recognize Article Title: Insulin signaling mediates neurodegeneration in glioma Article Snippet: Adult brains were dissected and fixed with 4% formaldehyde in phosphate-buffered saline for 20 min whereas adult NMJ were fixed 10 min; in both cases, samples were washed 3 × 15 min with PBS+0.4% triton, blocked for 1 h with PBS+0.4% triton+ BSA 5%, incubated overnight with primary antibodies, washed 3 × 15 min, incubated with secondary antibodies for 2 h, and mounted in Vectashield mounting medium, with DAPI in the case of the brains.min with PBS+0.4% triton, blocked for 1 h with PBS+0.4% triton+ BSA 5%, incubated overnight with primary antibodies, washed 3 × 15 min, incubated with secondary antibodies for 2 h, and mounted in Vectashield mounting medium, with DAPI in the case of the brains. ... The primary antibodies used were anti-repo mouse (1/200; DSHB) to recognize |