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Biosearch Technologies Inc custom stellaris tm probe designer
Custom Stellaris Tm Probe Designer, supplied by Biosearch Technologies Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/custom+designed+probes/designer+fish+probe+rna+stellaris/bio_rxiv__64898__2026__02__18__706626-319-5-10
Average 86 stars, based on 1 article reviews
custom stellaris tm probe designer - by Bioz Stars, 2026-10
86/100 stars

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Labeling:

Article Title: Germ Granule Evolution Provides Mechanistic Insight into Drosophila Germline Development
Article Snippet: .. Custom species-specific smFISH probes were designed using Biosearch Technologies Stellaris Probe Designer tool and purchased from Biosearch Technologies where all pgc probe sets were labeled with Quasar 570 dye, and all nos probe sets were labeled with ATTO 647N dye. ..

Article Title: Evolutionary changes in germ granule mRNA content are driven by multiple mechanisms in Drosophila
Article Snippet: .. Custom species specific smFISH probes were designed using Biosearch Technologies Stellaris Probe Designer tool and purchased from Biosearch Technologies where all pgc probe sets were labeled with Quasar 570 dye and all nos probe sets were labeled with ATTO 647N dye. ..

other:

Article Title: Differences in blastomere totipotency in 2-cell mouse embryos are a maternal trait mediated by asymmetric mRNA distribution
Article Snippet: Commercially available Stellaris® RNA FISH probes against mouse Gapdh (BioSearch Technologies; VSMF-3015-5), Oct4 (BioSearch Technologies; VSMF-3067-5) and custom-designed probes against mouse Cops3 (NCBI gene ID: 26572) utilizing the BioSearch Technologies design service, both labelled with Quasar® 670, were used for hybridization.

Article Title: Single-cell alternative splicing analysis with Expedition reveals splicing dynamics during neuron differentiation
Article Snippet: To verify alternative splicing of MXE event composed of exon 9 and 10 in PKM, we designed 3 probe sets (Custom Stellaris® FISH Probes, Biosearch Technologies, Inc., CA, Table S2 ) using the Stellaris® RNA FISH Probe Designer available online.

Article Title: Ubiquitous selfish toxin-antidote elements in Caenorhabditis species
Article Snippet: We designed 48 Custom Stellaris FISH Probes against slow-1 mRNA using the Stellaris RNA FISH Probe Designer (Biosearch Technologies, Inc., Petaluma, CA) available online at www.biosearchtech.com/stellarisdesigner .

Article Title: Functional probing of neuronal subtypes via intersectional expression of optogenetic actuators reveals non-linear components in a linear circuit.
Article Snippet: REAGENT or RESOURCE SOURCE IDENTIFIER Critical commercial assays Custom-designed Chrimson smFISH probes, Quasar® 670 Dye BioSearch Technologies SMF-1065-5-P_ChrimsonCel Deposited data Raw behavioral data This study https://doi.org/10.6084/ m9.figshare.28217246.v3 Codes for data analysis This study https://github.com/leiferlab/ kumar-touch-neuron-subtypes.git Experimental models: Organisms/strains Caenorhabditis elegans: CGZ2357 syIs595[mec17p::cGAL4; Pofm-1::RFP] V; syIs503[15xUAS:: chrimson::gfp; Pofm-1::GFP] II This study All TRN:: Chrimson C. elegans: CGZ2180 syIs595[mec-17p::cGAL4; Pofm-1::RFP] V; syIs390[15xUAS::Δpes-10::GFP:: let-858 3 ′ UTR + ttx-3p::RFP + 1kb DNA ladder(NEB)] III This study All TRN:: GFP C. elegans: CGZ257 unc-119(ed3) unkIs17[mec-17p::cGAL-N; unc-119(+)] III This study All TRN:: cGAL-N C. elegans: CGZ357 unc119(ed3) unkIs17[mec17p::cGAL-N; unc-119(+)] III; syIs300[15xUAS:: Δpes-10::GFP::unc-54 3 ′ UTR + ttx-3p::RFP] V This study All TRN:: cGAL-N; no GFP CTR C. elegans: CGZ1409 unc119(ed3) unkIs17[mec17p::cGAL-N; unc-119(+)] III; syIs503[15xUAS:: Crimson::gfp; Pofm-1::GFP] II This study All TRN:: cGAL-N; no Chrimson CTR C. elegans: CGZ2020 unkIs56[T20B3.14p::cGAL-C; ceh-22p::GFP]; syIs503[15xUAS::chrimson::gfp; Pofm-1::GFP] II; unc-119(ed3) unkIs17[mec-17p::cGAL-N; unc-119(+)] III This study ALM:: Chrimson C. elegans: CGZ2021 unkIs43[C10C5.7p::cGAL-C; ceh-22p::GFP] IV; syIs503[15xUAS::chrimson::gfp; Pofm-1::GFP]II; unc-119(ed3) unkIs17[mec17p::cGAL-N; unc-119(+)] III This study AVM:: Chrimson C. elegans: CGZ2401 unkls71[C10B5.3p::cGAL-4-C; ceh-22p::GFP] syIs503[15xUAS::chrimson::gfp; Pofm-1::GFP] II; unc-119(ed3) unkIs17[mec-17p:: cGAL-N; unc-119(+)] III This study PLM:: Chrimson C. elegans: CGZ518 unkIs36[svh-5p2::cGAL-C; ceh-22p::GFP]; syIs503[UAS::Chrimson::gfp; Pofm-1::GFP] II; unc-119(ed3) unkIs17[mec-17p:: cGAL-N; unc-119(+)] III This study AVM & PLM:: Chrimson C. elegans: CGZ2042 unkIs54[nlp-7p::cGAL-C; ceh-22p::GFP] V; syIs503[15xUAS::chrimson::gfp; Pofm-1::GFP] II; unc-119(ed3); unkIs17[mec-17p:: cGAL-4-N; unc-119(+)] III This study ALM & PLM:: Chrimson C. elegans: CGZ2211 unc-119(ed3) unkIs17[mec-17p:: cGAL-4-N; unc-119(+)]; unkIs56[T20B3.14p::cGAL-C; ceh-22p::GFP]; syIs300[15xUAS::Δpes-10:: GFP::unc-54 3 ′ UTR + ttx-3p::RFP] This study ALM:: GFP (Continued on next page) 12 Cell Reports 44, 116327, October 28, 2025

Fluorescence In Situ Hybridization:

Article Title: Single-mRNA detection in living S. cerevisiae using a re-engineered MS2 system
Article Snippet: The MS2 system has been widely used, in organisms ranging from bacteria to higher eukaryotes, to image single mRNAs in intact cells with high precision.. We have recently re-engineered the MS2 system for accurate detection of mRNAs in living Saccharomyces cerevisiae.. Previous MS2 systems affected the degradation of the tagged mRNA, which led to accumulation of MS2 fragments and to erroneous conclusions about mRNA localization and expression.

Imaging:

Article Title: Single-mRNA detection in living S. cerevisiae using a re-engineered MS2 system
Article Snippet: The MS2 system has been widely used, in organisms ranging from bacteria to higher eukaryotes, to image single mRNAs in intact cells with high precision.. We have recently re-engineered the MS2 system for accurate detection of mRNAs in living Saccharomyces cerevisiae.. Previous MS2 systems affected the degradation of the tagged mRNA, which led to accumulation of MS2 fragments and to erroneous conclusions about mRNA localization and expression.

Control:

Article Title: Single-mRNA detection in living S. cerevisiae using a re-engineered MS2 system
Article Snippet: The MS2 system has been widely used, in organisms ranging from bacteria to higher eukaryotes, to image single mRNAs in intact cells with high precision.. We have recently re-engineered the MS2 system for accurate detection of mRNAs in living Saccharomyces cerevisiae.. Previous MS2 systems affected the degradation of the tagged mRNA, which led to accumulation of MS2 fragments and to erroneous conclusions about mRNA localization and expression.



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