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High ALDH expression has been reported for normal and cancer precursor cells of various lineages. The ALDEFLUOR assay is a widely published non-immunological method for the detection of ALDH-bright (ALDHbr) cells and can be used to detect cancer cells in hematopoietic, mammary, endothelial, mesenchymal, neural, and other tissues.

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• 1 year ago - submitted by Kyriaki-Barbara Papalois

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• 1 year ago - submitted by Kyriaki-Barbara Papalois

Reliability and innovation come together in Autostainer Link 48. Our trusted immunohistochemistry stainer is united with revolutionary software and connectivity options, delivering an outstanding level of integration that provides high productivity and efficient workflow.

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• 1 year ago - submitted by Kyriaki-Barbara Papalois

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• 1 year ago - submitted by Kyriaki-Barbara Papalois

Rapid 15 minute method for the isolation and purification of total RNA (including miRNA) from small input amounts of cultured animal cells, CTC, stem cells, immuno-sorted cells, and microdissected samples including laser-capture microdissection (LCM). The purified RNA is of the highest purity and integrity, and can be used in a number of qRT-PCR and digital PCR and other whole transcriptome applications.

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• 1 year ago - submitted by Kyriaki-Barbara Papalois

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• 1 year ago - submitted by Kyriaki-Barbara Papalois

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• 1 year ago - submitted by Kyriaki-Barbara Papalois

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• 1 year ago - submitted by Kyriaki-Barbara Papalois

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• 1 year ago - submitted by Kyriaki-Barbara Papalois

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• 1 year ago - submitted by Kyriaki-Barbara Papalois

cloud-based flow cytometry analysis platform bridging machine learning and analytical pipelines with classical analysis

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• 1 year ago - submitted by Meg Goswami

A Probabilistic Genome Simulator for Non-uniform Simple, Canonical, and Complex Structural Variations to Facilitate Benchmarking

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• 1 year ago - submitted by Zhen Zhang

for RNA, miRNA extraction

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• 1 year ago - submitted by Fatemeh VandRajabpour

eNRSA is an enhanced version of NRSA for analyzing nascent transcription profiles generated by PRO-seq, GRO-seq, (m)NET-seq, and Butt-seq data.

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• 1 year ago - submitted by huachang chen

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• 1 year ago - submitted by Moira Sheehan

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• 1 year ago - submitted by Moira Sheehan

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• 1 year ago - submitted by Moira Sheehan

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• 1 year ago - submitted by Moira Sheehan

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• 1 year ago - submitted by Moira Sheehan

Blueberry_DArTag_BI_Cornell_University 1.0 is a DArTag genotyping panel version 1 for blueberry targeting 3000 loci. DArTag assay uses custom designed oligos to amplify targeted SNPs, and their flanking sequences, prior to NGS sequencing. The sequenced amplicons are demultiplexed and targeted SNPs/haplotypes are analysed using DArT P/L’s proprietary pipeline (https://www.diversityarrays.com/services/targeted-genotying/). The markers were selected from a diverse set of 31 cultivated blueberry SHB and NHB parents and founders from North American breeding programs. The panel is suitable for genotyping tetraploid blueberry for breeding decisions and selection. Usage of the panel for hexaploid blueberry (i.e., Rabbit Eye) and diploid cranberry resulted in higher missing data and fewer polymorphic data points. Usage of the panel outside of Vaccinium corymbosum is likely to result in higher missing data and fewer data points. Panel developed in collaboration between DArT and Breeding Insight at Cornell University.

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• 1 year ago - submitted by Moira Sheehan