Literature DB >> 9671447

Optimized fixation and storage conditions for FISH analysis of single-cell suspensions.

S Murrell-Bussell1, D Nguyen, W D Schober, J Scott, J L Simpson, S Elias, F Z Bischoff, D E Lewis.   

Abstract

In our protocol to isolate and identify fetal cells in maternal peripheral blood, antibody (Ab)-stained cells are preserved with paraformaldehyde (PF) before batch flow cytometric sorting. However, PF fixation compromises the quality of subsequent interphase fluorescence in situ hybridization (FISH). We therefore examined the effect of PF concentrations and storage time in phosphate-buffered saline (PBS) on the quality of FISH signals. Cells were analyzed for changes in light scatter, morphology, and accessibility of target cell DNA. Fixation in 3% PF for 1 hr was ideal for both flow cytometry and subsequent FISH detection. However, beyond 10 days of storage, FISH quality deteriorated. (J Histochem Cytochem 46:971-973, 1998)

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Year:  1998        PMID: 9671447     DOI: 10.1177/002215549804600811

Source DB:  PubMed          Journal:  J Histochem Cytochem        ISSN: 0022-1554            Impact factor:   2.479


  2 in total

1.  Detection of ALK gene rearrangements in formalin-fixed, paraffin-embedded tissue using a fluorescence in situ hybridization (FISH) probe: a search for optimum conditions of tissue archiving and preparation for FISH.

Authors:  Leonard Hwan Cheong Tan; Elaine Do; Siew Meng Chong; Evelyn Siew Chuan Koay
Journal:  Mol Diagn       Date:  2003

2.  Multiplex cytokine profiling with highly pathogenic material: use of formalin solution in luminex analysis.

Authors:  Stuart D Dowall; Victoria A Graham; Thomas R W Tipton; Roger Hewson
Journal:  J Immunol Methods       Date:  2009-06-26       Impact factor: 2.303

  2 in total

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