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Multiprobe liquid

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The MultiProbe liquid is a laboratory instrument designed for automated liquid handling. It features multiple pipetting channels and can aspirate and dispense various liquid volumes precisely and efficiently.

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Lab products found in correlation

Multiprobe, by PerkinElmer (2 mentions)

Spelling variants of this product

MultiProbe (4 citations) Multiprobe II plus liquid handling system (2 citations) Multiprobe II EX Robotic Liquid Handling System (2 citations)

2 protocols using multiprobe liquid

1

High-Throughput DNA Library Quantification

Check if the same lab product or an alternative is used in the 5 most similar protocols
After in-solution hybrid selection, libraries were quantified using qPCR (KAPA Biosystems) with probes specific to the ends of the adapters. This assay was automated using Agilent’s Bravo liquid handling platform. Based on qPCR quantification, libraries were normalized to 2nM and then denatured using 0.1 N NaOH using Perkin-Elmer’s MultiProbe liquid handling platform. A subset of the samples prepared using forked, indexed adapters was quantified using qPCR, normalized to 2nM using Perkin-Elmer’s Mini-Janus liquid handling platform, and pooled by equal volume using the Agilent Bravo. Pools were then denatured using 0.1 N NaOH. Denatured samples were diluted into strip tubes using the Perkin-Elmer MultiProbe.
Do R., Stitziel N.O., Won H.H., Jørgensen A.B., Duga S., Merlini P.A., Kiezun A., Farrall M., Goel A., Zuk O., Guella I., Asselta R., Lange L.A., Peloso G.M., Auer P.L., Girelli D., Martinelli N., Farlow D.N., DePristo M.A., Roberts R., Stewart A.F., Saleheen D., Danesh J., Epstein S.E., Sivapalaratnam S., Hovingh G.K., Kastelein J.J., Samani N.J., Schunkert H., Erdmann J., Shah S.H., Kraus W.E., Davies R., Nikpay M., Johansen C.T., Wang J., Hegele R.A., Hechter E., Marz W., Kleber M.E., Huang J., Johnson A.D., Li M., Burke G.L., Gross M., Liu Y., Assimes T.L., Heiss G., Lange E.M., Folsom A.R., Taylor H.A., Olivieri O., Hamsten A., Clarke R., Reilly D.F., Yin W., Rivas M.A., Donnelly P., Rossouw J.E., Psaty B.M., Herrington D.M., Wilson J.G., Rich S.S., Bamshad M.J., Tracy R.P., Cupples L.A., Rader D.J., Reilly M.P., Spertus J.A., Cresci S., Hartiala J., Tang W.H., Hazen S.L., Allayee H., Reiner A.P., Carlson C.S., Kooperberg C., Jackson R.D., Boerwinkle E., Lander E.S., Schwartz S.M., Siscovick D.S., McPherson R., Tybjaerg-Hansen A., Abecasis G.R., Watkins H., Nickerson D.A., Ardissino D., Sunyaev S.R., O’Donnell C.J., Altshuler D., Gabriel S, & Kathiresan S. (2014). Multiple rare alleles at LDLR and APOA5 confer risk for early-onset myocardial infarction. Nature, 518(7537), 102-106.
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2

High-Throughput DNA Library Quantification

Check if the same lab product or an alternative is used in the 5 most similar protocols
After in-solution hybrid selection, libraries were quantified using qPCR (KAPA Biosystems) with probes specific to the ends of the adapters. This assay was automated using Agilent’s Bravo liquid handling platform. Based on qPCR quantification, libraries were normalized to 2nM and then denatured using 0.1 N NaOH using Perkin-Elmer’s MultiProbe liquid handling platform. A subset of the samples prepared using forked, indexed adapters was quantified using qPCR, normalized to 2nM using Perkin-Elmer’s Mini-Janus liquid handling platform, and pooled by equal volume using the Agilent Bravo. Pools were then denatured using 0.1 N NaOH. Denatured samples were diluted into strip tubes using the Perkin-Elmer MultiProbe.
Do R., Stitziel N.O., Won H.H., Jørgensen A.B., Duga S., Merlini P.A., Kiezun A., Farrall M., Goel A., Zuk O., Guella I., Asselta R., Lange L.A., Peloso G.M., Auer P.L., Girelli D., Martinelli N., Farlow D.N., DePristo M.A., Roberts R., Stewart A.F., Saleheen D., Danesh J., Epstein S.E., Sivapalaratnam S., Hovingh G.K., Kastelein J.J., Samani N.J., Schunkert H., Erdmann J., Shah S.H., Kraus W.E., Davies R., Nikpay M., Johansen C.T., Wang J., Hegele R.A., Hechter E., Marz W., Kleber M.E., Huang J., Johnson A.D., Li M., Burke G.L., Gross M., Liu Y., Assimes T.L., Heiss G., Lange E.M., Folsom A.R., Taylor H.A., Olivieri O., Hamsten A., Clarke R., Reilly D.F., Yin W., Rivas M.A., Donnelly P., Rossouw J.E., Psaty B.M., Herrington D.M., Wilson J.G., Rich S.S., Bamshad M.J., Tracy R.P., Cupples L.A., Rader D.J., Reilly M.P., Spertus J.A., Cresci S., Hartiala J., Tang W.H., Hazen S.L., Allayee H., Reiner A.P., Carlson C.S., Kooperberg C., Jackson R.D., Boerwinkle E., Lander E.S., Schwartz S.M., Siscovick D.S., McPherson R., Tybjaerg-Hansen A., Abecasis G.R., Watkins H., Nickerson D.A., Ardissino D., Sunyaev S.R., O’Donnell C.J., Altshuler D., Gabriel S, & Kathiresan S. (2014). Multiple rare alleles at LDLR and APOA5 confer risk for early-onset myocardial infarction. Nature, 518(7537), 102-106.
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