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Diversity of fruit quality associated traits within the RIL population. Top: Ripe fruit of the parental lines PI 414723 (left) and Dulce (right). Bottom: Distribution values of selected <t>metabolites</t> across the <t>RILs</t> population. Parental values are shown at green (PI 414723) and orange (Dulce). Accumulation values across RILs are provided at Additional file ; units are as detailed for parental values. Parental values (PI 414723/Dulce): sucrose: 4.5/52.1 mg/g; β-carotene: 1.4/9.7 ug/g F.W.; pH: 4.6/6.6; ethylene: 235/54 ppm/kg/hour; methyl 3-(methylthio)propionate: 0/34 ng compound/gr F.W.; ethyl butanoate: 4.6/23.3 ng compound/gr F.W.
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Diversity of fruit quality associated traits within the RIL population. Top: Ripe fruit of the parental lines PI 414723 (left) and Dulce (right). Bottom: Distribution values of selected <t>metabolites</t> across the <t>RILs</t> population. Parental values are shown at green (PI 414723) and orange (Dulce). Accumulation values across RILs are provided at Additional file ; units are as detailed for parental values. Parental values (PI 414723/Dulce): sucrose: 4.5/52.1 mg/g; β-carotene: 1.4/9.7 ug/g F.W.; pH: 4.6/6.6; ethylene: 235/54 ppm/kg/hour; methyl 3-(methylthio)propionate: 0/34 ng compound/gr F.W.; ethyl butanoate: 4.6/23.3 ng compound/gr F.W.
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Diversity of fruit quality associated traits within the RIL population. Top: Ripe fruit of the parental lines PI 414723 (left) and Dulce (right). Bottom: Distribution values of selected <t>metabolites</t> across the <t>RILs</t> population. Parental values are shown at green (PI 414723) and orange (Dulce). Accumulation values across RILs are provided at Additional file ; units are as detailed for parental values. Parental values (PI 414723/Dulce): sucrose: 4.5/52.1 mg/g; β-carotene: 1.4/9.7 ug/g F.W.; pH: 4.6/6.6; ethylene: 235/54 ppm/kg/hour; methyl 3-(methylthio)propionate: 0/34 ng compound/gr F.W.; ethyl butanoate: 4.6/23.3 ng compound/gr F.W.
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Diversity of fruit quality associated traits within the RIL population. Top: Ripe fruit of the parental lines PI 414723 (left) and Dulce (right). Bottom: Distribution values of selected <t>metabolites</t> across the <t>RILs</t> population. Parental values are shown at green (PI 414723) and orange (Dulce). Accumulation values across RILs are provided at Additional file ; units are as detailed for parental values. Parental values (PI 414723/Dulce): sucrose: 4.5/52.1 mg/g; β-carotene: 1.4/9.7 ug/g F.W.; pH: 4.6/6.6; ethylene: 235/54 ppm/kg/hour; methyl 3-(methylthio)propionate: 0/34 ng compound/gr F.W.; ethyl butanoate: 4.6/23.3 ng compound/gr F.W.
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Diversity of fruit quality associated traits within the RIL population. Top: Ripe fruit of the parental lines PI 414723 (left) and Dulce (right). Bottom: Distribution values of selected <t>metabolites</t> across the <t>RILs</t> population. Parental values are shown at green (PI 414723) and orange (Dulce). Accumulation values across RILs are provided at Additional file ; units are as detailed for parental values. Parental values (PI 414723/Dulce): sucrose: 4.5/52.1 mg/g; β-carotene: 1.4/9.7 ug/g F.W.; pH: 4.6/6.6; ethylene: 235/54 ppm/kg/hour; methyl 3-(methylthio)propionate: 0/34 ng compound/gr F.W.; ethyl butanoate: 4.6/23.3 ng compound/gr F.W.
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Cell-tracking microfluidics chip (A) Cell- and lineage-tracking custom microfluidics design (figure modified from Figure 1A in <xref ref-type=Bheda et al., 2020a ). The chip is designed with 16 independent microchambers, with each having its own media and cell inlet and outlet channels (represented by different colors), where different strains or conditions can be tested simultaneously. Each microchamber has 8 microchannels for trapping the yeast such that 8 regions containing cells of interest can be imaged per strain/condition ( Goulev et al., 2017 ). (B) Mold fabrication using photomasks and SU-8 photoresist. Photomasks are made from CAD files designed for each layer of the microfluidics chip, then printed onto slides. The mold is made by 2-layer photolithography using a silicon wafer. The process for each layer involves using a spin coater to evenly spread SU-8 photoresist on the wafer and UV treatment through each photomask to transfer the design onto the wafer. This process results in a negative replica mold that can be used repeatedly to prepare PDMS microfluidics chips. (C) Preparation of a PDMS chip stepwise from left to right. Liquid PDMS mix is poured into the replica mold and baked. The solidified PDMS is then assembled into a microfluidics chip by punching holes, treating with O 2 plasma, and attaching to a coverslip. For details see text. " width="250" height="auto" />
Cad File For The Microfluidic Chip Design, supplied by Mendeley Ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Mendeley Ltd cad file for the microfluidics chip design
<t>Cell-tracking</t> <t>microfluidics</t> chip (A) Cell- and lineage-tracking custom microfluidics design (figure modified from Figure 1A in <xref ref-type=Bheda et al., 2020a ). The chip is designed with 16 independent microchambers, with each having its own media and cell inlet and outlet channels (represented by different colors), where different strains or conditions can be tested simultaneously. Each microchamber has 8 microchannels for trapping the yeast such that 8 regions containing cells of interest can be imaged per strain/condition ( Goulev et al., 2017 ). (B) Mold fabrication using photomasks and SU-8 photoresist. Photomasks are made from CAD files designed for each layer of the microfluidics chip, then printed onto slides. The mold is made by 2-layer photolithography using a silicon wafer. The process for each layer involves using a spin coater to evenly spread SU-8 photoresist on the wafer and UV treatment through each photomask to transfer the design onto the wafer. This process results in a negative replica mold that can be used repeatedly to prepare PDMS microfluidics chips. (C) Preparation of a PDMS chip stepwise from left to right. Liquid PDMS mix is poured into the replica mold and baked. The solidified PDMS is then assembled into a microfluidics chip by punching holes, treating with O 2 plasma, and attaching to a coverslip. For details see text. " width="250" height="auto" />
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<t>Cell-tracking</t> <t>microfluidics</t> chip (A) Cell- and lineage-tracking custom microfluidics design (figure modified from Figure 1A in <xref ref-type=Bheda et al., 2020a ). The chip is designed with 16 independent microchambers, with each having its own media and cell inlet and outlet channels (represented by different colors), where different strains or conditions can be tested simultaneously. Each microchamber has 8 microchannels for trapping the yeast such that 8 regions containing cells of interest can be imaged per strain/condition ( Goulev et al., 2017 ). (B) Mold fabrication using photomasks and SU-8 photoresist. Photomasks are made from CAD files designed for each layer of the microfluidics chip, then printed onto slides. The mold is made by 2-layer photolithography using a silicon wafer. The process for each layer involves using a spin coater to evenly spread SU-8 photoresist on the wafer and UV treatment through each photomask to transfer the design onto the wafer. This process results in a negative replica mold that can be used repeatedly to prepare PDMS microfluidics chips. (C) Preparation of a PDMS chip stepwise from left to right. Liquid PDMS mix is poured into the replica mold and baked. The solidified PDMS is then assembled into a microfluidics chip by punching holes, treating with O 2 plasma, and attaching to a coverslip. For details see text. " width="250" height="auto" />
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Image Search Results


Diversity of fruit quality associated traits within the RIL population. Top: Ripe fruit of the parental lines PI 414723 (left) and Dulce (right). Bottom: Distribution values of selected metabolites across the RILs population. Parental values are shown at green (PI 414723) and orange (Dulce). Accumulation values across RILs are provided at Additional file ; units are as detailed for parental values. Parental values (PI 414723/Dulce): sucrose: 4.5/52.1 mg/g; β-carotene: 1.4/9.7 ug/g F.W.; pH: 4.6/6.6; ethylene: 235/54 ppm/kg/hour; methyl 3-(methylthio)propionate: 0/34 ng compound/gr F.W.; ethyl butanoate: 4.6/23.3 ng compound/gr F.W.

Journal: BMC Plant Biology

Article Title: Systems approach for exploring the intricate associations between sweetness, color and aroma in melon fruits

doi: 10.1186/s12870-015-0449-x

Figure Lengend Snippet: Diversity of fruit quality associated traits within the RIL population. Top: Ripe fruit of the parental lines PI 414723 (left) and Dulce (right). Bottom: Distribution values of selected metabolites across the RILs population. Parental values are shown at green (PI 414723) and orange (Dulce). Accumulation values across RILs are provided at Additional file ; units are as detailed for parental values. Parental values (PI 414723/Dulce): sucrose: 4.5/52.1 mg/g; β-carotene: 1.4/9.7 ug/g F.W.; pH: 4.6/6.6; ethylene: 235/54 ppm/kg/hour; methyl 3-(methylthio)propionate: 0/34 ng compound/gr F.W.; ethyl butanoate: 4.6/23.3 ng compound/gr F.W.

Article Snippet: All additional data files and a file describing the accumulation levels of metabolites across RILs and across biological repeats are available in the LabArchives repository [ ].

Techniques:

Cell-tracking microfluidics chip (A) Cell- and lineage-tracking custom microfluidics design (figure modified from Figure 1A in <xref ref-type=Bheda et al., 2020a ). The chip is designed with 16 independent microchambers, with each having its own media and cell inlet and outlet channels (represented by different colors), where different strains or conditions can be tested simultaneously. Each microchamber has 8 microchannels for trapping the yeast such that 8 regions containing cells of interest can be imaged per strain/condition ( Goulev et al., 2017 ). (B) Mold fabrication using photomasks and SU-8 photoresist. Photomasks are made from CAD files designed for each layer of the microfluidics chip, then printed onto slides. The mold is made by 2-layer photolithography using a silicon wafer. The process for each layer involves using a spin coater to evenly spread SU-8 photoresist on the wafer and UV treatment through each photomask to transfer the design onto the wafer. This process results in a negative replica mold that can be used repeatedly to prepare PDMS microfluidics chips. (C) Preparation of a PDMS chip stepwise from left to right. Liquid PDMS mix is poured into the replica mold and baked. The solidified PDMS is then assembled into a microfluidics chip by punching holes, treating with O 2 plasma, and attaching to a coverslip. For details see text. " width="100%" height="100%">

Journal: STAR Protocols

Article Title: Microfluidics for single-cell lineage tracking over time to characterize transmission of phenotypes in Saccharomyces cerevisiae

doi: 10.1016/j.xpro.2020.100228

Figure Lengend Snippet: Cell-tracking microfluidics chip (A) Cell- and lineage-tracking custom microfluidics design (figure modified from Figure 1A in Bheda et al., 2020a ). The chip is designed with 16 independent microchambers, with each having its own media and cell inlet and outlet channels (represented by different colors), where different strains or conditions can be tested simultaneously. Each microchamber has 8 microchannels for trapping the yeast such that 8 regions containing cells of interest can be imaged per strain/condition ( Goulev et al., 2017 ). (B) Mold fabrication using photomasks and SU-8 photoresist. Photomasks are made from CAD files designed for each layer of the microfluidics chip, then printed onto slides. The mold is made by 2-layer photolithography using a silicon wafer. The process for each layer involves using a spin coater to evenly spread SU-8 photoresist on the wafer and UV treatment through each photomask to transfer the design onto the wafer. This process results in a negative replica mold that can be used repeatedly to prepare PDMS microfluidics chips. (C) Preparation of a PDMS chip stepwise from left to right. Liquid PDMS mix is poured into the replica mold and baked. The solidified PDMS is then assembled into a microfluidics chip by punching holes, treating with O 2 plasma, and attaching to a coverslip. For details see text.

Article Snippet: The CAD file for the microfluidic chip design is available on Mendeley Data ( ).

Techniques: Cell Tracking Assay, Modification, Clinical Proteomics

Cell-tracking microfluidics chip (A) Cell- and lineage-tracking custom microfluidics design (figure modified from Figure 1A in <xref ref-type=Bheda et al., 2020a ). The chip is designed with 16 independent microchambers, with each having its own media and cell inlet and outlet channels (represented by different colors), where different strains or conditions can be tested simultaneously. Each microchamber has 8 microchannels for trapping the yeast such that 8 regions containing cells of interest can be imaged per strain/condition ( Goulev et al., 2017 ). (B) Mold fabrication using photomasks and SU-8 photoresist. Photomasks are made from CAD files designed for each layer of the microfluidics chip, then printed onto slides. The mold is made by 2-layer photolithography using a silicon wafer. The process for each layer involves using a spin coater to evenly spread SU-8 photoresist on the wafer and UV treatment through each photomask to transfer the design onto the wafer. This process results in a negative replica mold that can be used repeatedly to prepare PDMS microfluidics chips. (C) Preparation of a PDMS chip stepwise from left to right. Liquid PDMS mix is poured into the replica mold and baked. The solidified PDMS is then assembled into a microfluidics chip by punching holes, treating with O 2 plasma, and attaching to a coverslip. For details see text. " width="100%" height="100%">

Journal: STAR Protocols

Article Title: Microfluidics for single-cell lineage tracking over time to characterize transmission of phenotypes in Saccharomyces cerevisiae

doi: 10.1016/j.xpro.2020.100228

Figure Lengend Snippet: Cell-tracking microfluidics chip (A) Cell- and lineage-tracking custom microfluidics design (figure modified from Figure 1A in Bheda et al., 2020a ). The chip is designed with 16 independent microchambers, with each having its own media and cell inlet and outlet channels (represented by different colors), where different strains or conditions can be tested simultaneously. Each microchamber has 8 microchannels for trapping the yeast such that 8 regions containing cells of interest can be imaged per strain/condition ( Goulev et al., 2017 ). (B) Mold fabrication using photomasks and SU-8 photoresist. Photomasks are made from CAD files designed for each layer of the microfluidics chip, then printed onto slides. The mold is made by 2-layer photolithography using a silicon wafer. The process for each layer involves using a spin coater to evenly spread SU-8 photoresist on the wafer and UV treatment through each photomask to transfer the design onto the wafer. This process results in a negative replica mold that can be used repeatedly to prepare PDMS microfluidics chips. (C) Preparation of a PDMS chip stepwise from left to right. Liquid PDMS mix is poured into the replica mold and baked. The solidified PDMS is then assembled into a microfluidics chip by punching holes, treating with O 2 plasma, and attaching to a coverslip. For details see text.

Article Snippet: The CAD file for the microfluidics chip design used in is available at Mendeley Data ( https://data.mendeley.com/datasets/yr2nrysyyx/1 ) ( ).

Techniques: Cell Tracking Assay, Modification, Clinical Proteomics