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electrode microarray  (CombiMatrix)

 
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    CombiMatrix electrode microarray
    Electrode Microarray, supplied by CombiMatrix, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/customarraytm+12k+arrays/microelectrode+array/us09983204-474-4-8
    Average 90 stars, based on 1 article reviews
    electrode microarray - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    Microarray:

    Article Title: Microarray having a base cleavable linker
    Article Snippet: .. An example of an electrode microarray is a CombiMatrix CustomArrayTM 12 k, which has over 12,000 electrodes and an electrode density of approximately 17,778 electrodes per square centimeter. ..

    Article Title: Massively Parallel Interrogation of Aptamer Sequence, Structure and Function
    Article Snippet: .. Indeed, the Combimatrix electrode array microarray format has the potential to be used much like the Agilent arrays were used here but with an electronic readout. ..

    other:

    Article Title: From Molecules to Molecular Surfaces. Exploiting the Interplay Between Organic Synthesis and Electrochemistry
    Article Snippet: When this effort was begun, scientists at Combimatrix had illustrated an approach to accomplishing this for the generation of acid at selected sites on a microelectrode array.

    Article Title: Method for evaluating redox activity of nucleic acid molecule and nucleic acid molecule having redox activity
    Article Snippet: The conditions under which a redox reaction of a nucleic acid molecule to be evaluated was detected were considered. (1) Immobilization of Polynucleotide A known polynucleotide was immobilized, via a spacer, on an electrode of a commercially available electrochemical detection-type microarray (trade name: CombiMatrix ElectraSense microarray, manufactured by CombiMatrix) as shown below.

    Article Title: Microelectrode array biosensor for studying carbohydrate-mediated interactions
    Article Snippet: Platform: microelectrode array and instrumentation The microelectrode array ( ) and supporting instrumentation were developed by CombiMatrix (Mukilteo, WA; now CustomArray, Bothell, WA), as described in detail previously ( Cooper et al., 2010 ; Ghindilis et al., 2007 ; Roth et al., 2006 ).

    Generated:

    Article Title: From Molecules to Molecular Surfaces. Exploiting the Interplay Between Organic Synthesis and Electrochemistry
    Article Snippet: .. When this effort was begun, scientists at Combimatrix had illustrated an approach to accomplishing this for the generation of acid at selected sites on a microelectrode array.20 In this effort, the array was treated with aqueous base and then acid generated at selected electrodes in the array by the oxidation of water. ..



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    custom microarray customarraytm 12k arrays  (CombiMatrix)
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    Custom microarrays analysis . A) Bar plot of UCEs expressed across 4 mouse developmental stages tested (ES, E12.5, E14.5 and E16.5) based on the analysis of our UCE custom <t>microarray.</t> Blue bars indicate UCEs which show expression on a single strand, green columns indicate UCEs which show expression on both strands B) Venn diagram of UCE transcription results showing the overlap across the 4 stages analyzed. More than half (n = 140, 56%) of the transcribed UCEs are expressed in all the stages analyzed.
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    Custom microarrays analysis . A) Bar plot of UCEs expressed across 4 mouse developmental stages tested (ES, E12.5, E14.5 and E16.5) based on the analysis of our UCE custom microarray. Blue bars indicate UCEs which show expression on a single strand, green columns indicate UCEs which show expression on both strands B) Venn diagram of UCE transcription results showing the overlap across the 4 stages analyzed. More than half (n = 140, 56%) of the transcribed UCEs are expressed in all the stages analyzed.

    Journal: BMC Genomics

    Article Title: Promiscuity of enhancer, coding and non-coding transcription functions in ultraconserved elements

    doi: 10.1186/1471-2164-11-151

    Figure Lengend Snippet: Custom microarrays analysis . A) Bar plot of UCEs expressed across 4 mouse developmental stages tested (ES, E12.5, E14.5 and E16.5) based on the analysis of our UCE custom microarray. Blue bars indicate UCEs which show expression on a single strand, green columns indicate UCEs which show expression on both strands B) Venn diagram of UCE transcription results showing the overlap across the 4 stages analyzed. More than half (n = 140, 56%) of the transcribed UCEs are expressed in all the stages analyzed.

    Article Snippet: We therefore designed a custom microarray (CustomarrayTM 12K arrays from Combimatrix, Mukilteo, WA) encompassing 3 different probes on each DNA strand of UCEs (of the currently annotated 481 UCEs, probes could be designed for 475), as well as a large number of negative controls (exogenous sequences from bacteria and plants, negative controls used in the Affymetrix platform, rRNAs sequences), which were used to assess the levels of background signal.

    Techniques: Microarray, Expressing

    UCEs transcription and enhancer function overlap . Overlap between the enhancer dataset (Pennacchio et al, 2006) and the mouse microarray dataset in all samples analyzed, divided by stage. The yellow portion of each bar indicates UCEs that are only transcribed, the green portion UCEs that are transcribed and act as enhancers, the blue portion UCEs that are only transcribed.

    Journal: BMC Genomics

    Article Title: Promiscuity of enhancer, coding and non-coding transcription functions in ultraconserved elements

    doi: 10.1186/1471-2164-11-151

    Figure Lengend Snippet: UCEs transcription and enhancer function overlap . Overlap between the enhancer dataset (Pennacchio et al, 2006) and the mouse microarray dataset in all samples analyzed, divided by stage. The yellow portion of each bar indicates UCEs that are only transcribed, the green portion UCEs that are transcribed and act as enhancers, the blue portion UCEs that are only transcribed.

    Article Snippet: We therefore designed a custom microarray (CustomarrayTM 12K arrays from Combimatrix, Mukilteo, WA) encompassing 3 different probes on each DNA strand of UCEs (of the currently annotated 481 UCEs, probes could be designed for 475), as well as a large number of negative controls (exogenous sequences from bacteria and plants, negative controls used in the Affymetrix platform, rRNAs sequences), which were used to assess the levels of background signal.

    Techniques: Microarray

    UCE classification using External datasets . A) Comparison between the mouse enhancer dataset (Pennacchio et al. 2006) (green oval), our mouse development microarray dataset, (red oval), the human UCE expression dataset (Calin et al. 2007) (blue oval) and the mouse ES cell SOLiD expression dataset (Cloonan et al. 2008) (orange oval). B) Comparison of the SOLiD ES cell RNAseq dataset (Cloonan et al. 2008) for UCEs vs. randomly chosen non-transcribed genomic regions (outliers not shown).

    Journal: BMC Genomics

    Article Title: Promiscuity of enhancer, coding and non-coding transcription functions in ultraconserved elements

    doi: 10.1186/1471-2164-11-151

    Figure Lengend Snippet: UCE classification using External datasets . A) Comparison between the mouse enhancer dataset (Pennacchio et al. 2006) (green oval), our mouse development microarray dataset, (red oval), the human UCE expression dataset (Calin et al. 2007) (blue oval) and the mouse ES cell SOLiD expression dataset (Cloonan et al. 2008) (orange oval). B) Comparison of the SOLiD ES cell RNAseq dataset (Cloonan et al. 2008) for UCEs vs. randomly chosen non-transcribed genomic regions (outliers not shown).

    Article Snippet: We therefore designed a custom microarray (CustomarrayTM 12K arrays from Combimatrix, Mukilteo, WA) encompassing 3 different probes on each DNA strand of UCEs (of the currently annotated 481 UCEs, probes could be designed for 475), as well as a large number of negative controls (exogenous sequences from bacteria and plants, negative controls used in the Affymetrix platform, rRNAs sequences), which were used to assess the levels of background signal.

    Techniques: Comparison, Microarray, Expressing