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1.
Figure 2.

Figure 2. From: Explaining differences in saturation levels for Affymetrix GeneChip® arrays.

Standard Affymetrix eukaryotic protocol for hybridization, washing, staining and scanning (left) and our modified protocol (right).

Dmitriy Skvortsov, et al. Nucleic Acids Res. 2007 Jun;35(12):4154-4163.
2.
Figure 1.

Figure 1. From: Explaining differences in saturation levels for Affymetrix GeneChip® arrays.

Adsorption isotherms observed for Affymetrix microarrays. The observed adsorption isotherms (signal intensity versus target concentration) for Affymetrix microarrays exhibit different saturation intensities on both the log2 (left panel) and natural (right panel) scale.

Dmitriy Skvortsov, et al. Nucleic Acids Res. 2007 Jun;35(12):4154-4163.
3.
Figure 6.

Figure 6. From: Explaining differences in saturation levels for Affymetrix GeneChip® arrays.

Washing effect for specific and non-specific signal. (A) A boxplot of non-specifically bound probes intensities before and after the stringent wash. (B) before- versus after-wash scatterplot of specifically and non-specifically bound probe intensities; gray dots represent non-specific and black circles represent specific probe intensities.

Dmitriy Skvortsov, et al. Nucleic Acids Res. 2007 Jun;35(12):4154-4163.
4.
Figure 8.

Figure 8. From: Explaining differences in saturation levels for Affymetrix GeneChip® arrays.

Hybridization time effect. (A) The comparison of intensity ratios for spiked probes following 16 and 40 h of hybridization for PM (solid circles) and MM (open circles) probes. (B) shows the log2 difference in the wash effect for hybridization experiments with 16 and 40 h hybridization times for PM (solid circles) and MM (open circles) probes.

Dmitriy Skvortsov, et al. Nucleic Acids Res. 2007 Jun;35(12):4154-4163.
5.
Figure 4.

Figure 4. From: Explaining differences in saturation levels for Affymetrix GeneChip® arrays.

Scatterplot of intensities for corresponding probes resulting from the standard and modified protocols. Shown are the log2 intensities for spiked clones after the stringent wash from a chip processed according to the standard Affymetrix protocol versus the log2 intensities of the same probes on a chip that was processed according to the altered protocol; PM signal [red] and MM signal [blue].

Dmitriy Skvortsov, et al. Nucleic Acids Res. 2007 Jun;35(12):4154-4163.
6.
Figure 3.

Figure 3. From: Explaining differences in saturation levels for Affymetrix GeneChip® arrays.

Numerical solution of system (3). X-axis represents time in hours, Y-axis represents the fraction of chip that is occupied by particular targets. The colored lines represent the following: black, the fraction of unoccupied oligos; green, the fraction of oligos occupied by non-specifically absorbed targets; blue, the fraction occupied by intermediate products (partially zipped complexes with varying degrees of completion); orange, the fraction of all oligos bound to specific targets (fully and partially zipped); red, the fraction occupied by complete fully zipped duplexes.

Dmitriy Skvortsov, et al. Nucleic Acids Res. 2007 Jun;35(12):4154-4163.
7.
Figure 7.

Figure 7. From: Explaining differences in saturation levels for Affymetrix GeneChip® arrays.

Concentration effect. (A) The comparison of intensity ratios between hybridization experiments with clone concentrations of 1 nM and 10 nM for PM (black circles) and MM (open circles) probes versus the log2 intensity before the wash. (B) The observed log2 difference in the wash effect for 1 and 10 nM for PM (black circles) and MM (open circles) probes versus the log 2 intensity before the wash.

Dmitriy Skvortsov, et al. Nucleic Acids Res. 2007 Jun;35(12):4154-4163.
8.
Figure 5.

Figure 5. From: Explaining differences in saturation levels for Affymetrix GeneChip® arrays.

Washing effect. (A) The log2 observed intensities for spiked targets in the presence of complex background before the wash for PM (solid black) and MM (dashed black) probes, and after the wash for PM (solid gray) and MM (dashed gray) probes. Intensities are ordered by the pre-wash intensity of PM and MM probes. (B) The observed wash effect (pre/post wash intensity ratio) for spiked probes in the presence of complex background versus the log2 observed PM pre-wash intensity. Black and gray dots represent the PM wash effect after the first and second wash, respectively. Open black and gray circles represent the MM wash effect after the first and second wash, respectively.

Dmitriy Skvortsov, et al. Nucleic Acids Res. 2007 Jun;35(12):4154-4163.

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