Eliminates separate rRNA depletion step, preserves transcriptome coverage
The first-generation Affymetrix amplification method requires depletion of ribosomal RNA (rRNA) from RNA samples for optimal exon-level analysis. Conversely, the Ambion™ WT Expression Kit uses a novel reverse transcription (RT) priming method that eliminates the need for a separate rRNA depletion step. The kit includes RT primers designed using a proprietary oligonucleotide matching algorithm that eliminates primer sequences with homology to known ribosomal RNAs. The result is complete and unbiased coverage of the transcriptome, with rRNA amplification levels significantly lower than those of other methods.
Consistent results from less input RNA
With the Ambion WT Expression Kit, samples as small as 50ng of total RNA can be analyzed on Affymetrix GeneChip Human, Mouse, and Rat Exon and Gene 1.0 ST Arrays. Previous methods required 1μg of total RNA: often difficult or impossible to obtain from limited sources such as stem cells or small tissue samples. The modest requirement for input RNA permits the analysis of rare samples and provides for more efficient and cost-effective experimentation for most sample types. To demonstrate the performance of the WT Expression Kit, RNA from three sample types (HeLa cells, and Microarray Quality Control (MAQC) A and B samples) was prepared in triplicate using either the Affymetrix GeneChip WT cDNA Synthesis and Amplification Kit or the WT Expression Kit, and analyzed on Human Exon 1.0 ST Arrays. Total RNA (1μg) prepared by the Affymetrix protocol underwent an rRNA-depletion step while just 50ng total RNA (20-fold less) was prepared for microarray analysis using the WT Expression Kit. Both sets of samples were handled according to the manufacturers' recommendations. Direct correlation of log2 ratios for MAQC samples A and B was high, (r >0.94) at both the exon and transcript levels. Correlation of log2 ratios with gene expression data obtained using TaqMan™ Gene Expression assays for real-time PCR was also high for both kits.
Identify more differential expression with less RNA
In addition to its lower input RNA requirement, the WT Expression Kit provides a significant increase in sensitivity. A greater number of probe sets detected above background was obtained at the exon level with the WT Expression Kit as a result of an increased signal-to-noise ratio. A comparison of differential expression analysis results from the two methods indicated that, while differentially expressed genes and exons of MAQC A and MAQC B samples were similar between the two kits (78% and 89%, respectively), significantly more differential expression was observed on arrays hybridized with samples prepared using the WT Expression Kit. 499 more genes and 6,850 more exons were found to be differentially expressed in samples prepared using the Ambion kit, compared to samples prepared with the Affymetrix kit.
- Optimized for use with Affymetrix GeneChip Human, Mouse, and Rat 1.0 ST Arrays
- Allows RNA samples as small as 50ng to be analyzed on Affymetrix GeneChip Arrays
- Supports a streamlined workflow that does not require a separate rRNA depletion step
- Is ideal for high-sensitivity expression profiling
Expression Array Labeling, Gene Expression Analysis and Genotyping, Microarray Analysis, RNA Amplification
Shipping Condition: Approved for shipment on Wet or Dry Ice
|Kit, WT Expression|
|Expression Array Labeling, Gene Expression Analysis and Genotyping, Microarray Analysis, RNA Amplification|
|33μL First-Strand Enzyme Mix, 132μL First-Strand Buffer Mix, 165μL Second-Strand Enzyme Mix, 413μL Second-Strand Buffer Mix, 198μL IVT Enzyme Mix, 792μL IVT Buffer Mix, 10μL Control RNA 1mg/mL, 1.75mL Nuclease-free Water, 264μL 2nd-Cycle Buffer Mix, 66μL Random Primers, 264μL 2nd-Cycle Enzyme Mix, 66μL RNase H, 3.3mL Nucleic Acid Binding Buffer Concentrate, 660μL Nucleic Acid Binding Beads, 20mL Nucleic Acid Wash Solution Concentrate, 5mL Elution Solution, 10mL Nuclease-free Water, 40 8-Strip PCR Tubes and Caps, 4 U-Bottom Plate, 2 Reservoir|