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Invitrogen™ WT Expression Kit, high throughput

Generates amplified sense-strand cDNA ready for fragmentation and labeling using the Affymetrix™ GeneChip™ WT Terminal Labeling Kit

Brand:  Invitrogen™ 4440536

Additional Details : Weight : 0.00450kg

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Product Code. 15524334

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Description

Description

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 (see Product Bulletin for data).

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
  • For high-throughput robotics

Expression Array Labeling, Gene Expression Analysis and Genotyping, Microarray Analysis, RNA Amplification

Specifications

Specifications

Kit, WT Expression
No
Proprietary
≥ 50 ng total RNA
Ambion™
• 150 μl First-Strand Enzyme Mix (-20°C)
• 600 μl First-Strand Buffer Mix (-20°C)
• 650 μl Second-Strand Enzyme Mix (-20°C)
• 1.45 ml Second-Strand Buffer Mix (-20°C)
• 850 μl IVT Enzyme Mix (-20°C)
• 1.4 ml IVT Buffer Mix (-20°C)
• 10 μl Control RNA 1 mg/ml (-20°C)
• 1.45 ml 2nd-Cycle Buffer Mix (-20°C)
• 300 μl Random Primers (-20°C)
• 1 ml 2nd-Cycle Enzyme Mix (-20°C)
• 300 μl RNase H (-20°C)
• 12.5 ml Nucleic Acid Binding Buffer Concentrate (room temperature)
• 2.5 ml Nucleic Acid Binding Beads (4°C)
• 50 ml Nucleic Acid Wash Solution Concentrate (room temperature)
• 22 ml Elution Solution (4°C or room temperature)
Indirect Labeling
Total RNA
Affymetrix GeneChip™
96 Reactions
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For Research Use Only. Not for use in diagnostic procedures.