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Applied Biosystems™
ViiA™ 7 Array Card RNaseP Verification Kit
The ViiA™ 7 System TaqMan™ Low Density Array Instrument Verification RNase P kit is used to validate the performance of詳細を見る
| 製品番号（カタログ番号） | 数量 |
|---|---|
| 4432265 | 1 kit |
製品番号（カタログ番号） 4432265
価格（JPY）
320,900
Each
数量:
1 kit
The ViiA™ 7 System TaqMan™ Low Density Array Instrument Verification RNase P kit is used to validate the performance of the Applied Biosystems™ ViiA™ 7 Real-Time PCR Systems with the TaqMan™ Low Density Array Block Upgrade.
The ViiA™ 7 System TaqMan™ Low Density Array Instrument Verification RNase P kit contains an empty TaqMan™ Low Density Array and 8 vials of RNase P detection reagents to detect and quantitate genomic copies of the human RNase P gene, a single-copy gene encoding the RNA moiety of the RNase P enzyme. Each vial contains premixed reagents (1X TaqMan™ Universal PCR Master Mix, RNase P primers, and FAM™ dye-labeled probe) and template.
The ViiA™ 7 System TaqMan™ Low Density Array Instrument Verification RNase P kit must demonstrate the ability to distinguish between 5,000 and 10,000 genomic equivalents with a 99.7% confidence level for a subsequent sample run in a single well. To ensure accurate results, Applied Biosystems™ recommends that the performance of your instrument be verified every six months.
The ViiA™ 7 System TaqMan™ Low Density Array Instrument Verification RNase P kit contains an empty TaqMan™ Low Density Array and 8 vials of RNase P detection reagents to detect and quantitate genomic copies of the human RNase P gene, a single-copy gene encoding the RNA moiety of the RNase P enzyme. Each vial contains premixed reagents (1X TaqMan™ Universal PCR Master Mix, RNase P primers, and FAM™ dye-labeled probe) and template.
The ViiA™ 7 System TaqMan™ Low Density Array Instrument Verification RNase P kit must demonstrate the ability to distinguish between 5,000 and 10,000 genomic equivalents with a 99.7% confidence level for a subsequent sample run in a single well. To ensure accurate results, Applied Biosystems™ recommends that the performance of your instrument be verified every six months.
研究用途にのみご使用ください。診断目的には使用できません。
仕様
校正タイプRNase P Calibration, Instrument Verification Plate
使用対象（アプリケーション）Real Time PCR (qPCR)
使用対象 (装置)ViiA™ 7 System
フォーマット384-well Microfluidic Card
製品ラインViiA
数量1 kit
製品タイプArray Card RNaseP Verification Kit
Unit SizeEach
組成および保存条件
8 x Tubes with Standard Dilutions, Empty Array Card, Port 1 NTC, Port 2 Unknown A, Port 3 U, Store at -15°C to -25°C