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Laboratory chip technique

Manufactured by Agilent Technologies

The Laboratory-Chip technique is an analytical method that utilizes a miniaturized platform to perform various laboratory operations. It allows for the integration of multiple analytical processes on a single, compact device. The core function of this technique is to enable rapid and efficient analysis of small-volume samples, with applications in fields such as chemistry, biology, and diagnostics.

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2 protocols using laboratory chip technique

1

NK Precursor Gene Expression Analysis

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NK precursors (stage 1 and stage 2) were sorted according to their expression profiles described in supplementary figure 4a. Total RNA was extracted using RNeasy Micro Kit (Qiagen). The quality of the RNA obtained was evaluated using the Laboratory-Chip technique (Agilent Bioanalyzer) and subsequently preamplified according to the Ambion WTA expression protocol (Thermo Fischer). RNA was reverse transcribed into cDNA using the iScript protocol (Bio-Rad). QT-PCR was performed using the SsoAdvanced™ Universal SYBR® Green Supermix (BIO-RAD) and the MyCycler Thermal cycler system (Bio-Rad).Used primers: mNKG2D-S FW: AGTTGAGTTGAAGGCTTTGACTC, mNKG2D-S REV: ACTTTGCTGGCTTGAGGTC, DAP12 FW: GACTGTGGGAGGATTAAGTCC, DAP12 REV: AACACCAAGTCACCCAGAAC.
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2

NK Precursor Gene Expression Analysis

Check if the same lab product or an alternative is used in the 5 most similar protocols
NK precursors (stage 1 and stage 2) were sorted according to their expression profiles described in supplementary figure 4a. Total RNA was extracted using RNeasy Micro Kit (Qiagen). The quality of the RNA obtained was evaluated using the Laboratory-Chip technique (Agilent Bioanalyzer) and subsequently preamplified according to the Ambion WTA expression protocol (Thermo Fischer). RNA was reverse transcribed into cDNA using the iScript protocol (Bio-Rad). QT-PCR was performed using the SsoAdvanced™ Universal SYBR® Green Supermix (BIO-RAD) and the MyCycler Thermal cycler system (Bio-Rad).Used primers: mNKG2D-S FW: AGTTGAGTTGAAGGCTTTGACTC, mNKG2D-S REV: ACTTTGCTGGCTTGAGGTC, DAP12 FW: GACTGTGGGAGGATTAAGTCC, DAP12 REV: AACACCAAGTCACCCAGAAC.
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