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Gcs 3000 canner

Manufactured by Thermo Fisher Scientific
Sourced in United States

The GCS 3000 canner is a laboratory equipment designed for the hermetic sealing of test samples in cans or other containers. It provides a controlled environment for the preservation and storage of samples, ensuring their integrity during transportation and analysis.

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2 protocols using gcs 3000 canner

1

miRNA Profiling Using Affymetrix GeneChip

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The Affymetrix Genechip miRNA 4.0 array process was carried out according to the manufacturer’s instructions. 1000 ng RNA samples were labeled with the FlashTag™ Biotin using RNA Labeling Kit (Genisphere, Hatfield, PA, USA). The labeled RNA was further quantified, fractionated and hybridized to the miRNA microarray according to the standard protocol. The labeled RNA was then heated at 99 °C and then at 45 °C (for 5 mins at both temp). An Affymetrix® 450 Fluidics Station was used for RNA-array hybridization with agitation at 60 rotations per minute at 48 °C for 16 h. The chips were washed and stained using a Genechip Fluidics Station 450 (Affymetrix, Santa Clara, California, United States). The chips were then scanned with an Affymetrix GCS 3000 canner (Affymetrix, Santa Clara, California, United States). Using the Affymetrix® GeneChip™ Command Console software (AGCC) signal values were computed.
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2

Affymetrix GeneChip miRNA 4.0 Array Protocol

Check if the same lab product or an alternative is used in the 5 most similar protocols
The Affymetrix Genechip miRNA 4.0 array process was executed according to the manufacturer's protocol. 1000 ng RNA samples were labeled with the FlashTag™ Biotin RNA Labeling Kit (Genisphere, Hatfield, PA, USA). The labeled RNA was quantified, fractionated and hybridized to the miRNA microarray according to the standard procedures provided by the manufacture. The labeled RNA was heated to 99°C for 5 minutes and then to 45 °C for 5 min.
RNA-array hybridization was performed with agitation at 60 rotations per minute for 16 h at 48 °C on an Affymetrix GeneChip Hybridization oven 645. The chips were washed and stained using a Genechip Fluidics Station 450 (Affymetrix, CA, United States). The chips were then scanned with an Affymetrix GCS 3000 canner (Affymetrix).
MiRNA-Gene ontology (GO) analysis was performed by top 5 list of miRNAs that satisfy |fold change| ≥ 2 and p value < 0.05 between primary CRC group and paired PTM group. The miRNA-GO analysis was conducted through DIANA-mirPath v 3.0 software.
The genes targeted by miR-193a used heatmap to compare the expression levels in each CRC-PTM cell line set (SNU-2335A, SNU-2335D, SNU-2404A, SNU-2404B, SNU-2414A and SNU-2414B) and the heatmap were analyzed using “pheatmap” libarary in R program (v 4.0.0).
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