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Home › Dataset Library › Transcription profiling of mouse RAW 264.7 cells treated with the oxidant hypochlorous acid (HOCl) - dose response

Dataset: Transcription profiling of mouse RAW 264.7 cells treated with the oxidant hypochlorous acid (HOCl) - dose response

Hypochlorous acid (HOCl) is a potent oxidant that is produced endogenously in mammalian tissue by phagocytes. Exogenous exposure to HOCl...

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Hypochlorous acid (HOCl) is a potent oxidant that is produced endogenously in mammalian tissue by phagocytes. Exogenous exposure to HOCl also can occur following inhalation of chlorine gas. HOCl has been implicated as a source of oxidative stress associated atherosclerosis and other diseases. The purpose of this study was to identify dose-dependent transitions in cellular response to hypochlorous acid (HOCl), with a focus on understanding how various cellular defense and stress dose-responses overlap. Experiment Overall Design: RAW 264.7 cells were grown to 80-90% confluency in DMEM supplemented with supplemented with 10% fetal bovine serum (FBS), 10 mM HEPES, 100 U penicillin/ml, and 100 µg streptomycin/ml. Cells were treated with 0, 0.14, 0.35, 0.7, 1.4, 2.1, 2.8 or 3.5 mM HOCl in medium for 6 hr. Total RNA was isolated from cells with TRIzol according to manufacturer's instructions and then subjected to cleanup using RNase-Free DNase Set and RNeasy Mini kit. The resultant DNA-free RNA was diluted in RNase-free H2O and quantified by Nanodrop at 260 nm. The quality of RNA samples was confirmed using RNA Nano Chips with Agilent 2100 Bioanalyzer. RNA samples were stored at –70 oC until use. Experiment Overall Design: From 5 micrograms of total RNA, cDNA was synthesized using a one-cycle cDNA synthesis kit (Affymetrix Corp., Santa Clara, CA). cDNA was transcribed to cRNA which was then biotin-labeled using GeneChip IVT labeling kit. Fifteen micrograms of labeled cRNA were then hybridized to an Affymetrix Mouse Genome 430 2.0 Array at 45°C for 16 hr. Biological cRNA replicates (n = 3) were each hybridized to an individual array. After being washed using the GeneChip Fluidics Station 450, arrays were scanned using a GeneChip 3000 scanner and intensity values were extracted from the CEL file using Array Assist software (Stratagene, La Jolla, CA). Experiment Overall Design:

Species:
mouse

Samples:
25

Source:
E-GEOD-15457

Updated:
Dec.12, 2014

Registered:
Nov.11, 2014


Factors: (via ArrayExpress)
Sample
GSE15457GSM387601
GSE15457GSM387602
GSE15457GSM387605
GSE15457GSM387606
GSE15457GSM387645
GSE15457GSM387646
GSE15457GSM387647
GSE15457GSM387648
GSE15457GSM387649
GSE15457GSM387676
GSE15457GSM387677
GSE15457GSM387678
GSE15457GSM387679
GSE15457GSM387698
GSE15457GSM387699
GSE15457GSM387700
GSE15457GSM387701
GSE15457GSM387702
GSE15457GSM387703
GSE15457GSM387713
GSE15457GSM387714
GSE15457GSM387716
GSE15457GSM387750
GSE15457GSM387751
GSE15457GSM387752

Tags

  • atherosclerosis
  • gas
  • genome
  • serum

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