GSM4851835: MM099 ChIP-seq Fra-1; Homo sapiens; ChIP-Seq
Sample information curated by ChIP-Atlas
Antigen
Antigen Class
TFs and others
Antigen
FOSL1
Cell type
Cell type Class
Epidermis
Cell type
Melanoma cell line
NA
NA
Attributes by original data submitter
Sample
source_name
MM099 ChIP-seq Fra-1
cell line
MM099
cell type
melanoma cell line
chip antibody
Fra-1 antibody (sc-376148, Santa Cruz Biotechnology)
Sequenced DNA Library
library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
For Omni-ATAC-seq, cells were detached by trypsinization, counted and processed according to downstream protocols. For ChIP-seq, cells were grown and processed 15-cm dishes. A total of 20 million cells per ChIP sample were collected. ChIP samples were prepared following the 'Myers Lab ChIP-seq Protocol v011014'. OmniATAC-seq was performed as described previously [Corces et al., 2017]. 50,000 cells were pelleted at 500 RCF at 4°C for 5 min, medium was carefully aspirated and the cells were washed and lysed using 50 uL of cold ATAC-Resupension Buffer (RSB) (see Corces et al., 2017 for composition) containing 0.1% NP40, 0.1% Tween-20 and 0.01% digitonin by pipetting up and down three times and incubating the cells for 3 min on ice. The lysis was washed out by adding 1 mL of cold ATAC-RSB containing 0.1% Tween-20 and inverting the tube three times. Nuclei were pelleted at 500 RCF for 10 min at 4°C, the supernatant was carrefully removed and nuclei were resuspended in 50 uL of transposition mixture (25 uL 2x TD buffer (see Corces et al., 2017 for composition), 2.5 uL transposase (100 nM), 16.5 uL DPBS, 0.5 uL 1% digitonin, 0.5 uL 10% Tween-20, 5 uL H2O) by pipetting six times up and down, followed by 30 minutes incubation at 37°C at 1000 RPM mixing rate. Samples were cleaned-up by MinElute. After MinElute clean-up and elution in 21 uL elution buffer, the transposed fragments were pre-amplified with Nextera primers by mixing 20 uL of transposed sample, 2.5 uL of both forward and reverse primers (25 uM) and 25 uL of 2x NEBNext Master Mix (program: 72°C for 5 min, 98°C for 30 sec and 5 cycles of [98°C for 10 sec, 63 °C for 30 sec, 72°C for 1 min] and hold at 4°C). To determine the required number of additional PCR cycles, a qPCR was performed [see Bruenrostro et al., 2015 for the determination of the number of cycles to be added]. The final amplification was done with the additional number of cycles, samples were cleaned-up by MinElute and libraries were further prepped using the KAPA Library Quantificaton Kit as previously described [Corces et al., 2017]. For ChIP-seq, 5-20 ng of precipitated DNA was used per sample to perform library preparation according to the Illumina Truseq DNA sample preparation guide. In brief, the immunoprecipitated DNA was end-repaired, A-tailed and ligated to diluted sequencing adapters (1/100). After PCR amplification (15 cycles) and bead purification (Agencourt AmpureXP, Analis).