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Sample GSM7056898 Query DataSets for GSM7056898
Status Public on Jan 23, 2024
Title NT_3
Sample type protein
 
Source name Microglia isolated from NT group
Organism Mus musculus
Characteristics cell type: Microglia
tissue: Brain
Treatment protocol 100000 B-NHL (A20) cells were injected iv to sublethally irradiated mice. On day 7, 10 Million CD19 CAR T cells were injected iv and mice were sacrificed on day 10. Brain was isolated and FACS sorted for microglia (CD45lo and CD11b) cells.
Growth protocol B-NHL cells were maintained in DMEM complete media with 10% FCS and Penstrip
Extracted molecule protein
Extraction protocol PamGene lysates were prepared according to manufacturers instructions with M-PER Mammalian Protein Extraction Reagent (ThermoFisher) containing Halt phosphatase and Halt protease inhibitor cocktails (ThermoFisher). Total protein was quantified using the Pierce BCA Protein Assay Kit (ThermoFisher).
Label PY20 FITC
Label protocol We used the STK PamGene Array according to instructions
 
Hybridization protocol 5 μg of protein per well was loaded onto the PamChip and the assay was run on a PamStation96 (PamGene International).
Scan protocol The degree of phosphorylation was measured in real time via the kinetic image capture program, Evolve (PamGene International) Following 60 min incubation, the signal intensities for each peptide were analyzed using BioNavigator Software (PamGene International).
Description Protein lysates with still active kinases, phosphorylation of spotted peptides on chip detected with FITC labeled anti-phospho antibody
Data processing Only peptides that showed kinetics (increase of signal in time) on at least 25 % of the arrays were included in the analysis. Nominal coefficient of variation (CV) was calculated per peptide using a 2-component error fit model using overall mean as input and was used as a filter to remove low-intensity spots. Only peptides that showed nominal CV <0.5 were included in the analysis. For kinase interpretation, a ranked list of putative kinases responsible for differences in the peptide phosphorylation was generated by upstream kinase analysis (UKA, PamGene International).
 
Submission date Feb 22, 2023
Last update date Jan 23, 2024
Contact name Robert Zeiser
Organization name Uniklinik_Freiburg
Department Inner Medicine 1
Street address Hugstetter Strasse 53
City Freiburg
ZIP/Postal code 79106
Country Germany
 
Platform ID GPL33157
Series (1)
GSE225811 Signaling in microglia during CAR Tcell induced Immune cell associated neurotoxicity syndrome (ICANS)

Data table header descriptions
ID_REF
VALUE raw signal

Data table
ID_REF VALUE
ACM1_421_433 6.419284344
ACM1_444_456 5.416737556
ACM4_456_468 5.737646103
ACM5_494_506 7.041504383
ACM5_498_510 6.287494659
ADDB_696_708 4.332775593
ADDB_706_718 5.660096645
ADRB2_338_350 6.177466393
AKT1_301_313 3.743754625
ANDR_785_797 6.227002621
ART_025_CXGLRRWSLGGLRRWSL 6.444507122
ATF2_47_59 2.647119045
BAD_112_124 4.779874325
BAD_69_81 5.05179882
BAD_93_105 8.05241394
CA2D1_494_506 6.503900528
CAC1C_1974_1986 6.879872322
CD27_212_224 5.888628483
CDC2_154_169 5.143984795
CDK7_163_175 5.767934799

Total number of rows: 97

Table truncated, full table size 2 Kbytes.




Supplementary data files not provided
Processed data are available on Series record

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