Autor: |
Uğurlu-Çimen, Deniz, Odluyurt, Deniz, Sevinç, Kenan, Özkan-Küçük, Nazlı Ezgi, Özçimen, Burcu, Demirtaş, Deniz, Enüstün, Eray, Aztekin, Can, Philpott, Martin, Oppermann, Udo, Özlü, Nurhan, Önder, Tamer T. |
Rok vydání: |
2021 |
DOI: |
10.6084/m9.figshare.14903765.v1 |
Popis: |
Additional file 1: Figure S1. Identification of proximal interactors of DOT1L via BioID and their effect on reprogramming. (a) Replicate immunoblot of Fig. 1b. (b) CRAPome analysis of WT-DOT1L proximal proteins identified via BioID assay. Y-axis shows the PSM values from MS data. (c) mRNA levels of shRNA targeted genes were assessed via qRT-PCR. β-actin was used as an internal control and gene expression levels are normalized to control shFF (firefly luciferase targeting shRNA) expressing cells. (d) mRNA levels of shAF9 targeted genes were assessed via qRT-PCR. β-actin was used as an internal control and gene expression levels are normalized to control shFF (firefly luciferase targeting shRNA) expressing cells. (e) Fold change in the number of Tra-1-60 positive colonies upon shAF9 expression. P values were determined by one sample t-test; * P |
Databáze: |
OpenAIRE |
Externí odkaz: |
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