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c-Abl (Montrer ABL1 Kits ELISA) promotes TGF-beta (Montrer TGFB1 Kits ELISA)-induced SKIP/Smad3 (Montrer SMAD3 Kits ELISA) interaction.
Upon step 1 catalysis, Cwc25 (Montrer CWC25 Kits ELISA) contacts with the branch-site region, and enhanced crosslinks of Prp8 (Montrer PRPF8 Kits ELISA) and Prp45 with nucleotides surrounding the branch-site were observed.
Rab1A (Montrer RAB1A Kits ELISA) regulates anterograde melanosome transport by recruiting kinesin-1 to melanosomes through interaction with SKIP
Results show that SNW1 directly associates with EFTUD2 (Montrer EFTUD2 Kits ELISA) and SNRNP200 and that disruption of SNW1 association with these proteins promotes the apoptosis of breast cancer cells.
A transcriptome-wide analysis revealed that SNW1 or PRPF8 (Montrer PRPF8 Kits ELISA) depletion affects the splicing of specific introns in a subset of pre-mRNAs, including pre-mRNAs encoding the cohesion protein sororin and the APC (Montrer APC Kits ELISA)/C subunit APC2.
High SKIP expression was detected in clinical HCC (Montrer FAM126A Kits ELISA) samples.
SKIP increased 5alpha-dihydrotestosterone (DHT) induced N-terminal/C-terminal AR interaction from 12-fold to almost 300-fold in a two-hybrid assay, and enhanced AR ligand-independent AF-1 (Montrer EFNA5 Kits ELISA) transactivation.
Arl8 (Montrer ARL5B Kits ELISA) and SKIP are required for lysosomes to distribute away from the microtubule-organizing center. We identify two kinesin light chain binding motifs in SKIP that are required for lysosomes to accumulate kinesin-1 and redistribute to the cell periphery.
SKIP is required for epithelial mesenchymal transition and invasiveness induced by TGF-beta1 (Montrer TGFB1 Kits ELISA) in transformed cells.
This suggests that transcription of stress response genes, unlike, e.g., the SNW1-sensitive mitosis-specific genes, can proceed uncoupled from regulators that normally function under physiological conditions.
interaction with vitamin D receptor (Montrer VDR Kits ELISA) helix H10 (Montrer H1F0 Kits ELISA) residues
This gene, a member of the SNW gene family, encodes a coactivator that enhances transcription from some Pol II promoters. This coactivator can bind to the ligand-binding domain of the vitamin D receptor and to retinoid receptors to enhance vitamin D-, retinoic acid-, estrogen-, and glucocorticoid-mediated gene expression. It can also function as a splicing factor by interacting with poly(A)-binding protein 2 to directly control the expression of muscle-specific genes at the transcriptional level. Finally, the protein may be involved in oncogenesis since it interacts with a region of SKI oncoproteins that is required for transforming activity.
SKI interacting protein
, nuclear protein SkiP
, nuclear protein skip
, SKI-interacting protein
, SNW domain-containing protein 1
, homolog of Drosophila BX42
, nuclear receptor coactivator NCoA-62
, nuclear receptor coactivator, 62-kD
, ski-interacting protein