Application
Fig1: Western blot analysis of FUS/TLS on K562 cells lysates using anti-FUS/TLS antibody at 1/1,000 dilution.Application
Fig2: ICC staining FUS/TLS in Hela cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.Application
Fig3: ICC staining FUS/TLS in MCF-7 cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.Application
Fig4: ICC staining FUS/TLS in SW480 cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.Application
Fig5: Immunohistochemical analysis of paraffin-embedded human kidney tissue using anti-FUS/TLS antibody. Counter stained with hematoxylin.Application
Fig6: Flow cytometric analysis of Hela cells with FUS/TLS antibody at 1/50 dilution (red) compared with an unlabelled control (cells without incubation with primary antibody; black). Alexa Fluor 488-conjugated goat anti rabbit IgG was used as the secondary antibody.| Product Name | FUS/TLS [JJ09-31] |
|---|---|
| Antibody Type | Primary Antibodies |
| Antigen Alias | 75 kDa DNA pairing protein antibody 75 kDa DNA-pairing protein antibody ALS6 antibody Amyotrophic lateral sclerosis 6 antibody fus antibody FUS CHOP antibody Fus like protein antibody FUS_HUMAN antibody FUS1 antibody Fused in sarcoma antibody Fusion (involved in t(12;16) in malignant liposarcoma) antibody Fusion derived from t(12;16) malignant liposarcoma antibody Fusion gene in myxoid liposarcoma antibody Heterogeneous nuclear ribonucleoprotein P2 antibody hnRNP P2 antibody hnRNPP2 antibody Oncogene FUS antibody Oncogene TLS antibody POMp75 antibody RNA binding protein FUS antibody RNA-binding protein FUS antibody TLS antibody TLS CHOP antibody Translocated in liposarcoma antibody Translocated in liposarcoma protein antibody |
| Product description | EWS and FUS/TLS are nuclear RNA-binding proteins. As a result of chromosome translocation, the EWS gene is fused to a variety of transcription factors, including ATF-1, in human neoplasias. In the Ewing family of tumors, the N-terminal domain of EWS is fused to the DNA-binding domain of various Ets transcription factors, including Fli-1, ETV1 and FEV. The EWS/Fli-1 chimeric protein acts as a more potent transcriptional activator than Fli-1 and can promote cell transformation. In human myxoid liposarcomas and myeloid leukemias, chromosomal translocation results in the fusion of the N-terminal region of FUS/TLS with the open reading frame of CHOP. In normal cells, FUS/TLS binds to the DNA-binding domains of nuclear steroid receptors and is also present in subpopulations of TFIID complexes, indicating a potential role for FUS/TLS in the processing of primary transcripts that are generated in response to hormone-induced transcription. |
| Immunogen | recombinant protein |
| Clonality | Monoclonal |
|---|---|
| Isotype | IgG |
| Host Species | Recombinant rabbit |
| Tested Applications | WBICC/IFIHCFC |
| WB:1:1,000 ICC:1:50-1:200 IHC:1:50-1:200 FC:1:50-1:100 |
|
| Species Reactivity | HumanMouseRat |
| Concentration | 1mg/ml |
| Alternative Names | 75 kDa DNA pairing protein antibody
75 kDa DNA-pairing protein antibody
ALS6 antibody
Amyotrophic lateral sclerosis 6 antibody
fus antibody
FUS CHOP antibody
Fus like protein antibody
FUS_HUMAN antibody
FUS1 antibody
Fused in sarcoma antibody
Fusion (involved in t(12 16) in malignant liposarcoma) antibody Fusion derived from t(12 16) malignant liposarcoma antibody Fusion gene in myxoid liposarcoma antibody Heterogeneous nuclear ribonucleoprotein P2 antibody hnRNP P2 antibody hnRNPP2 antibody Oncogene FUS antibody Oncogene TLS antibody POMp75 antibody RNA binding protein FUS antibody RNA-binding protein FUS antibody TLS antibody TLS CHOP antibody Translocated in liposarcoma antibody Translocated in liposarcoma protein antibody |
|---|---|
| Molecular Weight(MW) | 75 kDa |
| Cellular Localization | Nucleus. |
Application
Fig1: Western blot analysis of FUS/TLS on K562 cells lysates using anti-FUS/TLS antibody at 1/1,000 dilution.
Application
Fig2: ICC staining FUS/TLS in Hela cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.
Application
Fig3: ICC staining FUS/TLS in MCF-7 cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.
Application
Fig4: ICC staining FUS/TLS in SW480 cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.
Application
Fig5: Immunohistochemical analysis of paraffin-embedded human kidney tissue using anti-FUS/TLS antibody. Counter stained with hematoxylin.
Application
Fig6: Flow cytometric analysis of Hela cells with FUS/TLS antibody at 1/50 dilution (red) compared with an unlabelled control (cells without incubation with primary antibody; black). Alexa Fluor 488-conjugated goat anti rabbit IgG was used as the secondary antibody.| Positive Control | SW480, MCF-7, Hela, K562, human kidney tissue. |
|---|---|
| Application Notes | WB:1:1,000 ICC:1:50-1:200 IHC:1:50-1:200 FC:1:50-1:100 |
| Form | Liquid |
|---|---|
| Storage Instructions | Store at +4℃ after thawing. Aliquot store at -20℃ or -80℃. Avoid repeated freeze / thaw cycles. |
| Storage Buffer | 1*TBS (pH7.4), 1%BSA, 40%Glycerol. Preservative: 0.05% Sodium Azide. |
