Mouse Recombinant Monoclonal TLS/FUS antibody. Carrier free. Suitable for ICC/IF, WB, IHC-P and reacts with Mouse, Human, Rat samples.
pH: 7.2 - 7.4
Constituents: 100% PBS
ICC/IF | WB | IHC-P | IP | |
---|---|---|---|---|
Human | Tested | Tested | Tested | Not recommended |
Mouse | Tested | Tested | Tested | Not recommended |
Rat | Expected | Expected | Tested | Not recommended |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Rat | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Rat | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Rat, Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human, Rat, Mouse | Dilution info - | Notes - |
DNA/RNA-binding protein that plays a role in various cellular processes such as transcription regulation, RNA splicing, RNA transport, DNA repair and damage response (PubMed:27731383). Binds to nascent pre-mRNAs and acts as a molecular mediator between RNA polymerase II and U1 small nuclear ribonucleoprotein thereby coupling transcription and splicing (PubMed:26124092). Binds also its own pre-mRNA and autoregulates its expression; this autoregulation mechanism is mediated by non-sense-mediated decay (PubMed:24204307). Plays a role in DNA repair mechanisms by promoting D-loop formation and homologous recombination during DNA double-strand break repair (PubMed:10567410). In neuronal cells, plays crucial roles in dendritic spine formation and stability, RNA transport, mRNA stability and synaptic homeostasis (By similarity).
TLS, FUS, RNA-binding protein FUS, 75 kDa DNA-pairing protein, Oncogene FUS, Oncogene TLS, POMp75, Translocated in liposarcoma protein
Mouse Recombinant Monoclonal TLS/FUS antibody. Carrier free. Suitable for ICC/IF, WB, IHC-P and reacts with Mouse, Human, Rat samples.
pH: 7.2 - 7.4
Constituents: 100% PBS
What are the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:
For more information, read more on recombinant antibodies.
Conjugation ready
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. This conjugation-ready format is designed for use with fluorochromes, metal isotopes, oligonucleotides, and enzymes, which makes them ideal for antibody labelling, functional and cell-based assays, flow-based assays (e.g. mass cytometry) and Multiplex Imaging applications.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with 1 minute hands-on-time and 100% antibody recovery: available for fluorescent dyes, HRP, biotin and gold.
Collaborations
This antibody was developed by the Structural Genomics Consortium and manufactured by Abcam.
TLS/FUS also known as FUS and the FUS protein is an RNA-binding protein involved in various cellular processes. It has a molecular weight of approximately 53 kDa. Expressed extensively in the nucleus FUS/TLS relocates to the cytoplasm under stress conditions. It plays mechanical roles in transcription regulation RNA splicing and mRNA transport. Scientists sometimes refer to FUS as the 'fused in sarcoma' protein because of its involvement in gene fusion events.
The FUS protein aids in the maintenance and stabilization of mRNA molecules and participates in the formation of stress granules distinct cytoplasmic aggregates of proteins and RNAs. It forms part of a large protein complex alongside other RNA-binding proteins. FUS stabilizes pre-mRNA structures which affects protein expression patterns essential for cell survival and differentiation. Its ability to bind to RNA and DNA indicates its fundamental role in genomic stability.
The functions of FUS help regulate RNA metabolism-related pathways and cellular stress response pathways. FUS interacts with proteins like TAF15 and EWSR1 within these pathways showing a complex network of interactions that contribute to RNA maturation and stress granule dynamic formation. The activity of FUS in these pathways ultimately affects cellular homeostasis gene expression modulation and response to cellular stress.
FUS protein mutations or mislocalizations relate to neurodegenerative diseases such as amyotrophic lateral sclerosis (ALS) and frontotemporal lobar degeneration (FTLD). These conditions are characterized by the accumulation of FUS or FUS-related aggregates in the cytoplasm leading to neuronal cell death. FUS is also connected to other RNA-binding proteins like TDP-43 which also mislocalizes and forms aggregates in these disorders highlighting the importance of protein homeostasis and normal RNA metabolism in the prevention of these diseases.
We have tested this species and application combination and it works. It is covered by our product promise.
We have not tested this specific species and application combination in-house, but expect it will work. It is covered by our product promise.
This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
We do not recommend this combination. It is not covered by our product promise.
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In the unlikely event of one of our products not working as expected, you are covered by our product promise.
Full details and terms and conditions can be found here:
Terms & Conditions.
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of Rat colon tissue labelling TLS/FUS with Anti-TLS/FUS antibody [Z-FUS-5] - Mouse IgG2a (Chimeric) ab283272 at 1/100 dilution. Heat mediated antigen retrieval was performed using Tris/EDTA buffer pH 9. LeicaDS9800 (Bond™ Polymer Refine Detection) was used as the secondary antibody. Hematoxylin was used as a counterstain.
Nuclear staining on rat colon. The section was incubated with Anti-TLS/FUS antibody [Z-FUS-5] - Mouse IgG2a (Chimeric) ab283272 for 30 mins at room temperature and followed mouse specific IgG antibody for 8 mins.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
This data was developed using Anti-TLS/FUS antibody [Z-FUS-5] - Mouse IgG2a (Chimeric) ab283272, the same antibody clone in a different buffer formulation.
Anti-TLS/FUS antibody [Z-FUS-5] - Mouse IgG2a (Chimeric) ab283272 staining NIH/3T3 in HeLa cells. The cells were fixed with 4% paraformaldehyde (10 min), permeabilized with 0.1% Triton X-100 for 5 minutes. The cells were then incubated with Anti-TLS/FUS antibody [Z-FUS-5] - Mouse IgG2a (Chimeric) ab283272 at 1/50 dilution and Anti-beta Tubulin antibody [EPR16774] - Loading Control ab179513 (Rabbit monoclonal to beta Tubulin) at 1/20 dilution overnight at +4°C, followed by a further incubation at room temperature for 1h with a goat secondary antibody to mouse IgG (Alexa Fluor® 488) (Goat Anti-Mouse IgG H&L (Alexa Fluor® 488) ab150113 ) at 1/1000 dilution (shown in green) and a goat secondary antibody to rabbit IgG (Alexa Fluor® 594) (Goat Anti-Rabbit IgG H&L (Alexa Fluor® 594) ab150080) at 1/500 dilution (shown in red). Nuclear DNA was labelled in blue with DAPI.
Confocal image showing nuclear staining in NIH/3T3 cell line.
This data was developed using Anti-TLS/FUS antibody [Z-FUS-5] - Mouse IgG2a (Chimeric) ab283272, the same antibody clone in a different buffer formulation.
The expression molecular weight observed is consistent with what has been described in the literature (PMID: 30344044).
Lanes 1-2: Merged signal (red and green). Green - Anti-TLS/FUS antibody [Z-FUS-5] - Mouse IgG2a (Chimeric) ab283272 observed at 60 kDa. Red - loading control Anti-GAPDH antibody [EPR16891] - Loading Control ab181602 (Rabbit monoclonal [EPR16891] to GAPDH) observed at 36 kDa.
Lanes 1-2: Anti-TLS/FUS antibody [Z-FUS-5] - Mouse IgG2a (Chimeric) ab283272 Anti-FUS antibody was shown to react with FUS in HAP1 cells in Western blot. Loss of signal was observed when FUS knockout sample was used. Wild-type and FUS knockout samples were subjected to SDS-PAGE.
Anti-TLS/FUS antibody [Z-FUS-5] - Mouse IgG2a (Chimeric) ab283272 and Anti-GAPDH antibody [EPR16891] - Loading Control (Anti-GAPDH antibody [EPR16891] - Loading Control ab181602) were incubated at 4℃ overnight at 1 in 1000 dilution and 1 in 20000 dilution respectively. Blots were developed with Goat anti-Rabbit IgG H&L (IRDye® 680CW) preadsorbed (Goat Anti-Rabbit IgG H&L (IRDye® 680RD) preadsorbed ab216777) and Goat anti-Mouse IgG H&L (IRDye® 800RD) preadsorbed (Goat anti-Mouse IgG H&L (IRDye® 800CW) preadsorbed ab216772) secondary antibodies at 1 in 10000 dilution for 1 hour at room temperature before imaging.
70kDa band is the non-specific band according to KO validation.
This data was developed using Anti-TLS/FUS antibody [Z-FUS-5] - Mouse IgG2a (Chimeric) ab283272, the same antibody clone in a different buffer formulation.
All lanes: Western blot - Anti-TLS/FUS antibody [Z-FUS-5] - Mouse IgG2a (Chimeric) (Anti-TLS/FUS antibody [Z-FUS-5] - Mouse IgG2a (Chimeric) ab283272) at 1/1000 dilution
Lane 1: Wild type HAP1(human chronic myelogenous leukemia near-haploid cell line), whole cell lysate at 20 µg
Lane 2: FUS knockout HAP1(human chronic myelogenous leukemia near-haploid cell line), whole cell lysate at 20 µg
Lane 3: HeLa (human cervix adenocarcinoma epithelial cell), whole cell lysate at 20 µg
Lane 4: 293T (human embryonic kidney epithelial cell) whole cell lysate at 20 µg
All lanes: Western blot - Goat Anti-Rabbit IgG H&L (IRDye® 680RD) preadsorbed (Goat Anti-Rabbit IgG H&L (IRDye® 680RD) preadsorbed ab216777) at 1/10000 dilution
Predicted band size: 53 kDa
Observed band size: 60 kDa
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of Mouse stomach tissue labelling TLS/FUS with Anti-TLS/FUS antibody [Z-FUS-5] - Mouse IgG2a (Chimeric) ab283272 at 1/100 dilution. Heat mediated antigen retrieval was performed using Tris/EDTA buffer pH 9. LeicaDS9800 (Bond™ Polymer Refine Detection) was used as the secondary antibody. Hematoxylin was used as a counterstain.
Nuclear staining on mouse stomach. The section was incubated with Anti-TLS/FUS antibody [Z-FUS-5] - Mouse IgG2a (Chimeric) ab283272 for 30 mins at room temperature and followed mouse specific IgG antibody for 8 mins.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
This data was developed using Anti-TLS/FUS antibody [Z-FUS-5] - Mouse IgG2a (Chimeric) ab283272, the same antibody clone in a different buffer formulation.
The expression molecular weight observed is consistent with what has been described in the literature (PMID: 30344044).
70kDa band is the non-specific band according to KO validation.
Lane 1: 70 seconds
Lane 2: 26 seconds
This data was developed using Anti-TLS/FUS antibody [Z-FUS-5] - Mouse IgG2a (Chimeric) ab283272, the same antibody clone in a different buffer formulation.
All lanes: Western blot - Anti-TLS/FUS antibody [Z-FUS-5] - Mouse IgG2a (Chimeric) (Anti-TLS/FUS antibody [Z-FUS-5] - Mouse IgG2a (Chimeric) ab283272) at 1/1000 dilution
Lane 1: HeLa (human epithelial cell line from cervix adenocarcinoma), whole cell lysate at 20 µg
Lane 2: NIH/3T3 (mouse embryonic fibroblast), whole cell lysate at 20 µg
All lanes: Peroxidase-Conjugated Goat anti-Mouse IgG (H+L) at 1/10000 dilution
Predicted band size: 53 kDa
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of Human lung carcinoma tissue labelling TLS/FUS with Anti-TLS/FUS antibody [Z-FUS-5] - Mouse IgG2a (Chimeric) ab283272 at 1/100 dilution. Heat mediated antigen retrieval was performed using Tris/EDTA buffer pH 9. LeicaDS9800 (Bond™ Polymer Refine Detection) was used as the secondary antibody. Hematoxylin was used as a counterstain.
Nuclear staining on human lung carcinoma. The section was incubated with Anti-TLS/FUS antibody [Z-FUS-5] - Mouse IgG2a (Chimeric) ab283272 for 30 mins at room temperature and followed mouse specific IgG antibody for 8 mins.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
This data was developed using Anti-TLS/FUS antibody [Z-FUS-5] - Mouse IgG2a (Chimeric) ab283272, the same antibody clone in a different buffer formulation.
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of Human colon tissue labelling TLS/FUS with Anti-TLS/FUS antibody [Z-FUS-5] - Mouse IgG2a (Chimeric) ab283272 at 1/100 dilution. Heat mediated antigen retrieval was performed using Tris/EDTA buffer pH 9. LeicaDS9800 (Bond™ Polymer Refine Detection) was used as the secondary antibody. Hematoxylin was used as a counterstain. Nuclear staining on human colon. The section was incubated with Anti-TLS/FUS antibody [Z-FUS-5] - Mouse IgG2a (Chimeric) ab283272 for 30 mins at room temperature and followed mouse specific IgG antibody for 8 mins.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument.
This data was developed using Anti-TLS/FUS antibody [Z-FUS-5] - Mouse IgG2a (Chimeric) ab283272, the same antibody clone in a different buffer formulation.
Anti-TLS/FUS antibody [Z-FUS-5] - Mouse IgG2a (Chimeric) ab283272 staining TLS/FUS in HeLa cells. The cells were fixed with 4% paraformaldehyde (10 min), permeabilized with 0.1% Triton X-100 for 5 minutes. The cells were then incubated with Anti-TLS/FUS antibody [Z-FUS-5] - Mouse IgG2a (Chimeric) ab283272 at 1/50 dilution and Anti-beta Tubulin antibody [EPR16774] - Loading Control ab179513 (Rabbit monoclonal to beta Tubulin) at 1/20 dilution overnight at +4°C, followed by a further incubation at room temperature for 1h with a goat secondary antibody to mouse IgG (Alexa Fluor® 488) (Goat Anti-Mouse IgG H&L (Alexa Fluor® 488) ab150113 ) at 1/1000 dilution (shown in green) and a goat secondary antibody to rabbit IgG (Alexa Fluor® 594) (Goat Anti-Rabbit IgG H&L (Alexa Fluor® 594) ab150080) at 1/500 dilution (shown in red). Nuclear DNA was labelled in blue with DAPI.
Confocal image showing nuclear staining in HeLa cell line.
This data was developed using Anti-TLS/FUS antibody [Z-FUS-5] - Mouse IgG2a (Chimeric) ab283272, the same antibody clone in a different buffer formulation.
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