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Fused in Sarcoma (FUS) ELISA Kits

FUS encodes a multifunctional protein component of the heterogeneous nuclear ribonucleoprotein (hnRNP) complex. Additionally we are shipping FUS Antibodies (104) and FUS Proteins (7) and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
FUS 2521 P35637
FUS 233908 P56959
Anti-Rat FUS FUS 317385  
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Top FUS ELISA Kits at

Showing 5 out of 10 products:

Catalog No. Reactivity Sensitivity Range Images Quantity Supplier Delivery Price Details
Human 0.055 ng/mL 0.15-10 ng/mL 96 Tests Log in to see 9 to 11 Days
Mouse 0.058 ng/mL 0.15-10 ng/mL 96 Tests Log in to see 9 to 11 Days
  96 Tests Log in to see 11 to 13 Days
  96 Tests Log in to see 11 to 13 Days
  96 Tests Log in to see 11 to 13 Days

More ELISA Kits for FUS Interaction Partners

Human Fused in Sarcoma (FUS) interaction partners

  1. Study identifies a common mechanism of transport into neurites of proteins linked to the pathology of Alzheimer's disease (i.e. sAPP) and ALS (show IGFALS ELISA Kits) (i.e. FUS, TDP-43 (show TARDBP ELISA Kits) and SOD1 (show SOD1 ELISA Kits))

  2. RNA binding proteins TDP-43 (show TARDBP ELISA Kits) and FUS do not consistently fit the currently characterised inclusion models suggesting that cells have a larger repertoire for generating inclusions than currently thought.

  3. FUS-ERG is a transcriptional repressor of retinoic acid signaling. It acts in the context of a heptad of proteins (ERG, FLI1, GATA2, LYL1, LMO2, RUNX1 and TAL1) central to proper expression of genes maintaining a hematopoietic stem cell phenotype.

  4. FUS and EWS (show EWSR1 ELISA Kits) target genes involved in pathways at the RNA regulatory level

  5. FUS mutation seems indicated in sporadic early-onset ALS patients especially if showing predominant bulbar symptoms and an aggressive disease course.

  6. Results demonstrate that ALS-mutant forms of TDP-43, FUS, and SOD1 all perturb protein transport in the early secretory pathway between ER and Golgi compartments, and imply that restoring Rab1-mediated ER-Golgi transport is a novel ALS therapeutic target

  7. FUS-DDIT3 (show DDIT3 ELISA Kits) is uniquely regulated at the transcriptional as well as the post-translational level and that its expression level is important for myxoid liposarcoma tumour development.

  8. FUS-dependent motor degeneration is not due to loss of FUS function, but to the gain of toxic properties conferred by ALS mutations.

  9. FUS1 has roles in cancer, inflammation, and autoimmunity [review]

  10. Genetic polymorphisms in the TLS genes might serve as potential predictive biomarkers of prognosis of advanced NSCLC patients treated with platinum-based chemotherapy.

Mouse (Murine) Fused in Sarcoma (FUS) interaction partners

  1. The data of this study support the notion that expression of cytoplasmically mislocalized FUS with compromised RNA-binding capacity causes particularly prominent and harmful FUS pathology in the mouse nervous system.

  2. These results highlight the pivotal role of FUS in regulating GluA1 (show GRIA1 ELISA Kits) mRNA stability, post-synaptic function and fronto-temporal lobar degeneration-like animal behaviors.

  3. these studies establish potentially converging disease mechanisms in amyotrophic lateral sclerosis (ALS) and spinal muscular atrophy, with ALS-causative mutants acquiring properties representing both gain and loss of function.

  4. FUS/TLS depletion causes phenotypes possibly related to neuropsychiatric and neurodegenerative conditions, but distinct from ALS and ET, together with specific alterations in RNA metabolisms.

  5. It is associated with amyotrophic lateral sclerosis and its mutation causes accumulation of fus positive stress granules in neurons.

  6. Study provides evidence for loss of PRMT1 (show PRMT1 ELISA Kits) function as a consequence of cytoplasmic accumulation of FUS in the pathogenesis of amyotrophic lateral sclerosis, including changes in the histone code regulating gene transcription.

  7. our study provided evidence that a multistep process of FUS aggregation in the cell cytoplasm includes RNA-dependent and RNA-independent mechanisms.

  8. Activation of metabotropic glutamate (show GRIN1 ELISA Kits) receptors 1/5 in neocortical slices and isolated synaptoneurosomes increases endogenous mouse FUS and FUS(WT) protein levels but decreases the FUS(R521G) protein

  9. Study shows that neuronal aggregates formed by mutant FUS protein may aberrantly sequester survival motor neuron protein (SMN (show SMN1 ELISA Kits)) and concomitantly cause a reduction of SMN (show STMN1 ELISA Kits) levels in the axon, leading to axonal defects.

  10. FUS is a coregulator of MITF (show MITF ELISA Kits) activity and provide new insights into how the RANKL (show TNFSF11 ELISA Kits)/p38 MAPK (show MAPK14 ELISA Kits) signaling nexus controls gene expression in osteoclasts.

FUS Antigen Profile

Antigen Summary

This gene encodes a multifunctional protein component of the heterogeneous nuclear ribonucleoprotein (hnRNP) complex. The hnRNP complex is involved in pre-mRNA splicing and the export of fully processed mRNA to the cytoplasm. This protein belongs to the FET family of RNA-binding proteins which have been implicated in cellular processes that include regulation of gene expression, maintenance of genomic integrity and mRNA/microRNA processing. Alternative splicing results in multiple transcript variants. Defects in this gene result in amyotrophic lateral sclerosis type 6.

Gene names and symbols associated with Fused in Sarcoma (FUS) ELISA Kits

  • fused in sarcoma (FUS) antibody
  • fused in sarcoma (Fus) antibody
  • ALS6 antibody
  • D430004D17Rik antibody
  • D930039C12Rik antibody
  • ETM4 antibody
  • FUS/TLS antibody
  • Fus1 antibody
  • HNRNPP2 antibody
  • POMP75 antibody
  • Tls antibody

Protein level used designations for Fused in Sarcoma (FUS) ELISA Kits

75 kDa DNA-pairing protein , RNA-binding protein FUS , fus-like protein , fusion gene in myxoid liposarcoma , heterogeneous nuclear ribonucleoprotein P2 , oncogene FUS , oncogene TLS , translocated in liposarcoma protein , fusion, derived from t(12;16) malignant liposarcoma , hnRNP P2 , pigpen protein , protein pigpen , translocated in liposarcoma , fusion , pigpen , fusion (involved in t(12;16) in malignant liposarcoma) , 16) in malignant liposarcoma) , 16) malignant liposarcoma , fusion (involved in t(12 , fusion, derived from t(12

2521 Homo sapiens
233908 Mus musculus
414144 Gallus gallus
280796 Bos taurus
317385 Rattus norvegicus
479778 Canis lupus familiaris
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