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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 (52) and FUS Proteins (3) 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 antibodies-online.com

Showing 3 out of 3 products:

Catalog No. Reactivity Sensitivity Range Quantity Supplier Delivery Price Details
Human
96 Tests Log in to see 11 to 13 Days
$875.60
Details
Mouse
96 Tests Log in to see 11 to 13 Days
$875.60
Details
Cow
96 Tests Log in to see 11 to 13 Days
$1,029.60
Details

More ELISA Kits for FUS Interaction Partners

Human Fused in Sarcoma (FUS) interaction partners

  1. FUS is glycosylated with a high stoichiometry not only in the neural cells but also in the non-neural cell lines.

  2. The results of this study suggested that FUS mutations are the most frequent genetic cause in early-onset sporadic ALS patients of Chinese origin.

  3. Data show that induced pluripotent stem cells (iPSC)-derived motor neurons mimicked several neurodegenerative phenotypes including mis (show AMH ELISA Kits)-localization of fused-in sarcoma (FUS) gene product into cytosolic.

  4. miR (show MLXIP ELISA Kits)-141 and the FUS gene, which are inversely correlated, play significant functional roles in regulating human neuroblastoma (show ARHGEF16 ELISA Kits).

  5. pathological TDP-43 (show TARDBP ELISA Kits) and FUS may exert motor neuron pathology in amyotrophic lateral sclerosis through the initiation of propagated misfolding of SOD1 (show SOD1 ELISA Kits)

  6. iNeurons may provide a more reliable model for investigating FUS mutations with disrupted NLS (show ALDH1A2 ELISA Kits) for understanding FUS-associated proteinopathies in amyotrophic lateral sclerosis

  7. A subset of juvenile-onset familial/sporadic ALS (show IGFALS ELISA Kits) cases with FUS gene mutations reportedly demonstrates mental retardation or learning difficulty.

  8. Study implicates phosphorylation as an additional mechanism by which nuclear transport of FUS might be regulated and potentially perturbed in ALS and FTLD.

  9. prevalence of the FUS-ERG (show ERG ELISA Kits) gene fusion in a large cohort of pathologically and molecularly well characterized small blue round cell tumors, lacking other known gene rearrangements

  10. 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))

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

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