Fascin Homolog 2, Actin-Bundling Protein, Retinal (Strongylocentrotus Purpuratus) (FSCN2) ELISA Kits

FSCN2 encodes a member of the fascin protein family. Additionally we are shipping FSCN2 Antibodies (44) and FSCN2 Proteins (9) and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
FSCN2 238021 Q32M02
FSCN2 25794 O14926
Anti-Rat FSCN2 FSCN2 303741  
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Top FSCN2 ELISA Kits at antibodies-online.com

Showing 3 out of 7 products:

Catalog No. Reactivity Sensitivity Range Images Quantity Supplier Delivery Price Details
Human 0.938 ng/mL 1.56 ng/mL - 100 ng/mL A typical standard curve 96 Tests Log in to see 13 to 16 Days
Mouse < 0.416 ng/mL 0.78 ng/mL - 50 ng/mL   96 Tests Log in to see 11 to 18 Days
  96 Tests Log in to see 15 to 18 Days

More ELISA Kits for FSCN2 Interaction Partners

Mouse (Murine) Fascin Homolog 2, Actin-Bundling Protein, Retinal (Strongylocentrotus Purpuratus) (FSCN2) interaction partners

  1. These results demonstrate that, in C57BL/6Jmice, Fscn2 is essential for maintaining ear and eye function and that a null mutation of Fscn2 leads to progressive hearing loss and retinal degeneration.

  2. The results show that cross-talk through CD40-CD40L signaling drives elevated fascin expression in DCs to support acquisition of full T-cell responses.

  3. A quantitative trait locus on chromosome 5 modifies hearing loss associated with the fascin-2 variant of DBA/2J mice.

  4. Fascin and Daam1 coimmunoprecipitated from cell extracts, and silencing of fascin led to a striking loss of Daam1 localization to filopodial shafts. Purified fascin bound directly to Daam1; fascin recruited Daam1 to and stabilized Daam1 on actin bundles.

  5. The results of this study demonistrated that fascin-2 crosslinks function to slow actin depolymerization at stereocilia tips to maintain stereocilia length.

  6. Mutation in the Fscn2 gene underlies the early onset progressive hearing loss of DBA/2J mice attributed to the ahl8 locus.

Human Fascin Homolog 2, Actin-Bundling Protein, Retinal (Strongylocentrotus Purpuratus) (FSCN2) interaction partners

  1. Fascin induces melanoma tumorigenesis and stemness through regulating the Hippo pathway

  2. diffuse expression in 82% of undifferentiated/dedifferentiated endometrial carcinomas

  3. Tax-mediated transcriptional induction of Fascin requires NF-kappaB- and TRR-dependent promoter activation, and a promoter-independent, but PP2-sensitive signaling pathway.

  4. the serum fascin level is an effective indicator of tumor aggressiveness, and that it plays an important role in the prognosis of NSCLC, particularly for non-distant metastatic patients.

  5. Data indicate the specific contribution of fascin and cortactin during invadopodium formation.

  6. The filopodium: a stable structure with highly regulated repetitive cycles of elongation and persistence depending on the actin cross-linker fascin

  7. Fascin expression predicts survival after potentially curative resection of node-positive colon cancer.

  8. The 208delG mutation in the FSCN2 gene produces not only autosomal dominant retinitis pigmentosa but also ADMD (autosomal dominant macular degeneration)

  9. The photoreceptor-specific FSCN2 gene showed a relatively high number of sequence variations.

  10. The 208delG mutation in FSCN2 is not associated with hereditary retinal degeneration in the Chinese individuals examined.

  11. Real-time PCR-based genotyping method developed here is useful for investigations of allelic asymmetries within genomic regions with variations found in retinitis pigmentosa and retinl degeneration.

  12. In ovarian tumors fascin is associated with certain features of increased tumor aggressiveness.

  13. Higher fascin scores correlated positively with tumor differentiation of esophageal SqCC. Significantly worse prognosis in patients with high scores of fascin, poor differentiation, T4 stage, positive for lymph node metastasis and distant metastasis

  14. expression may play an essential role in regulation of progression of oral squamous cell carcinoma and contributes to the event of epithelial-mesenchymal transition in the early aggressiveness of OSCC

FSCN2 Antigen Profile

Antigen Summary

This gene encodes a member of the fascin protein family. Fascins crosslink actin into filamentous bundles within dynamic cell extensions. This family member is proposed to play a role in photoreceptor disk morphogenesis. A mutation in this gene results in one form of autosomal dominant retinitis pigmentosa and macular degeneration. Multiple transcript variants encoding different isoforms have been found for this gene.

Gene names and symbols associated with FSCN2

  • fascin actin-bundling protein 2, retinal (FSCN2) antibody
  • fascin actin-bundling protein 1 (FSCN1) antibody
  • fascin actin-bundling protein 2 (Fscn2) antibody
  • fascin actin-bundling protein 2, retinal (Fscn2) antibody
  • A930022G03 antibody
  • ahl8 antibody
  • C630046B20Rik antibody
  • fascin-2 antibody
  • RFSN antibody
  • RP30 antibody

Protein level used designations for FSCN2

fascin-2 , putative fascin 1 , retinal fascin , fascin 2, retinal

429198 Gallus gallus
100190193 Taeniopygia guttata
238021 Mus musculus
25794 Homo sapiens
483362 Canis lupus familiaris
303741 Rattus norvegicus
337926 Bos taurus
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