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FSCN2 encodes a member of the fascin protein family. Zusätzlich bieten wir Ihnen FSCN2 Proteine (9) und FSCN2 Kits (6) und viele weitere Produktgruppen zu diesem Protein an.
Showing 10 out of 39 products:
Guinea Pig Polyclonal FSCN2 Primary Antibody für WB - ABIN611269
Giordano, Whyte, Harlow, Franza, Beach, Draetta: A 60 kd cdc2-associated polypeptide complexes with the E1A proteins in adenovirus-infected cells. in Cell 1989
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Mouse (Murine) Polyclonal FSCN2 Primary Antibody für ELISA, IHC - ABIN451600
Vignjevic, Kojima, Aratyn, Danciu, Svitkina, Borisy: Role of fascin in filopodial protrusion. in The Journal of cell biology 2006
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Mouse (Murine) Polyclonal FSCN2 Primary Antibody für IHC, ELISA - ABIN334397
Ramakrishnan, Drescher, Khan, Hatfield, Drescher: HCN1 and HCN2 proteins are expressed in cochlear hair cells: HCN1 can form a ternary complex with protocadherin 15 CD3 and F-actin-binding filamin A or can interact with HCN2. in The Journal of biological chemistry 2012
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The results show that cross-talk through CD40 (zeige CD40 Antikörper)-CD40L (zeige CD40LG Antikörper) signaling drives elevated fascin (zeige FSCN1 Antikörper) expression in DCs to support acquisition of full T-cell responses.
A quantitative trait locus on chromosome 5 modifies hearing loss associated with the fascin-2 variant of DBA (zeige RPS19 Antikörper)/2J mice.
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.
The results of this study demonistrated that fascin-2 crosslinks function to slow actin depolymerization at stereocilia tips to maintain stereocilia length.
Mutation in the Fscn2 gene underlies the early onset progressive hearing loss of DBA (zeige RPS19 Antikörper)/2J mice attributed to the ahl8 locus.
Tax-mediated transcriptional induction of Fascin requires NF-kappaB- and TRR-dependent promoter activation, and a promoter-independent, but PP2-sensitive signaling pathway.
the serum fascin (zeige FSCN1 Antikörper) 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.
Data indicate the specific contribution of fascin (zeige FSCN1 Antikörper) and cortactin (zeige CTTN Antikörper) during invadopodium formation.
The filopodium: a stable structure with highly regulated repetitive cycles of elongation and persistence depending on the actin cross-linker fascin (zeige FSCN1 Antikörper)
Fascin (zeige FSCN1 Antikörper) expression predicts survival after potentially curative resection of node-positive colon cancer.
The 208delG mutation in the FSCN2 gene produces not only autosomal dominant retinitis pigmentosa but also ADMD (zeige ELOVL4 Antikörper) (autosomal dominant macular degeneration)
The photoreceptor-specific FSCN2 gene showed a relatively high number of sequence variations.
The 208delG mutation in FSCN2 is not associated with hereditary retinal degeneration in the Chinese individuals examined.
In ovarian tumors fascin (zeige FSCN1 Antikörper) is associated with certain features of increased tumor aggressiveness.
Higher fascin (zeige FSCN1 Antikörper) scores correlated positively with tumor differentiation of esophageal SqCC. Significantly worse prognosis in patients with high scores of fascin (zeige FSCN1 Antikörper), poor differentiation, T4 stage, positive for lymph node metastasis and distant metastasis
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.
, putative fascin 1
, retinal fascin
, fascin 2, retinal