Gelsolin (GSN) Peptide
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- Target See all Gelsolin (GSN) products
- Gelsolin (GSN)
- Origin
- Human
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Source
- Synthetic
- Application
- Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
- Characteristics
- This is a synthetic peptide designed for use in combination with anti-GSN antibody (Catalog #: ARP54299_P050). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
- Purification
- Purified
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- Application Notes
- Each Investigator should determine their own optimal working dilution for specific applications.
- Restrictions
- For Research Use only
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- Format
- Lyophilized
- Reconstitution
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
- Concentration
- 1 mg/mL
- Buffer
- Final peptide concentration is 1 mg/mL in PBS.
- Handling Advice
- Avoid repeated freeze-thaw cycles.
- Storage
- -20 °C
- Storage Comment
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- Target
- Gelsolin (GSN)
- Synonyms
- ADF Peptide, AGEL Peptide, CG1106 Peptide, DGS Peptide, Dmel\\CG1106 Peptide, gel Peptide, scin Peptide, cb107 Peptide, gsn Peptide, sb:cb107 Peptide, u-gelsolin Peptide, wu:fi16f06 Peptide, gelsolin Peptide, Gelsolin Peptide, gelsolin S homeolog Peptide, gelsolin a Peptide, GSN Peptide, Gel Peptide, Gsn Peptide, gsn.S Peptide, gsn Peptide, gsna Peptide
- Background
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GSN binds to the 'plus' ends of actin monomers and filaments to prevent monomer exchange. It is a calcium-regulated protein, which functions in both assembly and disassembly of actin filaments. Defects in the gene encoding GSN are a cause of familial amyloidosis Finnish type (FAF).The protein encoded by this gene binds to the 'plus' ends of actin monomers and filaments to prevent monomer exchange. The encoded calcium-regulated protein functions in both assembly and disassembly of actin filaments. Defects in this gene are a cause of familial amyloidosis Finnish type (FAF). Multiple transcript variants encoding several different isoforms have been found for this gene.
Alias Symbols: DKFZp313L0718, ADF, AGEL
Protein Interaction Partner: tax,ACTA1,ACTB,ACTG1,ACTN4,APP,AR,BCAR1,CASP3,CLIC5,CSK,FHIT,FN1,LIMK2,PIK3CG,PTK2B,PXN,TNIK,TOM1L1,VASP,VCL,VDAC1,ACTA1,ACTN4,APP,AR,CASP4,FN1,PIK3CA,PLCG1,PPM1B,PTK2,PTK2B,PTPN12,PXN,SRC,STK39,TOM1L1,VCL,VDAC1
Protein Size: 782 - Molecular Weight
- 83 kDa
- Gene ID
- 2934
- NCBI Accession
- NM_000177, NP_000168
- UniProt
- P06396
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