Gelsolin anticorps
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- Antigène Voir toutes Gelsolin (GSN) Anticorps
- Gelsolin (GSN)
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Reactivité
- Humain
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Hôte
- Souris
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Clonalité
- Monoclonal
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Conjugué
- Cet anticorp Gelsolin est non-conjugé
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Application
- Western Blotting (WB)
- Purification
- Purified by Protein A/G
- Immunogène
- Recombinant human full-length protein
- Clone
- CPTC-Gelsolin-1
- Isotype
- IgG1 kappa
- Top Product
- Discover our top product GSN Anticorps primaire
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- Indications d'application
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Positive Control: MCF cell lysate, Tonsil.
Known Application: Western Blot (0.5-1.0 μg/mL), Optimal dilution for a specific application should be determined.
- Restrictions
- For Research Use only
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- Concentration
- 200 μg/mL
- Buffer
- 10 mM PBS with 0.05 % BSA & 0.05 % azide.
- Agent conservateur
- Sodium azide
- Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Stock
- 4 °C,-80 °C
- Stockage commentaire
- Antibody with azide - store at 2 to 8°C. Antibody without azide - store at -20 to -80°C. Antibody is stable for 24 months. Non-hazardous. No MSDS required.
- Date de péremption
- 24 months
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- Antigène
- Gelsolin (GSN)
- Autre désignation
- GSN (GSN Produits)
- Synonymes
- anticorps ADF, anticorps AGEL, anticorps CG1106, anticorps DGS, anticorps Dmel\\CG1106, anticorps gel, anticorps scin, anticorps cb107, anticorps gsn, anticorps sb:cb107, anticorps u-gelsolin, anticorps wu:fi16f06, anticorps gelsolin, anticorps Gelsolin, anticorps gelsolin S homeolog, anticorps gelsolin a, anticorps GSN, anticorps Gel, anticorps Gsn, anticorps gsn.S, anticorps gsn, anticorps gsna
- Sujet
- Gelsolin (also known as brevin, Actin-depolymerizing factor or ADF), a proteinof leukocytes, platelets and other cells, severs Actin filaments in thepresence of submicromolar calcium, thereby isolating cytoplasmic Actin gels. It is a calcium-regulated, actin-modulating protein that binds to the plus (or barbed) ends of actin monomers or filaments, preventing monomer exchange (end-blocking or capping). It can promote the assembly of monomers into filaments (nucleation) as well as sever filaments already formed. Plays a role in ciliogenesis. Defects in GSN are the cause of amyloidosis type 5 (AMYL5), also known as familial amyloidosis Finnish type, typically characterized by cranial neuropathy and lattice corneal dystrophy. Severe systemic disease can develop in some individuals causing peripheral polyneuropathy, amyloid cardiomyopathy, and nephrotic syndrome leading to renal failure.
- Poids moléculaire
- 90kDa
- ID gène
- 2934
- UniProt
- P06396
- Pathways
- Caspase Cascade in Apoptosis, Regulation of Actin Filament Polymerization, Autophagy
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