Cofilin 2 anticorps (AA 1-166)
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- Antigène Voir toutes Cofilin 2 (CFL2) Anticorps
- Cofilin 2 (CFL2)
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Épitope
- AA 1-166
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Reactivité
- Humain
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp Cofilin 2 est non-conjugé
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Application
- Western Blotting (WB), Immunofluorescence (IF)
- Séquence
- MASGVTVNDE VIKVFNDMKV RKSSTQEEIK KRKKAVLFCL SDDKRQIIVE EAKQILVGDI GDTVEDPYTS FVKLLPLNDC RYALYDATYE TKESKKEDLV FIFWAPESAP LKSKMIYASS KDAIKKKFTG IKHEWQVNGL DDIKDRSTLG EKLGGNVVVS LEGKPL
- Réactivité croisée
- Humain, Souris, Rat
- Attributs du produit
- Polyclonal Antibodies
- Purification
- Affinity purification
- Immunogène
- Recombinant fusion protein containing a sequence corresponding to amino acids 1-166 of human CFL2 (NP_068733.1).
- Isotype
- IgG
- Top Product
- Discover our top product CFL2 Anticorps primaire
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- Indications d'application
- WB,1:500 - 1:2000,IF,1:50 - 1:100
- Commentaires
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HIGH QUALITY
- Restrictions
- For Research Use only
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- Format
- Liquid
- Buffer
- PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
- 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
- -20 °C
- Stockage commentaire
- Store at -20°C. Avoid freeze / thaw cycles.
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- Antigène
- Cofilin 2 (CFL2)
- Autre désignation
- CFL2 (CFL2 Produits)
- Synonymes
- anticorps NEM7, anticorps CFL2, anticorps zgc:77288, anticorps cf12, anticorps cofilin 2, anticorps cofilin 2 (non-muscle), anticorps cofilin 2 (muscle), anticorps cofilin 2, muscle, anticorps cofilin-2, anticorps CFL2, anticorps cfl2, anticorps Cfl2, anticorps cf12, anticorps LOC100359205
- Sujet
- This gene encodes an intracellular protein that is involved in the regulation of actin-filament dynamics. This protein is a major component of intranuclear and cytoplasmic actin rods. It can bind G- and F-actin in a 1:1 ratio of cofilin to actin, and it reversibly controls actin polymerization and depolymerization in a pH -dependent manner. Mutations in this gene cause nemaline myopathy type 7, a form of congenital myopathy. Alternative splicing results in multiple transcript variants.,CFL2,NEM7,cofilin-2,Signal Transduction,Cell Biology & Developmental Biology,Cytoskeleton,Microfilaments,Actins,TGF-b-Smad Signaling Pathway,CFL2
- Poids moléculaire
- 16 kDa/18 kDa
- ID gène
- 1073
- UniProt
- Q9Y281
- Pathways
- Caspase Cascade in Apoptosis
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