Filensin Protein (Myc-DYKDDDDK Tag)
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- Antigène Voir toutes Filensin (BFSP1) Protéines
- Filensin (BFSP1) (Beaded Filament Structural Protein 1, Filensin (BFSP1))
- Type de proteíne
- Recombinant
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Origine
- Humain
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Source
- HEK-293 Cells
- Purification/Conjugué
- Cette Filensin protéine est marqué à la Myc-DYKDDDDK Tag.
- Application
- Antibody Production (AbP), Standard (STD)
- Attributs du produit
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- Recombinant human Filensin protein expressed in HEK293 cells.
- Produced with end-sequenced ORF clone
- Pureté
- > 80 % as determined by SDS-PAGE and Coomassie blue staining
- Top Product
- Discover our top product BFSP1 Protéine
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- Indications d'application
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Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays - Commentaires
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The tag is located at the C-terminal.
- Restrictions
- For Research Use only
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- Concentration
- 50 μg/mL
- Buffer
- 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
- Stock
- -80 °C
- Stockage commentaire
- Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
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- Antigène
- Filensin (BFSP1) (Beaded Filament Structural Protein 1, Filensin (BFSP1))
- Autre désignation
- Filensin (BFSP1 Produits)
- Synonymes
- BFSP1 Protein, CP115 Protein, CP94 Protein, CTRCT33 Protein, LIFL-H Protein, Bfsp1 Protein, 115-kDa Protein, CP95 Protein, CP97 Protein, MGC84254 Protein, LOC100220461 Protein, beaded filament structural protein 1 Protein, beaded filament structural protein 1 L homeolog Protein, beaded filament structural protein 1, in lens-CP94 Protein, BFSP1 Protein, Bfsp1 Protein, bfsp1.L Protein
- Sujet
- This gene encodes a lens-specific intermediate filament-like protein named filensin. The encoded protein is expressed in lens fiber cells after differentiation has begun. This protein functions as a component of the beaded filament which is a cytoskeletal structure found in lens fiber cells. Mutations in this gene are the cause of autosomal recessive cortical juvenile-onset cataract. Alternate splicing results in multiple transcript variants.
- Poids moléculaire
- 74.4 kDa
- NCBI Accession
- NP_001186
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