CEP41 Protein (Myc-DYKDDDDK Tag)
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- Target See all CEP41 Proteins
- CEP41 (Centrosomal Protein 41kDa (CEP41))
- Protein Type
- Recombinant
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Origin
- Human
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Source
- HEK-293 Cells
- Purification tag / Conjugate
- This CEP41 protein is labelled with Myc-DYKDDDDK Tag.
- Application
- Antibody Production (AbP), Standard (STD)
- Characteristics
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- Recombinant human TSGA14 / CEP41 protein expressed in HEK293 cells.
- Produced with end-sequenced ORF clone
- Purity
- > 80 % as determined by SDS-PAGE and Coomassie blue staining
- Top Product
- Discover our top product CEP41 Protein
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Centrosomal Protein 41kDa (CEP41) (AA 1-373) protein (His tag)
custom-made CEP41 Origin: Mouse Host: HEK-293 Cells Recombinant > 90 % as determined by Bis-Tris PAGE, anti-tag ELISA, Western Blot and analytical SEC (HPLC)
Centrosomal Protein 41kDa (CEP41) (AA 1-373) protein (His tag)custom-made CEP41 Origin: Human Host: HEK-293 Cells Recombinant > 90 % as determined by Bis-Tris PAGE, anti-tag ELISA, Western Blot and analytical SEC (HPLC)
Centrosomal Protein 41kDa (CEP41) (AA 1-301) protein (GST tag)CEP41 Origin: Human Host: Wheat germ Recombinant ELISA, WB, AA, AP
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- Application Notes
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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 - Comment
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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.
- Storage
- -80 °C
- Storage Comment
- 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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- Target
- CEP41 (Centrosomal Protein 41kDa (CEP41))
- Alternative Name
- Tsga14,cep41 (CEP41 Products)
- Background
- This gene encodes a centrosomal and microtubule-binding protein which is predicted to have two coiled-coil domains and a rhodanese domain. In human retinal pigment epithelial cells the protein localized to centrioles and cilia. Mutations in this gene have been associated with Joubert Syndrome 15 an autosomal recessive ciliopathy and neurological disorder. Alternative splicing results in multiple transcript variants.
- Molecular Weight
- 41.2 kDa
- NCBI Accession
- NP_061188
- Pathways
- M Phase
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