Fukutin Protein (FKTN) (Transcript Variant 1) (Myc-DYKDDDDK Tag)
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- Target See all Fukutin (FKTN) Proteins
- Fukutin (FKTN)
- Protein Type
- Recombinant
- Protein Characteristics
- Transcript Variant 1
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Origin
- Human
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Source
- HEK-293 Cells
- Purification tag / Conjugate
- This Fukutin protein is labelled with Myc-DYKDDDDK Tag.
- Application
- Antibody Production (AbP), Standard (STD)
- Characteristics
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- Recombinant human Fukutin (transcript variant 1) 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 FKTN Protein
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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
- Fukutin (FKTN)
- Alternative Name
- Fukutin (FKTN Products)
- Synonyms
- FCMD Protein, fcmd Protein, im:7163166 Protein, zgc:162828 Protein, FKTN Protein, CMD1X Protein, LGMD2M Protein, MDDGA4 Protein, MDDGB4 Protein, MDDGC4 Protein, D830030O17Rik Protein, Fcmd Protein, fukutin Protein, fukutin S homeolog Protein, Fukutin Protein, FKTN Protein, fktn Protein, fktn.S Protein, Bm1_09375 Protein, Bm1_09380 Protein, Bm1_44655 Protein, Fktn Protein
- Background
- The protein encoded by this gene is a putative transmembrane protein that is localized to the cis-Golgi compartment, where it may be involved in the glycosylation of alpha-dystroglycan in skeletal muscle. The encoded protein is thought to be a glycosyltransferase and could play a role in brain development. Defects in this gene are a cause of Fukuyama-type congenital muscular dystrophy (FCMD), Walker-Warburg syndrome (WWS), limb-girdle muscular dystrophy type 2M (LGMD2M), and dilated cardiomyopathy type 1X (CMD1X). Alternatively spliced transcript variants have been found for this gene.
- Molecular Weight
- 53.5 kDa
- NCBI Accession
- NP_001073270
- Pathways
- Regulation of Carbohydrate Metabolic Process
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