FGF13 Protein (Transcript Variant 6) (Myc-DYKDDDDK Tag)
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- Target See all FGF13 Proteins
- FGF13 (Fibroblast Growth Factor 13 (FGF13))
- Protein Type
- Recombinant
- Protein Characteristics
- Transcript Variant 6
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Origin
- Human
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Source
- HEK-293 Cells
- Purification tag / Conjugate
- This FGF13 protein is labelled with Myc-DYKDDDDK Tag.
- Application
- Antibody Production (AbP), Standard (STD)
- Characteristics
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- Recombinant human FGF13 (transcript variant 6) 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 FGF13 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
- FGF13 (Fibroblast Growth Factor 13 (FGF13))
- Alternative Name
- Fgf13 (FGF13 Products)
- Synonyms
- FGF13 Protein, fgf2 Protein, fhf2 Protein, fgf13 Protein, FGF-13 Protein, xFGF13 Protein, FGF2 Protein, FHF-2 Protein, FHF2 Protein, Fhf2 Protein, zgc:101784 Protein, fibroblast growth factor 13 Protein, fibroblast growth factor 13 L homeolog Protein, fibroblast growth factor 13a Protein, FGF13 Protein, fgf13 Protein, fgf13.L Protein, Fgf13 Protein, fgf13a Protein
- Background
- The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth, and invasion. This gene is located in a region on chromosome X, which is associated with Borjeson-Forssman-Lehmann syndrome (BFLS), making it a possible candidate gene for familial cases of the BFLS, and for other syndromal and nonspecific forms of X-linked mental retardation mapping to this region. Alternative splicing of this gene at the 5&apos end results in several transcript variants encoding different isoforms with different N-termini.
- Molecular Weight
- 21.4 kDa
- NCBI Accession
- NP_378668
- Pathways
- Regulation of Cell Size
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