FGF13 Protein (Transcript Variant 6) (Myc-DYKDDDDK Tag)
Quick Overview for FGF13 Protein (Transcript Variant 6) (Myc-DYKDDDDK Tag) (ABIN2721060)
Target
See all FGF13 ProteinsProtein Type
Origin
Source
Application
Purity
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Protein Characteristics
- Transcript Variant 6
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Purification tag / Conjugate
- This FGF13 protein is labelled with Myc-DYKDDDDK Tag.
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Characteristics
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- Recombinant human FGF13 (transcript variant 6) protein expressed in HEK293 cells.
- Produced with end-sequenced ORF clone
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Fibroblast Growth Factor 13 (FGF13) (AA 1-245) protein (GST tag)
FGF13 Origin: Human Host: Wheat germ Recombinant WB, ELISA, AA, AP
Fibroblast Growth Factor 13 (FGF13) (AA 1-192) (Active) protein (His tag)FGF13 Origin: Rat Host: Escherichia coli (E. coli) > 97 % AcA, CC Active
Fibroblast Growth Factor 13 (FGF13) (AA 10-245) protein (His-IF2DI Tag)FGF13 Origin: Human Host: Escherichia coli (E. coli) Recombinant Greater than 90 % as determined by SDS-PAGE. WB, ELISA
Fibroblast Growth Factor 13 (FGF13) (AA 1-245) protein (His-IF2DI Tag)FGF13 Origin: Human Host: Escherichia coli (E. coli) Recombinant Greater than 90 % as determined by SDS-PAGE. WB, ELISA
Fibroblast Growth Factor 13 (FGF13) proteinFGF13 Origin: Rat Host: Escherichia coli (E. coli) Recombinant > 95 % WB, SDS, ELISA, IP
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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.
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Restrictions
- For Research Use only
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Concentration
- 50 μg/mL
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Buffer
- 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
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Storage
- -80 °C
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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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- FGF13 (Fibroblast Growth Factor 13 (FGF13))
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Alternative Name
- Fgf13
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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.
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Molecular Weight
- 21.4 kDa
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NCBI Accession
- NP_378668
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Pathways
- Regulation of Cell Size
Target
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