Fibroblast Growth Factor 13 (FGF13) (Middle Region) Peptid
FGF13
Reaktivität: Human
Wirt: Synthetic
BP, WB
Produktnummer ABIN976829
Kurzübersicht für Fibroblast Growth Factor 13 (FGF13) (Middle Region) Peptid (ABIN976829)
Target
FGF13
(Fibroblast Growth Factor 13 (FGF13))
Spezies
Human
Quelle
Synthetic
Applikation
Blocking Peptide (BP), Western Blotting (WB)
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Protein Region
- Middle Region
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Sequenz
- PKPLKVAMYK EPSLHDLTEF SRSGSGTPTK SRSVSGVLNG GKSMSHNEST
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Produktmerkmale
- This is a synthetic peptide designed for use in combination with anti-FGF13 Antibody(ARP55413_P050),. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
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Aufreinigung
- Purified
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Fibroblast Growth Factor 13 (FGF13) peptide (Ovalbumin)
FGF13 Reaktivität: Maus Wirt: Synthetic WB, Imm, SDS
Fibroblast Growth Factor 13 (FGF13) peptide (Ovalbumin)FGF13 Reaktivität: Ratte Wirt: Synthetic WB, Imm, SDS
Fibroblast Growth Factor 13 (FGF13) peptide (Ovalbumin)FGF13 Reaktivität: Human Wirt: Synthetic WB, Imm, SDS
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Applikationshinweise
- Each Investigator should determine their own optimal working dilution for specific applications.
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Beschränkungen
- Nur für Forschungszwecke einsetzbar
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Format
- Lyophilized
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Rekonstitution
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
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Konzentration
- 1 mg/mL
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Buffer
- Final peptide concentration is 1 mg/mL in PBS.
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Handhabung
- Avoid repeated freeze-thaw cycles.
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Lagerung
- -20 °C
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Informationen zur Lagerung
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- FGF13 (Fibroblast Growth Factor 13 (FGF13))
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Hintergrund
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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' end results in several transcript variants encoding different isoforms with different N-termini.
Alias Symbols: FGF2, FHF-2, FHF2, FGF-13
Protein Interaction Partner: FGF13,SCN8A,MAPK8IP2
Protein Size: 192 -
Molekulargewicht
- 21 kDa
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Gen-ID
- 2258
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NCBI Accession
- NM_033642, NP_378668
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UniProt
- Q92913
Target
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