Fibroblast Growth Factor 13 (FGF13) (Middle Region) Peptid
FGF13
Reaktivität: Human
Wirt: Synthetic
BP, WB
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- Target Alle FGF13 Produkte
- FGF13 (Fibroblast Growth Factor 13 (FGF13))
- Protein Region
- Middle Region
- Spezies
- Human
-
Quelle
- Synthetic
- Applikation
- Blocking Peptide (BP), Western Blotting (WB)
- Sequenz
- PKPLKVAMYK EPSLHDLTEF SRSGSGTPTK SRSVSGVLNG GKSMSHNEST
- 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.
- 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
-
- Applikationshinweise
- Each Investigator should determine their own optimal working dilution for specific applications.
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
-
- Format
- Lyophilized
- Rekonstitution
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
- Konzentration
- 1 mg/mL
- Buffer
- Final peptide concentration is 1 mg/mL in PBS.
- Handhabung
- Avoid repeated freeze-thaw cycles.
- Lagerung
- -20 °C
- Informationen zur Lagerung
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
-
- Target
- FGF13 (Fibroblast Growth Factor 13 (FGF13))
- Hintergrund
-
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
- Gen-ID
- 2258
- NCBI Accession
- NM_033642, NP_378668
- UniProt
- Q92913
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