| No | Size | Price | Availability | |
| ARP2258-61 | 50ul | 1500.00 | In Stock |  |
| ARP2258-61 | 100ul | 2000.00 | In Stock | |
| Source: | Rabbit | Gene Id: | 2258 |
| Isotype: | IgG | Swiss Prot: | Q92913 |
| purity: | Affinity purification |
| 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' end results in several transcript variants encoding different isoforms with different N-termini. [provided by RefSeq |
| Reactivity | Human, Mouse, Rat |
| Tested applications | WB |
| Clonality | Polyclonal Antibody |
| Calculated MW | 28 kDa |
| Recommended Dilutions |
WB 1:500-1:1000
|
| Immunogen | A synthetic peptide |
| Storage | Store at -20°C or -80°C in PBS with 0.02% sodium azide and 50% glycerol. Avoid freeze/thaw cycles. |
| Synonym | Fibroblast growth factor 13, FGF-13, Fibroblast growth factor homologous factor 2, FHF-2 |
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