FineTest
SKU:FNab03090
anti- FGF13 antibody
anti- FGF13 antibody
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Unlock the mysteries of fibroblast growth factors with our Anti-FGF13 Antibody, a meticulously crafted product available in a 100µg vial. FGF13, a critical member of the FGF family, is known for its involvement in neuronal development and various biological processes. With this highly specific antibody, you'll gain the ability to investigate the intricate role of FGF13 in neuronal and developmental studies with unprecedented accuracy and reliability.
Key Features:
- Outstanding Specificity: Our Anti-FGF13 Antibody is rigorously validated for its specificity, ensuring it accurately targets FGF13, minimizing the risk of cross-reactivity.
- Versatile Applications: Ideal for a broad spectrum of experimental techniques, including immunohistochemistry, Western blotting, and immunoprecipitation.
- Ample Quantity: The 100µg supply ensures you have enough reagents for multiple experiments.
- Top-Tier Quality: Manufactured to the highest industry standards, guaranteeing dependable and replicable results.
- Advance Your Research: Whether you're researching neuronal development, neurobiology, or cell signaling, our Anti-FGF13 Antibody is an indispensable tool for your research endeavors.
Unravel the secrets of fibroblast growth factor 13 and lead the way in groundbreaking research with our Anti-FGF13 Antibody.
Product Name
FGF13 antibody
Size
100µg
Form
liquid
Purification
Immunogen affinity purified
Purity
≥95% as determined by SDS-PAGE
Host
Rabbit
Clonality
polyclonal
Isotype
IgG
Storage
PBS with 0.02% sodium azide and 50% glycerol pH 7.3, -20℃ for 12 months (Avoid repeated freeze / thaw cycles.)
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.
IMMUNOGEN INFORMATION
Immunogen
fibroblast growth factor 13
Synonyms
FHF2
Observed MW
28 kDa
APPLICATION
Tested Application
ELISA, IHC, WB
Recommended Dilution
WB: 1:500 - 1:2000; IHC: 1:50 - 1:200
UNIPROT INFORMATION
UniProt ID
IMAGES


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