FGF-17 rabbit pAb

FGF-17 rabbit pAb

AO-06-ES4284-100

FGF-17 rabbit pAb 100μL

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€429.00
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Antibody Product Overview

ELK.NoES4284
Product nameFGF-17 rabbit pAb
ReactivityHuman;Rat;Mouse;
ApplicationsWB;IHC;IF;ELISA
Other nameFGF17; Fibroblast growth factor 17; FGF-17
Size100μL
Unit price ($)248
Human gene ID8822
Human Swiss-ProtO60258
SourceRabbit
IsotypeIgG
TargetFGF-17
Fields>>MAPK signaling pathway;>>Ras signaling pathway;>>Rap1 signaling pathway;>>Calcium signaling pathway;>>PI3K-Akt signaling pathway;>>Regulation of actin cytoskeleton;>>Pathways in cancer;>>Chemical carcinogenesis - receptor activation;>>Melanoma;>>Breast cancer;>>Gastric cancer
Gene nameFGF17
Protein nameFibroblast growth factor 17
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID
Mouse gene link
Mouse Swiss-ProtP63075
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID
Rat gene link
Rat Swiss-Prot
Rat Swiss link
ImmunogenThe antiserum was produced against synthesized peptide derived from the C-terminal region of human FGF17. AA range:267-216
SpecificityFGF-17 Polyclonal Antibody detects endogenous levels of FGF-17 protein.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWestern Blot: 1/500 - 1/2000. IHC-p: 1:100-1:300. ELISA: 1/10000. Not yet tested in other applications.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)
Observed band (KD)25kD
BackgroundThis gene encodes a member of the fibroblast growth factor (FGF) family. Member of the FGF family 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 protein is expressed during embryogenesis and in the adult cerebellum and cortex and may be essential for vascular growth and normal brain development. Mutations in this gene are the cause of hypogonadotropic hypogonadism 20 with or without anosmia. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2015],
Functiondevelopmental stage:Detected in embryos at E14.5, but not at E10.5 and E19.5. Preferentially expressed in the neuroepithelia of the isthmus and septum of the embryonic brain at E14.5.,function:May be a signaling molecule in the induction and patterning of the embryonic brain.,similarity:Belongs to the heparin-binding growth factors family.,tissue specificity:Preferentially expressed in the embryonic brain.,
Subcellular locationSecreted.
ExpressionPreferentially expressed in the embryonic brain.

Additional Images

Image 1
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Western Blot analysis of NIH-3T3 cells using FGF-17 Polyclonal Antibody. Secondary antibody(catalog#:RS0002) was diluted at 1:20000
Image 2
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Immunohistochemical analysis of paraffin-embedded human-brain, antibody was diluted at 1:100
Image 3
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Immunohistochemical analysis of paraffin-embedded human-brain, antibody was diluted at 1:100
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: AO-06-ES4284-100
: 10 Items
Hurry! only 10 items left in stock.

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