Mouse FGF9 (Fibroblast Growth Factor 9) ELISA Kit | MyBioSource MBS2510974 product information

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product summary

company name :

MyBioSource

product type :

ELISA/assay

product name :

Mouse FGF9 (Fibroblast Growth Factor 9) ELISA Kit

catalog :

MBS2510974

quantity :

24-Strip-Wells

price :

215 USD

product information

catalog number :

MBS2510974

products type :

ELISA Kit

products full name :

Mouse FGF9 (Fibroblast Growth Factor 9) ELISA Kit

products short name :

[FGF9]

other names :

[fibroblast growth factor 9; Fibroblast growth factor 9; fibroblast growth factor 9; fibroblast growth factor 9 (glia-activating factor); heparin-binding growth factor 9; fibroblast growth factor 9; Glia-activating factor; GAF; Heparin-binding growth factor 9; HBGF-9]

products gene name :

[FGF9]

other gene names :

[FGF9; FGF9; GAF; FGF-9; SYNS3; HBFG-9; HBGF-9; FGF-9; GAF; HBGF-9]

uniprot entry name :

FGF9_HUMAN

reactivity :

Mouse

sequence length :

208

specificity :

This kit recognizes Mouse FGF9 in samples. No Significant cross-reactivity or interference between Mouse FGF9 and analogues was observed.

storage stability :

Store at 4 degree C.

image1 heading :

Typical Testing Data/Standard Curve (for reference only)

other info1 :

Samples: Serum, Plasma, Biological Fluids. Assay Type: Sandwich. Detection Range: 62.5-4000pg/mL. Sensitivity: Min: 37.5pg/mL; Max: 4000pg/mL

other info2 :

Intra-assay Precision: Intra-assay Precision (Precision within an assay): 3 samples with low, mid range and high level Mouse FGF9 were tested 20 times on one plate, respectively. Inter-assay Precision: Inter-assay Precision (Precision between assays): 3 samples with low, mid range and high level Mouse FGF9 were tested on 3 different plates, 20 replicates in each plate.

products description :

Intended Uses: This ELISA kit applies to the in vitro quantitative determination of Mouse FGF9 concentrations in serum, plasma and other biological fluids.

ncbi gi num :

4503707

ncbi acc num :

NP_002001.1

ncbi gb acc num :

NM_002010.2

uniprot acc num :

P31371

ncbi mol weight :

23,441 Da

ncbi pathways :

Activated Point Mutants Of FGFR2 Pathway (645281); Adaptive Immune System Pathway (366160); Constitutive PI3K/AKT Signaling In Cancer Pathway (685535); DAP12 Interactions Pathway (685549); DAP12 Signaling Pathway (685550); Disease Pathway (530764); Downstream Signal Transduction Pathway (106385); Downstream Signaling Events Of B Cell Receptor (BCR) Pathway (576250); Downstream Signaling Of Activated FGFR Pathway (160957); FGFR Ligand Binding And Activation Pathway (106344)

ncbi summary :

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 protein was isolated as a secreted factor that exhibits a growth-stimulating effect on cultured glial cells. In nervous system, this protein is produced mainly by neurons and may be important for glial cell development. Expression of the mouse homolog of this gene was found to be dependent on Sonic hedgehog (Shh) signaling. Mice lacking the homolog gene displayed a male-to-female sex reversal phenotype, which suggested a role in testicular embryogenesis. [provided by RefSeq, Jul 2008]

uniprot summary :

FGF9: Plays an important role in the regulation of embryonic development, cell proliferation, cell differentiation and cell migration. May have a role in glial cell growth and differentiation during development, gliosis during repair and regeneration of brain tissue after damage, differentiation and survival of neuronal cells, and growth stimulation of glial tumors. Defects in FGF9 are the cause of multiple synostoses syndrome type 3 (SYNS3). Multiple synostoses syndrome is an autosomal dominant condition characterized by progressive joint fusions of the fingers, wrists, ankles and cervical spine, characteristic facies and progressive conductive deafness. Belongs to the heparin-binding growth factors family. Protein type: Cytokine. Chromosomal Location of Human Ortholog: 13q11-q12. Cellular Component: extracellular space; cytoplasm; extracellular region; basement membrane. Molecular Function: heparin binding; growth factor activity; fibroblast growth factor receptor binding. Biological Process: negative regulation of Wnt receptor signaling pathway; nerve growth factor receptor signaling pathway; embryonic skeletal development; negative regulation of transcription from RNA polymerase II promoter; signal transduction; positive regulation of vascular endothelial growth factor receptor signaling pathway; positive regulation of activin receptor signaling pathway; substantia nigra development; cell-cell signaling; positive regulation of MAPKKK cascade; protein import into nucleus; male sex determination; positive regulation of mesenchymal cell proliferation; positive regulation of cell proliferation; positive regulation of smoothened signaling pathway; chondrocyte differentiation; angiogenesis; regulation of timing of cell differentiation; embryonic gut development; positive regulation of cardiac muscle cell proliferation; embryonic limb morphogenesis; epidermal growth factor receptor signaling pathway; inner ear morphogenesis; fibroblast growth factor receptor signaling pathway; phosphoinositide-mediated signaling; male gonad development; osteoblast differentiation; positive regulation of cell division; insulin receptor signaling pathway; innate immune response; positive regulation of epithelial cell proliferation. Disease: Multiple Synostoses Syndrome 3

size1 :

24-Strip-Wells

price1 :

215 USD

size2 :

48-Strip-Wells

price2 :

410

size3 :

96-Strip-Wells

price3 :

490

size4 :

5x96-Strip-Wells

price4 :

2040

size5 :

10x96-Strip-Wells

price5 :

3590