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MULTI SCIENCES

Human FGF Basic Sandwich ELISA Kit

Human FGF Basic Sandwich ELISA Kit

SKU:EK1F03

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Product Details

Human FGF Basic Sandwich ELISA Kit

Brand MultiSciences
CatNum 70-EK1F03
Product Name Human FGF basic ELISA Kit
Customs Name Human FGF basic ELISA Kit
Application ELISA
Reactivity Human
Assay Type Sandwich ELISA
Suitable Sample Type serum, plasma, cell culture supernates
Format 96-well strip plate
Storage 4℃ (unopened) standard stored at -20℃, others stored at 4℃ (opened)
Shipping Condition 4℃
Sample Volume 20 μl
Sensitivity 0.39 pg/ml
Standard Curve Range 15.63 - 1000 pg/ml
Spike Recovery Range 92 % - 119 %
Mean Spike Recovery 1.1
CV of Intra plate 3.8 % - 6.5 %
CV of Inter plate 5.3 % - 10.2 %
Components 96-well polystyrene microplate coated with a monoclonal antibody against FGF basic
Human FGF basic Standard, lyophilized
FGF basic Detect Antibody
Standard Diluent
Streptavidin-HRP
Assay Buffer (10×)
Substrate (TMB)
Stop Solution
Washing Buffer (20×)
Plate Covers
Describtion This assay employs the quantitative sandwich enzyme immunoassay technique for the quantitative detection of human FGF basic. The Human FGF basic ELISA is for research use only. Not for diagnostic or therapeutic procedures.
Basic fibroblast growth factor, also known as bFGF, FGF2 or FGF-β, is a member of the fibroblast growth factor family. During both wound healing of normal tissues and tumor development, the action of heparan sulfate-degrading enzymes activates bFGF to mediate angiogenesis. In addition, it is synthesized and secreted by human adipocytes and the concentration of bFGF correlates with the BMI in blood samples. It is shown that low levels of FGF2 play a key role in the incidence of excessive anxiety. Additionally, bFGF is a critical component of human embryonic stem cell culture medium; the growth factor is necessary for the cells to remain in an undifferentiated state. bFGF, in conjunction with BMP4, promote differentiation of stem cells to mesodermal lineages. After differentiation, BMP4 and FGF2 treated cells generally produces higher amounts of osteogenic and chondrogenic differentiation than untreated stem cells.