Human AFGF/FGF1 (Acidic Fibroblast Growth Factor 1) ELISA Kit

Human AFGF/FGF1 (Acidic Fibroblast Growth Factor 1) ELISA Kit

Note: 

*: [96T/48T] 

#: It’s OK to keep the kit in 4℃, if the kit is scheduled to be used up in one week. Please keep the 

reagent in -20℃ for long-term storage or repeated use. 

The reagent in each vial is slightly more that its volume written on label, please take out the required 

volume by certain tools (such as transferpettor, measuring cylinder), rather than pouring directly. 

Test principle 

Human AFGF/FGF1 (Acidic Fibroblast Growth Factor 1) ELISA Kit

This ELISA kit uses Sandwich-ELISA as the method. The micro ELISA plate provided in this kit has 

been pre-coated with an antibody specific to Human AFGF/FGF1. Standards or samples are then added 

to the appropriate micro ELISA plate wells and combined to the specific antibody. Then a biotinylated 

detection antibody specific for Human AFGF/FGF1 and Avidin-Horseradish Peroxidase (HRP) 

conjugate is added to each micro plate well and incubated. Free components are washed away. The 

substrate solution is added to each well. Only those wells that contain Human AFGF/FGF1, 

biotinylated detection antibody and Avidin-HRP conjugate will appear blue in color. 

Human AFGF/FGF1 (Acidic Fibroblast Growth Factor 1) ELISA Kit

The 

enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color turn 

yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm ± 2  

nm. The OD value is proportional to the concentration of Human AFGF/FGF1. You can calculate the 

concentration of AFGF/FGF1 in the samples by comparing the OD of the samples to the standard 

curve. 

Sample collection and storage 

Serum - Allow samples to clot for 2 hours at room temperature or overnight at 4°Cbefore 

centrifugation for 20 minutes at approximately 1000×g. Collect the supernatant and carry out the 

assay immediately. Blood collection tubes should be disposable, non-pyrogenic, and non-endotoxin. 

Plasma - Collect plasma using EDTA-Na2 or heparin as an anticoagulant. Centrifuge samples for 15 

minutes at 1000×g at 2 - 8°C within 30 minutes of collection. Collect the supernatant and carry out 

the assay immediately. Avoid hemolysis, high cholesterol samples. 

Tissue homogenates– For general information, hemolysis blood may affect the result, so you should 

rinse the tissues with ice-cold PBS (0.01M, pH=7.4) to remove excess blood thoroughly. Tissue 

pieces should be weighed and then minced to small pieces which will be homogenized in PBS (the 

volume depends on the weight of the tissue. 9mL PBS would be appropriate to 1 gram tissue pieces. 

Some protease inhibitor is recommended to add into the PBS.) with a glass homogenizer on ice. To 

further break the cells, you can sonicate the suspension with an ultrasonic cell disrupter or subject it to 

freeze-thaw cycles. The homogenates are then centrifugated for 5minutes at 5000×g to get the 

supernate. 

Cell culture supernate – Centrifuge supernate for 20 minutes to remove insoluble impurity and cell 

debris at 1000×g at 2 - 8°C. Collect the clear supernate and carry out the assay immediately. 

Other biological fluids –Centrifuge samples for 20 minutes at 1000×g at 2 - 8°C. Collect the 

supernatant and carry out the assay immediately. (You can refer to our website for detailed processing 

Sample preparation – Samples should be clear and transparent and be centrifuged to remove 

suspended solids. 

Note: Serum and plasma to be used within 7 days when stored at 2-8°C, otherwise samples must be 

divided and stored at -20°C (≤1 month) or -80°C (≤6 months) to avoid loss of bioactivity and 

contamination. Avoid freeze-thaw cycles. When performing the assay slowly bring samples to room 

temperature. If the sample concentration is higher than the maximum standard value, please dilute it 

with appropriate factor according to the actual situation. (A pre-test is recommended to determine the 

dilute factor). 

Other supplies required 

Microplate reader with 450nm wavelength filter 

High-precision transferpettor, EP tubes and disposable pipette tips 

37°C Incubator, Deionized or distilled water 

Absorbent paper 

 Human AFGF/FGF1 (Acidic Fibroblast Growth Factor 1) ELISA Kit

Reagent preparation 

Bring all reagents to room temperature before use. 

Wash Buffer - Dilute 30mL of Concentrated Wash Buffer into 750 mL of Wash Buffer with deionized 

or distilled water. Put unused solution back at 4°C. If crystals have formed in the concentrate, you can 

warm it with 40°Cwater bath (Heating temperature should not exceed 50°C) and mix it gently until the 

crystals have completely dissolved. The solution should be cooled to room temperature before use. 

Standard- Centrifuge at 10,000×g for 1 minute, and reconstitute the Standard with 1.0mL of 

Reference Standard &Sample Diluent. Tighten the lid, let it stand for 10 minutes and turn it upside 

down for several times. After it dissolves fully, mix it thoroughly with a pipette. This reconstitution 

produces a stock solution of 2000pg/mL. Then make serial dilutions as needed (Making serial 

dilution in the wells directly is not permitted). The recommended concentrations are as follows:2000、

1000、500、250、125、62.5、31.25、0pg/mL . As if you want to make standard solution at the 

concentration of 1000pg/mL, you can take 0.5mL the standard at 2000pg/mL, add it to an EP tube 

with 0.5mL Reference Standard &Sample Diluent, and mix it. The procedures of making the 

remaining concentrations are all the same. The undiluted standard serves as the highest standard 

(2000pg/mL). The Reference Standard &Sample Diluent serves as the zero (0pg/mL). 

(500μL/tube，for example. Can also be diluted according to the actual amount，such as 200μL/tube)