Amplite® Fluorimetric Calcium Quantitation Kit *Red Fluorescence*
Example protocol
AT A GLANCE
Protocol summary
- Prepare assay reaction mixture (50 µL)
- Add calcium standards or test samples (50 µL)
- Incubate at room temperature for 5 - 30 minutes
- Monitor the fluorescence intensity at Ex/Em = 540/590 nm
Important notes
Thaw all the kit components to room temperature before starting the experiment.
PREPARATION OF STOCK SOLUTION
1. Rhod Red™ stock solution (200X):
Add 50 µL of sterile H2O into the vial of Rhod Red™ Indicator (Component A).
PREPARATION OF STANDARD SOLUTION
For convenience, use the Serial Dilution Planner: https://www.aatbio.com/tools/serial-dilution/36360
Prepare a calcium standard by diluting the appropriate amount of the 300 mM Calcium Standard (Component C) into H2O to produce a Calcium concentration ranging from 0 to 3 mM.
PREPARATION OF WORKING SOLUTION
Add 25 μL of Rhod Red™ stock solution (200X) into 5 mL of Assay Buffer (Component B) to make a total volume of 5.025 mL. Keep from light.
SAMPLE EXPERIMENTAL PROTOCOL
Table 1. Layout of calcium standards and test samples in a solid black 96-well microplate. CS= Calcium Standards (CS7 - CS1, 0.003 to 3 mM), BL=Blank Control, TS=Test Samples.
BL | BL | TS | TS |
CS1 | CS1 | ... | ... |
CS2 | CS2 | ... | ... |
CS3 | CS3 | ||
CS4 | CS$ | ||
CS5 | CS5 | ||
CS6 | CS6 | ||
CS7 | CS7 |
Table 2. Reagent composition for each well.
Well | Volume | Reagent |
CS1 - CS7 | 50 µL | Serial Dilutions (0.003 to 3 mM) |
BL | 50 µL | H2O |
TS | 50 µL | test sample |
- Prepare calcium standards (CS), blank controls (BL), and test samples (TS) according to the layout provided in Tables 1 and 2. For a 384-well plate, use 25 µL of reagent per well instead of 50 µL.
- Add 50 µL of working solution to each well of calcium standard, blank control, and test samples to make the total calcium assay volume of 100 µL/well. For a 384-well plate, add 25 µL of working solution into each well instead, for a total volume of 50 µL/well.
- Incubate the reaction for 5 to 30 minutes at room temperature, protected from light.
- Monitor the fluorescence intensity with a fluorescence plate reader at Ex/Em = 540/590 nm.
Citations
Authors: Li, Yue and Wang, ShiHui and Zhang, YouHua and Liu, ZhaoYuan and Zheng, YunZhe and Zhang, Kun and Chen, ShiYang and Lv, XiaoYing and Huang, MengWen and Pan, XingChao and others,
Journal: Nature Communications (2024): 1--16
Authors: Tian, Linlin and Li, Xiaodong and Ding, Yi and Li, Minli and Tang, Yunzhao and Li, Daiqing
Journal: Biochemical and biophysical research communications (2022): 116--122
Authors: Furukawa, Kyohei and Kono, Masaya and Kataoka, Tetsuro and Hasebe, Yukio and Jia, Huijuan and Kato, Hisanori
Journal: Nutrients (2021): 2144
Authors: Hai, Yang and Song, Peng and Wang, Xin and Zhao, Longhe and Xie, Qinjian and Li, Jianyin and Li, Yang and Li, Hongyu
Journal: Journal of pharmacological sciences (2019): 162--170
Authors: Wang, Xueting and Ding, Jie and Xiang, Zou and Jiang, Peipei and Du, Jing and Han, Xiaodong
Journal: Toxicon (2016): 45--55
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