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. Author manuscript; available in PMC: 2019 Dec 12.
Published in final edited form as: Cell Calcium. 1994 Jan;15(1):7–27. doi: 10.1016/0143-4160(94)90100-7

Table 3.

Global multi-exponential analysis of the intensity decay of Quin–2.a

τ1 = 0.62 ns τ2 = 1.31 ns τ3 = 10.40 ns χR2=3.2
< τ1 = 0.54 ns τ2 = 1.32 ns τ3 = 10.32 ns χR2=3.0>b
[Ca2+] nm α1c α2 α3 f1 f2 f3 τ¯(ns)
8 0.402 0.540 0.058 0.160 0.452 0.388 4.60
< 0.579 0.391 0.030 0.276 0.455 0.269 3.45 >
38 0.328 0.381 0.290 0.055 0.136 0.811 8.47
<0.481 0.419 0.089 0.153 0.318 0.529 5.82 >
100 0.129 0.365 0.505 0.014 0.082 0.904 9.45
<0.608 0.270 0.122 0.170 0.184 0.646 7.02 >
602 0.010 0.192 0.798 0.001 0.029 0.970 10.07
<0.544 0.276 0.180 0.117 0.145 0.738 0.786 >
a

In buffer at pH 7.2, 20°C, 343 nm excitation, emission observed through a Coming 3-75 filter

b

The numbers in angular brackets are after 20 min of focused illumination (60–70% photobleaching)

c

The intensity decays were fit to the multi-exponential model, I(t)=Σαietη. The fractional intensity of each component is give by fi=αiτiΣαjτj; The following values were obtained for a global double exponential fit: τ1 = 1.02 ns; τ2 = 10.31 ns; χR2=5.1; < τ1 = 0.83 ns; τ2 = 9.69 ns; χR2=12.0>