| Water content |
Nearly all samples contain 50–80% water |
ca 10% of all samples are hydrates or contain 1–10 molecules of crystallization. (Threlfall, 1995 ▸; Infantes et al., 2003 ▸) |
| Absorption cross-section at 8.05 keV (Cu Kα) and 17.997 keV |
Lysozyme, 1.04 and 0.080 mm−1; Insulin, 1.02 and 0.078 mm−1
|
Indicative absorption coefficient for this sample: 1.736 and 0.804 mm−1
|
| Typical incident wavelength (Å) |
1.5–0.9 |
1.5–0.4 |
| Typical beam size |
Large range of available sizes and often adjustable |
Crystal smaller than beam |
| Typical crystal size |
3–200 µm in any dimension |
20–50 µm in all dimensions |
| Flux in incident beam (photons s−1) |
1012
|
1010
|
| Applicable no. of space groups |
65 |
230 |
| Multiplicity due to symmetry |
1–4 |
1–10 |
| Molecular weight (Da) |
>20000 |
<900 |
| Unit-cell size / number of reflections |
>50 Å axes |
<50 Å axes, <5000 unique reflections, <100000 reflections per dataset |
| Typical diffraction limit (Å) |
3.5–1.5 |
Beyond 0.8 |
| No. of scans on one crystal |
1 (but depends on the phasing technique used) |
3–6 depending on instrument geometry |