Expression of subtypes of AC and IP3R in HEK-PR1 cells
| Subtype | Percentage |
|---|---|
| AC1 | 12 ± 3 |
| AC2 | 0 |
| AC3 | 56 ± 7 |
| AC4 | 0 |
| AC5 | 0 |
| AC6 | 5 ± 1 |
| AC7 | 17 ± 3 |
| AC8 | 0 |
| AC9 | 10 ± 3 |
| IP3R1 | 19 ± 1 |
| IP3R2 | 46 ± 3 |
| IP3R3 | 35 ± 1 |
| Subtype | Percentage |
|---|---|
| AC1 | 12 ± 3 |
| AC2 | 0 |
| AC3 | 56 ± 7 |
| AC4 | 0 |
| AC5 | 0 |
| AC6 | 5 ± 1 |
| AC7 | 17 ± 3 |
| AC8 | 0 |
| AC9 | 10 ± 3 |
| IP3R1 | 19 ± 1 |
| IP3R2 | 46 ± 3 |
| IP3R3 | 35 ± 1 |
QPCR was used to measure relative levels (percentage of total) of mRNA encoding isoforms of AC and IP3R in HEK-PR1 cells. Results are means ± SEM from three experiments, each performed in duplicate. The absence of AC2, AC4, and AC8 is consistent with a previous semiquantitative RT-PCR analysis, although a low level of AC5 was detected (Ludwig and Seuwen, 2002). The preponderance of IP3R2 and IP3R3 in HEK cells is consistent with results from immunoblotting (Wojcikiewicz, 1995).
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