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hCaV 1.2
Cav1.2 is the major pore-forming alpha subunit of long-lasting (L-type) voltage-gated Ca2+ channels in the heart. The channels are present in the membranes of most excitable cells, where they mediate the entry of Ca2+ into cells upon depolarization. Cav1.2-containing channels play an important role in the heart, particularly in modulating ventricular and atrial contraction. The Cav1.2 protein binds to dihydropyridines, a class of drugs used to treat hypertension. Mutations in the CACNA1C gene encoding Cav1.2 have been implicated in long QT syndrome, Brugada syndrome, and bipolar disease
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| About the Channel |
| Aliases | CaV1.2, L-type calcium channel, α-1c subunit, dihydropyridine receptor (DHPR) |
| Description | human CaV1.2 ion channel |
| Gating inhibitors | isradipine, diltiazem, nifedipine, nimodipine |
| Pore blockers | Cd2+, efonidipine, mibefradil, Pb2+ |
| Activators | BayK-8644, FPL-4176 |
| Gene name | CACNA1C |
| Accession # (human) | NP_000710 |
| Product | ICa(L) |
| Selectivity | Na+ > Li+ > Ba2+ > Sr2+ ≥ Ca2+ |
| Distribution | Heart, brain, prostate, smooth muscle, placenta, spinal cord, adrenal gland |
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| About the Host Cell Line |
| Expression stability | N. A. |
| Expression rate | N. A. |
| Pharmacology validation | Nifedipine (IC50=50nM) |
| Selection antibiotic | |
| Packaging | Cryopreserved, 3 vials |
| Storage requirements | Liquid N2 |
| Quantity in vial | 3x 2E6 cells/vial |
| Host cell | HEK-293 |
| Growth media | DMEM/F12 + 5% FBS, P/S |
| Related products | division-arrested cells, total RNA |
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