HOMEPRODUCTSION CHANNEL CELL LINES ⇒ CAV 1.2

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


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
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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