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Antibodies

Cav1.2 Antibody, Clone S57: RPE

Product Sizes
100 ug
£506.00
SMC-300D-RPE-100UG
About this Product
SKU:
SMC-300D-RPE
Additional Names:
Voltage-dependent L-type calcium channel subunit alpha-1C, Cav1.2, Calcium channel, L type, alpha-1 polypeptide, isoform 1, cardiac muscle, Voltage-gated calcium channel subunit alpha Cav1.2, DHPR alpha-1 subunit, CACH3, CACN4, CACNL1A2, alpha-1 subunit voltage-dependent calcium channel, calcium channel voltage-dependent L type alpha 1C subunit1, calcium channel L type, alpha 1 polypeptide isoform 1 cardiac muscle, calcium channel cardiac dihydropyridine-sensitive alpha-1 subunit, voltage-gated L-type calcium channel Cav1.2 alpha 1 subunit splice variant 10
Application:
Antibody Microarray, Immunocytochemistry, Immunofluorescence, Immunohistochemistry, Immunoprecipitation, Western Blot
Buffer:
95.46mM Phosphate, 2.48mM MES and 2mM EDTA
CE/IVD:
RUO
translate.label.attr.clone:
S57
Clonality:
Monoclonal
Conjugate:
R-PE
Concentration:
1 mg/ml
Extra Details:
Cav1.2, encoded by the CACNA1C gene, is a major subunit of the L-type voltage-gated calcium channel family, best known for its role in cardiac excitation-contraction coupling. However, beyond the heart, Cav1.2 is highly expressed in the brain, where it regulates calcium influx critical for neuronal excitability, synaptic plasticity, and gene transcription. Dysregulation of Cav1.2 has been implicated in a range of neurological and neuropsychiatric disorders. Mutations in CACNA1C are causally linked to Timothy syndrome, a rare multisystem disorder characterized by cardiac arrhythmias, autism spectrum features, and cognitive impairment. Additionally, variants in CACNA1C have been associated with Brugada syndrome and are increasingly recognized as genetic risk factors for bipolar disorder, schizophrenia, and major depressive disorder. In the context of neurodegenerative disease, altered Cav1.2 function may contribute to disrupted calcium homeostasis, oxidative stress, and neuronal vulnerability-hallmarks of conditions such as Alzheimer's and Parkinson's disease. Its role in activity-dependent gene expression also positions Cav1.2 as a key modulator of long-term neuronal survival and plasticity. Given its dual importance in cardiac and neural physiology, Cav1.2 is a promising target for therapeutic strategies aimed at restoring calcium signaling balance in both neurodevelopmental and neurodegenerative disorders.
Host:
Mouse
Immunogen:
Fusion protein amino acids 1507-1733 (intracellular carboxyl terminus) of rabbit Cav1.2
Isotype:
IgG1
Purification:
Protein G Purified
Reactivities:
Hamster, Human, Mouse, Rat
Shipping Conditions:
Blue Ice
Specificity:
Detects ~240kDa (varies with cell background due to glycosylation).
Storage Conditions:
See Manual
Supplier:
StressMarq Biosciences
Type:
Antibody: Monoclonal Antibody