epitope corresponding to amino acids 1721-2000 mapping within an internal region of L-type Ca++ CP α1C of human origin
Modification Notes
Voltage-dependent Ca++ channels mediate Ca++ entry into excitable cells in response to membrane depolarization, and they are involved in a variety of Ca++-dependent processes, including muscle contraction, hormone or neurotransmitter release and gene expression. Calcium channels are highly diverse, multimeric complexes composed of an ?-1 subunit, an intracellular ?-subunit, a disulfide linked ?-2/? subunit and a transmembrane ?-subunit. Ca++ currents are characterized on the basis of their biophysical and pharmacologic properties and include L-, N-, T-, P-, Q-, and R- types. L-type Ca++ currents initiate muscle contraction, endocrine secretion, and gene transcription, and can be regulated through second-messenger activated protein phosphorylation pathways. L-type calcium channels may form macromolecular signaling complexes with G protein-coupled receptors, thereby enhancing the selectivity of regulating specific targets.
Key Feature
Clonality
Polyclonal
Isotype
IgG
Host Species
Rabbit
Tested Applications
WBIPIFELISA
recommended for detection of L-type Ca++ CP α1C of mouse, rat and human origin by WB, IP, IF and ELISA:
Species Reactivity
HumanMouseRat
Concentration
1mg/ml
Purification
Affinity purified
Target Information
Alternative Names
epitope corresponding to amino acids 1721-2000 mapping within an internal region of L-type Ca++ CP &alpha 1C of human origin
Tissue Specificity
epitope corresponding to amino acids 1721-2000 mapping within an internal region of L-type Ca++ CP α1C of human origin