Our Anti-Pan-KChIP K+ channel mouse monoclonal primary antibody from NeuroMab is produced in-house from hybridoma clone K55/82. It detects human, mouse, and rat Pan-KChIP K+ channel, and is purified by Protein A chromatography. It is great for use in CHiP, IHC, ICC, IP, WB.
The Kv channel-interacting proteins (KChIP1, kChIp2, kChIp3, and kChIp4) are members of the family of voltage-gated potassium (Kv) channel-interacting proteins (KCNIPs), which belong to the recoverin or neuronal calcium sensor (NCS) family branch of the EF-hand superfamily. They serve as auxiliary channel subunits and interact with Kv4 alpha subunits to form native Kv4 channel complexes. KChiP subunits regulate Kv4 channels through various mechanisms including altering: channel density, inactivation kinetics, rate of recovery from inactivation, and cell surface delivery.
Fusion protein amino acids 1-216 (full length) of rat KChIP1b (accession number Q8R426) produced recombinantly in E. Coli
Human, Mouse, Rat
AB_10673406
Aliquot and store at ≤ -20°C for long term storage. For short term storage, store at 2-8°C. For maximum recovery of product, centrifuge the vial prior to removing the cap.
Liquid
Produced by in vitro bioreactor culture of hybridoma line followed by Protein A affinity chromatography. Purified mAbs are >90% specific antibody.
10 mM Tris, 50 mM Sodium Chloride, 0.065% Sodium Azide pH 7.4
WB: 1:1000
IHC: 1:250
ICC: 1:250
Unconjugated
No cross-reactivity reported
Each new lot of antibody is quality control tested by western blot on rat whole brain lysate and confirmed to stain the expected molecular weight band.
These antibodies are to be used as research laboratory reagents and are not for use as diagnostic or therapeutic reagents in humans.
United States
24 months from date of receipt
Shipped on ice packs
Kv channel-interacting protein 1 (KChIP1) (A-type potassium channel modulatory protein 1) (Potassium channel-interacting protein 1)
Menegola, M. , et al. 2006. Unanticipated region- and cell-specific downregulation of individual KChIP auxiliary subunit isotypes in Kv4.2 knock-out mouse brain.. Journal of Neuroscience, 2137-42.
Heath, N.C., et al. 2014. The expression pattern of a Cav3-Kv4 complex differentially regulates spike output in cerebellar granule cells.. Journal of Neuroscience, 8800-8812.
Carlessi, L., et al. 2014. Functional and molecular defects of hiPSC-derived neurons from patients with ATM deficiency.. Cell Death Disease, e1342-e1342.
Sun, W., et al. 2011. DPP6 establishes the A-type K(+) current gradient critical for the regulation of dendritic excitability in CA1 hippocampal neurons.. Neuron, 1102-15.
Tozakidou, M., et al. 2010. Molecular and functional remodeling of I(to) by angiotensin II in the mouse left ventricle.. Journal of Molecular and Cellular Cardiology, 140-151.
Schwenk, J., et al. 2008. NMR analysis of KChIP4a reveals structural basis for control of surface expression of Kv4 channel complexes.. The Journal of Biological Chemistry, 18937-18946.
Pruunsild, P., et al. 2012. Subcellular localization and transcription regulatory potency of KCNIP/Calsenilin/DREAM/KChIP proteins in cultured primary cortical neurons do not provide support for their role in CRE-dependent gene expression.. Journal of Neurochemistry, 29-43.
Jerng, H.H. , et al. 2008. Multiple Kv channel-interacting proteins contain an N-terminal transmembrane domain that regulates Kv4 channel trafficking and gating.. The Journal of Biological Chemistry, 36046-36059.
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