15 results for "Kv11.1" in Products
Kv11.1 Products
| Reactivity: | Human, Mouse, Rat |
| Details: | Rabbit Polyclonal |
| Applications: | IHC, WB |
| Reactivity: | Human, Mouse |
| Details: | Rabbit IgG Polyclonal |
| Applications: | IHC, WB |
![Western Blot: Kv11.1 AntibodyAzide and BSA Free [NBP3-03109]](https://resources.bio-techne.com/images/products/Kv11.1-Antibody-Western-Blot-NBP3-03109-img0004.jpg "Western Blot: Kv11.1 AntibodyAzide and BSA Free [NBP3-03109]")
| Reactivity: | Human |
| Details: | Rabbit Polyclonal |
| Applications: | IHC |
![Immunohistochemistry-Paraffin: Kv11.1 Antibody [NBP3-14389]](https://resources.bio-techne.com/images/products/Kv11.1 "Immunohistochemistry-Paraffin: Kv11.1 Antibody [NBP3-14389]")
| Applications: | WB, ELISA, MA, AP |
![Western Blot: Kv11.1 Overexpression Lysate [NBL1-12154]](https://resources.bio-techne.com/images/products/hERG-Overexpression-Lysate-Adult-Normal-Western-Blot-NBL1-12154-img0002.jpg "Western Blot: Kv11.1 Overexpression Lysate [NBL1-12154]")
![Western Blot: Kv11.1 Overexpression Lysate [NBP2-10603]](https://resources.bio-techne.com/images/products/Kv11-1-Overexpression-Lysate-Native-Western-Blot-NBP2-10603-img0002.jpg "Western Blot: Kv11.1 Overexpression Lysate [NBP2-10603]")
KV11.1 (hERG) channel blocker; inhibits rapid delayed rectifier K+ current (IKr)
| Alternate Names: | Tikosyn,UK 68798 |
| Chemical Name: | 1-(4-Methanesulphonamidophenoxy)-2-[N-(4-methanesulphonamidophenethyl)-N-methylamino]ethane |
| Purity: | ≥98% (HPLC) |
KV11.1 (hERG) channel blocker; inhibits rapid delayed rectifier K+ current (IKr)
| Chemical Name: | N-[4-[[1-[2-(6-Methyl-2-pyridinyl)ethyl]-4-piperidinyl]carbonyl]phenyl]methanesulfonamide dihydrochloride |
| Purity: | ≥98% (HPLC) |
H1 antagonist. Also KV11.1 (hERG) and Kir6 (KATP) channel blocker
| Chemical Name: | α-[4-(1,1-Dimethylethyl)phenyl]-4-(hydroxydiphenylmethyl)-1-piperidinebutanol |
| Purity: | ≥98% (HPLC) |
Orally active, potent H1 antagonist; also KV11.1 (hERG) channel blocker
| Alternate Names: | Hismanal |
| Chemical Name: | 1-[(4-Fluorophenyl)methyl]-N-[1-[2-(4-methoxyphenyl)ethyl]-4-piperidinyl]-1H-benzimidazol-2-amine |
| Purity: | ≥98% (HPLC) |
Kv11.1 (hERG) channel blocker
| Chemical Name: | 1-[[[5-(4-Chlorophenyl)-2-furanyl]methylene]amino]-3-[4-(4-methyl-1-piperazinyl)butyl]-2,4-imidazolidinedione dihydrochloride |
| Purity: | ≥97% (HPLC) |
KV11.1 (hERG) and KV4.3 channel activator; antiarrhythmic
| Chemical Name: | N-[4-Bromo-2-(1H-tetrazol-5-yl-phenyl]-N'-[3-(trifluoromethyl)phenyl]-urea |
| Purity: | ≥99% (HPLC) |
KV11.1 (hERG) channel activator; antiarrhythmic
| Chemical Name: | N,N'-Bis[2-hydroxy-5-(trifluoromethyl)phenyl]urea |
| Purity: | ≥98% (HPLC) |
Blocks IKr, hERG and L-type Ca2+ channels; class III antiarrhythmic
| Chemical Name: | (±)-N-[4-[4-(Ethylheptylamino)-1-hydroxybutyl]phenyl]methanesulfonamide hemifumarate |
| Purity: | ≥98% (HPLC) |
Calmodulin antagonist. Inhibits myosin light chain kinase
| Chemical Name: | N-(6-Aminohexyl)-5-chloro-1-naphthalenesulfonamide hydrochloride |
| Purity: | ≥98% (HPLC) |
