<--- Back to Details
First PageDocument Content
Biology / Ion channels / Cardiac electrophysiology / Physiology / KCNE1 / KvLQT1 / Electrophysiology / Cardiac arrhythmia / Cardiac action potential / Potassium channel / Long QT syndrome / G418
Date: 2016-05-11 07:50:20
Biology
Ion channels
Cardiac electrophysiology
Physiology
KCNE1
KvLQT1
Electrophysiology
Cardiac arrhythmia
Cardiac action potential
Potassium channel
Long QT syndrome
G418

B’SYS GmbH CHO KVLQT1/minK Cell Line Specification Sheet © B’SYS GmbH

Add to Reading List

Source URL: www.bsys.ch

Download Document from Source Website

File Size: 248,71 KB

Share Document on Facebook

Similar Documents

B’SYS GmbH  CHO KVLQT1/minK Cell Line Specification Sheet © B’SYS GmbH

B’SYS GmbH CHO KVLQT1/minK Cell Line Specification Sheet © B’SYS GmbH

DocID: 1rn53 - View Document

Assay Catalogue  The Ionchannel Company Ion channels & Transporters		 Organ system - screening list

Assay Catalogue The Ionchannel Company Ion channels & Transporters Organ system - screening list

DocID: 1qANP - View Document

Microsoft Word - Cui_lecture_program.docx

Microsoft Word - Cui_lecture_program.docx

DocID: 1oR0c - View Document

The Danish National Research Foundation Centre for Cardiac Arrhythmia  The cardiac rhythm is governed by the electrical activity of the cardiomyocytes that regulate the 4050 mio. heart beats each year. Irregularities in

The Danish National Research Foundation Centre for Cardiac Arrhythmia The cardiac rhythm is governed by the electrical activity of the cardiomyocytes that regulate the 4050 mio. heart beats each year. Irregularities in

DocID: 14sfh - View Document

HIGHLIGHTS During 2006 we have made a number of important findings as stated shortly here: - In Danish patients with the common arrhythmia type atrial fibrillation mutations have been found in the genes coding for the fo

HIGHLIGHTS During 2006 we have made a number of important findings as stated shortly here: - In Danish patients with the common arrhythmia type atrial fibrillation mutations have been found in the genes coding for the fo

DocID: 13RLB - View Document