Common components of patch-clamp internal recording solutions can significantly affect protein kinase A activity

Brain Research

Volumn 828, Issue 1-2, 1999, Pages 169-173

  Vargas, Gricelly ^a   Yeh, Tsung Yin J ^a   Blumenthal, Donald K ^a   Lucero, Mary T ^a  

^a UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

Author keywords

Ion channel; Phosphorylation; Second messenger; Whole cell voltage clamp

Indexed keywords

ACETIC ACID; ALBUMIN; ASPARTIC ACID; CYCLIC AMP DEPENDENT PROTEIN KINASE; ETHYLENE GLYCOL; GLUCONIC ACID; ION CHANNEL; PHOSPHATE; POTASSIUM FLUORIDE; SULFATE; TRIMETHYLAMINE;

ANIMAL EXPERIMENT; ARTICLE; CHELATION; CHEMICAL REACTION; ENZYME ACTIVITY; ENZYME STABILITY; HYPERPOLARIZATION; MOUSE; NONHUMAN; OSMOLALITY; PATCH CLAMP; PHOSPHORYLATION; PRIORITY JOURNAL; SECOND MESSENGER; VOLTAGE CLAMP;

ANIMALS; ASPARTIC ACID; CALCIUM; CELLS, CULTURED; CESIUM; CHELATING AGENTS; CHLORIDES; CYCLIC AMP-DEPENDENT PROTEIN KINASES; EGTAZIC ACID; ENZYME ACTIVATION; ENZYME INHIBITORS; FLUORIDES; GLUCONATES; ION CHANNELS; ISOQUINOLINES; METHYLAMINES; OLFACTORY RECEPTOR NEURONS; PATCH-CLAMP TECHNIQUES; PHOSPHATES; PHOSPHORYLATION; POTASSIUM COMPOUNDS; RATS; SECOND MESSENGER SYSTEMS; SERUM ALBUMIN, BOVINE; SULFONAMIDES; SULFURIC ACID ESTERS; TETRAETHYLAMMONIUM;

EID: 0033562480     PISSN: 00068993     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0006-8993(99)01306-2     Document Type: Article

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