Optimizing the culture environment in the IVF laboratory: Impact of pH and buffer capacity on gamete and embryo quality

Reproductive BioMedicine Online

Volumn 21, Issue 1, 2010, Pages 6-16

  Swain, Jason E ^a  

^a UNIVERSITY OF MICHIGAN   (United States)

Author keywords

embryo; HEPES; hydrogen ion; MOPS; oocyte; pH

Indexed keywords

3 ( N MORPHOLINO)PROPANE SULPHONIC ACID; 3 ( N,N BIS[ 2 HYDROXYETHYL]AMINO) 2 HYDROXYPROPANE SULPHONIC ACID; 4 (2 HYDROXYETHYL) 1 PIPERAZINEETHANESULFONIC ACID; BICARBONATE; BUFFER; CARBON DIOXIDE; EDETIC ACID; MORPHOLINE DERIVATIVE; SULFONIC ACID DERIVATIVE; UNCLASSIFIED DRUG;

APOPTOSIS; CALIBRATION; CELL CULTURE; CELL PH; CRYOPRESERVATION; CULTURE MEDIUM; EMBRYO; EMBRYO CULTURE; EMBRYO DEVELOPMENT; EMBRYO TRANSFER; EQUILIBRIUM CONSTANT; FERTILIZATION; FERTILIZATION IN VITRO; GAMETE; HUMAN; INTRACYTOPLASMIC SPERM INJECTION; LABORATORY TEST; MEMBRANE STABILIZATION; NONHUMAN; OOCYTE; OOCYTE MATURATION; OSCILLATION; OSMOLALITY; QUALITY CONTROL; REVIEW; ROOM TEMPERATURE;

BUFFERS; CULTURE MEDIA; EMBRYO CULTURE TECHNIQUES; EMBRYO, MAMMALIAN; FERTILIZATION IN VITRO; HUMANS; HYDROGEN-ION CONCENTRATION; OOCYTES;

EID: 78650177927     PISSN: 14726483     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.rbmo.2010.03.012     Document Type: Review

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