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Examples
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(A) Oocytes were prepared and lysed for western blot as described in
PLoS ONE Alerts: New Articles Krishna Jagarlamudi et al. 2009
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Oocytes were prepared from ovaries of 3-4 week old mice that were treated with PMSG, as described in
PLoS ONE Alerts: New Articles Krishna Jagarlamudi et al. 2009
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Oocytes were injected with syntaxin 1A mRNA alone or co-injected with syntaxin 1A and KCNQ2/Δ339-360 deletion mutant/Δ372-493 deletion mutant.
PLoS ONE Alerts: New Articles Noa Regev et al. 2009
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They report their findings in a paper entitled, "Reprogramming of Human Somatic Cells Using Human and Animal Oocytes."
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Oocytes were injected (50 nl per oocyte) with 5 ng/oocyte KCNQ2/1 ng/oocyte KCNQ2+KCNQ3
PLoS ONE Alerts: New Articles Noa Regev et al. 2009
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Oocytes (n = 140) were immunoblotted at the indicated time points.
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Oocytes were double stained for TPX2 (green) and nucleic acids (blue) at the times indicated relative to GVBD.
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Oocytes injected with siRNA duplex oligonucleotides were maintained in prophase I for either two or five hours (referred to as siTPX2-2h and - 5h, respectively), then meiotic maturation was allowed to proceed.
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Xenopus Oocytes δ-ACTX-Hv1a has been shown to inhibit inactivation of insect and mammalian voltage-gated Na
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Oocytes (n = 150) were immunoblotted using an anti-TACC3 antibody (left) and an antibody raised against xTACC3 phosphorylated on Ser626 (right).
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