Sentence examples for microscopy samples of from inspiring English sources

For electron microscopy, samples of SK-N-SH cells expressing L84V SOD1 and spinal cords from transgenic SOD1 L84V mice were decolorized, rehydrated, and rinsed in 0.1 M PBS.

After intravital microscopy, samples of jejunum were therefore collected to test TLR4, pNF-kB p65 and SIRT1 protein expression by western blotting.

For light microscopy, samples of lung tissue were embedded in paraffin, cut into 4 μm slices, and stained with hematoxylin and eosin.

For optical microscopy, samples of almond cells (unstained) were either suspended in buffer (undigested samples) or collected from the reaction vessel (digested samples), and then mounted on a glass slide, covered and viewed immediately.

For examination by light microscopy, samples of ileal effluent were immersed in Karnovsky's fixative (1.6% formaldehyde and 2% glutaraldehyde; 0.08M sodium cacodylate; pH 7.2), and left to fix at room temperature for at least 24 h.

Light microscopy samples consisted of fragments fixed immediately in 2.5% glutaraldehyde in 0.1 M cacodylate buffer (pH 7.2, 3 h, 4°C), washed in 0.1 M cacodylate buffer, then postfixed in OsO4 and embedded in Epon.

Compared to fluorescent microscopy, sample preparation of SECM is simple without any staining or labeling procedure.

We spray gold for 20 s for preparation of electron microscopy samples.

Although this method demonstrates the possibility of using microscopy samples, further investigation is warranted which applies these techniques to fresh sputum samples.

After in vivo microscopy, tissue samples of the cremaster muscle were taken for immunohistochemistry. Blood samples were collected by cardiac puncture for the determination of systemic leukocyte counts using a Coulter ACT Counter (Coulter Corp., Miami, FL, USA).

Light microscopy (LM) samples of the different cell suspensions obtained during the protocol were prepared by cytocentrifugation.