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References in periodicals archive ?
1 1:100 California Napsin A Cell Marque, Rocklin, Polyclonal Ready-to-use California dilution Antibody Antigen Retrieval TTF-1 Envision Flex TRS Tris-EDTA (pH 9.
It was found that all the 53 positive isolates were also positive by modified 3-D test for AmpC [beta]-lactamase and the disk test using tris-EDTA.
DNA was extracted as described elsewhere (5), purified with polyvinyl-pyrrolidone, and stored at -20[degrees]C in Tris-EDTA buffer.
These solutions and water were used as washes after localization of [lambda] DNA stained with a 1:100 000 dilution of SYBR Gold (Molecular Probes) in Tris-EDTA.
5 mL phenol saturated with Tris-EDTA was preheated to 55[degrees]C, and 700 [micro]L of this mixture was added to the frozen, ground cells.
Staining with Vistra Green and measurement of cell-free plasma DNA were done on a LightCycler real-time PCR system (Roche) by fluorescent signal detection according to the following protocol: Human placental DNA calibrators (Sigma) were dissolved in Tris-EDTA buffer (1 mmol/L Tris-HCl, 1 mmol/L EDTA, pH 8.
Purified DNA was solubilized in Tris-EDTA buffer (10 mmol/L Tris-HCI, 1 mmol/L EDTA, pH 8) and stored at -20 [degrees]C.
Disks were washed four times with Tris-EDTA buffer (Tris 10 mM, pH 7.
5% sodium lauryl sarcosine in Tris-EDTA buffer) for 1 hour at 37 [degrees] C, replaced with ESP buffer (0.
In a room separate from the area in which samples were prepared and the PCR was set up, the oligonucleotides were dissolved In Tris-EDTA buffer (1 mmol/L Tris-HCI, nC 8.