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The sections were picked from the knife with 2.3 M sucrose and floated on 1% ovalbumin (Sigma, Cat No.A5378) in 0.1 M Na-cacodylate buffer for at least one hour before incubation with specific or non-reactive antibody (50 µg/ml), at RT for one hour.
The sections were picked from the knife with 2.3 M sucrose and floated on 1% ovalbumin (Sigma, Cat No. A5378) in 0.1 M Na cacodylate buffer for at least one hour before incubation with specific or non-reactive antibody (50 µg/ml), at RT for one hour.
Similar(58)
Sections were picked up from the knife with a loop dipped in 2.3 M sucrose and transferred to a formvar/carbon coated copper grid.
Sections were picked onto Superfrost Plus or Apes coated Superfrost slides.
Ultrathin sections were picked up in a mix of 1.8% methylcellulose and 2.3 M sucrose (1 1).
Sections were picked up on copper grids and stained with alcoholic uranyl acetate and Reynold's lead citrate.
Sections were picked up using 2.3 M sucrose and mounted on formvar-coated copper grids before labeling.
Sections were picked up on copper grids and stained with alcoholic uranyl acetate and Reynolds lead citrate.
Travel times of the reflection and refraction signals were picked from these record sections and used to construct a P-wave velocity model.
Briefly, protein bands were picked from the SDS gel.
Twenty clones were picked from each PCR product.
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