ライフサイエンスコーパス: electrophorese

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1 ions of F6P or ATP in the running buffer and electrophoresed.

2 one- and two-dimensional polyacrylamide gel electrophoreses.

3 This method electrophoreses a biological sample (e.g., serum) contai

4 ly sulfated flavanoids and flavonoids can be electrophoresed and resolved under reverse polarity at p

5 dephosphorylated when cellular proteins are electrophoresed and the separated PTPases are renatured

6 The purified samples were electrophoresed and transferred to nitrocellulose for de

7 ome information derived from two-dimensional electrophoreses and mass spectrometry of prostate cancer

8 by sodium dodecyl sulfate-polyacrylamide gel electrophoreses and silver staining revealed a 50-kDa pr

9 mples at equilibrium is rapidly quenched and electrophoresed at -40 degrees C.

10 Two-dimensional blue native (BN) electrophorese combined with SDS-PAGE yielded NOX4 to re

11 to snapshot imaging, in which molecules are electrophoresed for a constant time in an apparatus of c

12 r two near-IR dye-labeled sequencing primers electrophoresed in a capillary gel column were found to

13 When the dye/primer conjugates were electrophoresed in a cross-linked polyacrylamide gel ele

14 y, and mammary gland (female) were isolated, electrophoresed in agarose gels, and transferred to nylo

15 olubilized by n-dodecyl beta-D-maltoside and electrophoresed in blue native-polyacrylamide gels (BN-P

16 recovered in low-salt nuclear extracts, and electrophoresed in multigels consisting of nine individu

17 aining of extracts of Methanosarcina barkeri electrophoresed in polyacrylamide gels revealed an addit

18 Extracted proteins were electrophoresed on 7.5% polyacrylamide gels, transferred

19 as been treated with the hydroxyl radical is electrophoresed on a native gel.

20 Complete-digest fragments are electrophoresed on agarose gels, poststained, and imaged

21 R amplicons were digested with MspI and were electrophoresed on agarose gels.

22 Polymerase chain reaction products were electrophoresed on denaturing gels and exposed to radiog

23 Reaction products are electrophoresed on polyacrylamide gels for visualization

24 s having different native gel mobilities are electrophoresed on separate lanes of a denaturing gel to

25 sitive screening method that is performed by electrophoresing one lane of a Sanger dideoxy terminatio

26 H under normal polarity these species can be electrophoresed only if a pressurized capillary is emplo

27 hile residual primer, nucleotides, and salts electrophorese out of the system.

28 y a longer untagged target sequence as it is electrophoresed through a DNA-containing hydrogel plug i

29 body-antigen association, an antigen zone is electrophoresed through a zone of immobilized antibody.

30 Fluorescently labeled antigen is electrophoresed through each immobilized antibody zone,

31 altered mobility of single-stranded segments electrophoresed through non-denaturing polyacrylamide ge

32 labeled with a fluorophore and a biotin are electrophoresed through the SA hydrogel for binding and

33 o release the target molecule, which is then electrophoresed to a recovery chamber for subsequent PCR

34 The three pools were electrophoresed together on two-dimension SDS gels, and

35 Extracts of AS-induced cells electrophoresed under nonreducing conditions possessed u

36 linked dimers and monomers when samples were electrophoresed under nonreducing conditions.

37 wild-type, and master donor viruses are then electrophoresed under SSCP conditions.

38 The technique involves electrophoresing up to 10 or more DNA fragments on a pol

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