ライフサイエンスコーパス: electrophorese

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 turation/renaturation cycle and products are electrophoresed again.

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

6 These proteins were electrophoresed and the Coomassie Brilliant Blue (CBB)-p

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

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

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

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

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

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

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

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

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

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

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

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

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

20 y, using blue native gel and two-dimensional electrophoreses, nano-LC-MS/MS, immunogold EM, and stimu

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

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

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

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

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

26 Reaction products are electrophoresed on polyacrylamide gels for visualization

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

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

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

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

31 Sodium-dodecyl-sulfate poly acrylamide gel electrophoreses (SDS-PAGE) indicated that the integrity

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

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

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

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

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

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

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

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

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

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

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