ライフサイエンスコーパス: co-purification

1 ed by co-immunoprecipitation and/or in vitro co-purification.

2 tatistical noise inherent in observations of co-purifications.

3 evidences based on interaction conservation, co-purification and 3D domain contacts (iPfam, 3did).

4 single-stranded DNA-binding protein through co-purification and biochemical studies.

5 Co-purification and co-precipitation analyses demonstrat

6 For the first time, we show by co-purification and electron microscopy that mycobacteri

7 the pilus fibres, as measured using in vivo co-purification and in vitro pilus polymerization assays

8 As shown by co-purification and thermal inactivation studies, the 4'

9 med biochemically by co-immunoprecipitation, co-purification, and glutathione S-transferase pull-down

10 activity associated with CtBP/BARS is also a co-purification artefact.

11 in vitro electrophoretic mobility shift and co-purification assays.

12 eracts with ExsD in bacterial two-hybrid and co-purification assays.

13 ctrophoretic mobility gel shift analysis and co-purification assays.

14 hods employed included an overlay technique, co-purification, co-immunoprecipitation, and the use of

15 Co-purification experiments confirmed that LeuRS, LysRS,

16 Indeed, co-purification experiments indicate association of OsaC

17 Co-purification experiments of ChlB with Strep-ChlN sugg

18 -C from individual subunits was derived from co-purification experiments performed with various combi

19 ts of mass spectrometry results from protein co-purification experiments, yeast two-hybrid interactio

20 igomeric CsgG complexes were confirmed using co-purification experiments.

21 By several independent criteria, including co-purification, immunoprecipitation, and gel filtration

22 e co-immunoprecipitation of the proteins and co-purification in the glutathione S-transferase (GST) p

23 polymerase (RNAP), we noticed the consistent co-purification of a 110-kDa polypeptide.

24 491)-affinity chromatography resulted in the co-purification of a member of the G12 family.

25 In this report, I describe the co-purification of a novel 70-kDa RNA helicase (RH70) an

26 Co-purification of AcrZ with AcrB, in the absence of bot

27 Isolation of this protein resulted in the co-purification of another unique protein called heat re

28 tubulin was suggested by the following: (i) co-purification of betaARK with tubulin from brain tissu

29 Co-purification of BMPs 2-7 with BMP1 prodomain sequence

30 ed enzymatic activities of GRP94 may reflect co-purification of contaminant enzymes, rather than intr

31 Namely, co-purification of different protein complexes as mediat

32 DDeltaD3 from M. acetivorans resulted in the co-purification of endogenous subunit L with each tagged

33 ith other ethylene receptors was obtained by co-purification of ETR1 with tagged versions of ERS1, ET

34 The co-purification of guanine nucleotide on the beta-tubuli

35 particles, and highly sensitive as shown by co-purification of homologues of the yeast pre-mRNA spli

36 We recently documented the co-purification of members of the LIV-1 subfamily of ZIP

37 ay be at least partially responsible for the co-purification of NDP kinase with DnaK.

38 Co-purification of p110 with CK2 from Sf-9 cells that ov

39 ification of the unwinding activity revealed co-purification of P68 RNA helicase.

40 n studies were performed to test and compare co-purification of PCR inhibitors in samples extracted f

41 Pheromone induction greatly decreased the co-purification of PrgX.

42 with similar properties demonstrated precise co-purification of protein recognized by all antibodies

43 nes without use of detergents and observed a co-purification of PspA, a membrane-stress response prot

44 ciated with NDP kinase from all tissues, but co-purification of pyruvate kinase was seen only in live

45 from yeast nuclear extracts resulted in the co-purification of Rad1, Rad7, Rad10, Rad16, Rad23, RPA,

46 ired for its association with CTR1, based on co-purification of tagged ETR1 mutants and CTR1 after ex

47 e receptor signaling complex was obtained by co-purification of the ethylene receptor ETR1 with a tag

48 The co-purification of the two polypeptides with transcripti

49 KAP 220 from rat testis extracts resulted in co-purification of the type II PKA holoenzyme.

50 ing (His)6-tagged p110 or p33 results in the co-purification of the well characterized p39 and p90 su

51 Co-purification of two different epitope-tagged forms of

52 Co-purification of Ung and Ndk through multicolumn low p

53 -tagged 54 kDa isoform (His54) were shown by co-purification on a Ni-NTA column to interact in Strept

54 en two proteins based on similarity of their co-purification patterns derived from MS data.

55 Using a co-purification strategy, we have identified a Ran GTPas

56 Co-purification studies demonstrate that SseA directly b

57 ination of gel filtration chromatography and co-purification studies demonstrates that SBP2 does not

58 electrophoretic mobility shift assays and co-purification studies showed that Rep-(1-160) did not

59 Pull down experiments completed by co-purification study prove that DauA and DctA interact

60 Using co-expression and co-purification, we have been able to isolate a CaM-IQ m

61 By performing protein co-purifications, we show that EspG(5) interacts with se

62 ursor is highly and specifically enriched by co-purification with at least two different small regula

63 ified ER as confirmed by co-fluorescence and co-purification with known ER proteins.

64 dentify novel telomerase regulators by their co-purification with the telomerase holoenzyme.

65 Here, using co-purification with TOC159 from Arabidopsis, we discove