ライフサイエンスコーパス: we purified

1 We purified 8-amino-flaviolin and demonstrated that it is rev

2 To gain further insight into the involved mechanism, we purified a native effector complex of III-B Cmr-alpha from

3 We purified a stable, active complex consisting of all four p

4 nderstand how chlamydial supercoiling levels are regulated, we purified and analyzed three putative Chlamydia trachomatis

5 Here, we purified and assessed the origin, concentration and conten

6 We purified and compared the transcriptomes of pre-HSCs, HSCs

7 to the first-in-class proteasome inhibitor (PI) bortezomib, we purified and investigated patient-derived AL PCs, in compa

8 We purified and reconstituted IAR into large unilamellar vesi

9 To test this model, we purified and reconstituted the Mps2-Bbp1 complex from yeas

10 To identify as yet unknown interaction partners of NFAT, we purified biotin-tagged NFATc1/alphaA, NFATc1/betaC, and NF

11 We purified both fission yeast and human Aip1 and investigate

12 We purified budding yeast Arp2/3 complex held in or near the

13 In the present investigation, we purified carnosine N-methyltransferase from rat muscles ab

14 We purified, cloned, and characterized 13 IgGs specific for s

15 Here, we purified different classes of soluble and membrane-bound c

16 To elucidate heterochromatin organization and regulation, we purified Drosophila melanogaster HP1a interactors, and per

17 To do this, we purified exosomes from culture medium of eosinophils and c

18 We purified, for the first time, a WTA transporter and have r

19 We purified His-tagged ribosomes from Escherichia coli cells

20 Using this protocol, we purified human TRPV3.

21 Here, we purified iPSC-derived human dopaminergic neurons (DaNs) us

22 To gain insights into the molecular mechanisms of HOTAIR, we purified it in a stable and homogenous form in vitro, and

23 how SPIN1 functions as a transcriptional coactivator, here we purified its interacting proteins.

24 We purified KSP+ cells using flow cytometry with anti-KSP ant

25 To analyze an RNA-dependent interaction with chromatin, we purified native nucleosomes from mouse ES cells and detect

26 We purified nuclear extracts and quantified nuclear factor-ka

27 To study the strain-dependent conformations of PrP(Sc), we purified proteinase-resistant PrP(Sc) (PrP(RES)) from mous

28 We purified R.PabI homologs from Campylobacter coli (R.CcoLI)

29 We purified recombinant allergens that are recognized by pati

30 Here, we purified recombinant DDX43 protein to near homogeneity and

31 Here, we purified recombinant FA core complex to reveal the functio

32 We purified recombinant Go-opsin1 and found that it absorbs i

33 Here, we purified recombinant human SPCA1a from Saccharomyces cerev

34 Therefore we purified SpAin1 and quantified its ability to dynamically

35 To uncover how centrosomes sustain and regulate force, we purified SPBs from budding yeast and used laser trapping t

36 Thus, we purified StmPr1 from the S. maltophilia strain K279a cultu

37 We purified the AR9 nvRNAP from infected B. subtilis cells an

38 proteins associated with the nuclear exosome, in this work, we purified the complex with Rrp6-TAP, identified the co-puri

39 gy coupling and transport kinetics are complicated in vivo, we purified the major lysine transporter (Lyp1) of yeast and

40 ed in the model thaumarchaeon Nitrososphaera viennensis and we purified the recombinant enzyme from the uncultivated thau

41 To characterize the biochemical properties of GIMAP6, we purified the recombinant GIMAP6 to homogeneity and reveale

42 Using a chemical biology approach, we purified the sigma2 receptor from tissue, revealing its id

43 vation of TRPV1 in the presence of different phospholipids, we purified the TRPV1 protein from HEK-293 cells and incorpor

44 We purified thermostable wild type and QUAD opsins, with or w

45 We purified these cells to generate TCRbeta chain libraries p

46 We purified to homogeneity functional Asn, Glu, and Ile tRNAs

47 We purified trace-active derivatives of kynurenine and identi

48 We purified trans factors that recognize the motifs and ident

49 o evaluate the effect of the mutation on protease activity, we purified WT and Ubl mutant PLP2 and found that the proteas

50 Furthermore, we purified zebrafish MTH1 and solved the crystal structure o