ライフサイエンスコーパス: Sephacryl

1 y sequential chromatography on protein A and Sephacryl 300.

2 lex that contained BC plus BCCP emerged from Sephacryl 400 with an apparent molecular mass greater th

3 Chromatography of whole egg jelly on a Sephacryl 500 column resulted in isolation of the major

4 ther supporting matrices, such as Sepharose, Sephacryl, cellulose or pustulan.

5 Its molecular size, based on Sephacryl column fractionation of ammonium sulfate preci

6 r= 2 x 10(7) were isolated by gel sieving on Sephacryl HR S500 in buffered balanced salts solution pl

7 We chromatographed rat intestinal cytosol on Sephacryl S-100 and found that PCTV budding activity app

8 Following Sephacryl S-100 chromatography, CIA activity was identif

9 fied using a combination of zinc chelate and sephacryl S-100 column chromatography.

10 Two interacted with the matrix of a Sephacryl S-100 column.

11 40 in endotoxemic sera, as confirmed by both Sephacryl S-100 gel filtration and p40-specific immunopr

12 Sephacryl S-100 gel filtration chromatography analysis o

13 tography of native intestinal cytosol over a Sephacryl S-100 HR column that FABP1 (14 kDa) eluted in

14 -Sephacel, molecular sieve chromatography on Sephacryl S-100, chromatofocusing on Polybuffer exchange

15 p procedure consisting of DEAE, heparin, and Sephacryl S-200 chromatography.

16 hydrophobic interaction, Sephadex G-100 and Sephacryl S-200 gel filtration chromatographies, and sod

17 other glycosphingolipids by TLC overlay and Sephacryl S-200 gel filtration.

18 followed by affinity chromatography using a Sephacryl S-200 HR column.

19 Following gel filtration chromatography on Sephacryl S-200 in the presence of Mn(2+), PP1(C) coelut

20 y silver staining using glutathione-agarose, Sephacryl S-200, and DEAE-cellulose chromatography.

21 e were further purified by chromatography on Sephacryl S-200.

22 d by gel filtration column chromatography on Sephacryl S-200.

23 d by gel filtration column chromatography on Sephacryl S-200.

24 erial chromatography with DEAE-Sepharose and Sephacryl S-200.

25 enyl-Sepharose CL-4B and gel filtration with Sephacryl S-200.

26 ximately 9% of the hsp70 in lysate, and upon Sephacryl S-300 chromatography the GR.hsp90 assembly act

27 Renatured rTromp1 was passed through a Sephacryl S-300 gel exclusion column previously calibrat

28 L-6B ion exchange chromatography followed by Sephacryl S-300 gel filtration.

29 ially purified by approximately 900 folds by Sephacryl S-300 HR gel filtration, Matrex gel orange A d

30 radient centrifugation and gel filtration on Sephacryl S-300 indicated that neither heat shock nor Ma

31 tionation of the ATP-agarose flow-through on Sephacryl S-300 separates free thioredoxin from apo-nNOS

32 On Sephacryl S-300, the native enzyme has a molecular mass

33 y during gel filtration chromatography using Sephacryl S-300.

34 a molecular mass of approximately125 kDa on Sephacryl S-300.

35 ing gel filtration of B. subtilis lysates on Sephacryl S-400 and specifically bound to ribosomal prot

36 xing method with modified alkaline lysis and Sephacryl S-500 DNA purification procedures.

37 ized proteoglycans (PGs) were analyzed using Sephacryl S-500 HR gel chromatography.

38 In RAO-3 cells, Sephacryl-S 300 gel filtration and DEAE-Sepharose ion ex

39 vity in the soluble fraction was purified by Sephacryl S100 and DEAE Sephacel.

40 ximately 60,000 (LOS:sCD14) as determined by Sephacryl S200 chromatography.

41 5S-enkephalin precursor cleaving activity by Sephacryl S200 gel filtration chromatography and by a si

42 use of wheat germ agglutinin chromatography, Sephacryl S300 gel filtration chromatography, anti-FLAG

43 aphy steps (Q-Sepharose, hydroxyapatite, and Sephacryl S300) followed by sodium dodecyl sulfate analy

44 ed extensively by DEAE-Sepharose, Biorex 70, Sephacryl S300, and Mono Q chromatography.

45 on five columns: DEAE-Sepharose, Biorex 70, Sephacryl S300, Mono Q, and DNA-cellulose.

46 Mono Q, Sephacryl S300HR, and hydroxylapatite column chromatogra

47 recombinant alpha A-crystallins purified by Sephacryl size-exclusion chromatography.

48 acrophages elicited by the administration of Sephacryl to RAG-2-/- mice did not immunostain for 12/15