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