ライフサイエンスコーパス: eluate

1 nd a non-ER-containing fraction (250 mM NaCl eluate).

2 ld not be recovered with glycine as the only eluate.

3 adhesion molecules were not detected in the eluate.

4 e proteins are released and recovered in the eluate.

5 and anti-Crry Abs were present in glomerular eluates.

6 and endogenous serum components in the BEAD eluates.

7 tibody positive-control (NAb-PC) in the BEAD eluates.

8 tion into small-volume (tens of microliters) eluates.

9 set of autoantigens was observed only in RA eluates.

10 al P antigens could be demonstrated in these eluates.

11 cytometry and Western blot analysis of EGTA eluates.

12 ored only fractionally by addition of column eluates.

13 erferences; (3) elution/acidification of the eluate; (4) complexation of chromium with 1,5-diphenylca

14 ncentrations (0.1-0.5mM) of EDTA, monitoring eluate absorbance at 280 nm as well as at 215 nm, adding

15 ng complex was reconstituted from the column eluate after displacement of SDS with nonionic detergent

16 nanocarriers, Dex was already detectable in eluates after 6h when applying nanocrystals on intact sk

17 synthesized adhesives and the DOX-containing eluates against Streptococcus mutans through agar diffus

18 The DM-GRASP-Sepharose eluate also contains a potent neurite stimulating activi

19 Column eluates also showed some relative concentration of IgG a

20 bands were present in N-acetyl-D-glucosamine eluates, although their % distribution changes in favor

21 automated analysis of lipid extracts and TLC eluates and suggests that indirect high-performace (HP)T

22 ceptor (ER)-containing fraction (150 mM NaCl eluate) and a non-ER-containing fraction (250 mM NaCl el

23 E column, the derivatized phenols in the SPE eluate are analyzed by GC/MS.

24 out further processing the resulting FISHing eluates are suitable for BEAMing (beads, emulsion, ampli

25 ormed to interpret the DOM chemical space of eluates, as well as permeates and wash liquids with mole

26 ptors apoER2 and Lrp1 were identified in the eluate by mass spectrometry.

27 , called sequential analysis of fractionated eluates by SRM (SAFE-SRM), to plasma from cancer patient

28 ermined by tandem MS of TAP-TbRACK1 affinity eluates, co-sedimentation in a sucrose gradient, and co-

29 LC-MS analysis of eluates confirmed DSF retained major cranberry and blueb

30 The organic eluate containing extracted analytes was evaporated and

31 (-) mutant was incubated with a pneumococcal eluate containing native PspA, there was decreased depos

32 SMR acquired a chromatogram by measuring the eluate density.

33 DNase treatment of IVGG or Id column eluates did not affect anti-Id blocking activity.

34 Importantly, the urea-glycine eluates differed from the conventional eluates in having

35 radiolabeled with (68)Ga by adding generator eluate directly to a vial containing the cold precursors

36 serum samples are carried over to final BEAD eluates due to formation of protein complexes with ADA o

37 C plate dimensions and refined design of the eluate exit system.

38 GFbeta2 treatment elevated IOP and increased eluate fibronectin and PAI-1 content.

39 ound a higher zinc release in the batch test eluates for all granules, ranging from 15% higher to 687

40 red with subsaturating doses of the four IgG eluates for up to 144 hr.

41 This eluate fraction stimulated DNA synthesis in quiescent Ba

42 ries of labeled compounds in the appropriate eluate fraction.

43 ibeprin or avebetrin was done using buffered eluate fractions (600-800 MBq, pH 2) of an SnO2-based ge

44 Subsequently, nanoliter eluate fractions are collected at a rate of one fraction

45 A Western blot (immunoblot) of the eluate fractions revealed a correlation between peak Nef

46 Column flowthrough and eluate fractions were compared for their ability to bloc

47 biological activity of IL-6 complexes in the eluate fractions were probed using five IL-6 ELISAs and

48 Same complement analysis was performed in eluate from a control column after in vitro perfusion of

49 cal surface compared with incubation with an eluate from a PspA(-) strain.

50 (OCN) is described for direct deposition of eluate from a thermal field-flow fractionation (ThFFF) s

51 A gel activity assay revealed that the eluate from C16-serinol-Sepharose contained three serine

52 The eluate from the first dimension is actively modulated us

53 also detected by far-Western analysis in the eluate from the wild-type RNA column but not from the mu

54 The eluate from the wild-type RNA column contained a 65-kDa

55 detected by immunoblot in soluble fractions eluated from RBC units stored for more than 35 days, but

56 tivity was greatly enriched in the high-salt eluates from a D' affinity column.

57 f SLE APAD combining sites was observed with eluates from anti-DNA Id affinity columns; however, no c

58 In eluates from both patient and control, immunoadsorbent c

59 rom autoimmune MRL/lpr mice are not found in eluates from class II molecules of MHC-identical C3H mic

60 Eluates from donor hearts placed in vimentin/complete Fr

61 and casein (a milk protein) were analyzed in eluates from dried blood spots by enzyme-linked immunoso

62 of 17 inflammatory markers were measured in eluates from dried blood spots using a bead-based multip

63 Using eluates from FLAG-NEIL1 immunoprecipitates from human ce

64 Eluates from gel regions equivalent to 38 kDa were analy

65 i-Id blocking activity was recorded for IVGG eluates from human cationic myeloma columns devoid of th

66 In two recipients, eluates from immunoadsorbent columns were analyzed for C

67 e-3-phosphate dehydrogenase were absent from eluates from lung and liver.

68 were also recovered from the isothiocyanate eluates from microcystin-Sepharose by a rebinding intera

69 Furthermore, acid eluates from recombinant or cellular MR1 proteins enhanc

70 ected above 200 kDa in wheat germ agglutinin eluates from solubilized cells suggests that some recept

71 This protein was not detected in the eluates from the mutant or the antisense RNA columns.

72 sputum specimens) were positive by PCR with eluates from the smears.

73 Eluates from the Zymo kits also tested positive for DNA

74 mination, similar in appearance to dsDNA, in eluates from the Zymo, Qiagen, and ChargeSwitch kits.

75 The eluates from these kidneys did not contain ANA, anti-dsD

76 lyacrylamide gel electrophoresis analysis of eluates from these supports shows that five polypeptides

77 Plasma antibody eluates from two patients were used to select for phage

78 Immunoblotting of the eluate gave a single diffuse band at approximately 73 kD

79 The post-processed eluate has been used to radiolabel DOTATOC in yields of

80 The compartmentalization of the HPLC-eluate in a segmented flow was performed with droplet si

81 immunoprecipitation and concentration of the eluate in the microchannel, IEF-micropillar-MALDI-MS is

82 ycine eluates differed from the conventional eluates in having significantly greater reactivity to gl

83 the residual drug and human IgG in the BEAD eluates indicate that the BEAD efficiently removed the h

84 g site) activity in human anti-DNA Id column eluates indicates that epibodies from IVGG are relativel

85 ized for online ethanol-postprocessed (68)Ga eluate investigating various parameters, such as buffer

86 The eluate is reduced to < 1.0 mL and reconstituted in 10/90

87 hot-cell system,(68)Ga(3+) of the generator eluate is trapped on a cation exchanger cartridge (100 m

88 then eluted, using pH 2.5 glycine-saline and eluates neutralized to pH 7.4.

89 derivatization are: 500muL of isopropanolic eluate obtained by SPE combined with 500muL of derivatiz

90 the other hand, interference was observed in eluate obtained from C18 SPE column.

91 step yields a highly concentrated PCR-ready eluate of nucleic acids devoid of PCR inhibitors that ar

92 mately 50-kDa, and 34/31-kDa polypeptides in eluates of CaM affinity columns, suggesting the presence

93 rat hepatoma cells were treated with CE and eluates of CDSF at a range of 1-25 mug/ml.

94 CE and eluates of CDSF demonstrated dose-dependent inhibition o

95 The eluates of filters showed trapped bacteria determined by

96 The eluates of filters used for leukoreduction were also ass

97 Distinct protein compositions were found in eluates of lung and liver extracts processed in a like m

98 -actinin Abs were present in sera and kidney eluates of lupus mice with active nephritis.

99 el electrophoresis of the microcystin-biotin eluates of the three fractions revealed a complex patter

100 tibody against rat HB-EGF indicated that the eluate peak contained immunoreactive proteins of 22 and

101 lls was also tyrosine phosphorylated by this eluate peak.

102 Pretreatment of microvesicles, RBC eluate preparations, and HDL with phosphatidylinositol-s

103 PNH RBC that were exposed to HDL, RBC eluate preparations, or microvesicles demonstrated decre

104 More important, DOX-containing eluates promoted inhibition of MMP-1 activity when compa

105 bber (EPDM) or thermoplastic elastomer (TPE) eluates, reflect the stronger mechanical stress of batch

106 than the resin, generating more concentrated eluate relative to the amount of Pu loaded onto the foam

107 In contrast, immunoblotting of the peptide eluate revealed no copurifying Galphaq/11, Galphai1/2, G

108 te molar mass, size and concentration of the eluate species.

109 tion column to a micro T-junction, where the eluate stream is compartmentalized into picoliter drople

110 pproximately 20 microL/min of the 3.0 mL/min eluate stream to the mass spectrometer, eliminating the

111 ate nanoflow liquid chromatography (nano-LC) eluate streams at high frequencies and high peak resolut

112 Eluate that was adsorbed to NC1 hexamer from rat glomeru

113 Kidney eluate that was depleted of alpha3(IV)NC1 antibodies sti

114 ombinant PP-1C distinguished proteins in the eluates that bound PP-1C from those that bound PP-2AC.

115 ve major polypeptides in the affinity column eluate, the activity of interest was assigned to the pro

116 beled simply by addition of (68)Ga generator eluate to a cold kit.

117 entalization prevents peak dispersion during eluate transport and conserves the chromatographic perfo

118 3.5, 30 min and 2.5 mL for pH, contact time, eluate volume, respectively.

119 Our experimental analysis of eluate vs feed concentrations of Li and competing ions d

120 The final concentration of DNA in the eluate was 5x10(6), 14x10(6), and 8x10(6) copies/microL

121 The eluate was analyzed by capillary LC fractionation follow

122 s, the digest was subjected to HPLC, and the eluate was analyzed for argpyrimidine.

123 Each corneal eluate was collected and stored at -70 degrees C until a

124 column (MICC), and error-depleted DNA in the eluate was collected for downstream gene assembly.

125 The eluate was concentrated with two consecutive filtration

126 The eluate was concentrated, and the phthalate metabolites w

127 After concentration, the calmodulin eluate was further purified by successive high pressure

128 ushed with sterile saline, and the collected eluate was submitted for PCR amplification of IS6110 seq

129 romycin content of the serum samples and GCF eluates was determined with an agar diffusion bioassay.

130 NA (but not antihistone) reactivity in these eluates was due to cross-reactive anti-dsDNA antibodies.

131 and other components] plus (99m)Tc generator eluate) was examined.

132 t alpha3(IV)NC1 domain, and serum and kidney eluate were examined for antibodies to both native and r

133 ure model using human anterior segments, and eluates were analyzed for fibronectin and PAI-1 content.

134 None of the adhesives eluates were cytotoxic to the human dental pulp stem cel

135 The salt eluates were examined for the presence of both DNA repli

136 The eluates were IgM free and > or =95% IgG2.

137 The eluates were noncytotoxic in micro-CDC assays.

138 ound peptides were eluted with acid, and the eluates were pooled and submitted to high-pressure liqui

139 The eluates were subjected to analysis of total protein, SDS

140 All eluates were tested for specificity against a variety of

141 nity for DNA than antibodies also present in eluates which blocked anti-DNA combining sites.

142 Immunoprecipitation of the affinity column eluate with a Galpha(13) antibody demonstrated that 8-Br

143 carinii lysate and the 200 mM methylmannose eluate with antibody against the major surface glycoprot

144 beyed in the range of 0.07-3.0 mug mL(-1) in eluate, with the squared correlation coefficient (R(2))

145 Glycosidase digestion of the 2 m eluate yielded protein bands of M(r) 90,000 and 60,000 t