ライフサイエンスコーパス: heat-inactivate

1 benzolamide or when the exogenous enzyme was heat inactivated.

2 Killing was abolished when the serum was heat inactivated.

3 gnificantly if the serum in the cultures was heat-inactivated.

4 ot seen with injection of HEPES buffer, with heat-inactivated 8-amino-cADPR, or in cells pretreated w

5 mice to intratracheal challenge with live or heat-inactivated A. fumigatus spores.

6 coli and subsequent in vitro reactions with heat-inactivated acceptor fractions derived from Mycobac

7 d by DAT blocker GBR12935 and is absent when heat-inactivated alpha-synuclein is dialyzed into these

8 at 1, 10, 25, or 50 hemolytic units (HU) or heat-inactivated alpha-toxin was intrastromally injected

9 was dose and time dependent, was elicited by heat-inactivated and infectious viruses, and did not dep

10 erived from an eIF4G2 mutant strain could be heat inactivated, and this inactivation could be reverse

11 and embryoid bodies dropped after culture in heat-inactivated anti-Neu5Gc antibody-negative human ser

12 division, whereas cells injected with either heat-inactivated antibodies or control scrambled peptide

13 Heat-inactivated antibody or control antibodies had a mu

14 nor secreted products were suppressive, and heat-inactivated, antibody-coated tachyzoites, which eff

15 However, TFII-I is heat-inactivated at temperatures lower than that require

16 eclined over time when cells were exposed to heat-inactivated ATCV-1.

17 These heat-inactivated B. pertussis Ag/LPS-stimulated mast cel

18 Addition of EMD 57033 to heat-inactivated beta-cardiac myosin is followed by refo

19 ression in mast cells stimulated with LPS or heat-inactivated Bordetella pertussis Ag.

20 UV- and heat-inactivated C pneumoniae EBs also stimulated VSMC p

21 Formalin and heat-inactivated C. pneumoniae activated the transcripti

22 Heat-inactivated C. pneumoniae failed to stimulate produ

23 rly (IM) with MOMP, MOMP-ISCOMs, and live or heat-inactivated C. trachomatis serovar D.

24 cavengers, and catalytically active (but not heat-inactivated) catalase and SOD.

25 tibody is introduced into the cells, whereas heat-inactivated CE and antibodies are ineffective.

26 Heat-inactivated chronic-stage plasma can "neutralize" t

27 s observed when normal rabbit serum (NRS) or heat-inactivated complement was used.

28 y inhalation to A. fumigatus viable conidia, heat-inactivated conidia (HIC), or HEPA-filtered air twi

29 ells incubated with aHUS serum compared with heat-inactivated control, TTP, and normal serum.

30 Upon treatment with heat-inactivated Corynebacterium parvum, urinary nitrite

31 volar forearm of 15 healthy volunteers with heat-inactivated cowhage spicules previously soaked in t

32 curred after treatment of colonic loops with heat-inactivated CPE, antibody alone, or bovine serum al

33 n contrast, control rabbits, inoculated with heat-inactivated culture supernatants from the same cell

34 Using heat-inactivated D39 (HI-D39) and sterile peritoneal dia

35 lture medium, purified DspB protein, but not heat-inactivated DspB, restored the ability of the mutan

36 d, intraperitoneal administration of live or heat inactivated E. coli JE5505 lacking the abundant out

37 In wild-type (Wt) mice injected with heat-inactivated E. coli, hepatic TLR4 and TLR2 proteins

38 Heat-inactivated elastase was used as control.

39 cubated with human uracil DNA N-glycosylase, heat-inactivated enzyme or buffer.

40 etectable in cells scanned with noncoated or heat-inactivated enzyme-coated tips (n = 9).

41 n SsoPox-W263I activity and could reactivate heat-inactivated enzyme.

42 to medium supplemented with 10% unheated or heat-inactivated fetal bovine serum and incubated at 37

43 S phase in the presence of cytokines and 5% heat-inactivated fetal calf serum (HI-FCS).

44 Heat-inactivated formulations and subunit vaccines are s

45 winged and unwinged aphids challenged with a heat-inactivated fungal pathogen, and found that immune

46 Live but not heat-inactivated fungal spores resulted in recruitment o

47 , gamma globulin-depleted ovine serum or 25% heat-inactivated, gamma globulin-depleted bovine serum.

48 mM MgCl2 or with this buffer and either 25% heat-inactivated, gamma globulin-depleted ovine serum or

49 We have previously shown that the heat-inactivated gram-negative bacterium Brucella abortu

50 Inoculation of live or heat-inactivated gram-positive bacteria with macrophages

51 (AP) in normal human serum (NHS) but not by heat-inactivated (HI) serum.

52 Liposomes containing heat-inactivated HindIII or an endonuclease specific for

53 ed with soluble CD4 (sCD4) or, as a control, heat-inactivated HIV.

54 artificial DNA and RNA both in buffer and in heat-inactivated human blood serum.

55 an neutrophils in the presence or absence of heat-inactivated human immune serum.

56 de inhibits the agglutination of pig RBCs by heat-inactivated human serum at concentrations similar t

57 Incubation in 10% heat-inactivated human serum increased adherence to endo

58 Heat-inactivated IgE was less effective and the monoclon

59 e contralateral side that received saline or heat-inactivated IL1beta.

60 The active cytolysin, when compared with heat-inactivated ILY, did not appear to be chemotactic f

61 Heat-inactivated immune serum induced passive cutaneous

62 Opsonization with heat-inactivated immune serum reduced the amount of atta

63 ither live (infection/inflammation model) or heat-inactivated (inflammation model) cultures in a thig

64 In contrast, PBMCs treated with a heat-inactivated inoculum exhibit normal susceptibility

65 When FVIII is heat inactivated, it loses function and much of its immu

66 imed via intranasal inoculation with live or heat-inactivated Lactobacillus plantarum or Lactobacillu

67 Heat-inactivated, live attenuated varicella vaccine was

68 that E. coli Hsp90 promotes reactivation of heat-inactivated luciferase in a reaction that requires

69 Heat-inactivated M. bovis induced a slight increase in t

70 Mouse serum and heat-inactivated mouse serum inhibited TNF-alpha product

71 had been pretreated with normal mouse serum, heat-inactivated mouse serum, or complement- deficient (

72 However, upon removal of heat-inactivated mycoplasmas, 32D cells quickly became a

73 In vitro, heat-inactivated, naive or sensitized baboon sera contai

74 The synergy was reduced when SCP was either heat inactivated or coinstilled with a peptide inhibitor

75 and phagocytosis were still seen if PHS was heat inactivated or omitted altogether.

76 ese effects were attenuated if the serum was heat-inactivated or if hyaluronidase was added.

77 gammaR-expressing cells occurred with either heat-inactivated or non-heat-inactivated sera, was block

78 dition, the use of other vaccines, including heat-inactivated or replication-defective varicella-zost

79 TP plasma that was preincubated with EDTA or heat-inactivated, or to control plasma.

80 heat-inactivated ovine or bovine serum or in heat-inactivated ovine or bovine serum depleted of gamma

81 rain L011 were incubated in vitro for 2 h in heat-inactivated ovine or bovine serum from which gamma

82 Strains 82-25 and L101, incubated for 2 h in heat-inactivated ovine or bovine serum or in heat-inacti

83 Intranasal immunization using heat-inactivated P. acnes-based vaccines provided a simp

84 Finally, DC-pulsed with heat-inactivated P. aeruginosa protected CD8(-/-) but no

85 mong them, miR393 and miR166 were induced by heat-inactivated P. sojae hyphae, indicating that they m

86 We showed that live, but not heat-inactivated, P. aeruginosa inhibited phagocytosis a

87 tensive corneal epithelial erosions, whereas heat-inactivated PASP produced no erosions.

88 PASP and heat-inactivated PASP were injected into rabbit corneas,

89 The addition of PCSK9, but not heat-inactivated PCSK9, to the medium of cultured hepato

90 th pig IFN-gamma (but not human IFN-gamma or heat-inactivated pig IFN-gamma) induced human CD4(+) and

91 Neither ATP alone nor ATP with heat-inactivated PKC rescued a rundown of SOC.

92 ivated platelets and undetected in serum and heat-inactivated platelets, and in platelets prepared fr

93 ceptor (Ldlr(-/-) ) mice were immunized with heat-inactivated pneumococci, which were shown to induce

94 unized with control serum, antiserum against heat-inactivated pneumolysin (HI-PLY), or antiserum agai

95 killed Staphylococcus aureus opsonized with heat-inactivated pooled human serum significantly improv

96 in or of oligonucleotide or when protein was heat-inactivated prior to forming proteoliposomes.

97 Injection of 20 ng active protease IV or heat-inactivated protease IV (200 ng) had no effect on o

98 ction with purified protease IV but not with heat-inactivated protease IV (P < or = 0.0001).

99 Neither active nor heat-inactivated protease IV altered the growth of bacte

100 200 ng active purified protease IV or 200 ng heat-inactivated protease IV.

101 ignificantly reduced; neither PTX alone, nor heat-inactivated PTX had any effect on quinpirole-induce

102 Positive PCR results were also obtained with heat-inactivated pus (24 horses) and blood (23 horses) s

103 roduction scheme and compared to traditional heat-inactivated rAAV preparations in vitro and in vivo,

104 buffer media containing zymosan-activated or heat-inactivated rat sera in the presence of protein kin

105 mosan-activated (4 or 10 mg/mL) rat sera, or heat-inactivated rat sera.

106 r [Na+]i and [Na+]i/[K+]i ratios relative to heat-inactivated rat sera.

107 vival was not affected in mice that received heat-inactivated rmIL-13.

108 recombinant (r)PASP (10 microg/20 microL) or heat-inactivated rPASP was intrastromally injected into

109 culated with live RSV, UV light-treated RSV, heat-inactivated RSV, or medium.

110 augmented by recent RSV infection but not by heat-inactivated RSV.

111 d to SR after exposure to saline alone or to heat-inactivated RSV.

112 al mouse microglia and astrocytes exposed to heat-inactivated S. aureus in vitro.

113 lopment was demonstrated by the inability of heat-inactivated S. aureus to induce proinflammatory cyt

114 ubation in pH 4.5 buffer or by incubation of heat-inactivated segments in alpha-expansin or a fungal

115 red with rabbit complement 10- to 60-fold in heat-inactivated sera from human vaccinees.

116 Heat-inactivated sera from rhesus monkeys that were natu

117 Heat-inactivated sera from skin grafted F344 rats were a

118 occurred with either heat-inactivated or non-heat-inactivated sera, was blocked by addition of purifi

119 ains were resistant to killing by normal and heat-inactivated sera.

120 Passive transfer of heat-inactivated serum from infected and immune wild-typ

121 ons were performed in complement-depleted or heat-inactivated serum rather than control serum.

122 g untreated naive serum, but not C3-depleted heat-inactivated serum to the location of the parasites.

123 kill S. epidermidis when the gels contained heat-inactivated serum, C5-deficient serum, a streptococ

124 nectin increased by 511% after incubation in heat-inactivated serum, compared to that of organisms in

125 as determined by adding rabbit complement to heat-inactivated serum, using a two-color fluorescent dy

126 cidal activities of platelet-free plasma and heat-inactivated serum, while the activity of normal ser

127 get cells was blocked by human serum but not heat-inactivated serum.

128 fresh serum and only partially decreased in heat-inactivated serum.

129 EC by 58% compared to organisms incubated in heat-inactivated serum.

130 Further, when the heat-inactivated set-point-stage plasma pool was mixed w

131 n of splicing extracts and reconstitution of heat-inactivated splicing extracts from strains carrying

132 While heat-inactivated spores did not induce detectable levels

133 in sera of mice following immunization with heat-inactivated spores.

134 We show that both viable and heat-inactivated Staphylococcus aureus and lipoteichoic

135 titis media with effusion, administration of heat-inactivated Streptococcus pneumoniae into the middl

136 exposed to medium, Stx1 (0.01-100 ng/mL), or heat-inactivated Stx1 or Stx1 B subunit (100 ng/mL).

137 UV irradiation, whereas liposomes containing heat-inactivated T4 endonuclease V were ineffective.

138 UV-irradiated skin with liposomes containing heat-inactivated T4N5 did not restore immune function.

139 red with control cells or cells treated with heat-inactivated Tat.

140 ted by antibodies raised against Sug1, or by heat-inactivating temperature-sensitive Sug1 mutants wit

141 nfect the animals, and when such strains are heat inactivated they lose their ability to rescue the i

142 tive to the contralateral side that received heat-inactivated TNFalpha.

143 ity to restore the 'acid-growth' response to heat-inactivated tomato walls and by its similarity to e

144 nal toxin, because LT subunits, mutants, and heat-inactivated toxin were unable to trigger resistance

145 bit corneas (P < or = 0.05), whereas 1 HU or heat-inactivated toxin yielded negligible pathologic cha

146 RyRs to luminal Ca(2+) was not observed with heat-inactivated trypsin, indicating that digestion of l

147 i with potent ability to induce extension of heat-inactivated type I cell walls.

148 f C. albicans hyphae (Hyphae) but not by its heat-inactivated unicellular form.

149 idly lethal disease in N. vectensis and that heat-inactivated V. coralliilyticus and bacterial flagel

150 ricella vaccine (3625 pfu) or of a partially heat-inactivated vaccine (1125 or 439 pfu).

151 ed on the ability of a formaldehyde-treated, heat-inactivated vaccine to induce modest antibody respo

152 The immunogenicity of heat-inactivated varicella vaccine and effects on VZV pa

153 envelope-modified, formaldehyde-stabilized, heat-inactivated virion vaccine could produce higher-tit

154 cating virus since they were not elicited by heat-inactivated virus and the anti-SIV antibody respons

155 ation, but monocyte cultures inoculated with heat-inactivated virus or infected in the presence of AZ

156 Results obtained with heat-inactivated virus, neutralizing anti-EBV mAb 72A1 a

157 Extension of heat-inactivated walls from cucumber (Cucumis sativus cv

158 Mice were exposed to native or heat-inactivated white birch pollen extract (BPEx) intra

159 led to secrete TNF-alpha in response to both heat-inactivated whole bacteria and GBS-F, suggesting th

160 We show that both heat-inactivated whole GBS and a secreted proteinaceous

161 Both heat-inactivated whole GBS bacteria and a heat-labile so

162 equired opsonization of hyphae with fresh or heat-inactivated whole plasma.

163 Mice immunized with heat-inactivated, whole yeast-form cells (Y cells) of Ca

164 Helper adenoviruses can be effectively heat-inactivated with no effect on the infectivity of SV

165 ribose, raffinose, and maltose spiked into a heat-inactivated yeast culture broth supernatant that wa