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1 hiotreitol, ethylenediaminetetraacetic acid, heat inactivation).
2 ected in SDS-PAGE without reducing agent and heat inactivation.
3  of samples was tested both with and without heat inactivation.
4 ss that is resistant to N-ethylmaleimide and heat inactivation.
5  to the unbound state indicates irreversible heat inactivation.
6 mplate-primer, which likely protects against heat inactivation.
7 Mos(1-198)/SH2 enzyme is also more stable to heat inactivation.
8 liquefaction in thermo-protection buffer and heat inactivation.
9 s of ACSL6 were more resistant than ACSL4 to heat inactivation.
10 ediated cytotoxicity, which was inhibited by heat inactivation.
11  inhibitory activity was markedly reduced by heat inactivation.
12 esent in rhHSP60-2 were equally sensitive to heat inactivation.
13 plus rhHsp70-1 were all equally sensitive to heat inactivation.
14 RNA promoter protects the polymerase against heat inactivation.
15 LV RT and therefore is better protected from heat inactivation.
16 e of the mutants were also more sensitive to heat inactivation.
17 ven when other chaperones are present during heat inactivation.
18 l2 and ATP and formed complexes resistant to heat inactivation.
19 rus (PV) mutant with increased resistance to heat inactivation.
20 ctivity when standard titers were zero after heat inactivation.
21 cts human rhinovirus 14 (HRV14) from acid or heat inactivation.
22             Enhancement (i) was destroyed by heat inactivation (30 min, 56 degrees C); (ii) did not r
23  Glycodelin activity was totally reversed by heat inactivation (95 degrees C x 15 min) and neutralize
24   Simultaneous sputum liquefaction, bacteria heat inactivation (99 degrees C/30 min), and enrichment
25  is important to understand how formalin and heat inactivation affected the antigenicity and immunoge
26 strain fail to form mature spliceosomes upon heat inactivation, although commitment complexes and pre
27  neutralizing activity of human sera without heat inactivation and could account for neutralizing act
28 arvicidal activities were retained following heat inactivation and drying of the yeast into tabular f
29  the presence of heparin and was reversed by heat inactivation and the protease inhibitor leupeptin,
30                                              Heat inactivation and trypsin treatment of cytosol, as w
31 r PBMC AI, an effect that was increased with heat inactivation and was corrected with CVF treatment.
32 ccessory subunit, as judged by processivity, heat inactivation, and N-ethylmaleimide protection assay
33 cific ACAT inhibitor, and sensitivity toward heat inactivation, are essentially unaltered.
34 n the absence of plasma and was inhibited by heat inactivation, as well as by the terminal complement
35 ic peptide Cet1(232-265), protects Ceg1 from heat inactivation at physiological temperatures.
36 ne activity was unable to protect MKP-3 from heat inactivation but interfered with MEK1/2 activation
37 wo mutants were similar in susceptibility to heat inactivation, but one of those mutants and one othe
38  concentrations is shown to be stabilized to heat inactivation by E. coli molecular chaperones DnaK o
39                                   Complement heat-inactivation, C5 depletion, and C5a receptor inhibi
40 r and SLE or control plasma, with or without heat inactivation, cobra venom factor (CVF), or lipopoly
41 re vulnerable to proteolytic degradation and heat inactivation compared with the wild-type enzyme.
42                     These findings show that heat inactivation could obviate the need for category 3
43 the presence of plasma and its abrogation by heat inactivation, EDTA, and eculizumab.
44 in; this proteolytic action was inhibited by heat inactivation, EGTA, or ALLN.
45 ted lysate assay reactions can be stopped by heat inactivation (enabling ready control of selection s
46 activity potential of fermented yogurt while heat-inactivation, ensuring long shelf-life, modulates t
47                                              Heat inactivation experiments with the variants suggest
48       Several assay parameters such as serum heat-inactivation (HI) and dilution can alter WNV MIA se
49               However, it was protected from heat inactivation if both the 5' and 3' strands of the v
50 ncluded (i) proteinase K digestion (PKD) and heat inactivation; (ii) PKD and ethanol precipitation (E
51 tein expression, which were abrogated by Tat heat inactivation, immunodepletion, and cysteine mutatio
52  of different quality by exploiting standard heat inactivation in EPH.
53             To assess this, here we evaluate heat inactivation in milk for a panel of different influ
54 oral poliovirus vaccine seed stocks based on heat inactivation in the presence of MgCl2 did not compl
55 re vulnerable to proteolytic degradation and heat inactivation in vitro compared with the oligomeric
56 were abolished by both trypsin treatment and heat inactivation, indicating the protein nature of the
57                             We conclude that heat inactivation is a simple step that eliminates false
58 men were comparable to those obtained by the heat-inactivation method (except for subjects with therm
59                          This was not due to heat inactivation of A. actinomycetemcomitans AI-2 since
60                                              Heat inactivation of BPEx had no effect on the developme
61 the development of a large scale process for heat inactivation of clinical COVID-19 samples prior to
62 e introducing new technologies including the Heat Inactivation of clinical samples upon receipt into
63                   Serum pretreated by either heat inactivation of complement or immunoadsorption with
64   The same tautomer shift is also induced by heat inactivation of Fe(II)CBS, or by an Arg266Met repla
65 proteins, and (iii) thermoprotection against heat inactivation of firefly luciferase, and (iv) sequen
66                                              Heat inactivation of H. somnus culture filtrates partial
67                                              Heat inactivation of HIV-1 blocks nuclear localization o
68                                              Heat inactivation of human convalescent serum was shown
69                    Furthermore, we show that heat inactivation of human serum significantly lowered n
70                                        Using heat inactivation of influenza virus, we show that viral
71  by using industrial catering ovens for bulk heat inactivation of oropharyngeal/nasopharyngeal swab s
72                                      Neither heat inactivation of plasma nor ultrafiltration of plasm
73 Tat from Tat-containing conditioned media or heat inactivation of recombinant Tat abrogated those eff
74                                              Heat inactivation of restriction enzymes followed by lig
75 seropositivity were significantly reduced by heat inactivation of samples.
76            This attachment is not reduced by heat inactivation of the serum, suggesting complement in
77                                     In vitro heat inactivation of the temperature-sensitive prp5-1 mu
78 ted genuine infection included the fact that heat inactivation of the virus eliminated it, the levels
79  as early as 10 d after symptom onset, while heat inactivation of this plasma caused 77-95% abrogatio
80 o E6 and Calu-3), and is abrogated following heat-inactivation of the complement source.
81 taminating adenovirus infectious activity by heat inactivation or by purification.
82 tion in chicken macrophages was abrogated by heat inactivation or pre-exposure of the lysate to PMSF.
83 cell extract could be abrogated by dilution, heat inactivation, or chromatographic depletion.
84    The cytotoxicity of sCD44 was verified by heat-inactivation, pretreatment with a pan-caspase inhib
85     The cytotoxicity of sCD44 was blocked by heat-inactivation, pretreatment with a pan-caspase inhib
86                                      Because heat inactivation primarily denatures C1q, we used serum
87 this observation, biochemical properties and heat inactivation profiles of the genetically altered en
88 c activity, thrombin activation profile, and heat inactivation properties similar to those of wild-ty
89 r Ad5dl309 as a helper demonstrated that the heat inactivation protocol generally used does not remov
90                 We also demonstrate the bulk heat inactivation protocol inactivates a murine surrogat
91                                       Proper heat inactivation protocols are essential to ensure the
92  melting temperature and 20 degrees C in the heat-inactivation temperature.
93                                   Using bulk heat inactivation, the assay is no longer reliant on con
94 tects human rhinovirus 14 from both acid and heat inactivation through rhamnolipids.
95                 We have evaluated the use of heat inactivation to render TB samples safe to work with
96 bility of vRNA to protect the enzyme against heat inactivation, we established a novel assay, in conj