ライフサイエンスコーパス: secondary antibody

1 e cytotoxin saporin either directly or via a secondary antibody.

2 body fragments followed by an anti-human IgG secondary antibody.

3 lonal anti-BrdU antibody and FITC-conjugated secondary antibody.

4 orescent label was located on the primary or secondary antibody.

5 onstrated by complexing the Au particle to a secondary antibody.

6 -ir by using a Bodipy fluorophore conjugated secondary antibody.

7 diaminobenzidine and a peroxidase-conjugated secondary antibody.

8 with and anti-TrkA antibody and fluorescent secondary antibody.

9 l antibody to BrdU and a fluorescent-labeled secondary antibody.

10 mesenchymal antigens as well as a dye-linked secondary antibody.

11 el via reaction with a suitable biotinylated secondary antibody.

12 eradish peroxidase (HRP-labeled anti-PSA) as secondary antibody.

13 ignal generated via a fluorescently labelled secondary antibody.

14 ing the antifumonisin antibody and a labeled secondary antibody.

15 ntibodies and then with a fluorescent-tagged secondary antibody.

16 olled to prevent detection of mouse IgG by a secondary antibody.

17 noclonal antibody through interaction with a secondary antibody.

18 ion of coating antigen, primary antibody and secondary antibody.

19 measurements of attached DyLight649-labeled secondary antibody.

20 evelation using alkaline phosphatase-labeled secondary antibody.

21 crosslinking veltuzumab or rituximab with a secondary antibody.

22 fotyrosine primary and Cy3-labeled antimouse secondary antibodies.

23 he hydroxyl-terminated nanocrystals with the secondary antibodies.

24 jugate as well as affinity bound primary and secondary antibodies.

25 AM-1) antibodies followed by FITC-conjugated secondary antibodies.

26 t was used to separate fluorescently labeled secondary antibodies.

27 ith diaminobenzidine or by using fluorescent secondary antibodies.

28 yanine-conjugated and fluorescein-conjugated secondary antibodies.

29 of receptor and phosphotyrosine content with secondary antibodies.

30 yanine-conjugated and fluorescein-conjugated secondary antibodies.

31 horseradish peroxidase (HRP) labeled on the secondary antibodies.

32 ed by a cocktail of fluorescently conjugated secondary antibodies.

33 be quantitatively differentiated by adopting secondary antibodies.

34 by the immunoreaction with the biotinylated secondary antibodies.

35 smaller label displacement than traditional secondary antibodies.

36 e alkynes on ODFs with azide groups added to secondary antibodies.

37 proteins IL-6 and IL-8 using biotin-labeled secondary antibodies.

38 ody ESH8 followed by a phycoerythrin-labeled secondary antibody; (2) biotinylated C1C2 detected by ph

39 F4 monoclonal antibody and an anti-mouse IgG secondary antibody, a protease-resistant PrP was reporte

40 Secondary antibodies (Ab(2)) attached to carboxylated mu

41 Measurements employed goat antichicken secondary antibodies (Ab(2)) labeled with horseradish pe

42 ring horseradish peroxidase (HRP) labels and secondary antibodies (Ab(2)) linked to carbon nanotubes

43 Biotinylated secondary antibodies (Ab(2)) that bind specifically to s

44 ased on a competitive inhibition format with secondary antibodies (Ab2) conjugated to gold nanopartic

45 otinylated-horseradish peroxidase-conjugated secondary antibody, after which sections were reacted wi

46 and unprocessed whole blood samples by using secondary antibodies against human IgE labeled with 40 n

47 enhance the sensor response to biotinylated secondary antibody against CEA.

48 ing capacity (ABC) of a cell population, the secondary antibody amplification (psi), the particle-mag

49 concentration of 10(7)spores/mL, and with a secondary antibody amplification at a concentration of 1

50 After secondary antibody amplification, reactions were visuali

51 equal concentrations (10(7)spores/mL) with a secondary antibody amplification.

52 tected either by using peroxidase conjugated secondary antibodies and developing with diaminobenzidin

53 l antibodies (MAbs) and fluorescently tagged secondary antibodies and examined by confocal microscopy

54 or pathogen detection that avoids the use of secondary antibodies and is revealed by the photolumines

55 ity was controlled by omission of primary or secondary antibodies and pre-absorption test.

56 e bound bacterial toxins with a biotinylated secondary antibodies and streptavidin-coated MB resulted

57 tting with quantitation using [125I]-labeled secondary antibody and a phosphorimager.

58 lian Na-K-Cl cotransporter and a fluorescent secondary antibody and examined under a fluorescent micr

59 labeled with horseradish peroxidase (HRP) as secondary antibody and H(2)O(2) as the substrate.

60 hworks were treated with a rhodamine-labeled secondary antibody and sectioned, and the number of inge

61 d with labeled antibodies) or incubated with secondary antibody and then flat mounted (retinas from e

62 y antibodies and their corresponding labeled secondary antibodies, and surface-enhanced Raman scatter

63 s against complement components, fluorescent secondary antibodies, and the analysis of >150 images to

64 A secondary antibody (Aptamer-Antibody Assay) or a lectin

65 Polyclonal anti-immunoglobulin G (anti-IgG) secondary antibodies are essential tools for many molecu

66 The secondary antibody arm (antibody 679) recognizes a hista

67 pecific receptor molecule and the QD-labeled secondary antibody as a dual (fluorescence cum electroch

68 dwiching afterwards with AuNPs modified with secondary antibodies (AuNPs-sECAb) and detected using ch

69 Sensor responses were confirmed using a secondary antibody binding step, similar to the sandwich

70 e cytotoxin saporin either directly or via a secondary antibody, both resulted in prostate cancer cel

71 Imaging secondary antibodies bound to M1-AQP4 allowed us to infe

72 After flushing away excess reagents, secondary antibodies bound to their targets are then det

73 Our system not only eliminates secondary antibodies but also serves as a novel method p

74 nium ester as the chemiluminescent probe and secondary antibody-coated paramagnetic particles for the

75 ellular compartment with fluorescent primary-secondary antibody complexes, total internal reflection

76 competitive immunoassay that is amplified by secondary antibodies conjugated with Au nanoparticles.

77 t the virus env surface protein, followed by secondary antibodies conjugated with colloidal gold part

78 ke amplification strategy was set up using a secondary antibody conjugated to horseradish peroxidase

79 n anti-LfR antibody that was detected with a secondary antibody conjugated with a red-color fluoresce

80 ssed using a specific primary antibody and a secondary antibody conjugated with Alexa 488 fluorescent

81 fter washing, the sections were treated with secondary antibody conjugated with FITC.

82 proteolysis of VAMP2 as a marked decrease in secondary antibody-conjugated colloidal gold particles t

83 and neuraminidase, coupled with appropriate secondary antibody conjugates.

84 the basis for a mechanistic understanding of secondary antibody diversification and the subsequent ge

85 antigen-specific B cells undergo a phase of secondary antibody diversification in germinal centers (

86 (1 microL for the antigen, 1 microL for the secondary antibody-enzyme conjugate, and 200 nL for the

87 and specificity, followed by binding with a secondary antibody-enzyme conjugate.

88 rescein-labeled antibodies and enzyme-linked secondary antibodies for quantification of purified CTB.

89 CDK phosphorylation, and a Europium-labeled secondary antibody for signal detection.

90 NTs are modified and then decorated with the secondary antibody for tau protein.

91 ong-lived sources of rapid, isotype-switched secondary antibody-forming cell (AFC) responses.

92 toreactivity, yet, in an autoimmune context, secondary antibody gene rearrangements might also contri

93 specific antibodies followed by binding of a secondary antibody horseradish peroxidase (HRP) complex

94 s (CNSs) labeled with horseradish peroxidase-secondary antibodies (HRP-Ab2).

95 modify the binding of subsequent primary or secondary antibodies; (ii) the IgM MAbs bind primarily t

96 inity-purified antibodies ordinarily used as secondary antibodies in immunodetection protocols were b

97 ochemical methods using a peroxidase-labeled secondary antibody in albino mice revealed heavy labelin

98 sters is detectable using the anti-mouse IgG secondary antibody in the absence of the 3F4 monoclonal

99 xidase (HRP) was used as label on detection (secondary) antibodies in a sandwich immunoassay scheme.

100 ycoerythrin), and goat anti-mouse polyclonal secondary antibody (indodicarbocyanin).

101 apical PM was confirmed by microinjection of secondary antibodies into the bile canalicular-like spac

102 The amount of the bound secondary antibody is directly proportional to the conce

103 Secondary antibodies labeled with conventional organic d

104 Secondary antibodies labeled with two spectrally distinc

105 A secondary antibody labeled with dyes/quantum dots (QDs)

106 rmed with electron microscopy and the use of secondary antibody labeled with horseradish peroxidase.

107 ated emission depletion nanoscopy, we imaged secondary antibody labeling of monoclonal AQP4-IgGs with

108 ell, (2) primary antibody labeling well, (3) secondary antibody labeling well, and (4) readout buffer

109 clusters, and estimate the average number of secondary antibody labels per cluster.

110 no mass amplification and with sandwich-type secondary antibody mass amplification.

111 ube (SWNT) forest platforms with multi-label secondary antibody-nanotube bioconjugates for highly sen

112 w that antibody cross-linking (anti-MOG plus secondary antibody) of MOG on the surface of OLs results

113 ody and Horse Radish Peroxidase (HRP) tagged secondary antibody on the surface of GCE/f-MWCNT-Chit@Th

114 and horseradish peroxidase (HRP)-conjugated secondary antibody onto AgNPs-rGO modified-SPEs to fabri

115 ather lengthy and involve the use of labeled secondary antibodies or other agents to provide a signal

116 ng the antibody to the beads with Protein L, secondary antibody, or streptavidin: the high-stability

117 through of primary and peroxidase-conjugated secondary antibodies over the course of 3 min enhanced p

118 Cross-linking with secondary antibody overcame the inhibitory effect of ant

119 gnal response from label-free, sandwich with secondary antibody (pAb), and pAb functionalized with ir

120 icted by the limited availability of primary/secondary antibody pairs.

121 luorescent probe, covalently attached to the secondary antibody, plays a crucial role of indicating c

122 Unexpectedly, the anti-FLAG secondary antibody produced positive results with CaLas

123 me epitopes combined with a goat anti-rabbit secondary antibody produced very strong purple color in

124 cale in Escherichia coli and could thus make secondary antibody production in animals obsolete.

125 say where an alkaline phosphatase conjugated secondary antibody reacts with p-aminophenyl phosphate (

126 genes, which underlie the generation of the secondary antibody repertoire in B lymphocytes.

127 sfully primed the mice to mount an effective secondary antibody response after a single boost with TB

128 Secondary antibody response to rechallenge in passively

129 cterial numbers in a manner reminiscent of a secondary antibody response to rechallenge.

130 intravenous injection and does not induce a secondary antibody response when given to mice previousl

131 3d with low C3d/PPS14 ratios had an enhanced secondary antibody response.

132 al boosting, generated a strong long-lasting secondary antibody response.

133 centers and a detectable, although reduced, secondary antibody response.

134 rized to hFVIII generated normal primary and secondary antibody responses after immunization with the

135 reviously vaccinated participants manifested secondary antibody responses after receipt of low-dose A

136 ed the induction of long-lasting primary and secondary antibody responses post-RABV immunization.IMPO

137 lder avian influenza H5 strain might lead to secondary antibody responses to a single dose of more cu

138 can have distinct effects on the primary and secondary antibody responses to a T-cell-independent typ

139 We now show that TCI induces secondary antibody responses to coadministered antigens

140 uring efalizumab treatment, both primary and secondary antibody responses to phiX174, including IgM/I

141 influenza but failed to generate protective secondary antibody responses when challenged with influe

142 survival, (2) inhibition of primary but not secondary antibody responses, and (3) minimal drug toxic

143 tolerized mice exhibited normal primary and secondary antibody responses, suggesting that transient

144 lammatory context is required to induce B-1a secondary antibody responses.

145 anoparticles containing [Ru(bpy)(3)](2+) and secondary antibodies (RuBPY-silica-Ab(2)) are employed i

146 AM1 antibody and then incubated with labeled secondary antibody showed selective staining of retinal

147 ecognition event was displayed using labeled secondary antibody solution and subsequent signal amplif

148 dingly through a multiplex immunoassay using secondary antibodies specific to each patterned primary

149 "anchors," which were functionalized with a secondary antibody specific to the Fc region of the prim

150 osensor horseradish peroxidase (HRP) labeled secondary antibodies, specifically interacting with the

151 Immunogold and alkaline phosphatase secondary antibody staining both show antigen in seconda

152 In the presence of secondary antibodies the analytical sensitivity was impr

153 d with an anti-gp75 antibody and fluorescent secondary antibody, the cells are then fixed to prevent

154 fic antibodies and then with gold-conjugated secondary antibodies; the thin sections were examined by

155 shes survival of germinal center B cells and secondary antibody titers.

156 The assay uses infrared-labeled secondary antibodies to detect phospho-ERK, and the sign

157 ed with horseradish peroxidase (HRP) labeled secondary antibodies to the trans-membrane protein CD44.

158 By employing a more massive secondary antibody to amplify the signal arising from th

159 with the Ru-silica@Au nanocomposite labeled secondary antibody to form a sandwich-type immunocomplex

160 A or 20 min by ICGA without species-specific secondary antibodies under field conditions, thus allowi

161 and a fluorescein-isothiocyanate-conjugated secondary antibody was performed on cryostat sections of

162 lubilized, and then immunoprecipitation with secondary antibody was performed.

163 abbit anti-iNOS antibody was employed as the secondary antibody, was developed.

164 s amplification of gold-nanoparticle labeled secondary antibodies, we establish a detection limit of

165 antibodies bound to the surface-immobilized secondary antibodies, we observed this binding via chang

166 Then, the peroxidase-labeled secondary antibodies were added to bind these primary an

167 Afterward, fluorescein-conjugated secondary antibodies were applied to the wire for quanti

168 Secondary antibodies were fluorescein-conjugated anti-mo

169 in was placed on test line; species specific secondary antibodies were placed on the control line of

170 Multiple ODF-tagged secondary antibodies were then used to mark primary anti

171 Selected sets of the differently labeled secondary antibodies were then used to simultaneously ma

172 Protein immune detection requires secondary antibodies which must be carefully selected in

173 A secondary antibody, which was specific to the adenovirus

174 ti-5'-bromo-2'-deoxyuridine antibodies using secondary antibodies with red and green fluorescence, re

175 o the immunochemical complex by labeling the secondary antibody with a magnetically susceptible, micr

176 ng) or using a more robust reporter (e.g., a secondary antibody with biotin-streptavidin).