ライフサイエンスコーパス: indirect immunofluorescence

1 e also displayed viral protein expression by indirect immunofluorescence.

2 C-I, C-II, C-III, E, and J were detected by indirect immunofluorescence.

3 ic protein (GFAP) expression was detected by indirect immunofluorescence.

4 down assays, and protein colocalization with indirect immunofluorescence.

5 human colonic mucosa was determined by using indirect immunofluorescence.

6 oantibody development was assessedwith HeP-2 indirect immunofluorescence.

7 as localized exclusively to the cell wall by indirect immunofluorescence.

8 th a speckling over the entire neutrophil on indirect immunofluorescence.

9 liver/kidney microsome type 1 were sought by indirect immunofluorescence.

10 n-1 was demonstrated at the cell membrane by indirect immunofluorescence.

11 ndosome antigen 1 in STS26T Schwann cells by indirect immunofluorescence.

12 (2)) activation and P-selectin expression by indirect immunofluorescence.

13 esis, Byr4 localization was determined using indirect immunofluorescence.

14 uch as the mitotic spindle to be detected by indirect immunofluorescence.

15 merase chain reaction, Western blotting, and indirect immunofluorescence.

16 localize to the trans-Golgi network (TGN) by indirect immunofluorescence.

17 (APT)] revealed linear binding to the GBM by indirect immunofluorescence.

18 lasmic, diffuse, and nuclear, as measured by indirect immunofluorescence.

19 by ELISA and confirmed by immunoblotting and indirect immunofluorescence.

20 ANAs were assessed by indirect immunofluorescence.

21 was investigated using western blotting and indirect immunofluorescence.

22 Cultures were analyzed with TEM and indirect immunofluorescence.

23 the presence of periodontal pathogens using indirect immunofluorescence.

24 -linked immunosorbent assays (ELISAs) and by indirect immunofluorescence.

25 NMO-IgG is detected by indirect immunofluorescence.

26 -6 immunoglobulin G antibody was measured by indirect immunofluorescence.

27 alized in infected cell nuclei, as viewed by indirect immunofluorescence.

28 Indirect immunofluorescence analyses revealed distinct T

29 To address this, we performed a series of indirect immunofluorescence analyses using synchronously

30 everse transcription-PCR, Western blots, and indirect immunofluorescence analyses.

31 leocapsids was confirmed by Western blot and indirect immunofluorescence analyses.

32 Indirect immunofluorescence analysis localized endogenou

33 m three independent methodologies, i.e., (a) indirect immunofluorescence analysis of agarose-encapsul

34 Indirect immunofluorescence analysis of B. burgdorferi a

35 cting actual staining patterns observed upon indirect immunofluorescence analysis of indicated epitop

36 Indirect immunofluorescence analysis of Sed1p localizati

37 inase K treatment of intact treponemes, (ii) indirect immunofluorescence analysis of treponemes encap

38 Indirect immunofluorescence analysis revealed caveolin-1

39 Indirect immunofluorescence analysis revealed that OspE,

40 Indirect immunofluorescence analysis showed distinct loc

41 Indirect immunofluorescence analysis showed that L(pro)

42 Indirect immunofluorescence analysis showed that TbHA pr

43 Indirect immunofluorescence analysis using antibodies ag

44 zen sections of bovine retina-RPE-choroid by indirect immunofluorescence analysis.

45 Using indirect immunofluorescence and an anti-Rop antibody, we

46 Using indirect immunofluorescence and biochemical analysis, we

47 As shown by indirect immunofluorescence and biochemical fractionatio

48 haromyces cerevisiae plasma membrane by both indirect immunofluorescence and biochemical fractionatio

49 Erythrocytes were characterized by indirect immunofluorescence and by flow cytometry for de

50 ER-to-Golgi transport of gB was assessed by indirect immunofluorescence and by the acquisition of Go

51 Interestingly, indirect immunofluorescence and cell surface biotinylati

52 citrullinated filaggrin in rat esophagus by indirect immunofluorescence and citrullinated fibrinogen

53 -disulfide isomerase as determined by double indirect immunofluorescence and co-distribution with cal

54 c cycle antigens of HHV-8 were determined by indirect immunofluorescence and confirmed by immunoblots

55 Indirect immunofluorescence and confocal microscopy were

56 ntly expressed in HeLa cells and analyzed by indirect immunofluorescence and cysteine derivatization.

57 This was demonstrated by indirect immunofluorescence and eGFP fusions that examin

58 Salt-split skin indirect immunofluorescence and ELISA BP230 results were

59 PSGL-1 expression was examined via indirect immunofluorescence and flow cytometry before an

60 the majority of untreated cells analyzed by indirect immunofluorescence and formed discrete nuclear

61 cleus during HCMV infection as determined by indirect immunofluorescence and immunoblot analysis.

62 Indirect immunofluorescence and immunoelectron microscop

63 Indirect immunofluorescence and immunoelectron microscop

64 1(-/-) mouse embryonic fibroblasts (MEFs) by indirect immunofluorescence and immunogold electron micr

65 er, was localized in polytene chromosomes by indirect immunofluorescence and in diploid chromosomes b

66 Using indirect immunofluorescence and scanning electron micros

67 new FIDA methodology as well as by standard indirect immunofluorescence and solid-phase immunoassays

68 le and the life cycle using a combination of indirect immunofluorescence and subcellular fractionatio

69 tudied the distribution of the receptor with indirect immunofluorescence and used selective agonists

70 lated porcine Muller cells were evaluated by indirect immunofluorescence and Western blotting.

71 d with their antibody response determined by indirect immunofluorescence and Western immunoblotting,

72 cal characteristics, standard and salt-split indirect immunofluorescence, and bullous pemphigoid (BP)

73 and B was compared to detection by culture, indirect immunofluorescence, and enzyme immunoassay in 4

74 Soft X-ray, indirect immunofluorescence, and green fluorescent prote

75 ioimmunoprecipitation, ICA was determined by indirect immunofluorescence, and HLA class II genotyping

76 as determined by native fluorescence (EGFP), indirect immunofluorescence, and immunoelectron microsco

77 h caveolar membranes by immunoprecipitation, indirect immunofluorescence, and immunogold transmission

78 Finally, immunohistochemical staining, indirect immunofluorescence, and Western blotting analys

79 A human herpesvirus 7 (HHV-7) indirect immunofluorescence antibody avidity test was de

80 se-borne relapsing fever were tested with an indirect immunofluorescence assay (IFA) and an enzyme-li

81 lar endothelial cells (DMVEC) as detected by indirect immunofluorescence assay (IFA) and immunohistoc

82 alternative serologic diagnostic test to the indirect immunofluorescence assay (IFA) for scrub typhus

83 Diagnosis of E. chaffeensis infection by indirect immunofluorescence assay (IFA) is the reference

84 d in 2 independent laboratories using either indirect immunofluorescence assay (IFA) or a combination

85 gainst mouse-derived P. carinii was shown by indirect immunofluorescence assay (IFA) to bind surface

86 f human ehrlichioses is routinely made by an indirect immunofluorescence assay (IFA) using cultured e

87 of T. cruzi antibody titers as determined by indirect immunofluorescence assay (IFA).

88 g of influenza A virus-positive specimens by indirect immunofluorescence assay (IFA).

89 the identification of the 2009 H1N1 virus by indirect immunofluorescence assay (IFA).

90 Indirect immunofluorescence assay and in vitro organ cul

91 to HHV-8 lytic proteins were detected by an indirect immunofluorescence assay in serum samples of 10

92 Immunohistochemical staining and indirect immunofluorescence assay indicated that GH and

93 Currently, serological assays using either indirect immunofluorescence assay or enzyme-linked immun

94 The viral replication was analyzed by an indirect immunofluorescence assay to monitor NS1 express

95 convalescent-phase samples for scrub typhus indirect immunofluorescence assay using Bayesian latent

96 LAMP-2 expressed in Escherichia coli, and an indirect immunofluorescence assay using stably transfect

97 a antibody testing was performed by using an indirect immunofluorescence assay with Ehrlichia chaffee

98 In addition, an indirect immunofluorescence assay with whole trophozoite

99 w, calcofluor and Gram chromotrope staining, indirect immunofluorescence assay, and transmission elec

100 As determined by indirect immunofluorescence assay, no patient serum demo

101 ecific antigen expression was detected by an indirect immunofluorescence assay.

102 We tested serum antibodies by indirect immunofluorescence assay.

103 and normal levels of immunoreactivity in an indirect immunofluorescence assay.

104 n antibodies reactive with E. chaffeensis by indirect immunofluorescence assays (IFAs).

105 Indirect immunofluorescence assays and in situ hybridiza

106 Indirect immunofluorescence assays demonstrated that TIF

107 increase test sensitivity to that of current indirect immunofluorescence assays for LANA (80%-90%).

108 Indirect immunofluorescence assays performed on temperat

109 Indirect immunofluorescence assays that combined monoclo

110 Indirect immunofluorescence assays using an antibody tha

111 Western blots and indirect immunofluorescence assays were used to probe fo

112 In biochemical fractionations and indirect immunofluorescence assays, a fraction of endoge

113 were probed with IncA-specific antibodies in indirect immunofluorescence assays, IncA was detectable

114 anscription-PCR analysis and by double-label indirect immunofluorescence assays.

115 clear localization of L1 was demonstrated by indirect immunofluorescence assays.

116 contain antibodies reactive with E. canis by indirect immunofluorescence assays.

117 Plasma membrane expression was documented by indirect immunofluorescence before [(3)H]oleic acid upta

118 By indirect immunofluorescence, both R. rickettsii and List

119 invariable region 6 of VlsE, as assessed by indirect immunofluorescence, but not preimmune serum fro

120 ells using an antibody to either protein, by indirect immunofluorescence colocalization in both virus

121 Indirect immunofluorescence confirmed the presence of NF

122 the basal one-third of the epithelium, while indirect immunofluorescence confirmed the presence of st

123 Membrane floatation gradient and indirect immunofluorescence confocal microscopy analysis

124 Indirect immunofluorescence confocal microscopy demonstr

125 Indirect immunofluorescence confocal microscopy of preim

126 rized in vitro RPE model was determined with indirect immunofluorescence confocal microscopy.

127 analyzed their subcellular localizations by indirect immunofluorescence confocal microscopy.

128 ional associations between mercury and ANAs (indirect immunofluorescence; cutoff >/= 1:80).

129 )6 when transiently coexpressed as viewed by indirect immunofluorescence, deletion of U(L)26.5 codons

130 Finally, indirect immunofluorescence demonstrated that 14-3-3beta

131 Indirect immunofluorescence demonstrated that EAPII is p

132 Indirect immunofluorescence demonstrated that GPS2 and R

133 Indirect immunofluorescence demonstrated that PIAS1 and

134 Indirect immunofluorescence demonstrated the presence of

135 Podocyte nuclei were imaged using indirect immunofluorescence detection of antibodies agai

136 Using direct epifluorescence imaging and indirect immunofluorescence detection, we have confirmed

137 r in size, and biochemical fractionation and indirect immunofluorescence experiments show that, in bo

138 Here, we examined all ANA patterns by indirect immunofluorescence for 859 rheumatoid arthritis

139 and trigeminal ganglia were processed using indirect immunofluorescence for nNOS.

140 Indirect immunofluorescence for protein gene product (PG

141 cell surface, as shown by flow cytometry and indirect immunofluorescence for TRAIL-R1.

142 By indirect immunofluorescence, Fre3p was expressed on the

143 Indirect immunofluorescence (IF) microscopy revealed the

144 mucosal tissues from WT mice, as detected by indirect immunofluorescence (IF).

145 A random portion was also tested by indirect immunofluorescence (IFA).

146 Indirect immunofluorescence (IIF) and enzyme-linked immu

147 Indirect immunofluorescence (IIF) and enzyme-linked immu

148 chondrial antibodies (AMAs) were detected by indirect immunofluorescence (IIF) and found in approxima

149 the baseline and study-end serum samples by indirect immunofluorescence (IIF) for perinuclear ANCA (

150 hosphopeptidomannan, respectively and PAB by indirect immunofluorescence (IIF) in 271 sera, 169 with

151 ntibodies from HCV patients identify a novel indirect immunofluorescence (IIF) pattern on HEp-2 cells

152 ases of balamuthiasis that were diagnosed by indirect immunofluorescence (IIF) staining of serum for

153 -LKM-1 and PBC-specific AMA was confirmed by indirect immunofluorescence (IIF), and immunoblotting an

154 SLE autoantibodies using a bead-based assay, indirect immunofluorescence (IIF), and immunodiffusion.

155 vated PKD to cell nuclei, as revealed by PKD indirect immunofluorescence, imaging of a PKD-green fluo

156 We conducted indirect immunofluorescence, immunoblot, and immunopreci

157 nse to these same ligands was examined using indirect immunofluorescence, immunoblots, and radioligan

158 rns of expression and distribution of PCL by indirect immunofluorescence in both developing and adult

159 Cellular microtubules studied by indirect immunofluorescence in both mutant and revertant

160 Using indirect immunofluorescence in combination with fluoresc

161 Nuclear localization could be visualized by indirect immunofluorescence in HeLa cells transiently ex

162 imes during the follow-up evaluation through indirect immunofluorescence in rodent tissues, HEp-2 cel

163 Tagged L proteins were detectable, by indirect immunofluorescence in the case of EdtagL(MMc-my

164 During infection CdsF is detectable by indirect immunofluorescence in the inclusion membrane wi

165 ed by fluorescence in situ hybridization and indirect immunofluorescence in the presence of an inhibi

166 itation, electrophoretic mobility shift, and indirect immunofluorescence, in an attempt to elucidate

167 ith their role in measuring telomere length, indirect immunofluorescence indicated that both TRF1 and

168 A methodology was developed to quantify indirect immunofluorescence intensities, and to evaluate

169 However, indirect immunofluorescence is routinely negative, raisi

170 By indirect immunofluorescence, it is detected prominently

171 EFs infected with wild-type HSV as viewed by indirect immunofluorescence, it localized in densely sta

172 Three of the MAC-ELISA kits and 1 indirect immunofluorescence kit had comparable performan

173 anges in RPE phenotype were characterized by indirect immunofluorescence localization and Western blo

174 Indirect immunofluorescence localization studies in Plas

175 Indirect immunofluorescence localized the antigen recogn

176 We have used indirect immunofluorescence microscopy and confocal lase

177 IncG was confirmed in infected HeLa cells by indirect immunofluorescence microscopy and interaction w

178 , laminin, and fibronectin were evaluated by indirect immunofluorescence microscopy and/or Western bl

179 Indirect immunofluorescence microscopy demonstrated NBC

180 Using selective permeabilization indirect immunofluorescence microscopy in combination wi

181 se data, sucrose gradient centrifugation and indirect immunofluorescence microscopy indicated that mo

182 Indirect immunofluorescence microscopy indicated that St

183 Indirect immunofluorescence microscopy knockout analysis

184 ce microscopy serration pattern analysis and indirect immunofluorescence microscopy knockout analysis

185 n age, 66.6 years) were identified using the indirect immunofluorescence microscopy knockout analysis

186 Indirect immunofluorescence microscopy localized OSTalph

187 from patients with lichen sclerosus and did indirect immunofluorescence microscopy on normal skin wi

188 Indirect immunofluorescence microscopy performed on nond

189 Indirect immunofluorescence microscopy revealed that ASI

190 Indirect immunofluorescence microscopy revealed that CLI

191 Indirect immunofluorescence microscopy revealed that cyt

192 Indirect immunofluorescence microscopy revealed that del

193 Cytological studies using indirect immunofluorescence microscopy revealed that FIG

194 Indirect immunofluorescence microscopy revealed that GNA

195 l characterized subcellular fractions and by indirect immunofluorescence microscopy revealed that the

196 Subcellular fractionation studies and indirect immunofluorescence microscopy show that syntaxi

197 s insensitive to proteinase K digestion, and indirect immunofluorescence microscopy showed that BBA74

198 Indirect immunofluorescence microscopy showed that E is

199 Indirect immunofluorescence microscopy shows that, when

200 ivators, we fused Rob's CTD to SoxS and used indirect immunofluorescence microscopy to determine the

201 Activation of EGFR was analyzed by 1) indirect immunofluorescence microscopy, 2) immunoprecipi

202 of actively cycling cells, were localized by indirect immunofluorescence microscopy, in corneas of ne

203 racterized using morphology, histochemistry, indirect immunofluorescence microscopy, molecular biolog

204 dium chloride)-split human skin substrate by indirect immunofluorescence microscopy, not diagnosed ep

205 ly events of virus-host cell interaction via indirect immunofluorescence microscopy.

206 n microscopy, specialized histochemistry and indirect immunofluorescence microscopy.

207 receptors were assessed by western blot and indirect immunofluorescence microscopy.

208 Indirect-immunofluorescence microscopy detected host tyr

209 This included indirect immunofluorescence (neuronal nuclear and cytopl

210 ot of whole infected-culture extracts and by indirect immunofluorescence of infected monolayers at ti

211 alyzing the fluorescence histograms from the indirect immunofluorescence of the spores.

212 Second, indirect immunofluorescence on frozen liver sections and

213 ACA was detected by indirect immunofluorescence on HEp-2 cell substrate, and

214 Sensitivity was higher than indirect immunofluorescence on salt-split skin and immun

215 ization of human pol epsilon was examined by indirect immunofluorescence, pol epsilon appeared in dis

216 Indirect immunofluorescence produced highly similar stai

217 applied test to diagnose this disease is the indirect immunofluorescence reaction, however two sample

218 o encode a 63.1-kDa membrane protein that by indirect immunofluorescence resides in the ER.

219 process of deposition explains the negative indirect immunofluorescence results with DH serum.

220 Indirect immunofluorescence revealed a nonuniform patter

221 Indirect immunofluorescence revealed that both fluoresce

222 An affinity ligand blot immunoassay and indirect immunofluorescence revealed that the CspA mutan

223 Unexpectedly, indirect immunofluorescence reveals a translocation of m

224 Indirect immunofluorescence showed a sensitivity of 59.8

225 Indirect immunofluorescence showed reduced COL6A5 expres

226 lysis of monolayers 20 h after infection via indirect immunofluorescence showed specific labelling of

227 Indirect immunofluorescence showed that apical transport

228 Indirect immunofluorescence showed that most bacteria we

229 In comparison to the wild-type protein, indirect immunofluorescence showed that the mutant prote

230 Indirect immunofluorescence showed that, like p62, p90 l

231 Indirect immunofluorescence shows punctate localization

232 Indirect immunofluorescence shows that C/EBP beta is dif

233 Indirect immunofluorescence shows that CDPK1 localizes t

234 Indirect immunofluorescence shows that endogenous Sec1p

235 noclonal antibodies (MAbs), as determined by indirect immunofluorescence staining and flow-cytometric

236 Indirect immunofluorescence staining and western blot te

237 Furthermore, indirect immunofluorescence staining demonstrated that m

238 Indirect immunofluorescence staining of HeLa cells using

239 ed three patterns of ICP8 localization using indirect immunofluorescence staining of HSV-1-infected c

240 It was confirmed as Balamuthia by indirect immunofluorescence staining with rabbit anti-Ba

241 Furthermore, using indirect immunofluorescence staining, we showed that the

242 Indirect immunofluorescence studies also indicated that

243 ere processed for single- and double-labeled indirect immunofluorescence studies and examined with co

244 Indirect immunofluorescence studies for different recept

245 d for Western blot, immunoprecipitation, and indirect immunofluorescence studies of human MRP1.

246 Indirect immunofluorescence studies revealed a preferent

247 Indirect immunofluorescence studies revealed that gM col

248 Cell fractionation as well as indirect immunofluorescence studies showed that c-Myc or

249 were processed for single- and double-label indirect immunofluorescence studies to show their innerv

250 Indirect immunofluorescence studies with anti-SMRTe anti

251 Indirect immunofluorescence studies with selective perme

252 ere processed for single- and double-labeled indirect immunofluorescence studies.

253 wo-hybrid screen, coimmunoprecipitation, and indirect immunofluorescence studies.

254 Previous indirect-immunofluorescence studies observed that the HS

255 Indirect-immunofluorescence studies using an ORF 3 pepti

256 An indirect-immunofluorescence study of the MEQ S42D mutant

257 antibodies by 3 methods: Crithidia luciliae indirect immunofluorescence test (CLIFT), a commercial F

258 Western blot analysis and a newly developed indirect immunofluorescence test (IFT).

259 Our results correlated well with an indirect immunofluorescence test and demonstrated that v

260 y and nephrotic-range proteinuria using both indirect immunofluorescence testing (IIFT) and ELISA.

261 Direct and indirect immunofluorescence testing confirmed the clinic

262 lobulins and/or complement along the BMZ and indirect immunofluorescence testing showing circulating

263 logy, direct immunofluorescence testing, and indirect immunofluorescence testing were utilized and co

264 Indirect immunofluorescence tests showed that the dog wa

265 Using indirect immunofluorescence tests, the dog was seroposit

266 inked immunosorbent assays (MAC-ELISAs), and indirect immunofluorescence tests.

267 Furthermore, we find by using indirect immunofluorescence that hUpf1p is detected only

268 Here, we show by indirect immunofluorescence that Sp1 phosphorylated on s

269 Furthermore, we show by indirect immunofluorescence that TPZ leads to a localiza

270 As determined by indirect immunofluorescence, the axons of Us9-null infec

271 he ZBRK1 binding protein BRCA1 were shown by indirect immunofluorescence to be present in replication

272 We used indirect immunofluorescence to demonstrate that the full

273 Using a combination of indirect immunofluorescence to detect endogenous protein

274 We used indirect immunofluorescence to examine the developmental

275 e humoral rejection ACR in renal allografts, indirect immunofluorescence using a monoclonal anti-C4d

276 HNE ANCAs were measured by indirect immunofluorescence using a previously undescrib

277 Indirect immunofluorescence using antibodies specific fo

278 Indirect immunofluorescence using antibodies to a conser

279 Indirect immunofluorescence using antibodies to two diff

280 t the rat central nervous system by means of indirect immunofluorescence using the tyramide signal am

281 Indirect immunofluorescence was performed with anti-Smad

282 omodeoxyuridine to detect proliferation, and indirect immunofluorescence was performed.

283 Using indirect immunofluorescence, we detected MPZL3 protein i

284 Using indirect immunofluorescence, we labeled sections for the

285 Using indirect immunofluorescence, we show here that epitope-t

286 For analysis based on indirect immunofluorescence, we used biochip mosaics of

287 in was confirmed in hBMVEC by immunoblot and indirect immunofluorescence; we show that hBMVEC express

288 Electrophysiologic recording and indirect immunofluorescence were combined to study local

289 Immunohistochemistry and indirect immunofluorescence were used to assess tissue s

290 Western and protein dot blot analyses and indirect immunofluorescence were used to define the temp

291 Indirect immunofluorescence with a composite substrate o

292 We identified horizontal cells by indirect immunofluorescence with antibodies to calretini

293 d using transmission electron microscopy and indirect immunofluorescence with confocal microscopy, an

294 Indirect immunofluorescence with Crithidia luciliae and

295 bodies raised in mice and rabbits reacted by indirect immunofluorescence with E. bieneusi but not wit

296 clear antibodies (ANAs) was determined using indirect immunofluorescence with HEp-2 cells as substrat

297 hritis were examined by light microscopy and indirect immunofluorescence with IgG-subclass-specific m

298 ll isolates were screened immunologically by indirect immunofluorescence with monoclonal antibodies t

299 Indirect immunofluorescence with rat hippocampal neurona

300 r B. henselae immunoglobulin G antibodies by indirect immunofluorescence, with 97.3% specificity and