ライフサイエンスコーパス: immunoblot

1 (2) device area (>10x increase over previous immunoblots).

2 sequential EIAs without the inclusion of an immunoblot.

3 to assess PKARIalpha disulfide formation by immunoblot.

4 Signaling pathways in cells were analyzed by immunoblots.

5 yzed by histology, immunohistochemistry, and immunoblots.

6 transcription polymerase chain reaction, and immunoblots.

7 nadvertently used as loading control for the immunoblots.

8 easured with G-LISA, cell fractionation, and immunoblots.

9 ice and analyzed by immunohistochemistry and immunoblots.

10 r poultry species was assessed in inhibition immunoblots.

11 ular localization, caspase 3 activation, and immunoblots.

12 ata analysis was still made with the correct immunoblots.

13 itu hybridization, proliferation assays, and immunoblots.

14 alyzed by histology, immunofluorescence, and immunoblots.

15 l populations by techniques such as ELISA or immunoblotting.

16 f CXCR3 and CCR7 by immunohistochemistry and immunoblotting.

17 acterized by competition studies, ELISAs and immunoblotting.

18 ionylated serpins A1 and A3 were assessed by immunoblotting.

19 molecular integrity was assessed by SDS-PAGE immunoblotting.

20 pparent molecular mass (~40 kDa) observed by immunoblotting.

21 HLA-DM expression was analyzed by means of immunoblotting.

22 ancer cell lines by immunohistochemistry and immunoblotting.

23 d haptoglobin were also validated by western immunoblotting.

24 tive comparisons of selected key proteins by immunoblotting.

25 despite no change in total TPBG detected by immunoblotting.

26 which is a convenient alternative method to immunoblotting.

27 tive real-time polymerase chain reaction and immunoblotting.

28 , 17d, and 25b inhibited pERK1/2 and pAkt by immunoblotting.

29 inoculation or tick bite were collected for immunoblotting against B. miyamotoi membrane-associated

30 Immunoblotting against the protein extracts revealed dif

31 Immunoblotting along with cryo-EM showed gingipain expre

32 Proteomics and immunoblot analyses demonstrated that, compared to stand

33 oxisomes is essential for fertilization, and immunoblot analyses hinted at the presence of unprocesse

34 High-resolution 2-D gel electrophoresis and immunoblot analyses revealed that transgenic soybean see

35 Fluorescence microscopy and immunoblot analyses were used to monitor levels of alpha

36 led MCT4), and SLC2A1 (also called GLUT1) by immunoblot analyses.

37 RNA-Seq and immunoblotting analyses showed that MEOX1 knockdown decr

38 ay crystallography, protein engineering, and immunoblotting analyses, here we investigated the struct

39 ng co-immunoprecipitation followed by MS and immunoblotting analyses, we demonstrate the association

40 expression and activity were assessed using immunoblot analysis and a two-electrode voltage clamp te

41 His-tagged CesA5 from Physcomitrella patens Immunoblot analysis and mass spectrometry confirmed enri

42 Interestingly, immunoblot analysis demonstrated that melioidosis patien

43 vealed decreased 5' UTR usage of Hnrnph1 and immunoblot analysis identified a corresponding decrease

44 ial expression was performed via qRT-PCR and immunoblot analysis in the defined model nerve cell line

45 vo well counting (r(2)=0.9375; P<0.0001) and immunoblot analysis of NIS protein (r(2)=0.65; P<0.0001)

46 Subcellular fractionation and immunoblot analysis revealed that ATP sulfurylase isofor

47 Toll-like receptor 4 (TLR4) stimulation, and immunoblot analysis were performed on these Burkholderia

48 ied as measurably decreased and validated by immunoblot analysis were two light harvesting complex bi

49 cell-cycle arrest, in which RNA sequencing, immunoblot analysis, and RNA interference revealed to be

50 , adoptive cell transfer to ischemic muscle, immunoblot analysis, ELISAs, immunostainings, flow cytom

51 We also used immunoblot analysis, immunohistochemical staining, and o

52 Using immunoblot analysis, we detected PTPN7 in both human and

53 lin B1/CDK1 complex confirmed by qRT-PCR and immunoblot analysis.

54 Immunoblotting analysis confirmed the S-acylation of fiv

55 eine-cysteine crosslinked samples, capillary immunoblotting analysis demonstrated that depletion of S

56 f ubiquitylation events in ask1 estimated by immunoblotting analysis in this work.

57 Immunoblotting analysis using methyllysine-specific anti

58 These data are confirmed by immunoblotting analysis, which showed a significant redu

59 omains of the 35 antibodies were analyzed by immunoblot and by epitope mapping using phage display.

60 thermore, PrP(D) characteristics analyzed by immunoblot and conformational stability immunoassay were

61 antibodies (MOG-Abs) were first detected by immunoblot and enzyme-linked immunosorbent assay nearly

62 e removed and analyzed by histology, western immunoblot and gene expression analysis.

63 mall hairpin RNAs and cells were analyzed by immunoblot and immunofluorescence microscopy.

64 orta in the CKD-bMPOKO mice was confirmed by immunoblot and immunohistochemistry, respectively.

65 patients and protein levels were measured on immunoblot and immunohistochemistry; we tested the corre

66 Using immunoblot and phosphoproteomic approaches, we correlate

67 We used immunoblot and quantitative polymerase chain reaction to

68 e also examined for protein expression using immunoblot and reverse phase protein array (RPPA) and th

69 nts was generated and analyzed by native dot immunoblot and transduction assays.

70 Tumor samples were collected and analyzed by immunoblots and immunohistochemistry.

71 PK1) in the enteric ganglia were assessed by immunoblots and immunostaining.

72 interfering RNAs in BE cells and analyzed by immunoblots and in immunoprecipitation and ubiquitin lig

73 vectors that express microRNAs, analyzed by immunoblots and real-time polymerase chain reaction (PCR

74 idual components of the ETC were assessed by immunoblotting and cellular complex IV activity was anal

75 Parallel native PAGE, immunoblotting and Complex I activity assays furthermore

76 ol mice and this finding was corroborated by immunoblotting and electrophoretic mobility shift assays

77 expression by RNA sequencing, and performed immunoblotting and ELISA.

78 Instead, using immunoblotting and enzyme-linked immunosorbent assays (E

79 activity were examined using real-time PCR, immunoblotting and flow cytometry.

80 phages was investigated by quantitative PCR, immunoblotting and flow cytometry.

81 Here, using subcellular fractionation, immunoblotting and fluorescence, siRNA-based gene knockd

82 Immunoblotting and histochemical analysis confirmed the

83 were collected at the end of each study for immunoblotting and histological studies.

84 d in the spinal cord, which was confirmed by immunoblotting and immunocytochemical labelling.

85 molecular, transmission electron microscopy, immunoblotting and immunofluorescence analyses, we studi

86 Here, using immunoblotting and immunofluorescence staining, qRT-PCR,

87 Our immunoblotting and immunostaining analyses revealed that

88 Immunoblotting and immunostaining of brain samples from

89 We conducted immunoblotting and in vivo microdialysis procedures in M

90 ariance in a limited cohort was supported by immunoblotting and is consistent with mechanisms previou

91 nd an array of biochemical methods including immunoblotting and kinase assays, we show that sirtuin 2

92 Immunoblotting and kinetic and MS/MS experiments reveale

93 the Luminex Multiplex assay, ELISA, PCR, and immunoblotting and linked to the presence of EETs.

94 tch, respectively, and were then analyzed by immunoblotting and mass spectrometry for autophagy, apop

95 them using transmission electron microscopy, immunoblotting and mass spectrometry.

96 al cancer cell lines, which were analyzed by immunoblotting and proliferation and colony formation as

97 Through a series of immunoblotting and quantitative PCR (qPCR) experiments,

98 eme limiting dilution assays as well as with immunoblotting and quantitative real-time PCR for the ex

99 We confirmed these results by immunoblotting and selected protease and glycosidase act

100 Immunoblotting and selective reaction monitoring were us

101 Immunoblotting and sequence-translation analysis was per

102 We quantified protein changes with immunoblotting and t-SP by measuring dendritic spine mor

103 By using immunoblotting and ultra-performance liquid chromatograp

104 two EIA strategies were followed by Western immunoblotting and when used in an MTTT, respectively.

105 ther cytokines and analyzed them by imaging, immunoblot, and functional assays and enzyme-linked immu

106 Single-gene quantitative real-time PCR, immunoblot, and immunofluorescence analyses confirmed th

107 Single-gene RT-qPCR, immunoblot, and immunofluorescence analyses confirmed th

108 ray, quantitative polymerase chain reaction, immunoblot, and immunofluorescence analyses.

109 immunoassay (EIA) followed by a supplemental immunoblot, and modified two-tiered testing (MTTT) relie

110 number and by immunohistochemical staining, immunoblot, and quantitative reverse transcription polym

111 died by flow cytometry, confocal microscopy, immunoblot, and real-time polymerase chain reaction.

112 e and control mice were analyzed by qRT-PCR, immunoblot, and transepithelial electrical resistance.

113 ssed by real-time polymerase chain reaction, immunoblots, and immunostaining.

114 Using cell viability assays, LC3B immunoblots, and live-cell fluorescence microscopy, we r

115 eactivity to chicken muscle were analyzed in immunoblots, and proteins recognized by the majority of

116 analyzed by histology, immunohistochemistry, immunoblots, and quantitative polymerase chain reaction.

117 of Crt) were analyzed by immunofluorescence, immunoblots, and/or quantitative reverse-transcription p

118 allelic exchange, quantitative PCR analyses, immunoblotting, and (13)C-heme uptake experiments, we de

119 otein modeling, immunofluorescence staining, immunoblotting, and an enzymatic assay to evaluate the c

120 n were assessed using reverse protein array, immunoblotting, and chromatin immunoprecipitation (ChIP)

121 Using chromogenic substrate assays, immunoblotting, and ELISA, we analyzed expression media,

122 sgenic technology, CRISPR-Cas9 gene editing, immunoblotting, and fluorescence resonance energy transf

123 rected mutagenesis, Click O-GlcNAc labeling, immunoblotting, and immunofluorescence and EM imaging, w

124 kers by real-time polymerase chain reaction, immunoblotting, and immunofluorescence.

125 MLECs were authenticated by CD31 immunoblotting, and immunofluorescent staining of establ

126 y cell cultures along with quantitative PCR, immunoblotting, and immunohistochemistry, we tested whet

127 ne knock-in technology and quantitative PCR, immunoblotting, and immunoprecipitation assays, we show

128 Using several mutant mouse strains, immunoblotting, and microcomputed tomography, we demonst

129 lyses of AKT-related genes using microarray, immunoblotting, and real-time quantitative PCR indicated

130 thological evaluation, immunohistochemistry, immunoblotting, and RNA sequencing.

131 Since immunoblots are time-consuming, laborious, and challengi

132 A recombinant immunoblot assay (RIBA) was used as a confirmatory assay

133 In the immunoblot assay, binding of IgE antibody was observed w

134 Immunoblot assays performed with fish-allergic patients

135 protein expression, immunoprecipitation and immunoblot assays, transmission EM of exosomes, and axon

136 quantitative polymerase chain reaction, and immunoblot assays.

137 unohistochemistry, biochemical, RT-qPCR, and immunoblotting assays revealed that Sema3d inhibits para

138 NAJC7 exceeded genome-wide significance, and immunoblotting assays showed depletion of DNAJC7 protein

139 MTT, qPCR and immunoblotting assays tested the effects of cottonseed e

140 Here, using immunofluorescence immunoblotting assays, co-immunoprecipitation, siRNA-med

141 with endocytosis, Lucifer Yellow-based, and immunoblotting assays, identified an elaborate signaling

142 s, fluorescence microscopy, and pulldown and immunoblotting assays, we show that alpha-dystrobrevin (

143 Using a combination of immunoblotting, co-immunoprecipitation, and myosin-bindi

144 ainst the target are purchased and tested by immunoblot comparing parental and KO.

145 Immunoblotting confirmation further supported this obser

146 In a set of sarcoma cell lines, immunoblotting confirmed nuclear localization of YAP1 an

147 Western immunoblotting confirmed that autophagy is not activated

148 lyzed them by histology, immunofluorescence, immunoblot, cytokine and chemokine magnetic bead, and DN

149 Immunoblotting data agreed with mRNA changes.

150 An examination of crwn mutants using protein immunoblots demonstrated that CRWN4 abundance depends on

151 Western immunoblotting demonstrated a 60% elevation of myocardia

152 ll among the three fractions tested, with 1D immunoblots demonstrating a slight predominance of IgE r

153 PCR (qRT-PCR) analysis of the porA mRNA and immunoblot detection of MOMP in C. jejuni showed that di

154 Circular dichroism, UV-Vis spectroscopy, and immunoblotting determined their capacity to (i) bind to

155 allergy diagnostics and a newly established immunoblot diagnostic system.

156 ion, and knockdown via mimics and anti-miRs, immunoblotting, dual luciferase reporter assay, in vivo

157 production, and cell death were evaluated by immunoblotting, ELISA, and cell death assays, respective

158 Here, using immunoblotting, ELISA, and surface plasmon resonance ana

159 ohistochemistry, real-time quantitative PCR, immunoblotting, ELISA, siRNA-mediated gene silencing, pl

160 iginal data were available for most EMSA and immunoblot experiments, those corresponding to the publi

161 Immunoblotting experiments confirmed that HP-bicarbonate

162 his nonapoptotic death pathway, we performed immunoblotting experiments in the presence and absence o

163 valuated INF2 cleavage as an explanation for immunoblot findings.

164 Cells were analyzed by immunoblots, flow cytometry, or RNA-sequencing analysis

165 Here, using metabolic assays, immunoblotting, flow cytometry analyses, and siRNA-media

166 Using immunoblotting, flow cytometry, and LC-MS-based glycolip

167 ochondrial integrity by immunocytochemistry, immunoblotting, flow cytometry, and real-time PCR to qua

168 ed and tumors were collected and analyzed by immunoblotting for levels of RNF128, p53, and acetylated

169 lamide Gel Electrophoresis (BN-PAGE) and dot immunoblotting for quantifying various photosystem II (P

170 s, a strong signal at ~70kDa was detected by immunoblotting, for which mass spectrometry revealed Dre

171 niques, including site-directed mutagenesis, immunoblotting, FRET, and proximity-ligation assays, we

172 ms of TRAF2, along with immunoprecipitation, immunoblotting, gene expression, and immunofluorescence

173 ucture of recombinant CLEC3A by SDS-PAGE and immunoblot, glycan analysis, matrix-assisted laser desor

174 nfirmed that eyes with more intense bands on immunoblot had fewer recurrences (P = .041).

175 In this study, we used mutational analysis, immunoblotting, HEK293 cells, and immunofluorescence mic

176 , which were analyzed by immunofluorescence, immunoblots, high-performance liquid chromatography (to

177 cate (WCS) and a C6 EIA, with a supplemental immunoblot if either EIA was positive or equivocal.

178 analyzed by RNA sequencing, flow cytometry, immunoblots, immunofluorescence, or reverse transcriptio

179 In addition, immunoblotting, immunofluorescence, confocal imaging, an

180 including cell biology, RT-quantitative PCR, immunoblotting, immunofluorescence, flow cytometry, and

181 Immunoblotting, immunofluorescence, immunohistochemistry

182 atiometric calcium imaging with quantitative immunoblotting, immunofluorescent confocal microscopy, a

183 Sanger sequencing, immunoblotting, immunohistochemical testing, flow cytome

184 were analyzed by histology, RNA sequencing, immunoblots, immunohistochemistry, hydroxyproline, and m

185 Immunoblotting, immunohistochemistry, and enzyme treatme

186 on and livers were collected and analyzed by immunoblotting, immunohistochemistry, histology, and rea

187 cells and transfected HEK293T cells through immunoblotting, immunohistochemistry, luciferase activit

188 ncluding efflux assays, immunoprecipitation, immunoblotting, immunohistochemistry, paracellular perme

189 Whole-exome sequencing, immunoblotting, immunophenotyping, and in vitro assays o

190 ned a wide array of approaches, ranging from immunoblotting, immunoprecipitation, mass spectrometry,

191 Immunoblotting, immunopurification, mass spectrometry an

192 We used electrophysiology studies, immunoblotting, immunostaining, and renal clearance to e

193 ish allergen parvalbumin was not detected by immunoblotting in 6/26 extracts.

194 We validated these data by quantitative immunoblotting in striatal cell lines and human HD brain

195 analyzed by histology, immunohistochemistry, immunoblots, in situ hybridization, and quantitative rea

196 Additionally, immunoblotting indicated that yeast coq11Delta mutants a

197 clusters of differentiation 9, 63, and 81 by immunoblot) indicated that most serum EV were exosomes.

198 Immunoblotting is widely used for the detection of prote

199 n array of biochemical approaches, including immunoblotting, kinase assays, immunoprecipitation, and

200 We used structural modeling, immunoblotting, live cell imaging, and split green fluor

201 La cells, along with immunoprecipitation and immunoblotting, live-cell imaging, and protein-stability

202 Immunoblotting, mass spectrometry, and ultrafast spectro

203 We present here a new immunoblotting method, which is characterized by excepti

204 nockout mice, subcellular fractionation, and immunoblotting methods, we addressed the relationship of

205 ter than published serial sampling), with 25 immunoblots/mm(2) device area (>10x increase over previo

206 s, and HEK293T cells, which were analyzed by immunoblot, mobility shift, and immunoprecipitation assa

207 Herein, we used a combination of immunoblotting, neuropharmacological and transgenic proc

208 8a, the independent replicate immunoblots of Fig.

209 Immunoblotting of FECD ex vivo specimens revealed an acc

210 for choline/methyl metabolite measurements, immunoblotting or gene expression of relevant enzymes.

211 f antiapoptotic BCL2 family members based on immunoblotting or RNA transcript levels correlated poorl

212 ficient (GWC), Toxoplasma gondii (T. gondii) immunoblot, or T. gondii-specific polymerase chain react

213 number of intense bands on aqueous T. gondii immunoblot (P = .006), and increased when venous vasculi

214 HCV assay that was performed on an automated immunoblot platform using a fourth-generation HCV recomb

215 e urothelial tissue for PCR, microarray, and immunoblot procedures.

216 ration markers to be assayed in combined IEF-immunoblotting procedures; the latter ones showing optim

217 tified by transcriptome sequencing, qRT-PCR, immunoblotting, protein interaction studies, knockdown a

218 Here, using murine ventricular myocytes, immunoblotting, proximity ligation as-says, and nitric o

219 uses after drug treatment were determined by immunoblotting, proximity ligation, replicon DNA replica

220 Immunoblot, pulse labeling, and ribosome profiling analy

221 By immunoblotting pyrin after infection, we observed that w

222 Immunoblot quantification with a TpnT-specific mAb indic

223 Cells were analyzed by immunoblot, quantitative polymerase chain reaction, chro

224 Cells were analyzed by immunoblots, quantitative real-time polymerase chain rea

225 In this work, using ChIP-sequencing, immunoblotting, quantitative PCR, and computational anal

226 proaches, along with immunoprecipitation and immunoblotting, quantitative RT-PCR, and ELISAs, we foun

227 situ hybridization, primary cell isolation, immunoblotting, quantitative RT-PCR, and liquid chromato

228 Here, using isolated MV, immunoblotting, quantitative RT-PCR, FACS analysis, and

229 r cell lines, siRNA-mediated gene silencing, immunoblotting, quantitative RT-PCR, promoter-reporter a

230 in cell migration and invasion assays and by immunoblots, real-time polymerase chain reaction, and li

231 opment and analyzed by immunohistochemistry, immunoblotting, real-time polymerase chain reaction, and

232 myocytes, lucigenin chemiluminescence assay, immunoblotting, real-time polymerase chain reaction, imm

233 with knockdown of LKB1 or other proteins by immunoblotting, real-time quantitative polymerase chain

234 and RhCG, were quantified by real-time PCR, immunoblots, reporter assays, biotin-tagged promoter pul

235 ll lines via indirect immunofluorescence and immunoblotting, respectively.

236 h quantitative polymerase chain reaction and immunoblotting, respectively.

237 In addition, PCR or immunoblot results obtained from homogenates of bladder

238 ttern of DMT1 regulation was corroborated by immunoblotting results in diabetic mice showing that BBM

239 Immunoblotting results revealed that the astrocytes prop

240 Flow cytometric and immunoblotting results suggest that CurDD can induce Hep

241 Immunoblotting revealed a decrease of AQP5 protein abund

242 e-negative breast cancer cell viability, and immunoblotting revealed that impaired growth is due to p

243 Mass spectrometry and immunoblotting revealed that the costimulatory factor in

244 lished; cells and spheroids were analyzed by immunoblots, reverse transcription polymerase chain reac

245 By immunoblotting, RIP9, OTP86, OZ1 and ORRM1 were shown to

246 using HEK 293T cells and immunofluorescence, immunoblotting, RNAi, subcellular fractionation, co-immu

247 Using immunoprecipitation and immunoblotting, RT-quantitative PCR, and ChIP assays, we

248 Immunoblots showed that the knockdown tumors had potenti

249 sed on the surface of CLL cells, and Western immunoblotting showed an inverse correlation between Wnt

250 Transcriptome analyses, real-time PCR, and immunoblotting showed consistent reductions in the expre

251 Immunoblotting showed elevated levels of gamma-H2AX, Bcl

252 N-beta than was the wild-type S. aureus, and immunoblotting showed that IFN-beta interacts with the b

253 Immunoblotting showed that procyanidin C1 and chlorogeni

254 Immunohistochemical and immunoblot staining of midbrain dopaminergic neurons and

255 Proteomic analysis and immunoblot studies revealed P497S mutant mice and UBQLN2

256 -activated protein kinase, and Src, shown by immunoblotting studies.

257 PDLIM1 through immunofluorescence staining, immunoblots, subcellular fractionation, and immunoprecip

258 Here, by applying immunoblotting, targeted phosphoproteomics and metabolit

259 Western immunoblotting techniques detected higher CML levels in

260 Immunoblot testing in cells with pathogenic SVBP variant

261 ation, enzyme immunoassay (EIA), and Western immunoblot tests against viral Ags.

262 c tests are the same enzyme immunoassays and immunoblots that are routinely used to detect the presen

263 monstrate by immunofluorescence staining and immunoblotting the presence of galectin-8 within the mit

264 In the immunoblotting, the patient's IgE reacted with 18 and 30

265 n the basolateral medium was investigated by immunoblotting, thin-layer chromatography with immunosta

266 , we introduce three-dimensional single-cell immunoblots to detect both cytosolic and nuclear protein

267 ophysiology, renal clearance techniques, and immunoblotting to examine effects of Kir4.1/Kir5.1 in th

268 human serum IgG4 were identified by means of immunoblotting to screen for potential bacterial allerge

269 Using immunoblotting to specifically examine the expression le

270 used electrophysiology, renal clearance, and immunoblotting to study Kir4.1 in the DCT and NCC in Kir

271 We employed affinity purification and immunoblotting to validate the interaction between STAT5

272 pared CTTT (WCS EIA followed by supplemental immunoblot) to MTTT (WCS EIA followed by C6 EIA) using M

273 pression in human cells and when assessed by immunoblotting under reducing and denaturing conditions,

274 and heated protein extracts was evaluated by immunoblotting using five allergen-specific antibodies a

275 .4%) for IgM and 86/295 (29.1%) for IgG, and immunoblot was positive in 21/191 (10.9%) for IgM and 50

276 IgE-immunoblotting was also conducted using sera from childr

277 Because immunoblotting was found to be inefficient for most of t

278 as9 gene-editing, MARCH6 overexpression, and immunoblotting, we found here that cholesterol stabilize

279 In addition, through immunoblotting, we found that AHAs overexpressed the NMD

280 ch-clamp recordings, confocal microscopy and immunoblotting, we found that both the GABRB3 (N328D) an

281 Using double-thymidine synchronization and immunoblotting, we observed that MELK inhibition delays

282 Using fluorescence microscopy and immunoblotting, we show here that the endogenously produ

283 tion mutants, quantitative PCR analyses, and immunoblotting, we show that the activation of the sigma

284 8a, 8d, 9, and in some cases the beta-actin immunoblots were erroneously described in the figure leg

285 Western immunoblots were performed with specific antibodies to A

286 Immunoblots were used to assess the underlying mechanism

287 Analytic isoelectric focusing and immunoblotting were conducted on cellular extracts of B.

288 e binding to beta-tubulin is demonstrated by immunoblotting, which allows for determination of the re

289 sphorylated CaMKII (immunohistochemistry and immunoblot) while decreasing the nuclear/cytosolic expre

290 HN13-derived antiserum was cross-reactive in immunoblots with all tested 32 field isolates, whereas o

291 n can be easily measured in cells by probing immunoblots with phosphospecific antibodies.

292 PO7, coupled with phosphopeptide mapping and immunoblotting with a phosphoserine-specific PKC substra

293 ifying 16 allergens based on two-dimensional immunoblotting with A. terreus susceptible patient sera.

294 e detection of His-tagged proteins relies on immunoblotting with anti-His antibodies.

295 rometry, followed by SDS-PAGE and subsequent immunoblotting with antibodies detecting 4 fish allergen

296 Using immunoblotting with CLCA1-specific antibodies and recomb

297 tial scanning fluorimetry, CD, SDS-PAGE, and immunoblotting with conformation-dependent and -independ

298 Rca-beta wild-type control, as evidenced by immunoblotting with custom antibodies and quantitative m

299 -polyacrylamide gel electrophoresis SDS-PAGE-immunoblotting with patient sera and rabbit serum anti-P

300 st increased family, as confirmed by western immunoblotting, with a stronger reactivity in SAU mastit