ライフサイエンスコーパス: antiserum

1 ed with the same strain of virus (homologous antiserum).

2 ing platelet-derived growth factor (PDGF)-BB antiserum.

3 onfirmed by immunoprecipitation using EcPTP1 antiserum.

4 ognizing LT-IIa or LT-IIb but not by anti-CT antiserum.

5 tochemistry (IHC) with an anti-XMRV specific antiserum.

6 be present at only low levels in primate PA antiserum.

7 -, 6-, and 3-fold higher than that of the PA antiserum.

8 viruses in the presence of homologous ferret antiserum.

9 with a specific rabbit and anti-T lymphocyte antiserum.

10 ge binding assays with and without anti-YaeT antiserum.

11 neutralization by A/Hong Kong/4801/2014-like antiserum.

12 s almost completely inhibited by anti-PM1665 antiserum.

13 reticulum (ER) membrane using Yke4p-specific antiserum.

14 used to raise rabbit polyclonal monospecific antiserum.

15 on and was immunostained by the anti-Apo A-I antiserum.

16 h the highest immunoreactivity to the rabbit antiserum.

17 sensitivity to neutralization by SU-specific antiserum.

18 ng administration of neutralizing anti-G-CSF antiserum.

19 rotein purification and lack of a high-titer antiserum.

20 sport, enabled potent bacterial killing with antiserum.

21 cross-reactivity against heterologous clade antiserum.

22 high HI titers to heterologous (D/OK) clade antiserum.

23 TbCentrin2, identified using phosphospecific antiserum.

24 then immunoprecipitated using a CMS-specific antiserum.

25 isolates were recognized by JGS4143-derived antiserum.

26 rway responses, mice were treated with CCL28 antiserum 1 hour before receiving the final CRA challeng

27 ntisera were screened and the combination of antiserum 1648 and a heterologous competitive hapten con

28 position and subsequent reaction with typing antiserum 35a.

29 Zip Tip immunocapture, a specific anti-Abeta antiserum (6E10), and matrix-assisted laser desorption i

30 -barrels, and beta-cylindrins (recognized by antiserum A11).

31 Importantly, IL-17-neutralizing antiserum abrogated the neurotrophic effect of splenocyt

32 The new factor 6d antiserum accurately identifies serotype 6C.

33 oelectron microscopy with an AcCYS1-specific antiserum, AcCYS1 was found in the apoplasm.

34 asmon resonance (SPR) revealed low nanomolar antiserum affinity for the key heroin metabolite, 6-acet

35 ed against small subdomains revealed that an antiserum against a 40-amino-acid region (residues 121 t

36 A neutralizing antiserum against AnxA1 and a nonselective antagonist of

37 st heat-inactivated pneumolysin (HI-PLY), or antiserum against cytotoxin-negative pneumolysin (psiPLY

38 body were, furthermore, also labeled with an antiserum against Dip-allatostatin I.

39 s and tissues, we raised a high titer rabbit antiserum against full-length mouse TTP.

40 then passively immunized with control serum, antiserum against heat-inactivated pneumolysin (HI-PLY),

41 Antiserum against one of these five proteins-A. aegypti

42 orneas from rabbits passively immunized with antiserum against psiPLY were examined up to 14 days aft

43 ttenuated by i.t. pretreatment with a rabbit antiserum against rat dynorphin1-13 but not antisera aga

44 Polyclonal antiserum against recombinant GP63 of T. cruzi (TcGP63)

45 srP(SRR1-BR) also neutralized PsrP function; antiserum against rPsrP(SRR1-BR) blocked TIGR4 adhesion

46 ent infected with MERS-CoV (NA 01) and human antiserum against SARS-CoV, human CoV NL63, and human Co

47 We also developed a specific antiserum against sbLPXRFa2, which revealed sbLPXRFa-imm

48 Also, a rabbit antiserum against the acidic domain of GPIHBP1 blocked L

49 Finally, antiserum against the Pel polysaccharide was generated,

50 immune cytokines, IFN-alpha or IFN-beta, or antiserum against the type I IFNs during the innate immu

51 ptens bound significantly to the same rabbit antiserum, albeit with less immunoreactivity than the he

52 ellar 'clutch' or addition of anti-flagellin antiserum also increased degU transcription and activity

53 The antiserum also lost the ability to kill the mutant strai

54 AgBR1 antiserum also partially protected mice from lethal mosq

55 Passive immunization with anti-Sse antiserum also significantly protects mice against subcu

56 on experiments carried out with NEV-specific antiserum and a set of plant endomembrane markers reveal

57 Furthermore, rabbit antiserum and antifecal antibodies were able to neutrali

58 entified by immunoblotting with monospecific antiserum and convalescent rat serum in addition to mass

59 Isolates reacting with group B antiserum and demonstrating wide beta-hemolysis should b

60 Kupffer cells were depleted with neutrophil antiserum and gadolinium chloride, respectively, before

61 nthesized to raise selective anti-OTC rabbit antiserum and highly specific monoclonal antibody (mAb).

62 hecal treatment with an interleukin-6 (IL-6) antiserum and in mice with protein kinase Cgamma (PKCgam

63 present in commercially available anti-BHV-1 antiserum and in real serum samples from cattle with res

64 epsin-digested fluoresceinated anti-F (ab')2 antiserum and T cells were detected with a specific rabb

65 ssed in Escherichia coli and used to prepare antiserum and to analyze the interaction of AgALP with m

66 labeling the hypothalamic sections with NPB antiserum and vasopressin or oxytocin antibody revealed

67 in was recognized by rabbit anti-C. irritans antiserum and was capable of eliciting immobilizing anti

68 lation site using phospho-specific anti-Y775 antiserum, and by mutational analysis.

69 f neutrophils by using rabbit antineutrophil antiserum, and immune responses and immunopathology were

70 rn analysis using phosphoamino acid-specific antiserum, and in vivo 32P labeling of PACT demonstrated

71 TbTOP2beta is not detected by beta-specific antiserum, and RNAi silencing results in no obvious phen

72 vitro kinase assay, phosphopeptide-specific antiserum, and the cdk inhibitor roscovitine to demonstr

73 d phosphate, detection by anti-phosphoserine antiserum, and the stabilizing effect of general serine

74 ing treatment with anti-tubular brush-border antiserum (anti-Fx1A).

75 treated with a neutralizing anti-mouse VEGF antiserum (anti-VEGF) or control serum daily from day -1

76 issues, and macrophages detected using BTN3A antiserum, are consistent with complex functions for BTN

77 Treatment with anti-asialo GM1 antiserum (ASGM1), which ablated circulating NK cells an

78 RBS deletions are able to escape polyclonal antiserum binding and are able to infect and be transmit

79 he factor involved is likely PEDF, as a PEDF-antiserum blocked the repulsing action.

80 The bactericidal activity of the rabbit antiserum can be fully inhibited by the type B LOS but n

81 was composed of immobilized anti-OTC rabbit antiserum (capture antibody) onto the membrane, the seco

82 n neutralization assays using defined animal antiserum confirmed MDCK cells as the preferred cell sub

83 stern blot analysis using an hMPV F-specific antiserum confirmed the expression of hMPV in recombinan

84 that chromatin immunoprecipitated with Bach1 antiserum contains ferritin DNA sequences.

85 In all cases, the expected antiserum-CPS binding signals were detected, prompting a

86 Anti-DBL5 antiserum cross-reacted with surface proteins of chondro

87 n problems associated with serology, such as antiserum cross-reactivity and one-way immunogenicity, i

88 R1(C)-ir were unchanged, suggesting that the antiserum crossreacts with another molecule in tissue.

89 Using a polyclonal antiserum, CSP1 was co-immunopurified with several hundr

90 Immunoblotting analysis using CfrB-specific antiserum demonstrated that CfrB was dramatically induce

91 ity H7N9 virus in the presence of polyclonal antiserum derived from ferrets infected with the same st

92 Antiserum derived from immunized macaques protected macr

93 The nsp6-specific peptide antiserum detected the replicase intermediate p150 (nsp4

94 However, the antiserum did not detect lubricin in synovial fluid or c

95 Furthermore, an anti-genogroup 1 human TTV antiserum did not react with any of the three TTSuV anti

96 The CBS antiserum did not recognize the correct molecular weight

97 d and characterized an anti-sEGFR polyclonal antiserum directed against a 31-mer peptide (residues 60

98 Antiserum directed against NF-IA, C/EBPalpha, or C/EBPbe

99 With the use of an antiserum directed against the rat NPB, immunoreactivity

100 or patients receiving antibiotics or anthrax antiserum during the prodromal phase of disease, multidr

101 l dynorphin content and spinal antidynorphin antiserum elicited a time-related reversal of abdominal

102 Among all reported nodal ECM components, the antiserum exhibited strong cross-reactivity against vers

103 immunoprecipitation of DNA fragments by GyrA antiserum following nalidixic acid treatment of cells.

104 d, and their expression was studied by using antiserum for GBS80 (backbone protein of pilus island-I)

105 re >90%, with the exception of polyvalent O1 antiserum, for which sensitivity was 88.9%.

106 ay and lineage-representative D/OK and D/660 antiserum found up to an approximate 10-fold loss in cro

107 s-tagged BMAA0742 was recognized by glanders antiserum from a horse, a human and mice, indicating tha

108 MPL antiserum was lower than the activity of antiserum from animals immunized with the nHgbAI/Freund'

109 Antiserum from mice immunized with the modified GNA1870-

110 Antiserum generated against an epitope in the amino-term

111 Antiserum generated against an epitope in the protein's

112 In addition, antiserum generated against this penguin virus did not i

113 propagation of H7N9 virus in virus-specific antiserum gives rise to mutant viruses carrying mutation

114 However, a U51-specific antiserum had no virus-neutralizing activity, suggesting

115 LasB antiserum identified the ATCC 19660 protease as modified

116 were detected by N-terminal peptide specific antiserum in IHH CM immunoprecipitated with chronically

117 M-mediated cell death was reversed by p75NTR antiserum in p75NTR(+)/trkA(-) 661w cells.

118 rats and the effects of spinal antidynorphin antiserum in pancreatic pain were assessed.

119 Antiserum in the 1918 flu epidemic, contaminated yellow

120 nt immunoreactive for specific P2X7 receptor antiserum in the kainate-induced seizure and non-seizure

121 Titration of the most commonly used GRP antiserum in tissues from wild-type and GRP mutant mice

122 by selective depletion with anti-asialo-GM1 antiserum in vivo and NK-cell-mediated cytolysis of B16L

123 o a previously described anti-peptide TcGP63 antiserum indicates that each antiserum recognizes disti

124 g the epitope recognized by the bactericidal antiserum induced by immunization with our conjugate vac

125 cocci were identified in a polyclonal rabbit antiserum induced in rabbits by whole group A streptococ

126 arthritis-related protein (Arp) and that Arp antiserum induces arthritis remission.

127 Indeed, rTF and an anti-rTF antiserum inhibited bacterial adhesion to human lung der

128 Anti-vimentin antiserum inhibited NK cell lysis of infected monocytes,

129 Antiserum inhibited the ability of recombinant MTP-1 to

130 Conversely, repeated administration of BDNF antiserum into the nucleus accumbens during chronic coca

131 f endothelial cells with the polyclonal GFAP antiserum is due to cross reactivity with another protei

132 -type and GRP mutant mice indicates that the antiserum is only selective for GRP at high dilutions.

133 One antiserum labeled a large group of cells and fibers, whi

134 The other antiserum labeled large club-like structures, which were

135 Furthermore, the OMgp antiserum labeled OMgp-null nodes, but not nodes from ve

136 ional inhibition of cell surface AnxA1 using antiserum (LCO1) significantly reduced cell invasion.

137 d that treatment with anti-IL-6-neutralizing antiserum led to reduced Akt phosphorylation, diminished

138 s of DNA sequences immunoprecipitated with J antiserum, localized J within subtelomeric regions rich

139 Further studies showed that the antiserum lost the recognition of both mutant cells and

140 Anti-TraM antiserum mediated in vitro opsonophagocytic killing of

141 vo Opsonization of Y. pestis with polyclonal antiserum modestly increased phagocytosis/killing by an

142 terologous anti-glomerular basement membrane antiserum (nephrotoxic serum, NTS) into presensitized mi

143 ypes of BoNTs (A-G) based on a lack of cross antiserum neutralization.

144 sensitive assay identified was one utilizing antiserum no.

145 Glycan microarray analysis of the antiserum obtained indicated that the combination of GH-

146 llel, in-register beta-sheets (recognized by antiserum OC) or antiparallel beta-sheets, beta-solenoid

147 bation of trypomastigotes with either TcGP63 antiserum or a purified TcGP63 C-terminal subfragment re

148 of the Wnt receptor, Frizzled3 (Fzd3), with antiserum or by short interfering RNA (siRNA) markedly r

149 itis was treated with neutralizing anti-gp96 antiserum or control serum.

150 Treating DC organisms with Asp14 antiserum or preincubating mammalian host cells with glu

151 Treatment with anti-PGE2 antiserum or the COX-2 inhibitor NS398 reversed the inhi

152 r, feeding of the anti-H. virescens cadherin antiserum or the partial cadherins, which contain the to

153 . conorii serum, Fab fragments of polyclonal antiserum, or no antibodies and then challenged 48 h lat

154 agonist APV, anti-p75(NTR) function-blocking antiserum, or previous tetanic stimulation.

155 nd nucleoproteins were also captured by this antiserum, our results were not affected due to the spec

156 Using specific antiserum, ovastacin was detected in cortical granules b

157 subsided in animals treated with neutrophil antiserum plus gadolinium chloride.

158 Antiserum prepared for this peptide was reactive with re

159 Pretreatment of mice with anti-MCP-1 antiserum prevented an increase in myeloperoxidase and e

160 nist, or by using an anti-AnxA1 neutralizing antiserum) prevented ROL- and Bt2cAMP-induced resolution

161 g, and mice that were administrated with Shr antiserum prior to the infection demonstrated a signific

162 Antiserum produced in mice against the conserved subdoma

163 cal difficulties of serotyping, primarily in antiserum production and quality control, can be overcom

164 Anti-JUNV glycoprotein rabbit antiserum protected Hartley guinea pigs from lethal intr

165 A rabbit antiserum raised against a synthetic peptide fragment en

166 Notably, antiserum raised against Chi3l1 or Sema7a phenocopied th

167 processed for immunocytochemistry, using an antiserum raised against DOR or MOR using diaminobenzidi

168 actinomycetemcomitans PGA cross-reacts with antiserum raised against polysaccharide intercellular ad

169 seen after passive administration of rabbit antiserum raised against PotD (P < 0.004).

170 Antiserum raised against recombinant ChiA was used to de

171 eins was studied with Western analysis using antiserum raised against the benzoquinone ring structure

172 Polyclonal antiserum raised against the spin trap 5,5-dimethyl-1-py

173 eurons were most effectively labeled with an antiserum raised against tyrosine hydroxylase (TH), the

174 Antiserum raised to recombinant purified OppA recognized

175 Unlike the outer glycan, an antiserum raised to the core glycan reacted with all Bac

176 Passive immunization of mice with a goat antiserum raised to the dPNAG-DT vaccine protected again

177 pregnancy malaria isolate, whereas anti-DBL6 antiserum reacted only to 3D7 surface protein.

178 Polyclonal H. ducreyi LspB antiserum reacted with a 64-kDa antigen present in the S

179 Factor 6d antiserum reacts with the new Streptococcus pneumoniae s

180 r weight protein in mouse retina but the CGL antiserum recognized the correct molecular weight protei

181 peptide TcGP63 antiserum indicates that each antiserum recognizes distinct TcGP63 proteins.

182 . actinomycetemcomitans cells with anti-ApiA antiserum reduced binding in a dose-dependent manner.

183 , immunization with either TraM or anti-TraM antiserum reduced significantly the colony counts in mic

184 nt of A. phagocytophilum organisms with OmpA antiserum reduces their abilities to infect HL-60 cells.

185 ide epitope as well as murine antigonococcal antiserum required functional properdin to kill C4BP-bin

186 C3 transfection or with an Atg8/LC3 specific antiserum, respectively.

187 the combination of P4 and serotype-specific antiserum resulted in 100% remission of bacteremia and r

188 hereas co-gavage with JGS4143 and alpha-HN13 antiserum resulted in 89% survival.

189 intact oocytes with either recmSLLP1 or its antiserum resulted in a significant (P < or = 0.05) inhi

190 3 virus in the presence of homologous ferret antiserum resulted in immune escape viruses containing a

191 Initial evaluation of polyclonal antiserum resulting from immunization with a KLH conjuga

192 of immune serum, or passive transfer of DbpA antiserum revealed that such treatment resulted in elimi

193 Use of a DPE2 antiserum revealed that the DPE2 protein is cytosolic.

194 ence was inhibited by pilus protein-specific antiserum SAN1518 significantly (p < 0.001) by 88.5 and

195 Using an antiserum screen of mutants generated from a C. perfring

196 vely homogeneous preparations of APFs and an antiserum selective for APFs (alphaAPF) compared with pr

197 Polyvalent O and O1 antiserum sensitivity and specificity were >90%, with th

198 l analyses using a phospho-synapsin-specific antiserum show that synapsin is a target of Ca(2+) calmo

199 In addition, a representative rabbit antiserum showed bactericidal activity against 14 of 18

200 mologous strain, and a representative rabbit antiserum showed bactericidal activity against nine of t

201 owed an intriguing binding pattern where the antiserum showed near complete specificity for MUC4 TR g

202 Passive immunization with each antiserum significantly lowered clinical severity compar

203 eatment of extracts with flap endonuclease 1 antiserum significantly reduced MHEJ.

204 f endocrine milieu were immunoreactive to an antiserum specific for eclosion hormone (EH), a neuropep

205 Antiserum specific for Leishmania amazonensis GP63 speci

206 imately 60 kDa) recognizable by a polyclonal antiserum specific for the NH2-terminal half.

207 Development of an antiserum specific to the second cytoplasmic loop of Pre

208 Anti-Jun and anti-Fos antiserum specifically inhibited protein-DNA complex for

209 Anti-JH antiserum specifically recognizes hemolymph-soluble Hex-

210 eas intracerebroventricular infusion of apoE antiserum stimulated feeding, implying that endogenous a

211 A growth assay using CfrB-specific antiserum strongly suggested that specific CfrB antibodi

212 el IHC experiments with tyrosine hydroxylase antiserum suggested that the D(2alphaPan) receptors rece

213 DNA binding sites, and the addition of Foxa2 antiserum supershifted the complex.

214 r in rabbits passively immunized with psiPLY antiserum than in control rabbits (P < or = 0.010).

215 r in rabbits passively immunized with HI-PLY antiserum than in control rabbits (P < or = 0.043).

216 methyl-1-pyrroline N-oxide (DMPO) polyclonal antiserum that specifically recognizes protein radical-d

217 Initiation of antibiotic or anthrax antiserum therapy during the prodromal phase is associat

218 Antiserum to 9Glc-NH(2)-TT was highly opsonic against an

219 Borrelia burgdorferi-infected C3H-scid mice, antiserum to a differentially expressed, 37-kDa spiroche

220 Western blot comparison of our antiserum to a previously described anti-peptide TcGP63

221 Rabbit antiserum to a selected E1 ectodomain-derived peptide di

222 NK cell lysis of infected monocytes, whereas antiserum to actin, another filamentous protein, did not

223 ion of cell-culture-grown HCV infectivity by antiserum to ApoE and, to a lesser extent, by ApoB furth

224 Moreover, administration of IsPDIA3 antiserum to B. burgdorferi-infected mice reduced the ab

225 1241 were prevented in rats when naloxone or antiserum to beta-endorphin was injected in the hindpaw

226 Antiserum to CcsB was used to show that CcsB is absent i

227 tation of CMS-containing DNA with a specific antiserum to CMS.

228 Passive immunization with antiserum to CP5-CRM or CP8-CRM protected mice against b

229 anti-DMPO (5,5-dimethyl-1-pyrroline N-oxide) antiserum to detect protein radical-derived DMPO nitrone

230 dy, we used FcRn-deficient mice and specific antiserum to determine the tissue distribution of FcRn i

231 atecholamine immunotoxin, saporin-conjugated antiserum to dopamine-beta-hydroxylase, on acute restrai

232 Since antiserum to folate receptors induces embryo resorption

233 Antiserum to HagB, but not HagA, blocked B. avium erythr

234 lonal antibody (RG-1), in addition to rabbit antiserum to HPV6 L2, to localize L2.

235 Rabbit antiserum to human keratin did not inhibit the reaction

236 Conversely, administration of antiserum to IFN-beta led to a more severe demyelinating

237 H36B (Ib/BCP(+)) for killing by HL-60 cells; antiserum to III-rBCP and III-rBCP(DeltaIgA) also opsoni

238 assive transfer of L. monocytogenes-specific antiserum to naive mice had no impact on priming antigen

239 ation in vivo, we generated phospho-specific antiserum to Orco(S289) and show that phosphorylation at

240 Antiserum to P450c17 co-immunoprecipitated P450c17 and b

241 as late as 24 h after infection, the rabbit antiserum to PAO1DeltaaroA was effective at reducing cor

242 white rabbits were passively immunized with antiserum to PLY, PPSV23, a mixture of PPSV23/PLY, or PB

243 d with hyperimmune and/or convalescent-phase antiserum to rapidly identify vaccine candidates.

244 p of Cdk9, we used a Thr-186-phosphospecific antiserum to screen a phosphatase expression library.

245 Using antiserum to SNMP infused directly into the sensillum ly

246 An antiserum to SPE-10 showed significant colocalization wi

247 me-linked immunosorbent assay using a rabbit antiserum to strain 26397.

248 The immunoreactivity of a rabbit antiserum to synthetic DOG1 peptides was assessed on two

249 chronically infected mice, and monospecific antiserum to the antigenic variation protein, VlsE, were

250 Antiserum to the Borrelia burgdorferi arthritis-related

251 Antiserum to the C-terminus (CT-2) labels both wild-type

252 e of these cells were double labeled with an antiserum to the glial protein S-100.

253 In IC-IDMS, antiserum to the HA of interest captured viral proteins

254 ular virus particles, and reactivity with an antiserum to the HMWP, identified it as the HMWP.

255 Antiserum to the HPV16 L2 peptide comprising residues 17

256 Using antiserum to the recombinant protein, Ac-GST-1 was immun

257 were on the spirochete's outer surface, and antiserum to these proteins reduced the adherence of B.

258 yme-linked immunosorbent assay (ELISA) using antiserum to virus-like particles of HuNoV GII/4.

259 ng Western immunoblot with an IRF-1-specific antiserum, to examine possible differences resulting fro

260 explore the function of ERbeta2 in brain, an antiserum (TwobetaER.1) targeting the 18 AA insert was d

261 However, we show here that the anti-OMgp antiserum used in previous studies to define the functio

262 We conclude that P2X7 antiserum used in this study is specific for and identif

263 l infection with JUNV strain Romero when the antiserum was administered 2 days after challenge and pr

264 The specificity of the antiserum was characterized by immunoprecipitation and W

265 e immunization experiment using pooled nHgbA antiserum was conducted in the experimental swine model

266 ramuscularly into chickens, the HN13-derived antiserum was cross-reactive in immunoblots with all tes

267 hesis in the secretory pathway, a polyclonal antiserum was generated against hephaestin, a multicoppe

268 Polyclonal Gpd2 antiserum was generated and localized Gpd2 at the surfac

269 ent assay (ELISA) activity of the nHgbAI/MPL antiserum was lower than the activity of antiserum from

270 Thus, the rabbit antiserum was not specific to DAO, even though it immuno

271 Because Pneumocystis-specific antiserum was only able to partially protect B cell-defi

272 Rabbit Shr antiserum was opsonizing, and mice that were administrat

273 li as a His tag fusion protein, and a rabbit antiserum was raised against the purified protein.

274 ate the role of the gasdermin gene family an antiserum was raised to a peptide highly homologous to a

275 The immunized-goat antiserum was shown to compete with the binding of all M

276 ive or passive vaccination with Shr, and Shr antiserum was tested for bactericidal activity.

277 Therefore, DbpA antiserum was tested to determine its ability to induce

278 A well-characterized rabbit polyclonal antiserum was used for immunohistochemical localization

279 The resultant antiserum was used for Western blotting of cell lysates,

280 In vivo administration of antineutrophil antiserum was used to evaluate the role of neutrophils i

281 MTP-1 formulated with AS03 adjuvant, and the antiserum was used to immunolocalize the anatomic sites

282 In GILZ immunoblots using a newly developed antiserum, we detected multiple species in extracts from

283 Using ferret-generated antiserum, we determined that CIV-H3N2 is antigenically

284 s which may complement those prevalent in PA antiserum, we evaluated whether sequences within the 2be

285 To test the specificity of our MOR1(C) antiserum, we examined MOR1(C)-ir in control and knockou

286 First, using anti-murine APOBEC3 antiserum, we showed that both APOBEC3 allelic variants

287 BDNF and a specific antiserum were examined for their effects on the perista

288 Pigs receiving this pooled nHgbA antiserum were protected from a homologous, but not a he

289 Mice receiving H3L-neutralizing antiserum were protected from a lethal challenge with 3

290 to overcome the neutralizing capacity of the antiserum were sequenced.

291 ents production of a polyvalent neutralizing antiserum, whereas the determinants dictating their trap

292 ve in Western blots with rabbit anti-megalin antiserum, whereas the insect cell-derived proteins reac

293 The available treatment for snakebite is antiserum which does not provide enough protection again

294 local trivalent vaccine and guinea pig FMDV antiserum, which is routinely used as tracing/detecting

295 Treatment with an FSH-antiserum, which suppressed primordial follicle formatio

296 ell selectivity of anti-asialoganglioside M1 antiserum, which was previously used to conclude the pro

297 to capture and detect anti-BSA antibody from antiserum with a colorimetric response, demonstrating ou

298 Preabsorption of the antiserum with metastin peptide fragment (45-54)-NH2 (1

299 eficient mice, and preadsorption of the OMgp antiserum with recombinant versican V2 blocked nodal lab

300 of ascites-derived monoclonal antibodies or antiserum with type A erythrocytes or the use of in vitr