ライフサイエンスコーパス: antiserum

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

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

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

4 -, 6-, and 3-fold higher than that of the PA antiserum.

5 sport, enabled potent bacterial killing with antiserum.

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

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

8 s almost completely inhibited by anti-PM1665 antiserum.

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

10 used to raise rabbit polyclonal monospecific antiserum.

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

12 cross-reactivity against heterologous clade antiserum.

13 h the highest immunoreactivity to the rabbit antiserum.

14 sensitivity to neutralization by SU-specific antiserum.

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

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

17 d proteins that reacted with the BM2 peptide antiserum.

18 TbCentrin2, identified using phosphospecific antiserum.

19 then immunoprecipitated using a CMS-specific antiserum.

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

21 onfirmed by immunoprecipitation using EcPTP1 antiserum.

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

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

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

25 position and subsequent reaction with typing antiserum 35a.

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

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

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

29 Using a peptide-specific antiserum, abundant expression of BRAK protein was found

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

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

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

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

34 im of this study was to develop a polyclonal antiserum against a polypeptide analog of segment 1-25 o

35 A neutralizing antiserum against AnxA1 and a nonselective antagonist of

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

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

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

39 tron microscopy demonstrated that polyclonal antiserum against phiE125 reacted with the tail of phi10

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

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

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

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

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

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

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

47 female adult peripheral chemosensory system, antiserum against the AgOR7 polypeptide labels most sens

48 tivity in mouse was investigated by using an antiserum against the epsilon-sarcoglycan protein.

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

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

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

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

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

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

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

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

62 e report the generation of an antihuman CRF1 antiserum and provide the first immunohistochemical desc

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

78 The antiserum bound to a single 53 kDa protein and immunopre

79 lation of MKK3/6 detected by phosphospecific antiserum but did not affect the poly(IC)-induced gel mi

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

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

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

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

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

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

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

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

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

89 Antiserum derived from immunized macaques protected macr

90 A VHY-specific antiserum detected a protein with an apparent molecular

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

92 as shown by Western blotting with polyclonal antiserum developed against a HumA peptide.

93 Because the antiserum developed recognizes the tumoral GHRH receptor

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 secretion by hybridomas, but I-A(d)-specific antiserum did not.

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

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

100 An antiserum directed against the alpha-subunit specificall

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

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

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

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

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

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

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

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

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

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

111 Antiserum from mice immunized with the modified GNA1870-

112 Antiserum generated against an epitope in the amino-term

113 Antiserum generated against an epitope in the protein's

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

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

116 Btk(-/-) mice 4 to 9 days postinfection with antiserum harvested 6 to 9 days postinfection from MAV-1

117 LasB antiserum identified the ATCC 19660 protease as modified

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

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

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

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

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

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

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

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

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

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

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 h a polyclonal antibody, although monoclonal antiserum labelled only astrocytes.

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

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

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

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

141 Anti-TraM antiserum mediated in vitro opsonophagocytic killing of

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 against a single protein variant was

163 Antiserum produced in mice against the conserved subdoma

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

165 To circumvent the problems associated with antiserum production, we began the development of a syst

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

167 The specificity of anti-CRF-R1 antiserum R221 was demonstrated using transfected hCRF1-

168 the protein were analyzed with a polyclonal antiserum raised against a peptide corresponding to the

169 A rabbit antiserum raised against a synthetic peptide fragment en

170 Notably, antiserum raised against Chi3l1 or Sema7a phenocopied th

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

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

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

174 Antiserum raised against recombinant ChiA was used to de

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

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

177 Antiserum raised to recombinant purified OppA recognized

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

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

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

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

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

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

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

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

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

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

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

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

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

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

192 Double immunolabelling with CRH antiserum revealed that CART increased the number of CRH

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

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

195 Immunogold labeling using AufA antiserum revealed the presence of amorphous material ex

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

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

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

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

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

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

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

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

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

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

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

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

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

231 Since antiserum to folate receptors induces embryo resorption

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

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

234 Rabbit antiserum to human keratin did not inhibit the reaction

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

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

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

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

239 Antiserum to P450c17 co-immunoprecipitated P450c17 and b

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

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

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

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

244 Using antiserum to SNMP infused directly into the sensillum ly

245 An antiserum to SPE-10 showed significant colocalization wi

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

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

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

249 Antiserum to the Borrelia burgdorferi arthritis-related

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

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

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

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

254 Antiserum to the HPV16 L2 peptide comprising residues 17

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

271 A polyclonal rabbit antiserum was previously developed to a purported purifi

272 A high-titer rabbit antiserum was raised against the MBP-hTTP fusion protein

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 an effort to obtain DAO cDNAs, this antiserum was used to screen a tobacco cDNA expression l

283 Using a DtxR-specific antiserum we confirmed the presence of a DtxR-like prote

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

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

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

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

288 restingly, while characterizing a PDZ-RhoGEF antiserum, we found that a transfected PDZ-RhoGEF constr

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

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

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

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

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

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

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