ライフサイエンスコーパス: hemocyanin

1 immunized with trinitrophenyl-keyhole limpet hemocyanin.

2 -fold) after conjugation with keyhole limpet hemocyanin.

3 2) mimics the spectroscopic signature of oxy-hemocyanin.

4 -dependent Ag, phosphocholine-keyhole limpet hemocyanin.

5 g dose groups challenged with keyhole limpet hemocyanin.

6 ow insect hexamerins might have evolved from hemocyanin.

7 ization of male SJL mice with keyhole limpet hemocyanin.

8 nserved copper-binding histidine residues of hemocyanin.

9 reased by conjugating them to keyhole limpet hemocyanin.

10 ITC-labeled tetanus, OVA, and keyhole limpet hemocyanin.

11 equenced lepidopteran hexamerin or arthropod hemocyanin.

12 host-restricted responses to keyhole limpet hemocyanin.

13 against 2,4,6 trinitro-phenyl-keyhole limpet hemocyanin.

14 hed control Ig, conjugated to keyhole limpet hemocyanin.

15 o oligosaccharides present on keyhole limpet hemocyanin.

16 A, as well as to the model Ag keyhole limpet hemocyanin.

17 T cell-dependent (TD) Ag DNP-keyhole limpet hemocyanin.

18 r after immunization with DNP-keyhole limpet hemocyanin.

19 T cell-dependent antigen TNP-keyhole limpet hemocyanin.

20 h UO(2)(2+)-DCP conjugated to keyhole limpet hemocyanin.

21 immunoglobulin conjugated to keyhole limpet hemocyanin.

22 ell and chemically coupled to keyhole limpet hemocyanin.

23 hapten, conjugated to BSA or keyhole limpet hemocyanin.

24 icant homology to the sequences of arthropod hemocyanins.

25 Inhibition of anti-keyhole limpet hemocyanin Ab response was dose-dependent in FR104 recip

26 nitrophenol hapten-conjugated keyhole limpet hemocyanin adsorbed to Imject aluminum hydroxide-contain

27 mmunity to model Ags (OVA and keyhole limpet hemocyanin), affecting all major T-dependent Ig classes,

28 a substantial Ab response to keyhole limpet hemocyanin after completion of anti-CD40L Ab treatment,

29 r, mDCs(ICOS) pulsed with the keyhole limpet hemocyanin Ag during the maturation phase were better st

30 en and secondary responses to keyhole limpet hemocyanin Ag.

31 ion of IgE in response to DNP-keyhole limpet hemocyanin/alum and Nippostrongylus brasiliensis infecti

32 nation with GM2 conjugated to keyhole limpet hemocyanin and administered with QS-21 (GMK) for 96 week

33 hemocyanin in comparison with keyhole limpet hemocyanin and C. concholepas hemocyanin, which was char

34 CD4+ T cell sensitization to keyhole limpet hemocyanin and CD8+ T cell sensitization to MART-1 melan

35 ykynurenine (3OHKYN)-modified keyhole limpet hemocyanin and characterized it using 3OHKYN-modified am

36 nses to two soluble proteins, keyhole limpet hemocyanin and chicken egg albumin.

37 The presence of both hemocyanin and cryptocyanin in one animal provides an ex

38 f tumor Ig protein coupled to keyhole limpet hemocyanin and emulsified in an immunologic adjuvant.

39 immune deviation induced with keyhole limpet hemocyanin and IFA did not affect corneal allograft reje

40 okine-matured DCs loaded with keyhole limpet hemocyanin and MHC-I alone or MHC-I/II-restricted tumor-

41 fferent immunogenic carriers, keyhole limpet hemocyanin and N-alpha-palmitoyl-S-[2,3-bis(palmitoyloxy

42 ponses to the T-dependent Ags keyhole limpet hemocyanin and OVA, as well as reduced Ag-specific B cel

43 duction of antibodies against keyhole limpet hemocyanin and Pneumovax in mice, indicating that APRIL

44 ponse to trinitrophenol (TNP)-keyhole limpet hemocyanin and tetanus/diphtheria vaccine, CD40Ltg+ mice

45 n or trinitrophenylated (TNP) keyhole limpet hemocyanin and the type 2 T-independent Ags TNP-Ficoll o

46 was conjugated to the carrier keyhole limpet hemocyanin and used to immunize mice.

47 cyanin is closely associated with crustacean hemocyanins and suggests that cryptocyanin arose as a re

48 en synthesized, conjugated to keyhole limpet hemocyanin, and administered with the immunologic adjuva

49 caffeine covalently linked to keyhole limpet hemocyanin, and recombinant antibody techniques were use

50 were synthesized, coupled to keyhole limpet hemocyanin, and used to produce rabbit antisera.

51 nd immunoblots using anti-AGE-keyhole limpet hemocyanin antibody, aminoguanidine inhibited glucose-in

52 L-selectin-deficient mice to keyhole limpet hemocyanin are indistinguishable from wild-type control

53 n, sarcoplasmic calcium-binding protein, and hemocyanin are the most relevant.

54 Il5 Collectively, our data demonstrate that hemocyanins are able to trigger the release of proinflam

55 Hemocyanins are giant oxygen transport proteins found in

56 Hemocyanins are multimeric copper-containing hemolymph p

57 ed after immunization with PC-keyhole limpet hemocyanin but at significantly lower levels than those

58 4-hydroxy-3-nitrophenylacetyl-keyhole limpet hemocyanin, but GrB-deficient mice produced normal amoun

59 igh doses of (4-hydroxy-3-nitrophenyl)acetyl-hemocyanin, but maintenance of affinity maturation.

60 m plasma of mice immunized to keyhole limpet hemocyanin, but not from naive or OVA-immunized mice, we

61 din L-733,560 was conjugated to succinylated hemocyanin by water-soluble carbodiimide and was used as

62 ounterligands (fibrinogen and keyhole limpet hemocyanin) by 50%, but did not affect adhesion to fibro

63 CTL, and development of anti-keyhole limpet hemocyanin CD4+ T cells, rejection of allogeneic or syng

64 phiX 174 and nuclear protein-keyhole limpet hemocyanin) characterized by a reduction in number and s

65 ere defective in adherence to keyhole limpet hemocyanin-coated glass, iC3b-mediated phagocytosis, and

66 MH6, was then contrasted with keyhole limpet hemocyanin conjugate vaccine in a subsequent experiment

67 zed with the native 38C13 IgM-keyhole limpet hemocyanin conjugate vaccine.

68 ], MH6, and MH7) or a control keyhole limpet hemocyanin conjugate vaccine.

69 cinated with the CD20 peptide keyhole limpet hemocyanin conjugates had a 25% decrease in CD19(+) sple

70 Both keyhole lymphet hemocyanin conjugates induced IgM and IgG antibodies aga

71 ty of three synthetic globo H-keyhole limpet hemocyanin conjugates plus the immunologic adjuvant QS-2

72 as free glycopeptides or as keyhole lymphet hemocyanin conjugates.

73 hetic model that structurally mimics the oxy-hemocyanin core, whereas the Cu(II)(2) protein reacted w

74 ltiple members of the hemocyanin gene family-hemocyanin, cryptocyanin, phenoloxidase, and hexamerins-

75 mmunized with nitrophenylated-keyhole limpet hemocyanin, Dbc1(-/-) mice produce significantly increas

76 immunized with trinitrophenyl-keyhole limpet hemocyanin, dbh-/- mice produced less Th1 cytokine-depen

77 The inhibition of hemocyanin-derived phenoloxidase activity is discussed,

78 unized with PA1 conjugated to keyhole limpet hemocyanin developed high anti-peptide (1/13,000), but l

79 gen, 2,4-dinitrophenyl hapten-keyhole limpet hemocyanin (DNP(23)-KLH).

80 he molt cycle and reaches levels higher than hemocyanin during premolt.

81 t from those generated by the keyhole limpet hemocyanin-epitope conjugates.

82 ptide [SLS(10-30)] coupled to keyhole limpet hemocyanin evoked antibodies in rabbits that completely

83 Within some spider lineages, however, hemocyanin evolution has been a dynamic process with ext

84 ion and cytokine secretion by keyhole limpet hemocyanin-experienced CD4(+) T cells.

85 mice with 3H1 conjugated with keyhole limpet hemocyanin Freund's adjuvant induced humoral and cellula

86 Rhodamine and fluorescein-labeled hemocyanin from Megathura crenulata (KLH) were prepared

87 ture of a high molecular weight protein, the hemocyanin from Octopus vulgaris, under solution conditi

88 The results show that the hemocyanin from the mollusc and that from the arthropod

89 ural and immunological properties, including hemocyanins from Concholepas concholepas, Fissurella lat

90 sts that cryptocyanin arose as a result of a hemocyanin gene duplication.

91 rphae in order to infer the evolution of the hemocyanin gene family and estimate spider relationships

92 etween cryptocyanin and other members of the hemocyanin gene family shows that cryptocyanin is closel

93 results suggest that multiple members of the hemocyanin gene family-hemocyanin, cryptocyanin, phenolo

94 We have obtained hemocyanin gene sequences from numerous representatives

95 Our hemocyanin gene tree is largely consistent with the prev

96 the last number of years, the oxygen carrier hemocyanin, has demonstrated several immune- and physiol

97 muscle of Macrobrachium rosenbergii whereas, hemocyanin (HC) was identified as an allergen in Macrobr

98 tertiary, and quaternary structures of squid hemocyanin (Hc) were characterised, and the relationship

99 led binuclear "type 3" Cu sites are found in hemocyanin (Hc), tyrosinase (Tyr), and the multicopper o

100 e the reaction coordinate of O(2) binding to Hemocyanin (Hc).

101 Immunization with DNP-keyhole limpet hemocyanin, heat-killed Brucella abortus, or infection w

102 n, aggrecan, collagen, entactin, fibrinogen, hemocyanin, heparan sulphate, laminin, myosin, proteogly

103 d to immunocyanin monomers of keyhole limpet hemocyanin (IC(KLH)) to create the MCV ICKLH-SOO9.

104 using the standard therapy of keyhole limpet hemocyanin Id + GM-CSF.

105 e immunogenic carrier protein keyhole limpet hemocyanin (Id-KLH).

106 h2 cells, lymphoid cells from keyhole limpet hemocyanin-immune mice bearing healthy corneal allograft

107 en-specific IgG1 responses to keyhole limpet hemocyanin immunization, regulated CD4(+) T-cell CD40L e

108 s of Th1 cells in response to keyhole limpet hemocyanin immunization.

109 droxy-3-nitrophenylacetyl/keyhole lymphocyte hemocyanin) immunization.

110 -hydroxy-3-nitrophenyl acetyl-keyhole limpet hemocyanin immunized animals; recall responses were also

111 lper 2 response (ovalbumin or keyhole limpet hemocyanin in alum) and is only seen with T cell-depende

112 fter immunization with OVA or keyhole limpet hemocyanin in CFA, NK cell-deficient (NK-T+) mice develo

113 roinflammatory response for F. latimarginata hemocyanin in comparison with keyhole limpet hemocyanin

114 0,000-mug doses of intranasal keyhole limpet hemocyanin in conjunction with adjuvant intranasal diese

115 s in isopods, we discuss a possible role for hemocyanins in lignin decomposition.

116 e to the T cell-dependent Ag, keyhole limpet hemocyanin, in the PDE7A(-/-) mice was found to be signi

117 Hemocyanins induce a potent Th1-dominant immune response

118 s preclinical models, such as keyhole limpet hemocyanin-induced Ab responses, alloantigen-induced T c

119 Octopus hemocyanin is composed of ten subunits, each of which co

120 TCR Id protein conjugated to keyhole limpet hemocyanin (KLH) (TCR Id:KLH) and injected with a chemic

121 ulated the production of anti-keyhole limpet hemocyanin (KLH) Ab, increasing anti-KLH IgG, IgG2a, and

122 ive subcutaneous boosts of Id/keyhole limpet hemocyanin (KLH) administered with adjuvant.

123 ) idiotype (Id) conjugated to keyhole limpet hemocyanin (KLH) and administered with granulocyte-monoc

124 tive was covalently linked to keyhole limpet hemocyanin (KLH) and monophosphoryl lipid A (MPLA) to fo

125 lsed with 2 foreign proteins, keyhole limpet hemocyanin (KLH) and tetanus toxoid (TT), as well as an

126 on with two conjugates, Tn(c)-keyhole limpet hemocyanin (KLH) and Tn(c)-palmitic acid (PAM) with the

127 pic mAb MK2-23, conjugated to keyhole limpet hemocyanin (KLH) as a carrier and given with Bacillus Ca

128 a matrix peptide (Flu-MP) and keyhole limpet hemocyanin (KLH) as control antigens.

129 Subjects were fed keyhole limpet hemocyanin (KLH) before subcutaneous immunization and bo

130 ty, we bound thiolated MEP to keyhole limpet hemocyanin (KLH) by using succinimidyl-4-(N-maleimidomet

131 generated to the glycoprotein keyhole limpet hemocyanin (KLH) can cross-link with reactive carbonyl r

132 on of the glycopeptide to the keyhole limpet hemocyanin (KLH) carrier protein completed the preparati

133 jugated to maleimide-modified keyhole limpet hemocyanin (KLH) carrier protein through backbone Cys re

134 ns plus GM-CSF, or linkage to keyhole limpet hemocyanin (KLH) carrier protein were increasingly poten

135 To solve this problem, the keyhole limpet hemocyanin (KLH) conjugates of a series of GM3 derivativ

136 1-82 alphaS, human betaS, and keyhole limpet hemocyanin (KLH) control proteins induced no symptoms or

137 olunteers were immunized with keyhole limpet hemocyanin (KLH) first orally and then parenterally or o

138 s and the immunogenic protein keyhole limpet hemocyanin (KLH) for 24 h and then combined.

139 ynthesized, and conjugated to keyhole limpet hemocyanin (KLH) for examining its immunogenicity.

140 6OXY(Gly)(4)OH) conjugated to keyhole limpet hemocyanin (KLH) has shown early proof-of-efficacy in ro

141 r immunity induced by s.c. Id-keyhole limpet hemocyanin (KLH) immunization.

142 initrophenol (TNP)-conjugated keyhole limpet hemocyanin (KLH) in a specific pathogen-free environment

143 ith the cocaine immunogen GNC-keyhole limpet hemocyanin (KLH) in preventing cocaine self-administrati

144 uenza matrix peptide (MP) and keyhole limpet hemocyanin (KLH) in two healthy subjects.

145 Mice immunized with the Ag keyhole limpet hemocyanin (KLH) mixed with HKL generated a KLH-specific

146 n cocaine immunoconjugate GND-keyhole limpet hemocyanin (KLH) or with the anti-cocaine mAb GNC92H2 we

147 sing Id chemically coupled to keyhole limpet hemocyanin (KLH) plus granulocyte macrophage colony-stim

148 ed to the immunogenic protein keyhole limpet hemocyanin (KLH) protects mice from tumor challenge with

149 hapten to maleimide-activated keyhole limpet hemocyanin (KLH) provided a PI3P immunogen, which was su

150 e of the transgenic mice with keyhole limpet hemocyanin (KLH) resulted in a decrease in anti-KLH IgG

151 s of inflammation including a keyhole limpet hemocyanin (KLH) study and a collagen-induced arthritis

152 ds demonstrated efficacy in a Keyhole Limpet Hemocyanin (KLH) study in rats, where the blockade of PI

153 ed and covalently linked with keyhole limpet hemocyanin (KLH) to generate Id/KLH.

154 genic foreign carrier protein keyhole limpet hemocyanin (KLH) using glutaraldehyde has shown promisin

155 Keyhole limpet hemocyanin (KLH) was beneficial in earlier studies.

156 and to peptides conjugated to keyhole limpet hemocyanin (KLH) were characterized by their ability to

157 r methods, to protein carrier keyhole limpet hemocyanin (KLH) were studied in mice.

158 mimetics of GXM conjugated to keyhole limpet hemocyanin (KLH) with glutaraldehyde developed Abs to GX

159 (TNP-LPS) or T-dependent (TNP-keyhole limpet hemocyanin (KLH)) Ag.

160 Following challenge with TNP-keyhole limpet hemocyanin (KLH), Ab production in these mice was hapten

161 onjugated to ovalbumin (OVA), keyhole limpet hemocyanin (KLH), and a bis-maleimide; KLH conjugates ar

162 Rats were immunized with keyhole limpet hemocyanin (KLH), and blood samples were taken.

163 n exogenous, nonself antigen, keyhole limpet hemocyanin (KLH), by releasing IL-4 in the microenvironm

164 of a foreign helper protein, keyhole limpet hemocyanin (KLH), can augment the efficacy of tumor lysa

165 ith a single dose of 20 mg of keyhole limpet hemocyanin (KLH), followed by s.c. immunization with KLH

166 gen conjugated to the protein keyhole limpet hemocyanin (KLH), has been in clinical evaluation.

167 eeks later by DCs pulsed with keyhole limpet hemocyanin (KLH), HLA-A*0201-positive restricted influen

168 response to PC conjugated to keyhole limpet hemocyanin (KLH), T15 Id(+) Abs constitute >90% of the s

169 Ab immunization protocol (mAb-keyhole limpet hemocyanin (KLH)-Calmette-Guerin bacillus (BCG), an auto

170 However, keyhole limpet hemocyanin (KLH)-priming of IFN-gko mice readily elicite

171 ultured with HDK-1 T cells (a keyhole limpet hemocyanin (KLH)-specific CD4+ Th1 clone) in the presenc

172 tective clone (N-MoPn), and a keyhole limpet hemocyanin (KLH)-specific cell line (KLH-1).

173 ith ovalbumin peptide or with keyhole limpet hemocyanin (KLH).

174 umin and a secondary antigen, keyhole limpet hemocyanin (KLH).

175 e, 2,4,6-trinitrophenyl (TNP)-keyhole limpet hemocyanin (KLH).

176 48 h before immunization with keyhole limpet hemocyanin (KLH).

177 n following immunization with keyhole limpet hemocyanin (KLH).

178 icle before immunization with keyhole limpet hemocyanin (KLH).

179 nant HPV16/18 E7 antigens and keyhole limpet hemocyanin (KLH; an immunological tracer molecule) and d

180 3 after immunization with Ars-keyhole limpet hemocyanin, (KLH) and at day 6, large clusters of Ars-sp

181 C with conjugates of primary (keyhole limpet hemocyanin; KLH) and recall (Bet v 1) Ags (H4B4*KLH and

182 immunized intranasally with a keyhole limpet hemocyanin-linked peptide, corresponding to the prominen

183 However, every hemocyanin maintains downregulated key M2 cytokine genes

184 We present evidence that hemocyanin may act as a causative agent of hyperpigmenta

185 Efficacy experiments in a keyhole limpet hemocyanin model in rats demonstrated that administratio

186 tibodies were raised by using keyhole limpet hemocyanin modified in vitro by 4-hydroxynonenal (4-HNE)

187 Imaging of DNA, keyhole limpet hemocyanin, mouse monoclonal IgG, and glucose oxidase on

188 -nitrophenyl(5) conjugated to keyhole limpet hemocyanin (NP(5)- KLH) or infected with HSV-1, and the

189 -hydroxy-3-nitrophenyl acetyl-keyhole limpet hemocyanin (NP-KLH) and NP-OVA develops within ectopic l

190 phenyl acetyl (NP)-conjugated keyhole limpet hemocyanin (NP-KLH) or ovalbumin(323-337) peptide, using

191 Sequencing of the subunit of the hemocyanin of Octopus dofleini has been completed from a

192 ata, and Megathura crenulata (keyhole limpet hemocyanin), on cultures of peritoneal macrophages.

193 h a secondary Th2 response to keyhole limpet hemocyanin or A. fumagatus extract, or by intranasal rIL

194 immature DCs with the neoAgs keyhole limpet hemocyanin or human immunodeficiency virus-1 p24 gag pri

195 en-activated BALB/c Th1 clones, specific for hemocyanin or ovalbumin, did not ameliorate EAE.

196 condary Th2 lung responses to keyhole limpet hemocyanin or primary responses to Nippostrongylus larva

197 ee cell type cluster complex, keyhole limpit hemocyanin or tetanus toxoid-reactive Th cells promoted

198 Ags fluorescein-labeled (FL) keyhole limpet hemocyanin or trinitrophenylated (TNP) keyhole limpet he

199 to Pneumovax, IgG response to keyhole limpet hemocyanin, or cytokine response to LPS).

200 and B cell-deficient mice to keyhole limpet hemocyanin over 6 mo and observed diminished IL-2 produc

201 esponses by immunization with keyhole limpet hemocyanin plus IFA.

202 ared a conjugate vaccine (GD2-keyhole limpet hemocyanin plus immunological adjuvant QS-21) that consi

203 phosphocholine conjugated to keyhole limpet hemocyanin, ppc1-5 NAA B cells mounted a quick IgM Ab re

204 h the foreign helper protein, keyhole limpet hemocyanin, prior to intratumoral delivery and combining

205 ginal tumor, including (1) Id-keyhole limpet hemocyanin protein, (2) Id single-chain variable fragmen

206 In this study, hemocyanin purified from the hemolymph of Nephrops norve

207 an F(2)Pab peptide coupled to keyhole limpet hemocyanin recognized a p53(1-39) peptide phosphorylated

208 CLEC12A-mediated delivery of keyhole limpet hemocyanin resulted in enhanced proliferation and cytoki

209 , a comparison of Octopus and horseshoe crab hemocyanin reveals a similar active site, in a striking

210 Lastly, the conserved hemocyanin sequences allow for the inference of spider r

211 Analyses of concatenated hemocyanin sequences resolved deep nodes in the spider p

212 eptide 184- 198 conjugated to keyhole limpet hemocyanin showed significant pulmonary eosinophilia (39

213 Ag (keyhole limpet hemocyanin)-specific Th1/Th2 responses of fetal-derived

214 nation with the TCR linked to keyhole limpet hemocyanin, specific anti-TCR humoral responses were ind

215 unization with trinitrophenyl-keyhole limpet hemocyanin, specific ASC could be isolated from all immu

216 on protein, however, enhances keyhole limpet hemocyanin- specific T-cell proliferation and 2,4,6-trin

217 ce, were able to suppress the keyhole limpet hemocyanin-specific delayed-type hypersensitivity inflam

218 A-stimulated spleen cells nor keyhole limpet hemocyanin-specific proliferation of spleen cells was al

219 r upon 6-h coculture with the keyhole limpet hemocyanin-specific Th1 clone HDK-1 in the presence of A

220 ncubation with HDK-1 T cells (keyhole limpet hemocyanin-specific TH1 clone) or with 5S8 T cells (dini

221 reconstituted with a clone of keyhole limpet hemocyanin-specific Th2 cells and trinitrophenyl-specifi

222 The sera raised against keyhole limpet hemocyanin-SV1 hapten, showed binding values of 50-75% a

223 similar in sequence, size, and structure to hemocyanin, the copper-containing oxygen-transport prote

224 nse to the T-dependent Ag DNP-keyhole limpet hemocyanin, the Tg mice exhibited severely impaired seco

225 ed with 2,4, 6-trinitrophenyl-keyhole limpet hemocyanin (TNP-KLH).

226 ease-inducing (TNP-conjugated keyhole limpet hemocyanin [TNP-KLH]) and disease-inhibiting (anti-CD3)

227 This represents the first molluscan hemocyanin to be completely sequenced.

228 tratumoral VVHY, VVGMCSF, and keyhole limpet hemocyanin (to produce CD4 help) generated splenic HY-sp

229 Hemocyanin transcripts were highly abundant in the hepat

230 However, the mechanisms by which hemocyanins trigger innate immune responses, leading to

231 to the coupled binuclear Cu active sites in hemocyanin, tyrosinase, and catechol oxidase, in O(2) ac

232 Coupled binuclear Cu proteins include hemocyanin, tyrosinase, and catechol oxidase.

233 ensitization to a neoantigen, keyhole limpet hemocyanin, using a unique model of human nasal allergic

234 elin as compared with Ghr2 or keyhole limpet hemocyanin vaccinated controls.

235 hypersensitivity response to keyhole limpet hemocyanin was diminished.

236 coupling the glycopeptide to keyhole limpet hemocyanin was examined; although both IgM and IgG antib

237 llowing immunization with DNP-keyhole limpet hemocyanin was significantly decreased for all IgG subcl

238 s, the primary Ab response to keyhole limpet hemocyanin was unaltered over a 20-day period.

239 ns, bacteriophage phiX174 and keyhole limpet hemocyanin, was also evaluated.

240 nant filarial protein Ags and keyhole limpet hemocyanin, we sensitized T cells from uninfected, nonat

241 gh-affinity antibodies to TNP-keyhole limpet hemocyanin were severely impaired, even after adoptive t

242 Hemocyanins were phagocytosed and slowly processed.

243 e response to recall antigen (keyhole limpet hemocyanin) were normal.

244 (GAD), but not the control Ag keyhole limpet hemocyanin, were eliminated in NODJg mu(null) mice.

245 inistered soluble protein Ag, keyhole limpet hemocyanin, were enhanced when mice were treated with pe

246 h or without conjugation with keyhole limpet hemocyanin, were fused with P3/NS1/1-Ag4-1 myeloma cells

247 keyhole limpet hemocyanin and C. concholepas hemocyanin, which was characterized by an increase in th

248 e, the biophysical interactions of shellfish hemocyanin with known phenoloxidase inhibitors are prese

249 nse, we investigated the effects of mollusks hemocyanins with varying structural and immunological pr