ライフサイエンスコーパス: RCA

1 RCA formation substantially reduced root respiration and

2 RCA fractional flow reserve increased significantly (P=0

3 RCA has also attracted significant attention in the fiel

4 RCA I injection led to a dose- and time-dependent decrea

5 RCA increased the growth of simulated 40-d-old maize pla

6 RCA is a linear DNA amplification technique that can use

7 RCA vessel wall thickness was significantly increased in

8 RCA-based analysis of condyloma specimens from a patient

9 RCA-FRET provides simple, rapid, sensitive, and specific

10 16 patients; LAD was affected in 16 (72.3%), RCA in 14 (63.3%), and LCX in 8 (36.4%) cases.

11 and AOC upon thermal treatment (RCH: 20-30%, RCA: 44-55%) without altering color properties.

12 NA) with a linear range spanning 6 (SNA), 7 (RCA), or 8 (Con A) orders of magnitude.

13 the efficiency of PP encapsulation was 79% (RCA) and 88% (RCH).

14 The Rubisco activase (RCA) gene from each species was sequenced.

15 n due to the inhibition of Rubisco activase (RCA) under moderately elevated temperatures.

16 e gamma-subunit (AtpC) and Rubisco activase (RCA) were identified by matrix-assisted laser-desorption

17 logical regulators of complement activation (RCA) can attenuate this foreign body-induced activation,

18 to the regulators of complement activation (RCA) family.

19 of the regulators of complement activation (RCA) gene family.

20 Regulators of complement activation (RCA) inhibit complement-induced immune responses on heal

21 te host regulators of complement activation (RCA) into their viral envelopes and, as a result, escape

22 surface regulators of complement activation (RCA) to resist antibody-dependent complement-mediated ly

23 termed regulators of complement activation (RCA).

24 gs to the regulators of complement activity (RCA) family.

25 ration of regulators of complement activity (RCA) into the viral envelope afforded complement resista

26 ling predicts that root cortical aerenchyma (RCA) could improve N acquisition in maize (Zea mays).

27 gly, we found that root cortical aerenchyma (RCA) is formed constitutively in OsEPF1OE lines regardle

28 Root cortical aerenchyma (RCA) is induced by hypoxia, drought, and several nutrien

29 he toxic lectin Ricinus communis agglutinin (RCA) I into the sciatic nerve.

30 pe I (SNA), and Ricinus communis agglutinin (RCA) on polycrystalline gold electrodes was optimized an

31 (Con A), 10 fM (Ricinus communis agglutinin (RCA), or 100 fM (SNA) with a linear range spanning 6 (SN

32 ases, including Ricinus communis agglutinin (RCA), saporin, and abrin II.

33 Also, RCA allowed the direct quantification of RNA targets at

34 A) technology, rolling circle amplification (RCA) and DNAzymes.

35 tative (q)PCR, rolling circle amplification (RCA) and droplet digital (dd)PCR assays were used to qua

36 that utilizes rolling circle amplification (RCA) and magnetic microbeads as a signal enhancement met

37 Rolling-circle amplification (RCA) and ramification amplification (RAM, also known as

38 on isothermal rolling circle amplification (RCA) and rapid time-gated Forster resonance energy trans

39 ow-temperature rolling circle amplification (RCA) and strand displacement amplification (SDA).

40 inear ligation-rolling circle amplification (RCA) are restricted by the sophisticated operation steps

41 (PLP)-mediated rolling circle amplification (RCA) bioassay and an (2) agarose bead-based microfluidic

42 ligation-based rolling circle amplification (RCA) can distinguish single-nucleotide variants, which i

43 Rolling circle amplification (RCA) combined with padlock probe recognition of a DNA ta

44 t of real-time rolling circle amplification (RCA) for protein targets, we have developed a novel type

45 uencing error, Rolling Circle Amplification (RCA) has been used to improve library preparation by amp

46 Rolling circle amplification (RCA) is an isothermal enzymatic process where a short DN

47 Rolling circle amplification (RCA) is frequently applied for fluorescence in situ imag

48 the dendritic rolling circle amplification (RCA) is introduced.

49 Isothermal rolling circle amplification (RCA) is used to detect nucleic and non-nucleic acid biom

50 on followed by rolling circle amplification (RCA) labeling of the cleavage products.

51 s amplified by rolling circle amplification (RCA) on magnetic particles.

52 ction (PCR) or rolling circle amplification (RCA) processes, taking advantage of real-time amplificat

53 In this paper, rolling circle amplification (RCA) products are detected in solution and on magnetic p

54 evaluated the rolling circle amplification (RCA) products that are based on anti-CD40 DNA aptamers a

55 NA circle in a rolling circle amplification (RCA) reaction.

56 consists of a rolling circle amplification (RCA) technique, responsible for the generation of nuclei

57 ion (LAMP) and Rolling Circle Amplification (RCA) techniques for c-MYC and BCR-ABL1 genes, allowing f

58 ostructures by rolling circle amplification (RCA) using boranephosphonate internucleotide linkages.

59 n this system, Rolling Circle Amplification (RCA) was used as a signal amplification method for both

60 he stand-alone rolling circle amplification (RCA) with capillary electrophoresis (CE) for specific an

61 Rolling circle amplification (RCA), an isothermal amplification technique that creates

62 niques such as rolling circle amplification (RCA), strand displacement amplification (SDA) and isothe

63 ne produced by rolling circle amplification (RCA), which results in increased stability and templated

64 combination of rolling circle amplification (RCA)-based nucleic acid amplification with an on-chip si

65 correction and rolling circle amplification (RCA)-based target enrichment to vastly improve NGS-based

66 on followed by rolling circle amplification (RCA).

67 synthesized by rolling-circle amplification (RCA).

68 y ligation and rolling circle amplification (RCA).

69 tectable using rolling circle amplification (RCA).

70 lication using rolling-circle amplification (RCA).

71 substrates for rolling circle amplification (RCA).

72 essfully using Rolling Circle Amplification (RCA).

73 uence within a rolling-circle amplification (RCA).

74 e ligation and rolling circle amplification (RCA).

75 e obtained via rolling circle amplification (RCA).

76 ing from the rolling circular amplification (RCA).

77 We herein demonstrate an RCA-based cascade amplification reaction that converts a

78 mit of detection of 10pM was obtained for an RCA time of 60min.

79 e obtain a limit of detection of 10pM for an RCA time of only 20min corresponding to a total assay ti

80 Here, we describe the integration of an RCA assay on a single-use polymer chip platform where ma

81 Root cause analysis (RCA) is a conventional method used to deal with errors t

82 , we developed reference component analysis (RCA), an algorithm that substantially improves clusterin

83 Through pull-down analysis, RCA bound predominantly to the region between the methyl

84 g mechanism, which splices the RCA-alpha and RCA-beta isoforms were probably gained from another gene

85 Pyrosequencing of domain amplicon and RCA PCR products generated 1.5 x 10(6) reads, including

86 Absolute decreases in mid-wall Ecc LAD and RCA and global Ecc were 3.0%, 3.4%, and 2.8%, respective

87 ted with lower (absolute) Ecc in the LAD and RCA regions (regression coefficient 0.37 per unit higher

88 Smokers had lower Ecc in the LAD and RCA regions compared with nonsmokers.

89 In addition, segmental function in LAD and RCA regions was reduced when individuals in the lowest 1

90 n by Ecc was noted (p < or = 0.01 in LAD and RCA territories).

91 abrin II shared one pattern, while ricin and RCA shared a distinct pattern.

92 flexor neck muscle, rectus capitis anterior (RCA), in the adult cat.

93 multaneously compared with a commercial anti-RCA IgG antibody in a multicapture agent, single target

94 r membrane proteins as recombinant antigens (RCA) and a whole-cell inactivated antigen vaccine (WCA),

95 Aptamer RCA II stimulated anti-M2e IgG antibody production to th

96 conjugated one of the aptamer RCAs (Aptamer RCA II) to M2e epitope peptide of influenza virus as a m

97 The results of our work suggest that aptamer RCA is a novel platform to boost the efficacy of vaccine

98 We demonstrated that all 4 aptamer RCAs significantly induced the signal transduction in ch

99 dates, 4 aptamer-based RCA products (aptamer RCAs) were generated, each consisting of two distinct ap

100 Finally, we conjugated one of the aptamer RCAs (Aptamer RCA II) to M2e epitope peptide of influenz

101 variants were introduced into an Arabidopsis RCA deletion (Deltarca) line.

102 rmed 'regulator of chromosome architecture' (RCA), cooperates with condensin to preserve the characte

103 an animal model for repetitive CO2 arousals (RCAs) and investigating the effect of deleting the gene

104 c death (AD) or resuscitated cardiac arrest (RCA).

105 ncreased by 60% in the right carotid artery (RCA) and decreased by 80% in the LCA.

106 for the detection of right coronary artery (RCA) and left circumflex artery (LCX) lesions (0.84 +/-

107 g a 1-minute proximal right coronary artery (RCA) and left coronary artery balloon occlusion at basel

108 proximal 40 mm of the right coronary artery (RCA) in 67 and from the proximal 35 mm of the left circu

109 onary sinus, from the right coronary artery (RCA) to the inferior vena cava, and from the RCA to the

110 d to measure proximal right coronary artery (RCA) wall thickness, and multidetector computed tomograp

111 ry (LAD), then in the right coronary artery (RCA), circumflex branch (LCx) and the left main coronary

112 inations and recorded right coronary artery (RCA), left coronary artery (LCA) and left anterior desce

113 lex artery (LCX), and right coronary artery (RCA).

114 left circumflex, and right coronary artery [RCA]).

115 the generation of nucleic acid amplicons as RCA products (RCPs).

116 Here we applied these DNA-assisted RCA techniques in capillary isoelectric focusing to reso

117 fy individual particles with single attached RCA products from blank particles.

118 The O. australiensis RCA enzyme was thermally stable up to 42 degrees C, cont

119 ng 8 DNA aptamer candidates, 4 aptamer-based RCA products (aptamer RCAs) were generated, each consist

120 A combination of both RCA and PCR provides a wide protein target dynamic range

121 combined features hold promise for bringing RCA-based molecular diagnostics closer to the point-of-c

122 NA sequence to Dk2, which, once amplified by RCA, codes for a fluorescence generating deoxyribozyme.

123 synthesis of scaffold and staple strands by RCA-based enzymatic reactions allows the generation of D

124 Red chicory (RCH) and red cabbage (RCA) are rich sources of polyphenols (PP), especially an

125 ion of small molecular entities that capture RCA with high affinity is an intriguing alternative, as

126 The incorporation of chicken RCA into NDV produced in embryonated eggs similarly prov

127 The concatameric RCA product hybridized to biotinylated oligonuclotides w

128 d PDGF-BB was amplified via the concatameric RCA product, and the diffraction gratings on the printed

129 Under low-N conditions, RCA formation increased rooting depth by 15% to 31%, inc

130 In contrast, RCA I injection into TMEV-infected mice induced lesions

131 ad of the DNA coils produced in conventional RCA, which makes it more convenient for downstream opera

132 (LAD), circumflex (LCX), and right coronary (RCA) territories.

133 alyzed patients with concomitant ULM and CTO-RCA, cardiac-death was significantly higher in patients

134 occlusion of the right coronary artery (CTO-RCA) in patients undergoing percutaneous interventions f

135 rventions and with or without associated CTO-RCA.

136 findings suggest that recanalization of CTO-RCA has significant impact on the long-term cardiac-mort

137 se, 522 had ULM lesions without residual CTO-RCA (493 ULM without CTO-RCA+29 ULM with treated CTO-RCA

138 ess frequently in patients with residual CTO-RCA (adjusted hazard ratios, 0.321 [95% confidence inter

139 as compared with those without residual CTO-RCA (adjusted hazard ratios, 2.163 [95% confidence inter

140 served in patients with ULM and residual CTO-RCA as compared with those without residual CTO-RCA (adj

141 ore frequently in patients with residual CTO-RCA as compared with those without residual CTO-RCA.

142 as compared with those without residual CTO-RCA.

143 d CTO-RCA), and 46 patients had residual CTO-RCA.

144 s with residual as compared with treated CTO-RCA (log-rank P=0.01) despite no difference in baseline

145 ULM without CTO-RCA+29 ULM with treated CTO-RCA), and 46 patients had residual CTO-RCA.

146 ithout residual CTO-RCA (493 ULM without CTO-RCA+29 ULM with treated CTO-RCA), and 46 patients had re

147 ting with a primitive form in cyanobacteria, RCA of chlorophytes evolved by integrating chloroplast t

148 with regular amounts of chlorogenic acid (D-RCA); during the last 6 d of the study, the weight-maint

149 g lipid oxidation increased with C-HCA and D-RCA (P < 0.05).

150 ion of VEGF signaling by AG-028262 decreased RCA I binding and internalization into tumor vessels.

151 The amplified dendritic RCA detection of DNA is further implemented to yield the

152 analyte sequence, resulting in the dendritic RCA-induced synthesis of the Mg(2+)-dependent DNAzyme un

153 functional hairpin structures, the dendritic RCA-stimulated multiplexed analysis of two different gen

154 mental engineering principles used to design RCA nanotechnologies, discuss recently developed RCA-bas

155 nanotechnologies, discuss recently developed RCA-based diagnostics and bioanalytical tools, and summa

156 ce and then investigated the arousals during RCA.

157 ase in intracoronary ECG ST-elevation during RCA occlusion from baseline to follow-up examination (P=

158 Angina pectoris during RCA occlusion tended to occur in fewer patients at follo

159 onstrate the mechanism of a nicking-enhanced RCA (NickRCA) strategy that allows several polymerases t

160 expressed recombinant RCA and leaf-extracted RCA, the kinetic properties of the two isoforms were stu

161 Following RCA, multiple fluorescently labeled signal probes were h

162 g of the diamond film was observed following RCA-1 treatment.

163 .03, and 0.92 +/- 0.05 vs. 0.75 +/- 0.09 for RCA, P = 0.02).

164 sites in a 200-nm mucin segment to be 4 for RCA, PNA, and UEA, and 1.8 for MALII.

165 rking it against a commercial instrument for RCA product (RCP) quantification and further investigate

166 4, 1.6, and 26 aJ was determined on pPGM for RCA, PNA, and UEA.

167 robe could in turn be used as a template for RCA.

168 ted, and this circular sequence was used for RCA.

169 ologies are unable to distinguish ricin from RCA 120, a nontoxic protein also found in the castor bea

170 These functional RCA based nanotechnologies have been utilized for biodet

171 the Kaposi's sarcoma-associated herpesvirus RCA homolog Kaposica as a model protein.

172 However, RCA has several limitations.

173 We present crystal structures of human RCA (MCP, DAF, and CR1) and a smallpox virus homolog (SP

174 rcle serves as a template for a novel hybrid RCA strategy that allows for exponential amplification a

175 lification (RAM, also known as hyperbranched RCA) are isothermal nucleic acid amplification technolog

176 Ricinus communis agglutinin I (RCA I), a galactose-binding lectin from castor beans, bi

177 ty of lectins Ricinus communis agglutinin I (RCA), peanut (Arachis hypogaea) agglutinin (PNA), Maacki

178 ) padlock probe annealing and ligation, (ii) RCA, and (iii) optomagnetic detection of RCA products.

179 Immuno-RCA, the specific detection of proteins via antigen-anti

180 ection methods, such as immuno-PCR or immuno-RCA, the bio bar code technique does not employ any enzy

181 aize recombinant inbred lines contrasting in RCA grown under suboptimal and adequate N availability i

182 There were no significant differences in RCA remodeling between genotypes.

183 NDV grown in RCA-expressing cells was resistant to complement by inco

184 Large genetic variation in RCA formation and the utility of RCA for a range of stre

185 N stress increased RCA formation by 200% in mesocosms and by 90% to 100% in

186 A formation are poorly understood, increased RCA formation appears be a promising breeding target for

187 These findings indicate RCA I preferentially binds to and is internalized by tum

188 The individual RCA amplicon molecules were counted on the surface using

189 After intravenous injection, RCA I bound strongly to tumor vessels but not to normal

190 for coating artificial surfaces with intact RCA are still missing.

191 H shock instead of heat shock and isothermal RCA reaction not only the procedure becomes easier, but

192 he posterior segment of the central isthmus (RCA to inferior vena cava distance).

193 ion of RCA members, particularly CD59 (a key RCA member that controls formation of the membrane attac

194 es the operation compared to linear ligation-RCA assays.

195 clinical application of conventional linear RCA is restricted by its unsatisfactory picomolar-level

196 The long RCA product was digested and analyzed by CE.

197 At 6 minutes, RCA I fluorescence of tumor vessels was largely diffuse,

198 l amplification (e.g. RPA, HDA, LAMP, NASBA, RCA, ICAN, SMART, SDA).

199 ol mice, infected with TMEV but receiving no RCA I, had inflammatory demyelinating lesions in the ant

200 The ability of RCA to produce single-stranded DNA tens of thousands of

201 first report to show that direct addition of RCA blockers into plasma from HCV-infected patients rend

202 Direct applicability of RCA-FRET to applied nucleic acid research was demonstrat

203 ps towards the integration and automation of RCA and potentially also other complex multi-step assays

204 Thus, blockage of RCA function represents a novel approach to restore acti

205 lts present an important proof of concept of RCA-FRET imaging with a strong potential to advance in s

206 Real-time detection of RCA or RAM products has been a challenge because of most

207 hromatography-based capture and detection of RCA products (RCPs) pre-labelled simultaneously with bio

208 ii) RCA, and (iii) optomagnetic detection of RCA products.

209 ication of HNB for colorimetric detection of RCA reaction further simplifies the assay.

210 wledge of precise structural determinants of RCA proteins critical for imparting the regulatory activ

211 essed this issue by examining the effects of RCA I on blood vessels of spontaneous pancreatic islet-c

212 gen deficit and stimulating the formation of RCA, second that an unknown EPF signalling pathway may b

213 that blockage of the biological function of RCA members rendered both HIV-1 virions and infected cel

214 Blockage of the biological function of RCA members, particularly CD59 (a key RCA member that co

215 e results illustrate the selective impact of RCA I on VEGF signaling in tumor blood vessels.

216 However, the integration of RCA on an automated chip platform is challenging due to

217 iologically functional CD59, a key member of RCA.

218 tic influenza target of 2 pM after 45 min of RCA, which is comparable to the corresponding laboratory

219 on-chip with an LOD of 20 pM after 45 min of RCA.

220 her investigated the effect of the number of RCA cycles and elongation times (ranging from 10 to 120

221 ave dissected the structural requirements of RCA proteins that are crucial for one of their two regul

222 The second round of RCA produces amplicon coils that anneal to detection pro

223 and ligation steps after the first round of RCA, and combines two amplification rounds in a one-pot

224 synthetic target with just a single round of RCA, comparable to recently reported procedures requirin

225 in the wild species to thermal stability of RCA, enabling Rubisco to remain active.

226 hat HCV may also use the similar strategy of RCA incorporation to escape ADCML.

227 Although potential fitness tradeoffs of RCA formation are poorly understood, increased RCA forma

228 istributed throughout the dendritic trees of RCA motoneurons, albeit with a strong bias to small-diam

229 ioanalytical tools, and summarize the use of RCA to construct multivalent molecular scaffolds and nan

230 The utility of RCA also depended on other root phenes and environmental

231 ariation in RCA formation and the utility of RCA for a range of stresses position RCA as an interesti

232 We evaluated the utility of RCA for N acquisition by physiological comparison of mai

233 On low-nitrate soils, the utility of RCA formation was 56% greater in coarser soils with high

234 The greater utility of RCA on low-potassium soils is associated with the fact t

235 w-phosphorus soils (7.5 muM), the utility of RCA was 2.9 times greater in plants with increased later

236 ion grade III had the highest risk for AD or RCA (P<0.001).

237 ted with a 3.5-fold increased risk for AD or RCA in the overall study population (hazard ratio=3.52;

238 ion is associated with a high risk for AD or RCA regardless if LVEF is <=35% or >35%.

239 average follow-up of 7.0+/-2.6 years, AD or RCA was observed in 28 (13.3%) and 33 (15.7%) patients,

240 of side branches is lower than in the LAD or RCA and there are no septal perforators with intramuscul

241 oise ratio was also measured on the in-plane RCA images.

242 The combination of PNA, RCA, and DNAzymes allows for sequence-specific and highl

243 lity of RCA for a range of stresses position RCA as an interesting crop-breeding target for enhanced

244 ction efficiency and simplify the procedure, RCA was not preceded with ligation, and a preformed circ

245 efined: proximal right coronary artery (prox RCA), mid and distal left anterior descending artery and

246 rnal mammary chain (IMC), high risk for prox RCA and mdLAD + dD from 1970 to 1995 and thereafter sole

247 dLAD + dD; and right IMC, high risk for prox RCA.

248 pidemia, and smoking contributed to proximal RCA thickening, independent of atherosclerotic plaque qu

249 d undetectable cccDNA when assessed by qPCR, RCA and ddPCR assays detected cccDNA in all-but-one nega

250 Other control mice that received RCA I alone did not develop inflammatory lesions.

251 protected from RMSF, whereas those receiving RCA developed disease similar to that of nonvaccinated R

252 Using expressed recombinant RCA and leaf-extracted RCA, the kinetic properties of th

253 cificity for ricin versus the highly related RCA 120 (1 to 10 000).

254 ibody that enhanced the activities of ricin, RCA, and abrin II to different extents, thus improving t

255 re oligonucleotides and amplified by a short RCA.

256 Moreover, since RCA products can be tailor-designed by manipulating the

257 g with a strong potential to advance in situ RCA toward easier sample preparation, higher-order multi

258 mic range by real-time monitoring of in situ RCA.

259 n photoluminescence from beta-actin-specific RCA and DNA probes freely diffusing in solution or nonsp

260 d dyes that hybridize to beta-actin-specific RCA products in HaCaT cells can afford washing-free imag

261 labeling method in combination with surface RCA as reporter system to achieve both high sequence spe

262 ation with random PCR amplification tagging (RCA-RA-PCR), high-throughput sequencing (Illumina HiSeq)

263 igned by manipulating the circular template, RCA has been employed to generate complex DNA nanostruct

264 We conclude that RCA can serve as a reliable method to replicate complex

265 We conclude that RCA development and stomatal development are linked by t

266 These results provide clear evidence that RCA is a major limiting factor in plant photosynthesis u

267 quantitative support for the hypothesis that RCA formation is a useful adaptation to suboptimal avail

268 ults are consistent with the hypothesis that RCA improves plant growth under N-limiting conditions by

269 Based on previous reports that RCA is heat-labile, the Rubisco activation state was mea

270 Previous research showed that RCA formation reduces the respiration and nutrient conte

271 The RCA genome contains E1 DNA acquired from the 293 cellula

272 The RCA product is a concatemer containing tens to hundreds

273 The RCA-produced long, single-stranded DNA with repeating un

274 The analyte activates the RCA process, leading to DNA chains consisting of the Mg(

275 eobacter DC5-80-3 cluster (also known as the RCA clade) is among the most abundant bacterial lineages

276 The AVN was supplied by the RCA in 89 patients, the LCX artery in 11 patients, and b

277 RCA) to the inferior vena cava, and from the RCA to the tricuspid valve annulus were measured.

278 cular function expressed as lower Ecc in the RCA (P<0.01) and left circumflex regions (P<0.05) measur

279 lysis revealed numerous polymorphisms in the RCA amino acid sequence from O. australiensis.

280 er within the proximal segment, while in the RCA their distribution is more uniform.

281 Linear products of the RCA contain multiple tandem copies of the template molec

282 Next, we prepared the RCA products that consist of these aptamers to increase

283 ernate splicing mechanism, which splices the RCA-alpha and RCA-beta isoforms were probably gained fro

284 anded loop domain that communicates with the RCA product.

285 To test the hypothesis that thermostable RCA can improve photosynthesis under elevated temperatur

286 ) were independently associated with thicker RCA vessel walls.

287 g the structure-switching aptamer, real-time RCA can be used to specifically quantitate PDGF down to

288 The aptamer can also be adapted to RCA on surfaces, although quantitation proved to be more

289 shown here that an excellent alternative to RCA labeling is tagging with gold nanoparticles followed

290 nal narrowing, and plaque was not related to RCA wall thickness.

291 Traditionally, RCA has been used to develop sensitive diagnostic method

292 v, and provide a framework for understanding RCA disease-related mutations and immune evasion.

293 Collateral flow index in the untreated RCA and left coronary artery changed from 0.071+/-0.082

294 Using RCA, we identified two distinct subtypes of cancer-assoc

295 both protein and DNA in a single test using RCA, the limit of detection for IL-8 and IL-6 was improv

296 ll as those within specific target genes via RCA-based enrichment.

297 stable up to 42 degrees C, contrasting with RCA from O. sativa, which was inhibited at 36 degrees C.

298 rs (P < .01) were positively correlated with RCA wall thickness.

299 A or B chains and low cross-reactivity with RCA 120.

300 a combination of antiretroviral therapy with RCA blockage, provirus activators, and therapeutic vacci