ライフサイエンスコーパス: marker protein

1 mature olfactory receptor neurons (olfactory marker protein).

2 ained the FXG-associated mRNA Omp (olfactory marker protein).

3 endrites (based on their immunostaining with marker proteins).

4 GAP43, PGP9.5, but the absence of olfactory marker protein.

5 receptors that were co-localized with an ER marker protein.

6 otein (GFAP), which is an astrocyte-specific marker protein.

7 usion protein colocalizes with a peroxisomal marker protein.

8 ized to expression of a neuronal or synaptic marker protein.

9 /mTOR is cofractionated with calnexin, an ER marker protein.

10 lant nucleorhabdovirus, and with a nucleolar marker protein.

11 the properties of tER sites using Sec13 as a marker protein.

12 eotide-gated channel subunits, and olfactory marker protein.

13 with the secretory pathway, but also a Golgi marker protein.

14 ells reduced the constitutive secretion of a marker protein.

15 izes with an antibody to lgp120, a lysosomal marker protein.

16 wed that they excluded a freely diffusing PM marker protein.

17 ning flotillin, a widely utilized lipid raft marker protein.

18 gth TDP-43, are frequently positive for this marker protein.

19 pericorneal tissue were immunostained for SC marker proteins.

20 an fluorescent protein with other individual marker proteins.

21 mulation and elevated expression of fat cell marker proteins.

22 ed without requiring colocalization with any marker proteins.

23 indicated by the differential expression of marker proteins.

24 ive glycosylation and colocalization with ER marker proteins.

25 in the absence of focal changes of neuronal marker proteins.

26 ely dispersing Golgi and trans-Golgi network marker proteins.

27 ibution to those of well-annotated organelle marker proteins.

28 tection of clinical diagnostic or prognostic marker proteins.

29 campal neurons and colocalizes with synaptic marker proteins.

30 normalities, including altered expression of marker proteins.

31 odies for quail cell nuclear antigen and SMC marker proteins.

32 ears to be a general feature of nuclear body marker proteins.

33 press normal amounts of four muscle-specific marker proteins.

34 n of mitotic Golgi also lacked detectable ER marker proteins.

35 ikely as a result of the lack of appropriate marker proteins.

36 expression of myofibroblast differentiation marker proteins.

37 hemical detection of somite and neural crest marker proteins.

38 istently co-labeled with stress granule (SG) marker proteins.

39 genic mice that express fluorescently tagged marker proteins.

40 distinct olfactory neurons express different marker proteins.

41 ssion of p53, p21(Cip1/Waf1), and other p53 "marker" proteins.

42 phometric quantification using the lysosomal marker protein 2 (LAMP-2) immunolabeling showed higher n

43 TPS+Vi showed (1) a higher level of a DsRed marker protein, (2) a higher level of ubiquitinated prot

44 he late endosomal marker lysosome-associated marker protein 3 (LAMP-3).

45 Human senescence marker protein 30 (SMP30), which functions enzymatically

46 on of expression of regucalcin or senescence marker protein 30 and L-gulonolactone oxidase.

47 ntained processes that express the olfactory marker protein, a marker common to mature OSN axons.

48 in the number of cells expressing olfactory marker protein, a marker of mature ORNs.

49 ic antibodies to ABCA2 and various organelle marker proteins, ABCA2 was found to colocalize with the

50 ing with the lipophilic dye Nile red and the marker protein ADRP.

51 These tumor endothelial marker proteins also exhibited increased expression in b

52 ner and showed lower expression of olfactory marker protein and growth-associated protein 43, indicat

53 kin with a lentivirus encoding a fluorescent marker protein and have mapped labeled columns of cells

54 is of Masson trichrome staining and fibrotic marker protein and mRNA expression 14 days after AKI rev

55 ly distinct from an apical zone of olfactory marker protein and odorant receptor-expressing cells.

56 f expressing odorant receptors and olfactory marker protein and of projecting axons to the olfactory

57 ls of NTE showed aberrant distribution of ER marker proteins and accumulation of NTE on the cytoplasm

58 ray analysis also indicates that mesenchymal marker proteins and certain growth factor receptors are

59 mbinations of fluorescent and bioluminescent marker proteins and employing multi-modality imaging tec

60 into cells that expressed immature neuronal marker proteins and increased cell number in cultures by

61 correlated with the distribution of defined marker proteins and nicotinic receptor binding sites det

62 ministration of DHA attenuated all ER stress marker proteins and reduced the accumulation of both ubi

63 ession of intestine-specific differentiation marker proteins and the tetraspanin CD63, which is invol

64 mbinations of fluorescent and bioluminescent marker proteins and used bioluminescence imaging and int

65 ioxidant defense capacity, stress/senescence marker proteins, and DNA repair mechanisms at the gene e

66 ll morphology and epithelial and mesenchymal marker proteins, and using cell migration and Matrigel i

67 , failed to incorporate classical lipid raft marker proteins, and were not disrupted by cholesterol e

68 Clinical markers, protein, and GeneChip analysis were used to ide

69 an papillomavirus (HPV) genomes that express marker proteins (antibiotic resistance genes and Green F

70 like particles, whereas a transmembrane raft marker protein appeared to associate with punctate Gag f

71 Fluorescent marker proteins are expressed at high levels within 1 we

72 arbors expressing a fluorescent postsynaptic marker protein as they arborized within the optic tectum

73 t solubility and lack of colocalization with marker proteins associated with raft domains.

74 o express short hairpin RNAs and fluorescent marker protein at high levels in hematopoietic cells and

75 ail; and the F ORF was replaced with that of marker protein beta-glucuronidase.

76 ting cell nuclear antigen (a nuclear mitosis marker protein), but not for nestin (a marker for NP cel

77 nstrate the quantitative analysis of disease-marker proteins by continuously separating the antibody-

78 Treatment of the mixed marker proteins by sequential strain-promoted and copper

79 onstrated that p65 co-sedimented with the ER marker protein calreticulin and myeloperoxidase precurso

80 Combinations of these marker proteins can be used in assays for rapid differen

81 ion of GKPID's capacity to bind the cortical marker protein - can be recapitulated by reintroducing a

82 f internalized cystatin C with the lysosomal marker proteins cathepsin D and legumain.

83 te in microdomains rich in the membrane raft marker protein caveolin-1.

84 ng), besides expressing CD34(+) cell lineage marker protein, CD34.

85 s indicated by up-regulation of cell surface marker proteins CD40, CD80, and CD86.

86 es exhibited the expected size and expressed marker proteins CD63, CD81, and heat shock protein (HSP)

87 ogy (electron microscopy), expressed exosome-marker proteins CD63, phosphatidylserine (flow cytometry

88 ons, viral mRNAs, microRNAs, and the exosome marker protein CD9.

89 Hepatocyte colonies also coexpressed marker proteins characteristic of adult hepatocytes and

90 eek, TM-associated TMSCs began expressing TM marker protein CHI3L1.

91 re dramatically decreased, and two apoptotic marker proteins, cleaved caspase 7 and cleaved poly(ADP-

92 In flies null for the CB marker protein coilin, CBs are absent and there are no l

93 often identified with antibodies against the marker protein coilin.

94 Despite recognition as the CB marker protein, coilin is primarily nucleoplasmic, and t

95 ly of Cajal bodies and relocalization of the marker protein, coilin, to nucleoli.

96 EDEs had usual exosome size and marker protein content, and significantly higher levels

97 colocalized with the mitochondrial-specific marker protein cytochrome oxidase subunit I.

98 eased the synthesis of early differentiation marker protein delta-crystallin in chicken lens epitheli

99 led differential, cell-selective labeling of marker proteins derived from two bacterial strains cocul

100 edial diploid bud, whereas mitochondrial GFP marker proteins distribute throughout the zygote and the

101 d in one of the haploid parents, each of the marker proteins distributes throughout the fused mitocho

102 py revealed that GNA colocalizes with the ER marker protein disulfide isomerase (PDI) and the COPI co

103 lization with the endoplasmic reticulum (ER) marker, protein disulfide isomerase.

104 lized with the luminal endoplasmic reticulum marker protein-disulfide isomerase (PDI) and that was in

105 e into cells that express the early neuronal marker protein doublecortin in the subventricular zone o

106 hondria, cofractionates with a mitochondrial marker protein during subcellular fractionation, and is

107 The recovery of marker proteins during synaptosome preparation was the s

108 NE decreased SMC marker proteins (eg, alpha-smooth muscle actin and desmi

109 ot sacrificed in an ADV backbone because the marker protein, EGFP, is expressed in R1881-stimulated A

110 itophorous vacuole as the degradation of the marker protein, Escherichia coli beta-lactamase, secrete

111 ostate-specific-membrane-antigen (PSMA) is a marker protein expressed primarily in prostate epitheliu

112 nullify Ggamma13 expression in the olfactory marker protein-expressing OSNs.

113 and the concomitant induction of mesenchymal marker protein expression and cell proliferation.

114 Marker protein expression and localization were determin

115 Using simultaneous germination assays and marker protein expression detection, we show that LepaDO

116 In contrast to results in rabbits, marker protein expression persisted in the lung in both

117 Cell proliferation and specific marker protein expression results also revealed that wit

118 r fewer mature ORNs, as defined by olfactory marker protein expression, and significantly greater num

119 GSI treatment also induced neuronal marker protein expression, as shown by Western blot anal

120 apes and structures, anatomic locations, and marker protein expression.

121 ith an accompanying restoration of olfactory marker protein expression.

122 Western blot analysis for the macrophage marker protein F4/80 in homogenates revealed not only th

123 Coilin is known as the marker protein for Cajal bodies (CBs), subnuclear domain

124 We have found that coilin, the marker protein for Cajal bodies (coiled bodies, CBs), is

125 chment on density gradients with caveolin, a marker protein for caveolae.

126 ated on sucrose gradients with caveolin-3, a marker protein for myocyte caveolae.

127 In addition, it is shown that a marker protein for plant microtubule organizing centers,

128 s small round foci partially associated with marker proteins for coiled bodies, suborganelles involve

129 pression of beta- and gamma-crystallins, the marker proteins for fiber differentiation, was not chang

130 ed into the bloodstream, suggesting possible marker proteins for follow-up serum proteomic studies.

131 nohistochemistry showed normal expression of marker proteins for muscular dystrophies.

132 he results indicate that, while the level of marker proteins for neurons and astrocytes remains the s

133 ells and divergent effects on the content of marker proteins for neutrophil granules.

134 ically, including analyses of representative marker proteins for nuclei and cytoplasm.

135 rall our studies identified candidate tissue marker proteins for ovarian cancer and demonstrate that

136 embrane domains in combination with cell-end marker proteins for polarity establishment.

137 Because Rab2, beta-COP, and p53/p58 are marker proteins for pre-Golgi intermediates (vesicular t

138 type was accompanied by the disappearance of marker proteins for renin cells (e.g., aldo-keto reducta

139 e epithelial layers, and these cells express marker proteins for stem/progenitor cells.

140 homogenates with no significant decrease in marker proteins for the other complexes of the electron

141 able human cell line expressing GFP-LC3, the marker-protein for autophagosomes.

142 anner, and svp1delta cells fail to recycle a marker protein from the vacuole to the Golgi.

143 act multicellular tissues using 20 different marker proteins from Arabidopsis thaliana, mostly belong

144 oteins mirrored that of total protein, while marker proteins from subcellular compartments were not r

145 -Golgi intermediate compartment, none of the marker proteins from this or any other cell compartments

146 localization with the foci of the DNA damage-marker proteins gammaH2A.X, 53BP1, and P-ATM.

147 Immunostaining for the pan-neuronal marker protein gene product (PGP) 9.5 revealed fibers wi

148 us wounds using an antibody to the neuroneal marker protein gene product (PGP) 9.5, we observed marke

149 Immunohistochemistry for the pan-neural marker protein gene product 9.5 (PGP9.5) and growth-asso

150 g experiments using the nonspecific neuronal marker Protein Gene Product 9.5 were performed in glabro

151 we labeled sections for the general neuronal marker, protein gene product 9.5.

152 oreactivity for CGRP and for a general nerve marker, protein gene product 9.5.

153 Sudomotor innervation was stained with 2 markers: protein gene product 9.5 (PGP 9.5), a general n

154 ey 293 cells that measures lipidation of the marker protein GFP-LC3 following amino acid starvation.

155 ead the GP64 or GP(64/F) protein and the two marker proteins GFP and GUS.

156 in, by antibody decoration, and by fusion to marker proteins (GFP or maltose binding protein).

157 Moreover, expression of the pGCIRES marker protein, GFP, directly correlated with the expres

158 transporter VGLUT2, several synaptic vesicle marker proteins, glutamate, the soluble N-ethylmaleimide

159 Olfactory epithelial cells from olfactory marker protein-green fluorescent protein (OMP-GFP) mice

160 relevance of A3G colocalization with P body marker proteins has not been established.

161 y using flow cytometry for a virally encoded marker protein, heat-stable antigen (HSA).

162 essing a green fluorescent protein-tagged ER marker protein (Hmg1p).

163 elatonin induced gene expression of the bone marker proteins; however, this does not occur until the

164 Glutathione S-transferase Pi (GSTpi) is a marker protein in many cancers and high levels are linke

165 dated by confirming the presence of specific marker proteins in cells.

166 how the dynamics of motility system-specific marker proteins in FrzE mutants as cells move forward an

167 l functions by studying excretion of urinary marker proteins in healthy human probands.

168 sera resulted in downregulation of synaptic marker proteins in hippocampal neurons.

169 and identification of clinical disease-state marker proteins in human serum.

170 Lumenal epitopes on marker proteins in secretory pathway compartments (p63,

171 AEM for imaging of fluorescent fusion-tagged marker proteins in studying cortical cytoskeletal and me

172 tterns appear to depend on distinct types of marker proteins in the cell cortex; in particular, the b

173 dentified AC hydrolase and known periplasmic marker proteins in the periplasmic fraction.

174 Although AdvSca1 cells do not express SMC marker proteins in vivo, they do express transcription f

175 Smn colocalizes with alpha-actinin, a Z-disc marker protein, in both skeletal and cardiac myofibrils.

176 ggered sustained expression of the ER stress marker proteins including phosphorylated eukaryotic init

177 , assessment of endothelial and inflammatory marker proteins (including tissue-type plasminogen activ

178 ed gene expression of BSP and the other bone marker proteins, including alkaline phosphatase (ALP); o

179 The endoplasmic reticulum stress marker proteins, including Grp78/Bip, phospho-eIF2alpha,

180 croglobulin and late endosomal and lysosomal marker proteins, including Rab7, mannose-6-phosphate rec

181 work did not colocalize with other organelle marker proteins, including three ER reticuloplasmins.

182 croglial cells that also contained olfactory marker protein, indicating neuronophagia within the olfa

183 ly label for bromodeoxyuridine and olfactory marker protein, indicating that neuronal cells born in v

184 lin-1 colocalized with endogenous desmosomal marker proteins, indicating efficient incorporation into

185 able high levels of the alkaline phosphatase marker protein into the bloodstream by transduced WAT.

186 Despite the sequestration of SG marker proteins into IB granules, canonical SGs are unab

187 gregation of some GFP-tagged plasma membrane marker proteins into rings around penetration sites, whi

188 APP, PS1, and p58 (an itinerant ER to Golgi marker protein) into transport vesicles from donor ER me

189 ice, induction of epithelial differentiation marker protein (involucrin), and change of cell cycle po

190 ies against IscS and IscU--two mitochondrial marker proteins involved in iron-sulphur cluster biosynt

191 raft-associated proteins included lipid raft markers, proteins involved in cell adhesion and membrane

192 n reaction measurements of expression of the marker protein ionized calcium-binding adapter molecule

193 Subsequent identification and validation of marker proteins is integral to rapid screening developme

194 e expression of nestin, the neural stem cell marker protein, is expressed in bulge-area stem cells of

195 The cortical marker protein Kar9 localizes to the bud tip and is requ

196 t is formed between the FHA domain of cancer marker protein Ki67 (Ki67FHA) and a peptide fragment of

197 glutamine synthetase (GS), the bipolar cell marker protein kinase C alpha (PKCalpha), and the horizo

198 Z-AT, and endoplasmic reticulum (ER) stress markers (protein kinase RNA-like ER kinase, activator tr

199 ophagosomes to colocalize with the autophagy marker protein LC3-II.

200 led to strong accumulation of the autophagic marker proteins LC3-II and p62, and decreased the proteo

201 lls with 80% of control cell mtDNA exhibited marker protein levels, cell morphology and invasive prop

202 The expression of the lens differentiation marker proteins, major intrinsic protein (MIP) and delta

203 rons to p75NGFR + cells (665%) and olfactory marker protein + mature neurons to p75NGFR + basal cells

204 yzed the effects of overexpression of P body marker proteins Mov10, DCP1a, and DCP2 on HIV-1 replicat

205 n with Tat export efficiency of a selectable marker protein, namely TEM-1 beta-lactamase.

206 S) cells and, along with two other stem cell marker proteins (Nanog and Sox2), together can convert h

207 Imaging of both Lifeact-GFP and the SG marker protein neuropeptide Y-mCherry reveals that SGs a

208 Marker proteins of differentiation declined over the fir

209 GW182 and its long isoform TNGW1 are marker proteins of GW/P bodies and bind to Argonaute pro

210 ivity was found to partially colocalize with marker proteins of inhibitory and excitatory synapses.

211 The cytoplasmic Vp1 does not colocalize with marker proteins of the endoplasmic reticulum.

212 some Bud1-GTPase module and the Tea cell-end marker proteins of the microtubule cytoskeleton, along w

213 ether ORs are expressed in mature [olfactory marker protein (OMP(+))] and/or immature [growth-associa

214 blocks the reappearance of mature, olfactory marker protein (OMP) (+) olfactory neurons as compared t

215 Antibodies to olfactory marker protein (OMP) and neuronal cell adhesion molecule

216 broaden our knowledge, we examined olfactory marker protein (OMP) expression in a sample of twenty-th

217 Mice from which the olfactory marker protein (OMP) gene has been deleted demonstrate a

218 n adenoviral vector to replace the olfactory marker protein (OMP) gene in olfactory receptor neurons

219 ing region, driven by the proximal olfactory marker protein (OMP) gene promoter, and shows expression

220 ough its function remains obscure, olfactory marker protein (OMP) has been implicated in olfactory tr

221 5)N relaxation measurements of the olfactory marker protein (OMP) including longitudinal relaxation (

222 Olfactory marker protein (OMP) is a highly expressed and phylogene

223 Olfactory marker protein (OMP) is a ubiquitous, cytoplasmic protei

224 Olfactory marker protein (OMP), a phylogenetically conserved prote

225 We found that olfactory marker protein (OMP), a protein expressed in mature ORNs

226 ls colabeled with antibody against olfactory marker protein (OMP), corroborating that mature ORNs exp

227 uble-label immunocytochemistry for olfactory marker protein (OMP), growth-associated protein (GAP-43)

228 essed for immunocytochemistry with olfactory marker protein (OMP), synaptophysin, synapsin 1, glial f

229 In animals heterozygous for the olfactory marker protein (OMP), this adaptive plasticity was stron

230 e prevented by genetic ablation of olfactory marker protein (OMP), which is exclusively expressed in

231 he absence of nasotoxic treatment, olfactory marker protein (OMP), which is specific for ORNs, was no

232 Immunohistochemical analyses of olfactory marker protein (OMP)-, calretinin- calbindin-, parvalbum

233 ), the pattern of expression of an olfactory marker protein (OMP)-lacZ fusion gene was analyzed in th

234 al along ORN axons were studied in olfactory marker protein (OMP)-null mice and genotypically matched

235 t quality perception is altered in olfactory marker protein (OMP)-null mice, we trained and tested ad

236 Ectopic olfactory marker protein (OMP)-stained fibers localized to the ext

237 zed as interacting partners of the olfactory marker protein (OMP).

238 ne associated protein (GAP) 43 and olfactory marker protein (OMP).

239 a by linking microtubule motor proteins to a marker protein on the cell cortex localized by external

240 x, and the minority of GINs express only one marker protein or peptide.

241 ing the intensities of a selected protein to marker proteins, or internal standards, a relative ratio

242 Plzf, Msx2, and Dlx5, and later of the bone marker proteins osteocalcin and alkaline phosphatase.

243 d the intensity and polarity of cytoskeletal marker proteins over time to characterize stereotyped ce

244 cluded calnexin and COPII, but not the ERGIC marker protein p58.

245 rganelles that are usually identified by the marker protein p80-coilin.

246 e nuclear organelles often identified by the marker protein p80-coilin.

247 tor neuron (SMN) protein complex, and the CB marker protein, p80 coilin.

248 olamine synthesis, tyrosine hydroxylase, the marker protein, placental alkaline phosphatase, was also

249 In RTT biopsies, olfactory marker protein-positive neurons displayed abnormal struc

250 ciated lipocalin (NGAL) has emerged an early marker protein, predicative of acute kidney injury (AKI)

251 We anticipate that the presence of the marker protein PV in the PV1-nucleus of the rodent hypot

252 further supported by a reduction of synaptic marker proteins Rab3 and cysteine-string protein (CSP/Dn

253 smic reticulum and Golgi, in comparison with marker proteins resident to these subcellular compartmen

254 ciated with nuclear retention of 40S subunit marker proteins, RpS2-GFP and RpS3-GFP.

255 Fluorescence microscopy with marker proteins showed that the alphaS-associated vesicl

256 ce typically rely on detection of a very few marker proteins, so are unsatisfactory.

257 Despite notable efforts, far-red marker proteins still need further optimization to match

258 on, histologic appearance, and expression of marker proteins strongly suggests the utility of this no

259 Further, expression of inflammatory marker proteins such as inducible nitric oxide synthase

260 ls showed decreased expression of adipogenic marker proteins, such as peroxisome proliferator-activat

261 The replicative phagosome lacks membrane marker proteins, such as the glycoprotein LAMP-1, that a

262 r type 1 (NR1) clusters with the presynaptic marker protein synapsin.

263 mpal CA3 it colocalized with the presynaptic marker proteins synaptophysin and the vesicular glutamat

264 le-cell marker Alexa-594 and two presynaptic marker proteins-synaptophysin-eGFP to monitor changes in

265 t associate with an authentic stress granule marker protein T-cell internal antigen 1 (TIA-1).

266 ing between the ER and the Golgi using Golgi marker proteins tagged with green fluorescent protein.

267 Previous studies identified a cell-end marker protein, Tea1, that is transported by cytoplasmic

268 GAPs that show homology to mammalian myelin marker proteins termed CNPases.

269 ation experiments with an extended subset of marker proteins tested in 45 different combinations reve

270 ffect membrane distribution of caveolin-1, a marker protein that is enriched in caveolae membrane mic

271 stigated the expression of immature neuronal marker proteins that signal the birth of new neurons in

272 rotransposons, and when fused to fluorescent marker proteins, the chromodomains target proteins to sp

273 of RabA4b cofractionated with Golgi membrane marker proteins, the majority of this protein labeled a

274 esponsible for the placement of the cell-end marker proteins, the Tea1-Tea4/Wsh3 complex, which recru

275 g cells in a stable line expressing a second marker protein, thus increasing the utility of a single

276 Injection of marker protein to visualize the spread of injected prote

277 s us to use immunofluorescence of endogenous marker proteins to assess kinetics from fixed cells.

278 of available organelle-specific fluorescent marker proteins to further evaluate cells during arbuscu

279 r envelope or endoplasmic reticulum membrane marker proteins to precisely map the nuclear volume.

280 cytoskeleton delivers the so-called cell-end marker proteins to the cell pole, which in turn polarize

281 nsible for the polarization of the dendritic marker protein transferrin receptor (TfR) in mature cell

282 LD from NAFLD, including the histopathologic marker protein tyrosine phosphatase 1b, AST/ALT ratio, g

283 arget of rapamycin (mTOR) targets, autophagy markers, protein ubiquitination, and the intracellular a

284 In addition, this system synthesizes a marker protein under control of the same promoter as the

285 localization of both IRS-1 and IRS-2 with ER marker proteins using immunofluorescent confocal microsc

286 n, immunostaining for beta-gal and olfactory marker protein was virtually eliminated in the bulb.

287 lgi and ER-to-Golgi intermediate compartment marker proteins was examined under specific conditions.

288 ssion of lens fiber-specific differentiation marker proteins was examined with western blot analysis

289 FORMED2 auxin transporter or plasma membrane marker proteins was not affected by loss of TWD1.

290 Sensitive immunohistochemistry with marker proteins was used to study reactions of astrocyte

291 system, a number of commonly used selectable marker proteins were assessed for their compatibility wi

292 The ER stress marker proteins were colocalized with APP accumulation i

293 Other Golgi-specific marker proteins were not affected under these conditions

294 es and expressed high levels of chondrocytic marker proteins when cultured on Pln.

295 n cells with absent or low expression of the marker protein, whereas lack of such methylation is evid

296 SMP30 was originally identified as an aging marker protein, whose expression decreased androgen inde

297 Here we present mGarnet, a robust monomeric marker protein with far-red fluorescence peaking at 670

298 ) exhibit aberrant apposition of presynaptic marker proteins with postsynaptic acetylcholine receptor

299 cardiovascular events, and for a macrophage marker protein, without increasing lesion macrophage con

300 expansin signal peptide, and the fluorescent marker protein YFP.