ライフサイエンスコーパス: protein A

1 CBU0077 MceA (mitochondrial Coxiellaeffector protein A).

2 alently modified by Protein-A (Glass/ZnO-NRs/Protein-A).

3 s specific genes, namely nuc, mecA, vanA and protein A.

4 ty of the ssDNA-binding protein, replication protein A.

5 ntaining multifunctional FHV RNA replication protein A.

6 cture of the C-proximal polymerase domain of protein A.

7 unoglobulin G to spheres functionalized with protein A.

8 ntains multifunctional viral RNA replication protein A.

9 uid chromatography (nanoLC) and, for histone proteins, a 2-d sample preparation that includes histone

10 The isolated protein, a 45-kDa monomer, lacks catalytic activity but

11 and virulence factors but increased surface protein A abundance.

12 Antiserum against one of these five proteins-A. aegypti bacteria-responsive protein 1 (AgBR1

13 tic monoclonal antibodies usually involves a protein A affinity capture step.

14 Protein A affinity capture was employed as a universal s

15 method which combines commercially available protein A affinity capture, targeted analyte isolation b

16 led to form BsAbs that were purified through protein A affinity chromatography to demonstrate industr

17 ally alter the pH at which a mAb elutes from protein A affinity resin.

18 for the first time, the implementation of a Protein-A affinity chromatography column as the first di

19 ophilum adhesins A. phagocytophilum invasion protein A (AipA), A. phagocytophilum surface protein (As

20 demonstrate that A. marginale outer membrane protein A (AmOmpA; AM854) contributes to the invasion of

21 ase rapidly hydrolyzes Staphylococcus aureus protein A, an important S. aureus virulence factor invol

22 rmed within the colloidal suspensions (i.e., Protein A and antibody binding) for tailored and specifi

23 ssociated membrane protein (VAMP)-associated protein A and B (VAPA and VAPB) have been reported to be

24 lar endothelial growth factor and surfactant protein A and B, but this effect was counteracted by sil

25 put method for generation of Bipods based on protein A and CH1 domain affinity capture.

26 topoisomerase 1, fibrillarin, and centromere protein A and discovered that they are homologous to vir

27 we show here in studies of human replication protein A and Escherichia coli single-stranded DNA bindi

28 roduction of parturition signals, surfactant protein A and platelet-activating factor, by the develop

29 odified by EDC-NHS crosslinkers, grafting of protein-A and finally interaction with anti-AFB(1) antib

30 oups using EDC-NHS crosslinkers, grafting of protein-A and immobilization of anti-AFB(1) antibodies.

31 ic Thermus thermophilus multidrug resistance proteins A and B (TmrAB), which not only shares structur

32 report that the ER-resident VAMP-associated proteins A and B (VAPA and VAPB) interact with the perox

33 acterized Borrelia adhesins, decorin-binding proteins A and B, have been shown to bind to 2 host rece

34 variants of the diverse pneumococcal surface proteins A and C (PspA and PspC) and zinc metalloproteas

35 ain-reaction assays for PorA (encoding porin protein A) and N. meningitidis genogroups.

36 says that combined monoclonal (outer surface protein A) and polyclonal antibodies were performed on a

37 nd nucleotide excision repair is replication protein A, and we find that its accumulation on UVB-dama

38 energy for the interaction of Glass/ZnO-NRs/Protein-A/Anti-OTA with OTA were calculated, analyzed an

39 r to form OTA-selective layer (Glass/ZnO-NRs/Protein-A/Anti-OTA).

40 vative functionalization method that exploit Protein-A/antibody affinity.

41 ndicate that the crown contains 12 copies of protein A arranged basally to apically in an N-to-C orie

42 choline expanded 54-fold, and the surfactant proteins A, B, and C expanded 144-, 4-, and 17-fold, res

43 idomic analysis of lipids and the surfactant proteins A, B, and C in lavage fluids from patients with

44 sicle-associated membrane protein-associated proteins A/B) and ACBD5 (acyl Co-A binding protein 5).

45 by combining interface exchange, asymmetric Protein A binding, and the scFv x Fab format.

46 Formed Glass/ZnO-NRs/Protein-A/BSA&Anti-OTA structures were integrated within

47 mbinant mouse FH and three FHR proteins (FHR proteins A-C).

48 lly when visualizing glial fibrillary acidic protein, a canonical marker for astrocytes.

49 NLR family CARD-containing 3 (NLRC3) protein, a caspase recruitment domain (CARD)-containing

50 ys identified features on the surface of the protein-a cationic patch and a unique hydrophobic loop-t

51 Catabolite control protein A (CcpA) is a master regulator of carbon source

52 resence of the histone H3-variant centromere protein A (CENP-A) [1].

53 Chromatin assembled with centromere protein A (CENP-A) is the epigenetic mark of centromere

54 ome segregation and are marked by centromere protein A (CENP-A) nucleosomes.

55 ovided by the histone H3 variant, centromere protein A (CENP-A), but the molecular mechanisms that un

56 tromere-specific histone variant, centromere protein A (CENP-A), using molecular dynamics simulations

57 involving the histone H3-variant centromere protein A (CENP-A).

58 e centromere-specific H3 variant, centromere protein A (CENP-A).

59 he centromeric histone H3 variant centromere protein A (CENPA) is an epigenetic mark that determines

60 large proportion of genes encoding membrane proteins, a central role for EMC as a TMD insertion fact

61 ecipitation analysis reveals that Centromere Protein A/ Centromeric Histone H3-like Protein (CENP-A/C

62 lutions make high-resolution studies of this protein a challenging task.

63 stion by studying the hepatitis C virus core protein, a chaperone that promotes viral genome dimeriza

64 In comparison to the parental m1 VacA protein, a chimeric protein (designated m2/m1) containin

65 f the Niemann-Pick disease type C-1a (NPC1a) protein, a cholesterol transporter, in germ cell migrati

66 t concentration for assessing performance of protein A chromatography resin during purification of mo

67 sk of homodimer contamination using a single Protein A chromatography step.

68 onoclonal antibody (mAb) purification during Protein A chromatography.

69 est increases in concentration of C-reactive protein, a circulating marker of inflammation, have been

70 antibodies targeting hMPV is the fusion (F) protein, a class I viral fusion protein mediating virus-

71 evealed that the highly surface-expressed M1 protein, a classical GAS virulence factor, was required

72 Biochemical analysis of the encoded proteins, a cobalamin (Cbl)-dependent S-adenosylmethioni

73 IgG, and detected 0.02-0.1 g/L human IgG in protein A column breakthrough at a flow velocity of 80 c

74 n IgG1 monoclonal antibody (mAb) purified by Protein A column elution, cation exchange chromatography

75 first depleting the sample of antibody on a protein A column, then specifically digesting HCPs while

76 Despite the variable nature of this protein, a common major histocompatibility complex class

77 The U2 SF3B1 protein, a common mutational target in haematopoietic ca

78 tes hypoxia responses by demethylating RACK1 protein, a component of hypoxia-inducible factor (HIF) u

79 een Hairless and Metastasis-associated (MTA) protein, a component of the NuRD complex.

80 body-named mAb-EspB-B7-that targets the EspB protein, a component within the bacterial type 3 secreti

81 ibition, and immunoprecipitation of the AGO1 protein--a component of the microRNA induced silencing c

82 id surfactants, including phospholipids, and proteins, a composition similar to pulmonary surfactants

83 % of bacterial proteomes consist of membrane proteins, a comprehensive understanding of their influen

84 thickness, cell infiltration, and surfactant protein A concentration in bronchoalveolar lavage fluid.

85 ield; p < 0.0001), and normalized surfactant protein A concentration was higher with flow-controlled

86 d to the accumulation of misfolded secretory proteins, a condition referred to as ER stress.

87 Suppressor-of-cytokine-2 (SOCS2) protein, a conserved program transcript, is expressed by

88 Serine/arginine-rich (SR) and SR-like proteins, a conserved family of RNA binding proteins acr

89 Both SARS-CoV-2 spike protein (S-protein), a critical element of the viral entry to the h

90 he mitochondrial single-stranded DNA-binding protein, a crucial protein involved in mtDNA replication

91 Although well-studied cold-shock protein A (CspA) family members are induced and function

92 iously unknown and cell cycle-regulated FlmG protein, a defining member of a new class of cytoplasmic

93 for the detection of non-structural 1 (NS1) protein, a dengue biomarker.

94 olves the histone variant CENP-A (centromere protein A), deposited by its chaperone, HJURP (Holliday

95 of a test protein to a long-lived reference protein, a dihydrofolate reductase (DHFR).

96 DNA-processing protein A (DprA) regulates the exit of pneumococcus from

97 were able to detect 27% to 173% more HCPs in protein A elution pools of five different antibodies and

98 contaminating parental mAbs by differential protein A elution starting from either a) purified paren

99 the nonfimbrial extracellular matrix binding protein A (EmaA), as observed by electron microscopy.

100 mportantly, expression of adipose FA binding protein (A-FABP) in macrophages facilitated metabolism o

101 rexpression of the human antiapoptotic Mcl-1 protein, a factor upregulated in AMs from patients at in

102 e show that PEs in serine-arginine-rich (SR) proteins, a family of 14 essential SFs, are differential

103 Previously we identified Lam/GramD1 proteins, a family of endoplasmic reticulum membrane pro

104 The 14-3-3 proteins, a family of highly conserved scaffolding prote

105 oteins (SRRPs), here named fibril-associated protein A (FapA), FapB, and FapC, and that each SRRP for

106 ng the 5-sided box-like shape of Rme2 reader proteins, a feature that has been hypothesized to impart

107 hnological production of small molecules and proteins, a field heavily relying on B. subtilis secreti

108 ectors (eg, alpha-toxin [hla] and Fn binding protein A [fnbA]), MgrA binding to fnbA promoter, and th

109 e SaeRS-modulated factor fibronectin-binding protein A (FnBPA) also contributed to the fermentative b

110 found that the S. aureus fibronectin binding protein A (FnBPA) is required for normal biofilm develop

111 nchored proteins such as fibronectin-binding protein A (FnBPA) that bind to host ligands (e.g. fibron

112 Fibronectin-binding protein A (FnBPA), a protein displayed on the outer surf

113 AB significantly altered the abundance of 76 proteins (a fold change >1.4, or <0.6, p-value <0.05) an

114 Unexpectedly, there is also evidence of egg protein-a food source generally reserved only for export

115 xameric coiled-coil bundle and an Fc-binding Protein A fragment, we generated the Hex nanocarrier tha

116 between alpha-syn and Pmel17 (premelanosomal protein), a functional amyloid that promotes melanogenes

117 The seven lipopolysaccharide transport (Lpt) proteins A-G move lipopolysaccharide from the inner to t

118 Antibodies were purified with protein A/G columns from nasal polyps (NP), matching pat

119 ploys neodymium magnetic sticks that capture protein A/G-coated paramagnetic beads bound to antibody-

120 The DEP domain containing 5 (DEPDC5) protein, a GATOR1 subunit, causes familial focal epileps

121 ty, triglycerides, liver enzymes, C-reactive protein, a genetic score representing insulin resistance

122 Rs were silanized and covalently modified by Protein-A (Glass/ZnO-NRs/Protein-A).

123 sitive strategy for the determination of tau protein, a hallmark of Alzheimer's disease (AD), involvi

124 Two of these proteins, a homolog of the adaptor protein 2 (AP-2) comp

125 Common to both viruses is the M2 protein, a homotetrameric transmembrane proton channel t

126 h formed by residues 106 to 145 of the prion protein, a hydrophobic and highly fibrillogenic disease-

127 rast, CYLD (cylindromatosis tumor-suppressor protein), a K63-specific deubiquitinase enriched in post

128 mRNA and subsequent decreases in ARGONAUTE6 protein, a key effector of RdDM.

129 ene, which results in overexpression of MDM2 protein, a key oncogenic process in DDLPS.

130 ic translation initiation factor 4E (EIF-4E) protein, a key regulator of gene translation and protein

131 flux, and of cAMP-responsive element-binding protein, a key transcription factor in hepatic regulatio

132 o leads to increased degradation of the Mfn2 protein, a key ubiquitylation target of Parkin on mitoch

133 pregulation of the programmed death ligand 1 protein-a key checkpoint molecule-in mregDCs is induced

134 f the stimulator of interferon genes (STING) protein-a key regulator of the innate immune response to

135 ucleocytoplasmic translocation of core clock proteins, a key step in circadian timekeeping, is not fu

136 ly, of the AMPA-receptor regulatory scaffold protein A-kinase anchoring protein (AKAP) 79/150.

137 ated T cells, affecting the abundance of Myc protein, a known regulator of ribosome biogenesis.

138 t KRAS have focused on inhibiting the mutant protein; a less explored approach involves targeting KRA

139 t application demonstrates the monitoring of protein A ligand density and foulant concentration for a

140 isation of both F-actin and actin regulatory proteins, a limitation we recently overcame for Toxoplas

141 d substrates and p97/VCP (valosin-containing protein), a major driver of ER-associated degradation (E

142 cted to APP (encoding amyloid beta precursor protein), a major player in Alzheimer's disease that is

143 tructural insights into the SARS-CoV-2 spike protein, a major determinant of transmissibility, and di

144 Prolyl hydroxylase domain (PHD)-2 protein, a major PHD in ECs, plays a critical role in in

145 the de-repression of thioredoxin-interacting protein, a major redox control molecule, and consequent

146 le the expression of glial fibrillary acidic protein, a marker for astrocytic activity, was elevated

147 ocal microscopy, we observed that this viral protein, a marker for viral replication complexes, local

148 2 diabetes and elevated levels of C-reactive protein, a marker of chronic inflammation.

149 s activates AKT/GSK3beta to stabilize Snail1 protein, a master regulator of epithelial-mesenchymal tr

150 turn enhance the stability of the PLETHORA2 protein, a master regulator of root stem cells.

151 Protein A* may elevate fitness by ensuring the product f

152 measuring the association of PTEN with MAGI proteins a mechanism for the induction of signalling by

153 Ethylene-responsive element binding protein, a member of the APETALA2/ethylene response fact

154 tors-the heteromeric macrophage growth locus protein A (MglA)-stringent starvation protein A (SspA) c

155 ated with antibody, followed by binding of a protein A-Micrococcal Nuclease (pA/MNase) fusion protein

156 he pentatricopeptide repeat domain 1 (PTCD1) protein, a mitochondrial leucine-specific tRNA binding p

157 IgG ELISA against trimeric SARS-CoV-2 spike protein, a muliplexed immunoassay, three live SARS-CoV-2

158 s (SYNV) is mediated by the viral matrix (M) protein, a multifunctional protein involved in transcrip

159 Although PBP1 is an essential protein, a mutant lacking PBP1 transpeptidase activity i

160 ng an I38T mutation in the polymerase acidic protein-a mutation that confers reduced susceptibility t

161 n (IFN)-inducible human myxovirus resistance protein A (MxA) associated with the endoplasmic reticulu

162 We investigated myxovirus resistance protein A (MxA), viperin, and tripartite-motif 21 (TRIM2

163 n (IFN)-inducible human myxovirus resistance protein A (MxA), which displays antiviral activity again

164 increased Sost mRNA(100-fold) and sclerostin protein, a negative regulator of bone formation(5000-fol

165 global conformational polymorphism of capsid proteins, a network formed by extended N arms, mortise-a

166 n factor/neuron-restrictive silencer factor) protein, a neuronal gene transcription repressor protein

167 , CXCL2, NFKBIZ, and TFRC, and release CXCL1 protein, a neutrophil chemoattractant.

168 ous domains outside the kinase region of the protein, a newly identified N-terminal domain that share

169 ically different nanoparticles, an exemplary protein, a noncovalent protein complex, a virus-like par

170 gnificant upregulation of claudin-1 mRNA and protein, a nonspecific claudin for blood vessels, and do

171 loop-helix (bHLH), Per-Arnt-Sim (PAS) domain protein, a novel type of hormone receptor.

172 oduce DESTINI (deep structural inference for proteins), a novel computational approach that combines

173 d FHL-1 was identified as neisserial surface protein A (NspA), which has previously been identified a

174 vity is particularly dependent on the EBV SM protein, a nuclear protein expressed early during lytic

175 n of XPA with DNA is a core function of this protein; a number of mutations in the DNA-binding domain

176 nding protein (MBP), N-utilisation substance protein A (NusA), human protein disulphide isomerase (PD

177 of the membrane domain of the Outer membrane protein A of Klebsiella pneumoniae (KpOmpA).

178 surface protein (Asp14), and outer membrane protein A (OmpA) are essential for optimal bacterial ent

179 rm the spontaneous folding of outer membrane protein A (OmpA) into preformed NDs.

180 Outer membrane protein A (OmpA) is a porin involved in Acinetobacter ba

181 l antibodies (MAbs) targeting outer membrane protein A (OmpA) of A. baumannii Five anti-OmpA MAbs wer

182 An anti-outer membrane protein A (OmpA) polyclonal antibody previously produced

183 ename BB0326 as periplasmic flagellar collar protein A or FlcA.

184 ein-3 (IGFBP-3), pregnancy-associated plasma protein A (PAPP-A2), IGF-II and IGFBP-5 in 838 children

185 or of the enzyme pregnancy-associated plasma protein-A (PAPP-A), which modulates IGF-I activity.

186 modulates this change is within the viral PA protein, a part of the virus polymerase gene that contri

187 It involves two proteins: a periplasmic one, MsrP, previously named YedY

188 We show key residues in outer capsid proteins, a pH-sensing histidine of a zinc finger within

189 rticular mRNAs to produce plasticity-related protein; a phenomenon exhibited during mGluR-mediated LT

190 r is composed of yellow and blue fluorescent proteins, a phosphopeptide binding domain, a MAPK substr

191 , food challenge (DBPCFC; <=500 mg of peanut protein), a positive skin-prick test (SPT) result (>=5 m

192 of CARM1 with post-synaptic density (PSD)-95 protein, a post-synaptic marker.

193 e-binding protein at the Jkappa site (RBP-J) protein, a potent OC inhibitor.

194 es were resistant to the human antiviral MxA protein, a prerequisite for zoonotic transmission and st

195 h functions to clear endogenous mannosylated proteins, a principle used to endow insulin analogs with

196 exes with peptides derived from internalized proteins, a process called cross-presentation.

197 oteasome system for selective degradation of proteins, a process vital to organismal fitness.

198 interacts with MYOSIN-RESEMBLING CHLOROPLAST PROTEIN, a proposed structural protein influential in st

199 ed by ALDH2) and Glu4Gly of BRCA1-associated protein (a protein encoded by BRAP).

200 ted that ataxia-telangiectasia mutated (ATM) protein, a protein kinase, is a direct target of miR-181

201 ondensates included the VSV nucleocapsid (N) protein, a protein previously shown to form liquid-like

202 The vaccinia virus (VACV) M1 ankyrin (ANK) protein, a protein with no previously ascribed function,

203 ts, can prevent isoprenylation of Rab-GTPase proteins, a protein family important for the regulation

204 duce three enhancements to CUT&RUN: A hybrid protein A-Protein G-MNase construct that expands antibod

205 RrCooJ was initially thought to be a unique protein, a proteome database search identified at least

206 (LOD) and the sensitivity range of anti-OTA/Protein-A/PSi immunosensors were estimated.

207 d by anti-OTA and BSA in this way a anti-OTA/Protein-A/PSi structure sensitive towards OTA was design

208 Interaction of OTA with anti-OTA/Protein-A/PSi surface resulted in the quenching of photo

209 free energy for the interaction of anti-OTA/Protein-A/PSi with OTA were calculated and analyzed usin

210 ein antigens, including pneumococcal surface protein A (PspA) and pneumolysin (Ply).

211 l culture harvest fluid without the need for Protein A purification or other sample preparations and

212 (+) channel tetramerization domain 5 (KCTD5) protein, a putative adaptor of cullin3 E3 ubiquitin liga

213 nificantly more cells express CD133 mRNA and protein, a putative stem cell marker, in allograft biops

214 division control protein 42 homolog (Cdc42) protein, a Ras superfamily GTPase, regulates cellular ac

215 dular design consisting of the fusion of two proteins: a recognition protein that binds a triggering

216 tion of ethionine instead of methionine into proteins, a reduction of histone-methylation, and ethyla

217 A 4D-LC/MS method (Protein-A-Reduction-RPLC-Digestion-RPLC/MS) was develope

218 rns at the reduced level, a 3D-LC/MS method (Protein-A-Reduction-RPLC-HILIC/MS) was also developed on

219 in p3 likely had changes in p12 (morphogenic protein), a region that was not polymorphic for the two

220 ew means of regulating the papillomavirus L2 proteins, a regulation that optimizes endocytic processi

221 e interaction of lipin 1beta with 14-3-3beta protein, a regulatory hub that facilitates the cytoplasm

222 outer surface protein C and decorin binding protein A, respectively, which are lipoproteins importan

223 tatic pairings from genetic screens of three proteins, a ribozyme and a protein interaction reveal 3D

224 ng for Neural retina-specific leucine zipper protein, a rod fate determinant during photoreceptor dev

225 tress-induced DNA damage markers replication protein A (RPA) and Ku.

226 gle-stranded DNA binding protein replication protein A (RPA) as a regulator of the deposition of newl

227 he subsequent recruitment of the replication protein A (RPA) complex to facilitate retrotransposition

228 Replication protein A (RPA) coordinates important DNA metabolic even

229 he ssDNA-binding protein complex replication protein A (RPA) in budding yeast (Saccharomyces cerevisi

230 CST resembles Replication Protein A (RPA) in that the two complexes harbor compara

231 hat the balance between RADX and Replication Protein A (RPA) is critical for DNA replication integrit

232 acts upon ssDNA bound by either replication protein A (RPA) or the recombinase Rad51.

233 gle-stranded DNA (ssDNA)-binding replication protein A (RPA) selectively restores XPF-ERCC1 endonucle

234 Replication protein A (RPA), a major eukaryotic ssDNA-binding protei

235 Here we show that replication protein A (RPA), an ssDNA-binding protein, interacts wit

236 created by A3A- colocalize with replication protein A (RPA), but not with A3A.

237 ing DNA is largely eliminated by replication protein A (RPA), likely because of the previously report

238 In the presence of replication protein A (RPA), MRN acts as a processivity factor for E

239 interacts with and ubiquitylates replication protein A (RPA), show profound defects in ICL repair.

240 Recent studies revealed that replication protein A (RPA), the major ssDNA-binding protein, is inv

241 Cell Nuclear Antigen (PCNA) and Replication Protein A (RPA), which are critical for DNA replication

242 (CENP-F), allowing ATR to engage replication protein A (RPA)-coated centromeric R loops.

243 interactions of human RAD52 with replication protein A (RPA)-coated ssDNA, and we monitored the fate

244 ded DNA (ssDNA) that is bound by replication protein A (RPA).

245 se/helicase Dna2, Top3-Rmi1, and replication protein A (RPA).

246 f all DNA metabolic processes is Replication Protein A (RPA).

247 tranded DNA binding heterotrimer replication protein A (RPA).

248 -like structure that is bound by replication protein A (RPA).

249 rotein [CRP], haptoglobin, and serum amyloid protein A [SAA]), inflammatory markers (matrix metallopr

250 ck Salivary Lectin Pathway Inhibitor (TSLPI) protein; a salivary gland protein that inhibits the func

251 The NIPPED-A protein, a scaffold for the SAGA and Tip60 histone modif

252 a binding motif for the quaking RNA binding protein, a sequence we show can significantly regulate m

253 To better understand the activity of this protein a series of mutants, targeted to the NADH co-fac

254 eta signaling pathway and alpha1-antitrypsin protein (a serine protease inhibitor) expression and dow

255 The Akt protein, a serine/threonine kinase, plays important role

256 MenB-FHbp (factor H binding protein), a serogroup B meningococcal (MenB) vaccine, wa

257 e partially controlled by the unessential A* protein, a shorter version of the essential A protein th

258 is especially advantageous for low-abundance proteins, a significant limitation of many multiplex MS

259 In contrast to globular proteins, a single protein sequence can aggregate into s

260 Salmonella invasion protein A (SipA) is a dual-function effector protein tha

261 uses it to complement its own nuclear export proteins (a site not targeted by current therapy), makin

262 . difficile is constructed mainly of S-layer protein A (SlpA), which is a key virulence factor and an

263 pability of surfactant-associated surfactant protein A (SP-A) and surfactant protein D (SP-D) to Mtb.

264 Surfactant protein A (SP-A) modulates host responses to infectious

265 Surfactant protein-A (SP-A) is an important mediator of pulmonary i

266 his protein family in particular, surfactant protein-A (SP-A).

267 ti-IgE omalizumab, antigen, and superantigen protein A (spA) by using the pertuzumab and trastuzumab

268 The staphylococcal protein A (spa) gene was sequenced for all isolates to d

269 irulence factor of S. aureus, staphylococcal protein A (SpA) in the presence of electroactive redox c

270 ptibility, biofilm formation, Staphylococcal protein A (spa) typing, SCCmec typing, and PCR-based ass

271 tions in transcription of alpha-toxin (hla), protein A (spa), and RNAIII, consistent with the hypothe

272 the abundant surface-exposed Staphylococcal protein A (SpA).

273 locus protein A (MglA)-stringent starvation protein A (SspA) complex and the DNA-binding protein pat

274 screened against three human galectin (hGal) proteins (a stable mutant of hGal1 (hGal-1), a C-termina

275 gosaccharides (HMOs) for four human galectin proteins, a stable mutant of hGal1 (hGal-1), a C-termina

276 a tissue-specific reduction of the IKAP/ELP1 protein, a subunit of the Elongator complex.

277 equence of the warthog and domestic pig RELA protein; a subunit of the NF-kappaB transcription factor

278 tronger structural similarity to Replication Protein A than the expected similarity to yeast Cdc13.

279 -seq utilizes a fusion of Tn5 transposase to Protein A that is targeted to chromatin by a specific an

280 cess to clarify wines removing heat unstable proteins, a theoretical study on the adsorption of three

281 metry data for chicken egg lysozyme, mutated Protein A, three wild-types of haloalkane dehalogenases,

282 by a specific antibody, which then tethers a protein A-Tn5 transposase fusion protein.

283 o-EM tomography mapping of the C terminus of protein A to the apical lobe, which correlates well with

284 Typically, they comprise two proteins, a toxin, and an antitoxin, encoded by adjacent

285 Tail tubular protein A (TTPA) is a structural tail protein of Klebsie

286 rylating and inactivating the retinoblastoma protein, a tumor suppressor that restrains G1- to S-phas

287 nce of specific antibodies against the GTF2b protein, a tumor-associate antigen (TAA) related to colo

288 phosphorylated and ubiquitinated replication protein A (ubq-pRPA), the latter of which is mediated by

289 r with other tumor biomarkers and C-reactive protein, a universal biomarker for infection and inflamm

290 rotein (CSA), CSB, or UV-stimulated scaffold protein A (UVSSA) homologs, whose orthologs are present

291 ide context, such as with the erythropoietin protein, a V3 polypeptide derived from HIV-1 gp120, or a

292 sicle-associated membrane protein-associated protein A (VAP-A).

293 ui is the surface bound virulence associated protein A (VapA).

294 of the proteoglycan versican and its linking protein, a vertebrate hyaluronan and proteoglycan link p

295 ional groups-carboxyl groups of Alb NPs, p19 protein, a viral protein that can bind and sequester sho

296 nant HSV-1 with a mutation in the gamma134.5 protein, a virulence factor, stimulates dendritic cell (

297 Protein A was covalently immobilized on the surface of P

298 the rBipA (recombinant Borrelia immunogenic protein A) Western blot.

299 ke domains, here we identify NopA (nucleolar protein A), which displays four regulator of chromosome

300 Labeling protein A with a His-tag that binds 5-nm Ni-nanogold all