ライフサイエンスコーパス: kDa

1 extrans of sizes ranging from 6 kDa to 2,000 kDa.

2 y associated with transport of molecules < 1 kDa), which are positioned by membrane remodeling GTPase

3 otein scaffolds characterized by small (1-10 kDa) size, stability, and versatility in drug-like roles

4 tin and fractioned to F1 (>10 kDa), F2 (3-10 kDa), and F3 (<3 kDa).

5 show that by increasing the PEG size from 10 kDa to 20 kDa, the electrical response upon binding of t

6 experimental scattering data on high MW (>10 kDa) PEO and the P(R(ee))'s crossover to the theoretical

7 on with pancreatin and fractioned to F1 (>10 kDa), F2 (3-10 kDa), and F3 (<3 kDa).

8 ), and interferon gamma inducible protein 10 kDa (IP-10) (53-fold) and an increase in interleukin-1 r

9 es the transcription of Pcp4l1 encoding a 10-kDa peptide, which inhibits the replication of multiple

10 to analyze the protein subunits (ca. 25-100 kDa) obtained after different levels of enzymatic digest

11 with peaks in both the 1-3 kDa and the >100 kDa size fractions.

12 BH could be reduced to mainly monomers (<100 kDa) after enzymatic digestion of nucleic acids, whereas

13 For small (<100 kDa) DNA-binding proteins, obtaining particle images wit

14 d linearization by materials larger than 100 kDa in the aged urine caused the observed transformation

15 We find that an ~100-kDa "mini" form of the ~800-kDa Nesprin-2 protein, which

16 ith a molecular weight of approximately 1000 kDa was found in all patient nasal lavage samples.

17 ase with molecular weight (MW) of 44 and 108 kDa.

18 We isolated an 11 kDa protein of the parasite cell wall and identified it

19 uld detect HCP with low molecular weight (11 kDa and 17 kDa) at a concentration as low as 1 ppm.

20 sults, in concert, indicate that the B19V 11-kDa protein interacts with cellular Grb2 to downregulate

21 While NS1 is essential, 11-kDa plays an enhancing role in viral DNA replication.

22 rminal peptides (TCPs), including a major 11-kDa fragment (TCP96), are produced through cleavage by h

23 udy, we confirmed the enhancement role of 11-kDa in viral DNA replication and elucidated the underlyi

24 ere, we elucidated a mechanism underlying 11-kDa protein-regulated B19V DNA replication.

25 A high-molecular-weight (HMW) isoform (110 kDa) that contains an additional large exon termed 4a wa

26 ctant and fractionate intact proteins (6-115 kDa).

27 decreases the size of the FAP label to ~8-12 kDa while preserving DiBs' unique properties: strong inc

28 s (>25 kDa) and could also work well for ~12 kDa as the lowest limit of molecular mass.

29 Ultrasonication of a 120 kDa BCOE copolymer mechanically remodels the polymer bac

30 The 120 kDa CTF was detected in the livers from humans and mice

31 outer membrane proteins (P28/OMP) and a 120-kDa surface protein, were also recognized as necessary f

32 latin solution in PLGA 75/25 acid capped (13 kDa Mw) dissolved in methylene chloride (DCM) was spray-

33 g peptides and proteins ranging from 1 to 14 kDa.

34 Compared with the 140-kDa N-terminal catalytic fragment of p261 (p261N), which

35 lysis of intact protein assemblies up to 147 kDa.

36 f the therapeutic antibody trastuzumab (~148 kDa), with a sequence coverage of 100% for light chains

37 A high molecular weight (148 kDa) PLGA at various concentrations was used to generate

38 Nanobodies are 12-15 kDa single-domain antibody fragments that can be deliver

39 minus and the small size of the nanobody (15 kDa) enable its oriented and tightly packed immobilizati

40 we identified a secreted glycoprotein of 15 kDa, designated as Ppal15kDa, using liquid chromatograph

41 lonal antibodies and their fragments (25-150 kDa) has been investigated using modern instrumentation

42 show that a 6 kDa affibody protein and a 150 kDa immunoglobulin-G antibody could be modified without

43 pically goes unresolved at masses above ~150 kDa.

44 re, by reducing the size of intact ADC (~150 kDa) to subfragments (~25 kDa), the identification of co

45 minant proteins (13, 17, 29, 50, 56, and 150 kDa).

46 d beta-gal, 465 kDa) and antibodies (ca. 150 kDa).

47 e and inter-strand organization within a 150-kDa oligomeric aggregate of the 42-residue variant of th

48 dies comprised of numerous copies of the 150-kDa ATI protein, which can provide stability and protect

49 does not apply to residues 11-24 in the 150-kDa oligomer.

50 omprised of numerous copies of the viral 150-kDa ATI protein.

51 extravasation of 0.58 kDa rhodamine and 153 kDa anti-VEGF monoclonal antibody (bevacizumab) upon IA

52 zes (i.e., molecular weights spanning 44-160 kDa).

53 low freezing rate caused appearance of a 160 kDa myosin-4 fragment in SDS-PAGE, further decreased wat

54 and protein complex ions ranging from 6-1600 kDa, exhibiting an average relative standard deviation (

55 rage sizes of 9.5, 22.8, 42.7, 82.0, and 165 kDa were compared.

56 Long-chain-conjugated Vi (165 kDa) induced a response in both wild-type and T cell-def

57 HCP with low molecular weight (11 kDa and 17 kDa) at a concentration as low as 1 ppm.

58 and Ehrlichia chaffeensis with the ompA, 17-kDa surface antigen gene, tsa56, msp2 (p44), and vlpt ge

59 crease DNA topoisomerase IIalpha protein 170 kDa expression levels in acquired resistance to etoposid

60 opoisomerase IIalpha protein (TOP2alpha) 170 kDa (TOP2alpha/170) is an important target for anticance

61 ormation of larger MW org-I compounds (12-18 kDa) in some samples.

62 A higher level of prolamines (15-18 kDa) in RB and DF-RB of PUSA1121 than PR111 was observed

63 nsively using PET is translocator protein 18 kDa (TSPO).

64 The translocator protein (18 kDa) (TSPO) is described as a biomarker for reactive gli

65 we measured the in vivo expression of the 18 kDa translocator protein (TSPO), an activated glial mark

66 emission tomography (PET) imaging of the 18 kDa translocator protein (TSPO), which is upregulated in

67 (NL-G-F) , and APPswe) together with 136 18-kDa translocator protein (TSPO) PET scans for microglial

68 Here, an 18-kDa IgE-reactive cyclophilin (Rhi o 2) was purified from

69 h-affinity complementation with LgBiT, an 18-kDa subunit derived from NanoLuc.

70 The translocator protein (TSPO), an 18-kDa transmembrane protein primarily found in the outer m

71 The 18-kDa translocator protein (TSPO) has been used in PET as

72 PET imaging of the 18-kDa translocator protein (TSPO) provides a biomarker for

73 enoxy-3-pyridinyl)acetamide) binds to the 18-kDa translocator protein (TSPO), a biomarker of glia.

74 Emission Tomography brain imaging of the 18-kDa translocator protein (TSPO), a microglial biomarker,

75 ind and prevent the aggregation of tOmpA (19 kDa) and OmpT (33 kDa).

76 , having an average molecular weight of 18.2 kDa and 3.6 nm in helical height, exhibits the highest a

77 combining a low molecular weight of about 2 kDa with an antibody-like binding specificity.

78 jejenum, but increased flux of 4, 10 and 20 kDa dextrans in T84 cells.

79 HA fragments with molecular weight (MW) <20 kDa.

80 ers and an extended mass-to-charge range (20 kDa m/z) and its performance capabilities and limits wer

81 by increasing the PEG size from 10 kDa to 20 kDa, the electrical response upon binding of tau improve

82 into a peptide profile ranging from 1 to 20 kDa.

83 With 20 kDa PEG, we demonstrate label-free tau detection in a wi

84 ineal) and a protein of approximately 80-200 kDa in the high molecular weight region.

85 the p53 monomer (~50 kDa) and tetramer (~200 kDa) were resolved to ~4.8 and ~7 angstrom, respectively

86 the H2B histone protein component of the 200-kDa nucleosome core particle (NCP) establish that methyl

87 s of two storage proteins - vicilin and a 21 kDa albumin.

88 cm(-2), the M(n) decreased from 93 kDa to 21 kDa, while samples not exposed to UVA light remained unc

89 CBX7)) whereas mCbx7 and hCBX7v3 encode a 22 kDa protein (p22(CBX7)).

90 tion 53 of the 191-amino-acid sequence of 22 kDa human GH (hGH) with serine (p.C53S).

91 ne encoding FKBP22 (FK506 Binding Protein 22 kDa) cause kyphoscoliotic Ehlers-Danlos Syndrome (kEDS).

92 NMR studies of the 220 kDa IsdH(N2N3):Hb complex reveal that it is dynamic, wit

93 ble enzyme active as an apparent trimer (220 kDa) composed of ~70 kDa monomers, with an optimum pH of

94 t protein size ladder ranging from 10 to 225 kDa, built from the same polypeptide blocks with no post

95 SNAP23 (synaptosome-associated protein of 23 kDa) deficiency blocks the activation of macroautophagy,

96 A 23-kDa IgE-reactive protein was identified as myosin light

97 isotopic resolution for pyruvate kinase (232 kDa) and beta-galactosidase (466 kDa), extending the lim

98 60 is obtained for pyruvate kinase (MW ~ 233 kDa); however, ion mobility resolution for bovine serum

99 ar mass of ~26 kDa (major component) and ~24 kDa (minor component).

100 Little is known about amisyn, a 24-kDa brain-enriched protein with a SNARE motif.

101 Nogo-A and observed exosomal release of a 24-kDa C-terminal Nogo-A fragment from cultured cells.

102 somal marker Alix, a Nogo-immunoreactive, 24-kDa protein is enriched in exosomes 2-fold after injury.

103 onal antibody, the authors found that the 24-kDa LAPTM4B isoform predominated in most, both healthy a

104 iometry, and domain interactions in the ~240 kDa BM3 dimeric complex.

105 Although sHSPs are 12-25 kDa polypeptides, most assemble into oligomers with >= 1

106 After M2 receptor stimulation, proNGF-B (25 kDa), which is involved in apoptotic processes, is stron

107 to 74% sequence coverage was obtained for 25 kDa antibody drug conjugate subunits in online LC-MS exp

108 f interchain disulfide bonds to generate ~25 kDa ADC subfragments, which are finally analyzed by LC-H

109 ful approach for RPLC of large proteins (>25 kDa) and could also work well for ~12 kDa as the lowest

110 SNAP25 (synaptosome-associated protein of 25 kDa) is mediated by a subset of Golgi zinc finger DHHC-t

111 metry, often focusing on the analysis of ~25 kDa protein subunits, offers the potential for complete

112 mAb by digesting the product into small ~25 kDa fragments, followed by an on-line peptide mapping an

113 f intact ADC (~150 kDa) to subfragments (~25 kDa), the identification of conjugated payload and its m

114 omatography (RPLC) column reduction, the ~25 kDa proteolytic fragments were analyzed using hydrophili

115 efficiently digested with CG generating a 25-kDa protein fragment, originating from the densely glyco

116 The 25-kDa fragment was present in the SF from OA patients, and

117 s (RSV) RNA polymerase, constituted of a 250 kDa large (L) protein and tetrameric phosphoprotein (P),

118 the densely glycosylated mucin domain (~250 kDa).

119 e (RdRP) resides within an approximately 250-kDa large protein (L), along with unconventional mRNA ca

120 Full-length 250-kDa L protein was expressed using a baculovirus expressi

121 The ~250-kDa L possesses all enzymatic activities necessary for i

122 dy with a molecular mass of approximately 26 kDa that inhibits VEGF-A.

123 ments with an apparent molecular mass of ~26 kDa (major component) and ~24 kDa (minor component).

124 alphaB-crystallin (HSPB5) and heat-shock 27-kDa protein (Hsp27, HSPB1) during amyloid formation by a

125 k we annotate 16 example proteins (up to 272 kDa) by de novo peptide sequencing and illustrate the ad

126 an apparent limiting molecular weight of 28 kDa.

127 ease the non-collagenous (NC) 1 domain, a 28-kDa peptide, designated NC1-peptide, from the C-terminal

128 munodominant membrane proteins, i.e., two 28-kDa outer membrane proteins (P28/OMP) and a 120-kDa surf

129 80% were achieved for carbonic anhydrase (29 kDa), 50% for aldolase (39 kDa), 46% for enolase (46 kDa

130 , such cleavage is regulated by the novel 29-kDa chaperone of the ER, ERp29.

131 trum using only a single polymer (M(n) = 290 kDa) by altering the initial emulsification conditions.

132 odal distribution with peaks in both the 1-3 kDa and the >100 kDa size fractions.

133 )= 350/450 nm) are present mostly in the 1-3 kDa size range, while peak-T associated fluorophores (E(

134 ly fused to an N-terminal HiBiT peptide (1.3 kDa), which produces bright luminescence upon high-affin

135 y folded ribonuclease inhibitor; R17, a 13.3 kDa system possessing folded and unfolded forms under sl

136 Mass spectrometry analysis identified a 3 kDa peptide, Hld (delta-toxin), present in GLP-1 positiv

137 -15) was identified in the small peptide (<3 kDa) fraction of the water extract of tempeh using LC-MS

138 d to F1 (>10 kDa), F2 (3-10 kDa), and F3 (<3 kDa).

139 The WPC hydrolysate and a permeate <=3 kDa were characterized by SDS-page, RP-HPLC and MALDI-TO

140 under normoxia and anoxia is greater than 3 kDa in size and is heat-stable.

141 The 3 kDa SdhF forms a single transmembrane helix and this hel

142 up level of analysis (fragments of ca. 25-30 kDa).

143 in the generation and nuclear import of a 30 kDa fragment comprising most of L1's C-terminal, intrace

144 mers, and molecular weights between 1 and 30 kDa can be targeted simply by altering the stoichiometry

145 , but in the case of high mass proteins (>30 kDa) the spectra are congested with overlapping isotope

146 roteins including the platelet-inhibitory 30 kDa family.

147 bly begins with the oxidative folding of ~30-kDa C-terminal propeptide (C-Pro) domains.

148 r non-reducing conditions and resolve at 300 kDa.

149 n crystalline GB1 and then applied to a >300 kDa precipitated complex of GB1 with full length human i

150 Full length lubricin (~300 kDa), was efficiently digested with CG generating a 25-k

151 The 300-kDa ClpP1P2 protease from Mycobacterium tuberculosis col

152 rPfs47 bound to a single 31-kDa band and the identity of this protein was determined

153 The functional ~310 kDa ectodomain of VAR2CSA is a multidomain protein that

154 ELMOD2 is a ~32 kDa protein first purified by its GTPase-activating prot

155 ine- and cAMP-regulated phosphoprotein of 32 kDa (DARPP32) or tyrosine hydroxylase (TH) in tissue sec

156 opamine and cAMP regulated phosphoprotein 32 kDa (DARPP-32) also known as phosphoprotein phosphatase-

157 ession pattern for two isoforms of 36 and 33 kDa.

158 e aggregation of tOmpA (19 kDa) and OmpT (33 kDa).

159 e noncovalent complexes up to pentamers (332 kDa) destroyed in FAIMS and not detected without it.

160 otein complex systems ranging from 53 to 336 kDa.

161 The 35 kDa OCP is structurally and functionally modular, consis

162 eptides with molecular weights from 12 to 35 kDa, with possible bioactivity, were identified by elect

163 ponent of the filaments is a glycosylated 35-kDa TSPV1 protein (TSPV1 GP24).

164 e 4B (LAPTM4B) have mainly focused on the 35-kDa isoform and its association with poor prognosis in c

165 evealed that mCbx7v1 and hCBX7v1 encode a 36 kDa protein (p36(CBX7)) whereas mCbx7 and hCBX7v3 encode

166 pid storage in ccRCC cells that had a low 36-kDa AnxA3 expression and 36/33 ratio.

167 These data suggest that 36-kDa AnxA3 negatively modulates the response to adipogeni

168 The 36-kDa AnxA3 silencing in ccRCC cells increased lipid stora

169 Here we describe a ~ 360 kDa ribosome-associated complex comprising the core Sec6

170 lied to protein complexes ranging from a 365 kDa CRISPR-Cas Csy ribonucleoprotein hetero-decamer, a 8

171 PAGE profiles, with bands close to 20 and 37 kDa.

172 SDS-PAGE, so too are detergent-insoluble, 37 kDa fragments of tau(9).

173 n had only peaks corresponding to 580 and 38 kDa.

174 responding to molecular weight lower than 38 kDa were noticed, while non-hydrolysed arabinoxylan had

175 VPS34 complex II (VPS34CII) is a 386-kDa assembly of the lipid kinase subunit VPS34 and three

176 nic anhydrase (29 kDa), 50% for aldolase (39 kDa), 46% for enolase (46 kDa), and 27% for glutamate de

177 Here, ~39 kDa class IV chitinase (HrCHI4) was purified from seabuc

178 reveal that main fractions of API (66.2-14.4 kDa) were migrated to oil-water interface for emulsion s

179 (~days) degrades the molecular weight to 4.4 kDa, > 10x smaller than control polymers in which lacton

180 DXR treatment increased flux of 4 kDa dextrans in mouse jejenum, but increased flux of 4,

181 en strain open reading frame (ORF) as a 17.4-kDa protein.

182 in vivo and ex vivo colon permeability to 4-kDa fluorescently labeled dextran and reduced ex vivo co

183 ical resistance [TEER] and permeability to 4-kDa fluorescently labeled dextran or 70-kDa rhodamine B-

184 en applied the workflow to characterize a 40 kDa 8-arm polyethylene glycol (PEG) functionalized with

185 o various hydrophilic solutes as large as 40 kDa, in contrast to synthetic giant unilamellar vesicles

186 d SAM-bound SAM-IV riboswitches (119-nt, ~40 kDa) to 3.7 angstrom and 4.1 angstrom resolution, respec

187 rylation of proline-rich Akt substrate of 40 kDa (PRAS40), an intrinsic inhibitory component of mTORC

188 channels is unclear and could involve the 40 kDa mitochondrial Ca(2+) uniporter (MCU) channel or the

189 se) to polyethylene glycol (PEG) of 20 to 40 kDa was previously shown to prolong the residence time o

190 methods caused increased extravasation of 40-kDa dextran from capillaries and postcapillary venules b

191 Analysis involved assessing 43 kDa Tar-DNA binding protein (TDP-43) accumulation in bra

192 rubiquitylated TAR DNA-binding protein of 43 kDa (TDP-43) in the central nervous system characterizes

193 transactive response DNA binding protein 43 kDa (TDP-43) accumulation.

194 e accumulation of TAR DNA-binding protein 43 kDa (TDP-43) proteinopathy, and the haplotype's large-sc

195 A-binding protein TAR DNA-binding protein 43 kDa (TDP-43).

196 reactive intermediate deiminase A (RidA, 43 kDa) were detected.

197 The 43 kDa subunit of the chloroplast signal recognition partic

198 ulation of medium to large proteins (HRP, 44 kDa and beta-gal, 465 kDa) and antibodies (ca. 150 kDa).

199 We describe the structure of this 450 kDa complex, interactions between its components, and th

200 % for aldolase (39 kDa), 46% for enolase (46 kDa), and 27% for glutamate dehydrogenase (56 kDa), and

201 arge proteins (HRP, 44 kDa and beta-gal, 465 kDa) and antibodies (ca. 150 kDa).

202 kinase (232 kDa) and beta-galactosidase (466 kDa), extending the limits of isotopic resolution for hi

203 hobicities and ranging in mass from 2 to 470 kDa.

204 his was associated with an induction of a 48-kDa active beta-catenin with a preserved hypophosphoryla

205 DCLK1 downregulation inhibited 48-kDa beta-catenin expression.

206 me inhibitor bortezomib did not block the 48-kDa beta-catenin, instead, caused a threefold accumulati

207 iparum CQ-resistance transporter PfCRT, a 49-kDa member of the drug/metabolite transporter superfamil

208 11-fold decrease in molecular weight to 2.5 kDa.

209 ith a low molecular weight (MW) range (0.5-5 kDa) in all soils and a slower (20-40 h) time-dependent

210 through papain hydrolysis and followed by 5 kDa membrane filtration.

211 H was fractionated into <1, 1-3, 3-5, and >5 kDa peptides by membrane ultrafiltration.

212 E6 increased ~5 kDa during maturation, becoming reactive with both TL an

213 ttaching methoxypolyethylene glycol (mPEG, 5 kDa).

214 8 significantly reduced levels of ~55 and 50 kDa forms of the tau protein without significant alterat

215 ly for large proteins (molecular weight > 50 kDa), which exhibit an average bioavailability of 1% to

216 supramolecular prisms (molecular weight >50 kDa) with tetratopic pyridinyl subunits serving differen

217 roscopy, structures for the p53 monomer (~50 kDa) and tetramer (~200 kDa) were resolved to ~4.8 and ~

218 designed that irreversibly bound a single 50 kDa cellular protein, identified by mass spectrometry as

219 l-length Dicer was undetectable; only an ~50-kDa fragment appeared in Western blots.

220 gether with varying amounts of ~170- and ~50-kDa Dicer fragments.

221 This massive (>500 kDa) protein has an N-terminal AAA (ATPase associated wi

222 ecomes overactive when associated with a 500-kDa multiprotein complex, as compared with the negligibl

223 clusters FXII and HK into a higher-order 500-kDa ternary complex.

224 streptavidin, with a molecular weight of 52 kDa, from 11,000 particles.

225 Da), and 27% for glutamate dehydrogenase (56 kDa), and up to 74% sequence coverage was obtained for 2

226 four proteins ranging in size from 29 to 56 kDa.

227 he most efficient technique for obtaining 57 kDa chenopodin isolate with higher processing capacity,

228 rved tongue region of the PHY domain of a 57-kDa photosensory module of Deinococcus radiodurans phyto

229 omic structures of the ectodomains of the 57-kDa spike protein VP5 from two related HRPVs revealing a

230 the structural description of the entire 575 kDa Y complex from one species.

231 ravital microscopy the extravasation of 0.58 kDa rhodamine and 153 kDa anti-VEGF monoclonal antibody

232 ucture reveals the intricate fold of the 584 kDa protein, comprising an N-terminal stalk, a dynein-li

233 (ee)) for low molecular weight (MW: 0.22-2.6 kDa) dilute PEO chains.

234 Additionally, we show that a 6 kDa affibody protein and a 150 kDa immunoglobulin-G anti

235 otides, and dextrans of sizes ranging from 6 kDa to 2,000 kDa.

236 and virulence of M. tuberculosis ESAT-6, a 6-kDa-secreted protein of region of difference 1, is known

237 ns (RNPs), composed of the ring-shaped Ro 60-kDa (Ro60) protein and noncoding RNAs called Y RNAs, are

238 allowing passage of proteins of at least 62 kDa throughout papillar tissue.

239 ITs reach these cells, we studied SS1P, a 63-kDa RIT that targets mesothelin-expressing tumors and ha

240 within a dataset for proteins as small as 64 kDa.

241 Intact tetrameric hemoglobin (64 kDa) and trimeric reactive intermediate deiminase A (Rid

242 ssign the side-chain methyl groups of the 64-kDa Mre11 nuclease and capping domains, which allowed us

243 heterogeneity, with multiple isoforms (45-65 kDa) generated by alternative splicing.

244 raphy, the enzyme presented approximately 65 kDa, and LC-MS/MS allowed the identification of a polyur

245 the Golgi reassembly stacking protein of 65 kDa (GRASP65) has been implicated in both Golgi stacking

246 20 nm and molecular weights greater than 65 kDa, through a combination of intra- and intermolecular

247 sk stratification and CMI specific to the 65 kDa phosphoprotein (pp65) CMV antigen were investigated.

248 l molecules, peptides, and proteins up to 66 kDa on three commercially available mass spectrometers f

249 We identified decreased expression of 37/67 kDa laminin receptor (LAMR), which binds laminin-beta1,

250 t protein (GFP) in cells that contain the 67 kDa isoform of glutamic acid decarboxylase (GAD67-GFP),

251 resolution for bovine serum albumin (MW ~ 68 kDa) is less than ~20, which arises from sample impuriti

252 DJ-1, a 20.7 kDa protein, is overexpressed in people who have bladder

253 charged Au(144) (SC(4) H(9) )(60) ions (33.7 kDa), which opens up exciting opportunities for the stru

254 marked contrast, short-chain Vi (9.5 to 42.7 kDa) conjugates induced a response in wild-type mice but

255 ivity of the BPP fraction was due to the 5-7 kDa amino-terminal fragment of Ara h 1.

256 odes 539 amino acids (molecular mass of 62.7 kDa); dsRNA2 dsRNA is 1,524 bp in length with an ORF tha

257 lectrophoresis with a molecular weight of ~7 kDa (7kDa-Abeta), is particularly toxic; however, the na

258 meric carrier was conjugated with a small (7 kDa) HER2-binding affibody peptide to produce a panel of

259 PI revealed major bands ranging from 50 to 7 kDa.

260 ibril formed in vitro spontaneously by a 9.7-kDa unglycosylated fragment of the human prion protein.

261 Cleaved CDCP1 isoform (70 kDa) was expressed to a varying degree in all samples bu

262 increased arginine methylation of HSPs of 70 kDa (HSP70); this methylation enhanced HSP70 binding and

263 Heat shock proteins of 70 kDa (Hsp70s) are ubiquitous and highly conserved molecul

264 eficiency in a zeta-associated protein of 70 kDa (ZAP-70)-deficient murine model.

265 an apparent trimer (220 kDa) composed of ~70 kDa monomers, with an optimum pH of 7.8.

266 The 70 kDa heat shock protein (HSP70) family of chaperones are

267 les but had no effect on extravasation of 70-kDa dextran or albumin.

268 to 4-kDa fluorescently labeled dextran or 70-kDa rhodamine B-dextran) and macrophage polarization.

269 es, indicated by electrical resistance or 70-kDa RITC-dextran permeability in primary endothelial cel

270 ng that requires extracellular heat shock 70-kDa protein (HSP70).

271 ntaining protein/p97 (VCP) and heat shock 70-kDa protein 8 (HSPA8).

272 RNAs with an additional protein mass of ~700 kDa on the small subunit, while the large subunit lacks

273 quantitative identification of HSP70 and 71 kDa heat shock cognate (HSC70) clients using a ubiquitin

274 /delta, cofilin-1, and heat shock cognate 71 kDa protein as novel biomarkers for poor neurologic outc

275 /delta, cofilin-1, and heat shock cognate 71 kDa protein into a multimarker predictive model along wi

276 nding ranging from molecular weight of 11-75 kDa.

277 ring complexes (MTCs) are large (250 to >750 kDa), conserved macromolecular machines that are essenti

278 es evidence that cancer cells overexpress 78-kDa glucose-regulated protein (GRP78) as a mechanism to

279 The 78-kDa glucose-regulated protein (GRP78), an endoplasmic re

280 osities and also to compare with a 64 and 79 kDa at a single, high concentration.

281 cken in the inactive dimeric state (about 80 kDa in size), as well as cGAMP-bound chicken STING in bo

282 PfGARP is a parasite antigen of 80 kDa that is expressed on the exofacial surface of erythr

283 encoding relatively large FGF proteins (~80 kDa).

284 ts sieving of proteins ranging from 20 to 80 kDa.

285 Csy ribonucleoprotein hetero-decamer, a 800 kDa GroEL homo-tetradecamer in its apo-form or loaded wi

286 ind that an ~100-kDa "mini" form of the ~800-kDa Nesprin-2 protein, which binds dynein and kinesin, i

287 in complexes ranging in size from 8.6 to 810 kDa are reported.

288 w MW beta-glucan (average > 1000, 524 and 82 kDa respectively) with 3 consequent meals on oat-derived

289 in a 6.5- angstrom structure of BurrH, an 82-kDa DNA-binding protein whose helical pseudosymmetry pre

290 process is demonstrated on proteins up to 83 kDa in size and can be conveniently carried out in water

291 odes 434 amino acids (molecular mass of 46.9 kDa).

292 NA ends, raising the question of how the ~90 kDa TOP1 protein is processed upstream of TDP1.

293 The molecular chaperone 90-kDa heat-shock protein (Hsp90) assists the late-stage fo

294 terized groups of client proteins for the 90-kDa heat shock protein (HSP90), a molecular chaperone th

295 lock copolymer with a molecular weight of 92 kDa was synthesized to conjugate with doxorubicin (DOX).

296 t 250 muW cm(-2), the M(n) decreased from 93 kDa to 21 kDa, while samples not exposed to UVA light re

297 up originally found and cloned cDNA for a 98-kDa type 1 transmembrane glycoprotein of unknown functio

298 ivo fluorescence imaging revealed that PEG30 kDa-conjugated rhDNase (PEG30-rhDNase) was retained in m

299 We quantify repeated reactions between sub-kDa thiolated species in real time and at concentrations

300 Trace analysis of sub-kDa reactants and products is obfuscated by labels, howe