ライフサイエンスコーパス: isoelectric point

1 key properties (aromaticity, hydropathy and isoelectric point).

2 ibuted over these sites can provide the same isoelectric point.

3 roteins was a substantially higher predicted isoelectric point.

4 separate bacteria by their surface charge or isoelectric point.

5 ntration and separation according to peptide isoelectric point.

6 eir primary structure, molecular weight, and isoelectric point.

7 e interfacial layer also increased below the isoelectric point.

8 culated molecular mass of 33 kDa and a basic isoelectric point.

9 acid of proteins, which causes the change in isoelectric point.

10 fer energy, (iv) beta turn frequency and (v) isoelectric point.

11 same monoisotopic masses but with differing isoelectric points.

12 tGPAT(-/-) liver mitochondria have different isoelectric points.

13 isoforms of AUF1 which migrated at multiple isoelectric points.

14 different phosphorylated forms with distinct isoelectric points.

15 progressively greater pH values exceed their isoelectric points.

16 hip between their order of elution and their isoelectric points.

17 having a wide range of molecular weights and isoelectric points.

18 forms, several of which differ only in their isoelectric points.

19 agnitude and separated on the basis of their isoelectric points.

20 , exist as two distinct forms with different isoelectric points.

21 e similar in deduced mass (11.4-12.2 kD) and isoelectric point (4.1-4.3).

22 Each is a basic glycoprotein (isoelectric point = 9.1-9.5) of approximately 28 kD and

23 Here we show that around the isoelectric point a different generic form of aggregatio

24 (TREN)-ferritin adducts include an increased isoelectric point, a shift in the Cr(TREN) UV/vis spectr

25 remains bound to a peptide of 17 kDa with an isoelectric point above 9, demonstrating that His(176) i

26 hat contains the predicted molecular weight, isoelectric point, accession number, and putative functi

27 ry peak of expression of genes encoding high-isoelectric point alpha-amylase during grain development

28 s association is of sufficient power to make isoelectric point an excellent predictor of spliceosomal

29 lex peptide mixtures on the basis of peptide isoelectric point and (2) the introduction of peptide pI

30 consistent relationship was observed between isoelectric point and ACE inhibition.

31 ptide mixtures based on their differences in isoelectric point and hydrophobicity but also eliminates

32 this partitioning can be predicted by their isoelectric point and hydrophobicity.

33 liana were purified based on native mass and isoelectric point and identified by mass spectrometry.

34 ne amelogenin ("rM179") was minimum near its isoelectric point and increased rapidly below and above,

35 Due to its high isoelectric point and its disordered structure, we propo

36 de gel electrophoresis (2-D PAGE) in similar isoelectric point and molecular mass ranges as studied b

37 ing of species-specific proteins, as well as isoelectric point and molecular weight sorting to facili

38 curated proteomes differ strongly in average isoelectric point and protein size, as well as transmemb

39 easing pH and strong agglomeration above the isoelectric point and settling in the presence of Ca.

40 l transit peptide sequences greatly affected isoelectric point and size distribution.

41 By taking into account the Ab isoelectric point and the net charge of the composite su

42 emonstrated with amidation to modify protein isoelectric point and through derivatization with quater

43 ite a difference of 5 pH units between their isoelectric points and despite displaying only 16% seque

44 ncated 25- to 27-kDa isoforms having various isoelectric points and electrophoretic mobilities were e

45 utralization breadth have relatively neutral isoelectric points and preferentially bind to envelope m

46 are consistently distinguished by more basic isoelectric points and specificity for epitopes shared b

47 ire devices can be used to determine rapidly isoelectric points and variations in receptor-virus bind

48 erms or motifs, or by limiting the range for isoelectric points and/or molecular weights and links to

49 structural equivalence with respect to mass, isoelectric point, and recognition by conformation-sensi

50 imilar to synaptopodin in terms of its size, isoelectric point, and sequence although synaptopodin is

51 tion of the high net charge, due to the high isoelectric point, and the relatively low intrinsic hydr

52 On the basis of molecular weights, isoelectric points, and Western immunoblots, the methyl-

53 explains the surprising observation that the isoelectric point appeared at approximately 3.0 when HCl

54 ypeptides with apparent molecular weight and isoelectric points appropriate for caveolin.

55 anogen bromide fragmentation, and calculated isoelectric point are all consistent with those determin

56 emistry and proteomics methods depend on the isoelectric point as a principal feature for protein and

57 nts of ~80- and ~100-kDa forms with the same isoelectric point as the 60-kDa species.

58 se of solution pH from 5.0 to 6.0 toward the isoelectric point as well as more rapid dissociation of

59 determined as 27648 Da and 19606 Da and the isoelectric points as 4.8 and 3.5, respectively.

60 Subsequently, we added estimates of protein isoelectric points as a feature to ANNs that classify sp

61 irmed by the pH at the anode being below the isoelectric point, as ascertained by pH titration.

62 th information on predicted protein size and isoelectric point, as well as any repeats, motifs or dom

63 beta-Filagenin has a calculated isoelectric point at 10.61 and a high percentage of arom

64 er Vsp and OspC proteins by a high predicted isoelectric point at 9.39.

65 mass of 48 kDa, a pH optimum of 7.0, and an isoelectric point at pH 4.4.

66 A mass spectrometry (MS)-compatible, isoelectric point-based separation method for removal of

67 ht of 26000 and an experimentally determined isoelectric point between 7.5 and 8.0.

68 ased it at pH > 7.5, indicating an effective isoelectric point between these limits.

69 This latter product migrated with an isoelectric point between those of antigen 85A and 85C b

70 a 26-kDa polypeptide that differed in their isoelectric points between the C57BL/6J and the DBA/2J i

71 ent and is consistent with the difference in isoelectric points between the proteins.

72 Moreover, NTHi P5 has a high theoretical isoelectric point, calculated as 9.58, which is not in a

73 ne adjustment of the buffer pH, close to the isoelectric point, can be used to slow down the transloc

74 c system-for example protein, DNA or RNA-the isoelectric point-commonly referred to as the pI-can be

75 d is likely facilitated by its difference in isoelectric point compared to the other VP sequences ass

76 eptides provided much faster measurements of isoelectric points compared with conventional isoelectri

77 It was demonstrated that the optimum pH and isoelectric point could be quite different.

78 ted on the basis of close proximity of their isoelectric points: D. chrysanthemi, D. chrysanthemi bv.

79 The Protein Isoelectric Point database (PIP-DB) has collected and co

80 Very small differences in peptide isoelectric points (deltapI approximately 0.01) could be

81 assay was applied to several mAbs of varying isoelectric points, demonstrating the suitability of Nan

82 ch is not in agreement with the experimental isoelectric point, determined as 6.3-6.8, or with its pr

83 ain complementarity determining region (CDR) isoelectric points did not correlate with silencing acti

84 o proteins with low molecular weight and low isoelectric points, distinguished fresh fillets from fro

85 kDa, WGA-reactive glycoprotein with a basic isoelectric point, distinguishing it from the acidic gly

86 y of the sample protein is reduced above the isoelectric point due to the decreased electrostatic att

87 on electrostatic attraction between the low-isoelectric-point enzyme and the microstructure, fabrica

88 of each protein such as molecular weight and isoelectric point, experimentally determined properties

89 somes have unique features (e.g., very basic isoelectric points, expressing the mutated tumor antigen

90 gical properties of MTases: structural fold, isoelectric point, expression pattern and cellular local

91 We experimentally determined the isoelectric point for the individual subunits.

92 pproximately 8.5 was found correspond to the isoelectric point for the prepared sol-gel ODS coatings.

93 , we found inducible oligomers and shifts in isoelectric points for peroxiredoxin 1 (Prdx-1), Prdx-3,

94 ds; P22 Xis, 116 amino acids) and have basic isoelectric points (for P22 Xis, 9.42; for lambda Xis, 1

95 asic protein (MBP1) is an exceedingly basic (isoelectric point >11) 14-kDa protein, comprising the co

96 parameters, such as crosslinking density and isoelectric point, have been tuned in order to optimize

97 fold more "extreme" proteins (low mass, high isoelectric point, hydrophobic) than previous mitochondr

98 Rates were correlated with the mineral's isoelectric point (IEP) and reactive surface area.

99 embled hexadecanethiol films on gold show an isoelectric point (IEP) around pH 4.

100 edicted molecular weight, (ii) the predicted isoelectric point, (iii) the accession number, and (iv)

101 rrelation between protein migration time and isoelectric point in CIEF-ESI-MS.

102 and also the effectiveness of using peptide isoelectric point in conjunction with peptide match prob

103 resumably normosialylated based on a neutral isoelectric point) in other glomerular diseases as well.

104 ial dilatational rheology was highest at the isoelectric point, indicating the dominant role of the c

105 y extracting peptides, on the basis of their isoelectric points, into an immiscible organic phase fro

106 molecular weight of RGS18 is 27,610 and the isoelectric point is 8.63.

107 Protein separation by isoelectric point is a critical part of 2-D gel electrop

108 he overcharging of the complex away from its isoelectric point is caused by changes of the bulk struc

109 ring study of gammaII-crystallins near their isoelectric point is presented.

110 ature ZP3, with respect to both mol. wt. and isoelectric point, is partly a consequence of the N-link

111 aphid proteins were expressed as heritable, isoelectric point isoform pairs, one derived from each p

112 own by zeta-potential versus pH profiles and isoelectric point measurements.

113 t to purification yields, thermal stability, isoelectric point, molar absorption coefficient, and eff

114 o acids in different physicochemical groups, isoelectric point, molecular weight, and length of prote

115 istribution of protein properties, including isoelectric point, molecular weight, number of exons, In

116 Below the isoelectric point, molecules partitioning into the excit

117 cognized a Mr 98,000 wall peroxidase with an isoelectric point near 4.2, and mWP19 recognized a Mr 58

118 SPSQRRSTS(V/K)(A/S)RR, yielding a predicted isoelectric point of 12.2 for this protein.

119 -A, with a molecular mass of 69.4 kDa and an isoelectric point of 3.5 was purified from papaya latex.

120 l primary sequence of MARCKS with an overall isoelectric point of 4.2 yet a very basic PSD (overall c

121 The protein had an acidic isoelectric point of 4.2-4.6, and was shown by periodate

122 It has a molecular weight of 63,000 and an isoelectric point of 4.6, and its hemolytic activity is

123 e protein with a subunit Mr of 18,800 and an isoelectric point of 4.6.

124 codes a putative protein of 30.2 kDa with an isoelectric point of 4.69.

125 The putative CP27 protein has an isoelectric point of 4.75 and features a distinct helix-

126 The enzyme has an isoelectric point of 4.78 and pH and temperature optima

127 The acyltransferase possesses an isoelectric point of 4.8, a relative molecular mass arou

128 s an apparent molecular mass of 18 kD and an isoelectric point of 4.8.

129 kD (designated the B2 subunit) and a native isoelectric point of 4.8.

130 had a subunit molecular mass of 26 kD and an isoelectric point of 4.9.

131 The NMTase had an isoelectric point of 5.15 and was reversibly inhibited b

132 The LFS has an isoelectric point of 5.2.

133 a 116-amino acid peptide of 13.5 kDa with an isoelectric point of 5.3 (residues 6-121), and His(176)

134 as an apparent molecular weight of 46,500 an isoelectric point of 5.5, and its pH optimum lies betwee

135 e-polyacrylamide gel electrophoresis, and an isoelectric point of 5.5.

136 sis showed a prominent spot of 23 kDa and an isoelectric point of 5.7.

137 e-averaged molecular mass of 44.6 kDa and an isoelectric point of 5.9.

138 subunit molecular mass of 124,350 Da and an isoelectric point of 6.0.

139 -averaged molecular mass of 24.1 kDa, and an isoelectric point of 6.0.

140 a calculated molecular weight of 46.3 and an isoelectric point of 6.0.

141 -averaged molecular mass of 124.3 kDa and an isoelectric point of 6.5.

142 ic Ag had a mass of 22 kDa (SDS-PAGE) and an isoelectric point of 6.75.

143 encodes a protein of 72 kDa with a predicted isoelectric point of 6.85.

144 calculated molecular weight of 29 kDa and an isoelectric point of 6.86.

145 ing frame of 181 amino acids and predicts an isoelectric point of 7.27.

146 predicted molecular weight of 24,444 and an isoelectric point of 7.7 and lacked the ability to form

147 r mass of 70 kD, a pH optimum of 6.2, and an isoelectric point of 8.1.

148 gest known profilins, and it had a predicted isoelectric point of 8.27.

149 nd to have a molecular mass of 25 kDa and an isoelectric point of 8.4.

150 oxin had a molecular weight of 26,000 and an isoelectric point of 8.5.

151 otease IV has a molecular mass of 26 kDa, an isoelectric point of 8.70, and optimum enzymatic activit

152 e a relative molecular mass of 55 000 Da, an isoelectric point of 9, and one FAD per protein.

153 a 149-amino acid peptide of 16.8 kDa with an isoelectric point of 9.3 (residues 131-279).

154 ed 12 transmembrane helices and predicted an isoelectric point of 9.4, both of which are characterist

155 , a predicted molecular mass of 9,647 Da, an isoelectric point of 9.81, and 90% to 95% sequence ident

156 mL) was treated with ammonium sulfate at the isoelectric point of alpha-Cbtx, and the pellet was diss

157 ein expression but did induce changes in the isoelectric point of Bim(EL) and its reactivity with an

158 H 7 as bulk water), a value that matches the isoelectric point of bubbles and oil droplets in indepen

159 ubility was observed at pH 4, confirming the isoelectric point of coconut protein.

160 The isoelectric point of cytochrome cM is 5.6 (without the h

161 exhibited positive surface charge, since the isoelectric point of DOPC is ca. 4.

162 The isoelectric point of each quantified protein was calcula

163 s, TPT could change the molecular weight and isoelectric point of effector proteins, induce their met

164 O2 deprivation resulted in a decrease in the isoelectric point of eIF4E, consistent with additional p

165 The isoelectric point of hCE-2 was approximately 4.9.

166 The experimentally determined isoelectric point of KcsA tetramer was 6.5-7.5, substant

167 significant shift toward lower values of the isoelectric point of maghemite upon selenium(IV) uptake,

168 These procedures predict an isoelectric point of our active component of 6.5-7.0 and

169 ecific 50-kilodalton nuclear protein with an isoelectric point of pH 6.0 detected in 92% (59 of 64) o

170 n purified approximately 16,000-fold, has an isoelectric point of pH 6.1 and yields three catalytical

171 Results indicate an isoelectric point of pH 8.6 and a critical coagulation c

172 n-based nanocapsules are unstable around the isoelectric point of protein.

173 of the GPI-anchor to the molecular mass and isoelectric point of PrP quasispecies under two-dimensio

174 astase also reduced the size and changed the isoelectric point of the A(2) peptide, as determined by

175 At pH = 6.0, near the isoelectric point of the chemisorbed cysteine, these mem

176 The isoelectric point of the enzyme was approximately 5.

177 evices also allowed for determination of the isoelectric point of the minute amounts of proteins immo

178 on procedure based on the molecular size and isoelectric point of the photoradiolabeled binding prote

179 ble to aggregation at pH values close to the isoelectric point of the protein (pH 4 and 5), at high i

180 e in charge density on the bead surface, the isoelectric point of the protein then dominates the mobi

181 oint for folding and only slightly below the isoelectric point of the protein, both the single domain

182 At best, these reagents perturb the isoelectric point of the protein.

183 eripherin/rds and a concomitant shift in the isoelectric point of the protein.

184 The predicted molecular mass and isoelectric point of the pTombetagal 4-encoded mature pr

185 The predicted isoelectric point of the putative apyrase matches the va

186 Aggregates tend to form near the isoelectric point of the virus, under the influence of c

187 The calculated isoelectric point of this protein is approximately 5.7.

188 lution isoelectric focusing to determine the isoelectric point of Wnt3A protein in conditioned medium

189 oteins of 60 and 59 amino acids with similar isoelectric points of 4.75 and 3.94, respectively.

190 t of native Hs11S was about 150-300 kDa with isoelectric points of 5.0-5.3, composed by four monomers

191 164-165 amino acid proteins with calculated isoelectric points of 5.2.

192 of 42,358 and 40,279 Daltons and calculated isoelectric points of 6.3 and 6.7, respectively.

193 molecular weight of around 7.3 kDa, a basic isoelectric points of 8.5 and the presence of typical CX

194 ifications contribute to the measured acidic isoelectric points of Cx26 and Cx32, whereas their low m

195 ints of the homomeric channels bracketed the isoelectric points of heteromeric Cx26/Cx32 channels.

196 the first report of the determination of the isoelectric points of individual mitochondria by capilla

197 The isoelectric points of MSSA and MRSA were found to be the

198 In this study, size, zeta-potential, and the isoelectric points of nanoparticles of the recombinant f

199 embly that correlated with a decrease in the isoelectric points of NCs, suggesting that the basic nat

200 rus transmission-competent F2 genotypes, the isoelectric points of the Buchnera proteins did not matc

201 The isoelectric points of the gap junction proteins connexin

202 The isoelectric points of the homomeric channels bracketed t

203 ane proteins that give rise to the effective isoelectric points of the organelles.

204 t the variable amino terminus determined the isoelectric points of the TnT isoforms expressed, and th

205 at are in good agreement with the respective isoelectric points of Tim9 and Tim10 were determined.

206 A protein's isoelectric point or pI corresponds to the solution pH a

207 re stable, reproducibly displayed a shift in isoelectric point, or changed in relative abundance at s

208 eptides of both hydrolysates showed that low isoelectric point peptides had antioxidant activity; how

209 kD proteins (pI 5.8-6.4) and 50-kD proteins (isoelectric point pH 6.7-6.8 and 5.8-6.2).

210 usting the pH value of preparations close to isoelectric point (pH 4-5).

211 re unstable to flocculation near the protein isoelectric point (pH 5.0), at high ionic strength (>100

212 We describe a novel isoelectric point photoswitching phenomenon in both wild

213 It has a low isoelectric point (pI 1.1) and, therefore, tends to be n

214 at pH above (pH 7.5) and below (pH 2.5) the isoelectric point (pI approximately 5.3).

215 eting CD25 [anti-Tac(scFv)-PE38] lowered its isoelectric point (pI) and decreased its toxicity in mic

216 ranslational modifications (PTMs) on protein isoelectric point (pI) and molecular weight and displays

217 proteins was affected by differences in the isoelectric point (pI) and the ion exchange properties o

218 employs the use of accurate mass and peptide isoelectric point (pI) as identification criteria, and r

219 The isoelectric point (pI) cutoff in these extractions depen

220 f integrated microfluidic platforms for fast isoelectric point (pI) determinations via free-flow elec

221 Proteins having an isoelectric point (pI) difference of 0.004 are shown to

222 otoheterotrophic life style and a low median isoelectric point (pI) for all predicted proteins, sugge

223 of OPN, 1, 25-(OH)2D3 induces a shift in OPN isoelectric point (pI) from 4.6 to 5.1.

224 se/direct IAP binding protein with low pH of isoelectric point (pI) from the mitochondria, and the ac

225 Prefractionation based on the isoelectric point (pI) is particularly attractive becaus

226 ble minor structural protein (ORF3), with an isoelectric point (pI) of 10.0 and a calculated molecula

227 We have noted that the Fv of anti-Tac has an isoelectric point (pI) of 10.2.

228 The protein is atypically cationic with an isoelectric point (pI) of 10.5.

229 alculated molecular mass of 29.11 kDa and an isoelectric point (pI) of 5.44.

230 atelet Mpl as an 85 to 92 kD protein with an isoelectric point (pI) of 5.5.

231 heoretical molecular mass of 87.8 kDa and an isoelectric point (pi) of 8.20.

232 rameters in the Protein Data Bank (PDB), the isoelectric point (pI) of a protein has been explored as

233 The experimental amino acid composition and isoelectric point (pI) of Fap1 were similar to that pred

234 e apparent higher molecular weight and lower isoelectric point (pI) of Hu-recA1PI than pd-A1PI.

235 value of pH approximately one unit below the isoelectric point (pI) of the protein, at a concentratio

236 f the buffer is merely one pH unit below the isoelectric point (pI) of the recombinant proteins, most

237 Isoelectric point (pI) values have long been a standard

238 contribution was ruled out by comparing the isoelectric point (pI) values to the adsorption of prote

239 ntibodies, to determine sCD44 concentration, isoelectric point (pI), and phosphorylation, respectivel

240 ome key parameters, such as applied voltage, isoelectric point (pI), bulk pH, and bulk conductivity,

241 Above the isoelectric point (pI), the individual protein molecules

242 A novel continuous-flow isoelectric point (pI)-based sorting technique has been

243 rystallins was associated with a decrease in isoelectric point (pI).

244 ous method for the estimation of the protein isoelectric point (pI).

245 and did not undergo charge inversion at its isoelectric point (pI=5.3) but remained anionic.

246 sses of ca. 61 kDa (unglycosylated) and high isoelectric points (pI 9.3-9.5).

247 hree fractions: one containing proteins with isoelectric points (pI values) higher than the pI of alb

248 lted in a cluster of ill-resolved peaks with isoelectric points (pI values) in the range 7.4 to 8.5.

249 n capabilities, using compounds with varying isoelectric points (pI) and pK(a) values over a range of

250 population was observed to exhibit distinct isoelectric points (pI) and, thus, distinct formal elect

251 wed differently charged 3C isoforms that had isoelectric points (pI) of 8.3 (55%) and 9.0 (45%), with

252 cIEF can also be used to determine the isoelectric points (pI) of antibody variants based on th

253 mn imaging detection (CIEF-WCID) method, the isoelectric points (pI) of complete intact polioviruses

254 ly discretized into fractions based on their isoelectric points (pI) without the use of carrier ampho

255 ion of acidic peptides (i.e., those with low isoelectric points (pI)) by matrix-assisted laser desorp

256 rogeneous organelles that likely have unique isoelectric points (pI), which are related to their surf

257 Analysis of hybrid CPs predicted that the isoelectric points (pI):charge value was 5.31:-2 for wil

258 ins (molecular mass [M(r)] 56 and 59 kDa and isoelectric point [pI] 5.2 and 5.3) in some, but not all

259 roteins in surface seawater exhibit alkaline isoelectric points (pIs of 8.10 and 8.37) and also acid

260 de mixtures based on the difference in their isoelectric points (pIs) after methyl esterification.

261 mns into three fractions, depending on their isoelectric points (pIs).

262 aganeite can be explained both by the higher isoelectric point/point-of-zero charge (9.6-10) of this

263 and the microstructure, fabricated from high-isoelectric-point proteins.

264 Gels formed close to the isoelectric point proved to be very resistant to simulat

265 Four proteins with isoelectric points ranging from ~5 to 9 were tested to s

266 laminosum and found to be identical in mass, isoelectric point, redox midpoint potential and (for pla

267 Remarkably, in the isoelectric point regime, the lambda-DNA interaxial spac

268 rley and wheat were found to differ in their isoelectric points, resistance to proteolysis, and conta

269 electively target peptides with low and high isoelectric points, respectively.

270 PEG at a pH that was close to the protein's isoelectric point resulted in rapid nucleation and growt

271 is shows that individual parameters, such as isoelectric point, sequence length, average hydropathy,

272 iently phosphorylated by PKR in vitro and an isoelectric point shift in B56alpha was detected in extr

273 AhRY9F mutant and wild-type AhR, but a basic isoelectric point shift was detected by two-dimensional

274 ed for polymers, by linking photolysis to an isoelectric point shift, which itself is linked to a sol

275 rizes RA-binding proteins according to their isoelectric point showed both CRABP I and CRABP II to be

276 These biomolecules have isoelectric points similar to C. parvum (pH approximatel

277 of apoptosis (IAP)-binding protein with low isoelectric point (Smac/DIABLO), and apoptosis-initiatin

278 to have an ER retention signal and an acidic isoelectric point, suggesting that it may be localized t

279 topes have significantly higher (more basic) isoelectric points than do nonantigenic regions.

280 surface varies, and if it is lower than the isoelectric point, that factor increases (rectification

281 At pH above the isoelectric point, the majority of the proteins involved

282 At pH 5.1, close to the isoelectric point, the osmotic pressure was lower at the

283 We found that if pH exceeds the isoelectric point, the rectification factor has a local

284 nding protein distinguishable by its neutral isoelectric point; the same binding protein was also det

285 L-FABP) is composed of isoforms differing in isoelectric point, their comparative structure and funct

286 and outer membrane proteins that have a high isoelectric point, thereby reducing their proton permeab

287 e of molecular mass, hydrodynamic radii, and isoelectric points through a nanofiber hydrogel scaffold

288 ated characteristics of biomolecules such as isoelectric points, titration curves and energies of pro

289 s of a sequence (e.g. surface composition or isoelectric point) to whole-genome data (e.g. absolute m

290 del peptides differing in hydrophobicity and isoelectric point using a combination of ion-exchange an

291 n of tubulin isotypes having a difference in isoelectric point values of 0.01, without the need for t

292 predicted molecular mass was 84 kDa, and the isoelectric point was 6.69, in agreement with rat brain

293 ular mass was determined to be 48 kD and the isoelectric point was at pH 6.1.

294 -polyacrylamide gel electrophoresis, and its isoelectric point was determined to be 7.8.

295 olyacrylamide gel electrophoresis, and their isoelectric points were determined to be greater than pH

296 Different isoelectric points were found in both PBPI (4.0-5.5) and

297 were not statistically significant, but the isoelectric points were shifted by PKG activation.

298 The isoelectric points were significantly more acidic than p

299 roteins with different molecular weights and isoelectric points when a low-femtomole amount was loade

300 log, and stationary growth phases differ in isoelectric point, with values ranging from 5.2 to 6.4.