ライフサイエンスコーパス: beta-galactosidase

1 Enzymatic assays confirmed its activity of beta-galactosidase.

2 f Streptococcus, a bacterial surface-exposed beta-galactosidase.

3 , and at 95% lactose depletion for K. lactis beta-galactosidase.

4 a selective artificial protein receptor for beta-galactosidase.

5 o carry beta-lactoglobulin but too small for beta-galactosidase.

6 hich only exons 1-4 were expressed, fused to beta-galactosidase.

7 d by the expression of senescence-associated beta-galactosidase.

8 cent protein EYFP and the enzymatic reporter beta-galactosidase.

9 interference with the enzymatic activity of beta-galactosidase.

10 or immobilization and controlled released of beta-galactosidase.

11 to enzymatic hydrolisis by Escherichia coli beta-galactosidase.

12 and kinetic binding studies with substituted beta-galactosidases.

13 isomerization is not a universal feature of beta-galactosidases.

14 d as support for the immobilization of model beta-galactosidases.

15 raminidase 1 (Neu1), neuraminidase 3 (Neu3), beta-galactosidase 1 (Glb1), and hexosaminidase B (HexB)

16 d peptides (1.6 kDa) and functional enzymes, beta-galactosidase (119 kDa) and Cre recombinase (37 kDa

17 ing a near-infrared fluorescent substrate of beta-galactosidase (9H-{1,3-dichloro-9,9-dimethylacridin

18 S. pneumoniae mutants deficient in NanA and beta-galactosidase A (BgaA) failed to form biofilms in v

19 ater increases in senescence associated (SA) beta-galactosidase, a known marker of cellular senescenc

20 beta-galactosidase, a lysosomal protein, was elevated 3.

21 1 green fluorescent protein (GFP)-AAP2BR and beta-galactosidase-AAP2BR fusion proteins, respectively,

22 X-gal analysis has shown strong beta-galactosidase activities in the prostate, brain, an

23 Some cerebral LLC exhibited beta galactosidase activity indicating a senescence phen

24 ent markers (increased senescence associated-beta galactosidase activity, p16, and p53 expression and

25 acZ were imaged with and without a stain for beta-galactosidase activity (S-Gal + ferric ammonium cit

26 We also found high beta-galactosidase activity accompanying tension wood di

27 as the gene responsible for the majority of beta-galactosidase activity against xyloglucan.

28 , and the induction of senescence-associated beta-galactosidase activity and cell morphology.

29 Analysis of beta-galactosidase activity and controlled release revea

30 , and the induction of senescence-associated beta-galactosidase activity and flat cell morphology.

31 hown by an increase in senescence-associated beta-galactosidase activity and formation of senescence-

32 me was effectively demonstrated in vitro for beta-galactosidase activity and in vivo in a mouse model

33 s, respectively, which by their lacZ encoded beta-galactosidase activity convert the inactive prodrug

34 determination of the fusion protein via its beta-galactosidase activity found 8.3 and 9.8 ng/mug (na

35 ed reporter assay linking LasR function with beta-galactosidase activity gave results consistent with

36 tic event enabled noninvasive measurement of beta-galactosidase activity in living cells, which corre

37 logy and expression of senescence-associated beta-galactosidase activity in MCF-7 breast cancer cells

38 ef-betaGal sensitively detects intracellular beta-galactosidase activity in several ovarian cancer li

39 y)UCA in Escherichia coli yields significant beta-galactosidase activity in vivo from a lacZ gene con

40 In both E. coli and V. cholerae the beta-galactosidase activity of transcriptional fusions o

41 scence was assessed as senescence-associated beta-galactosidase activity using flow cytometry, oxidat

42 beta-Galactosidase activity was detected in osteocytes o

43 rived from the transplanted BMC did not show beta-galactosidase activity, but after 6 mo, there were

44 tocyte senescence, as indicated by increased beta-galactosidase activity, elevated CDKN1A mRNA expres

45 etermined by a rise in senescence-associated beta-galactosidase activity, higher abundance of CDKN1A/

46 ns displayed increased senescence-associated beta-galactosidase activity, lower average telomere leng

47 ents induced increased senescence-associated beta-galactosidase activity, oxidative stress, early pho

48 ociated with decreased senescence-associated beta-galactosidase activity, preserved telomere length,

49 roliferative capacity, senescence-associated beta-galactosidase activity, the known senescence-induci

50 ression and cardiomyocyte-restricted nuclear beta-galactosidase activity, thus permitting simultaneou

51 scence, as assessed by senescence-associated beta-galactosidase activity, was induced by the passagin

52 Using the novel phenotype of periplasmic beta-galactosidase activity, we show that the periplasmi

53 h arrest and increased senescence-associated beta-galactosidase activity.

54 senescence and express senescence-associated beta-galactosidase activity.

55 ing sequence caused an 8.6-fold reduction in beta-galactosidase activity.

56 Cellular senescence was monitored by beta-galactosidase activity.

57 transcriptional fusion norA-lacZ for altered beta-galactosidase activity.

58 phology, and increased senescence-associated beta-galactosidase activity.

59 the reporter, and thereby reconstitution of beta-galactosidase activity.

60 t form, the hybrid reporter had undetectable beta-galactosidase activity.

61 ed cell morphology and senescence-associated beta-galactosidase activity.

62 inally become senescent, as determined by SA-beta-galactosidase activity.

63 nzymes possibly involved in apple softening, beta-galactosidase, alpha-arabinofuranosidase, polygalac

64 beta-Galactosidase also exhibited glycoproteineous prope

65 d by the expression of senescence-associated beta-galactosidase and 5-bromo-2-deoxyuridine incorporat

66 bgal10 xyl1 double mutant, deficient in both beta-galactosidase and alpha-xylosidase.

67 defects of ganglioside hydrolases, e.g., of beta-galactosidase and beta-hexosaminidases, and of GM2-

68 des can only be detected and qualified after beta-galactosidase and beta-N-acetylhexosaminidase diges

69 beta-Galactosidase and beta-N-acetylhexosaminidase were

70 Enzymes requiring Na(+) such as beta-galactosidase and clotting proteases are not activa

71 nstruct contained Renilla luciferase (RLuc), beta-galactosidase and firefly luciferase (FLuc) ORFs li

72 Microneedle-mediated intradermal delivery of beta-galactosidase and formaldehyde-inactivated botulinu

73 turn-ON probes for detection and imaging of beta-galactosidase and hydrogen peroxide.

74 scence markers, namely senescence-associated beta-galactosidase and increased p16(INK4a)/p19(ARF) exp

75 auses the induction of senescence-associated beta-galactosidase and inhibition of cell growth consist

76 We studied the enzymatic reaction for beta-galactosidase and its substrate (resorufin-beta-D-g

77 d by increased senescence-associated markers beta-galactosidase and p16 mRNA in aged CPCs.

78 radish peroxidase, alkaline phosphatase, and beta-galactosidase and substantially altered enzyme acti

79 ucture of a complex between Escherichia coli beta-galactosidase and the cell-permeant inhibitor pheny

80 the enzymatic activity of the cargo proteins beta-galactosidase and the enzymatic subunit of Clostrid

81 A demonstrated with the accurate modeling of beta-galactosidase and TRPV1 proteins at 3.2 A and 3.4 A

82 t complexes of peptides (derived from OVA or beta-galactosidase) and TRiC results in cross-priming of

83 re then labeled with an enzyme (streptavidin-beta-galactosidase), and single enzymes associated with

84 uncovered intracistronic complementation in beta-galactosidase, and investigated the role of cAMP in

85 , including p16, EGFP, senescence-associated beta-galactosidase, and the senescence-associated secret

86 nerated mice lacking both NPC1 and lysosomal beta-galactosidase, and therefore unable to generate GM2

87 ately 40-50% with B. circulans and A. oryzae beta-galactosidases, and at 95% lactose depletion for K.

88 bserve a fluctuation type of distribution of beta-galactosidase appearance in a growing culture, cons

89 t the solution structure of Escherichia coli beta-galactosidase ( approximately 465 kDa), solved at a

90 accompanies the use of senescence-associated beta-galactosidase as a collection of semiselective mark

91 nsduced with adenoviruses containing A20 (or beta-galactosidase as a control) were allografted into m

92 Using beta-galactosidase as a reporter for the null gene, deve

93 beta-Galactosidase as the reporter allows for the visual

94 egulatory system as recognition elements and beta-galactosidase as the reporter protein was designed

95 for inhibition of the hydrolytic activity of beta-galactosidase (Aspergillus oryzae) was evaluated.

96 ions, we established a senescence associated beta-galactosidase assay as a screening platform to rapi

97 hanced dramatically the dynamic range of the beta-galactosidase assay for cadBA activation.

98 aster staining reaction than the traditional beta-galactosidase assay in mouse embryos.

99 Using Northern hybridization and beta-galactosidase assays of an ace promoter-lacZ fusion

100 e for cytotoxicity and senescence-associated beta-galactosidase assays, which were compared with diss

101 nce with cellular growth on the high end for beta-galactosidase (at approximately 20,000 molecules pe

102 e lysosomal enzymes (alpha-glucosidase (AG), beta-galactosidase (B-GAL) and beta-N-acetylglucosamidas

103 ilk during treatment with several commercial beta-galactosidases (Bacillus circulans, Kluyveromyces l

104 e mutant was also 'leaking' as revealed by a beta-galactosidase-based assay employing a membrane impe

105 ary epithelial cells (PI-MECs)-are marked by beta-galactosidase (beta Gal) expression following pregn

106 ens (the DeltabioR DeltabioBFDA mutant), the beta-galactosidase (beta-Gal) activity of three plasmid-

107 y high amounts of galactose and considerable beta-galactosidase (beta-Gal) activity was observed.

108 beta-galactosidase (beta-gal) and beta-glucuronidase (be

109 ssay was implemented into the procedure with beta-galactosidase (beta-gal) as the detection enzyme.

110 we show that expression of an axon-targeted beta-galactosidase (beta-gal) from such vectors supports

111 e-mediated lysis was used to release endemic beta-galactosidase (beta-gal) from the bound bacterial c

112 In these animals, staining for beta-galactosidase (beta-gal) identifies cells in which

113 function and can solubilize heat-aggregated beta-galactosidase (beta-gal) in the absence of the Hsp7

114 We demonstrate that when beta-galactosidase (beta-gal) is expressed in LECs, beta

115 s work, specific immobilization of 6-phospho-beta-galactosidase (beta-Gal) on a self-assembled monola

116 sing mice in which the M9PROM was fused to a beta-galactosidase (beta-gal) reporter.

117 riple transgenic mice expressing ROSA26 stop beta-galactosidase (beta-gal), albumin Cre, and collagen

118 enzymes, namely pectin methylesterase (PME), beta-galactosidase (beta-Gal), endo-1,4-beta-D-glucanase

119 recombinant A20 adenovirus (rAd.A20) or rAd.beta-galactosidase (beta-gal), implanted, harvested 4 we

120 oli K12, which expresses the omega-domain of beta-galactosidase (beta-gal).

121 ges engineered with lacZ operon encoding for beta-galactosidase (beta-gal).

122 ps are electrostatically bound to an enzyme [beta-galactosidase (beta-Gal)], inhibiting enzyme activi

123 iposomes resulted in increased expression of beta-galactosidase(beta-gal) plasmid in rat brain tissue

124 -glucosidase/beta-xylosidase that also shows beta-galactosidase, beta-fucosidase, alpha-arabinofurano

125 es are electrostatically bound to an enzyme (beta-galactosidase, beta-Gal), inhibiting enzyme activit

126 in a reduction or absence of lysosomal acid beta-galactosidase (betagal) activity.

127 Using beta-galactosidase (betagal) as a model system, we have

128 ssed to cell fate reporter mice that express beta-galactosidase (betagal) in cells of AEC lineage.

129 Mice expressing beta-galactosidase (betagal) on a retina-specific promot

130 d a new model of memory inflation based on a beta-galactosidase (betagal)-recombinant adenovirus vect

131 Promoter fusions to a beta-galactosidase bgaH reporter revealed that transcrip

132 lycosides 7a-e and 8 were found to be modest beta-galactosidase (bGal) inhibitors.

133 Galectin-9 (Gal9), a beta-galactosidase-binding protein expressed by T-regs,

134 nts exhibit trans-alpha-xylosidase and trans-beta-galactosidase (but not trans-alpha-fucosidase) acti

135 ifferent analytes (Pd(0/2+), H(2)O(2), F(-), beta-galactosidase) can be created from the same core st

136 -kDa elastin-binding protein/spliced form of beta-galactosidase chaperone, enhancing secretion.

137 pombe tit1+ and tit1-Delta cells by using a beta-galactosidase codon-swap reporter whose catalytic a

138 In the current study we used a beta-galactosidase complementation method to screen a se

139 We used a beta-galactosidase complementation method to screen seve

140 ested PCR assay to detect NWM SFV DNA, and a beta-galactosidase-containing indicator cell line to ass

141 Importantly, endo-beta-galactosidase coupled with MALDI-MS allowed these t

142 med with LC-MS/MS, indicating that Chick pea beta-galactosidase (CpGAL) is a heterodimer.

143 studies provide an enhanced alternative for beta-galactosidase detection in expression and cell fate

144 ratracheal delivery of AAV1 was confirmed by beta-galactosidase detection in the distal pulmonary vas

145 S6KO) gene and lacz reporter cDNA coding for beta-galactosidase directed by the CerS6 promoter.

146 expression; expressed senescence-associated beta-galactosidase; displayed an enlarged, flattened phe

147 protein G domain but delays that of a large beta-galactosidase domain as a result of kinetic trappin

148 tal telencephalic expression of Dlx6 RNA and beta-galactosidase driven from a mutant Dlx6 locus.

149 beta-Galactosidase, encoded by lacZ, is usually detected

150 shell of oligonucleotides to the surface of beta-galactosidase enhances its cellular uptake of by up

151 Monastrell wines were also treated with beta-galactosidase enzyme addition and commercial enzyme

152 echniques (cold pre-fermentative maceration, beta-galactosidase enzyme addition and enzymatic prepara

153 beta-Galactosidase enzymes are used in the dairy industr

154 transgenic AlbuminCreXRosa26 mice expressing beta-galactosidase exclusively in hepatocytes.

155 ansgenic green fluorescence protein (GFP) or beta-galactosidase expressed from the ROSA26 locus was u

156 imised fluorescent-activated cell sorting of beta-galactosidase expressing cells (FACS-Gal) to compar

157 Immunogenicity of TRiC purified from OVA- or beta-galactosidase-expressing cells, that is, of endogen

158 Tests of the senescence-associated beta-galactosidase expression suggest that expression of

159 beta-galactosidase expression was predominantly found in

160 d a distinct profile of senescence including beta-galactosidase expression, autofluorescence, growth

161 resulting in decreased senescence-associated beta-galactosidase expression, increased self-renewal po

162 on-invasive imaging of Hmox1 expression, and beta-galactosidase for high-resolution mapping of expres

163 The level of beta-galactosidase from a gerA-lacZ fusion in superdorma

164 herichia coli l-arabinose promoter and bgaB (beta-galactosidase from Bacillus stearothermophilus) to

165 PatA (putrescine transaminase) activity and beta-galactosidase from cells with patA-lacZ transcripti

166 dvantageously used to optimally immobilise a beta-galactosidase from chick pea onto alkylamine glass

167 A beta-galactosidase from Cicer arietinum seeds has been p

168 Solubilisation of beta-galactosidase from Kluyveromyces lactis in Aerosol-

169 These results indicate that (i) levels of beta-galactosidase from lacZ fusions to operons encoding

170 The separation of beta-galactosidase from the test protein beta-lactoglobu

171 rly different GOS profiles of the commercial beta-galactosidases from Bacillus circulans, Kluyveromyc

172 ted GalCer-beta-galactosylceramidase and GM1-beta-galactosidase functions in the degradation of lacto

173 Expression of the kazrin-beta-galactosidase fusion protein faithfully reported en

174 edure using six cryo-EM structures of TRPV1, beta-galactosidase, gamma-secretase, ribosome-EF-Tu comp

175 ctive removal of the terminal galactose by a beta-galactosidase gave the Glc(1)Man(9)GlcNAc(2)-RNase

176 press either the BMP inhibitor noggin or the beta- galactosidase gene under the control of a BMP-resp

177 obe was able to image cells transfected with beta-galactosidase gene by chemiluminescence microscopy.

178 Herein, a recombinant reporter consisting of beta-galactosidase gene flanked by two estrogen receptor

179 wild-type RIMD2210633 strain marked with the beta-galactosidase gene lacZ (WBWlacZ), the mutant colon

180 n the rpoE mutant and the WT marked with the beta-galactosidase gene lacZ (WBWlacZ), the mutant strai

181 V. parahaemolyticus strains marked with the beta-galactosidase gene lacZ demonstrated that the Delta

182 as well as genes for gas vesicles, a second beta-galactosidase gene, and most but not all of the gen

183 rolysis approach (0.5L) using the commercial beta-galactosidase Godo-YNL2.

184 ed delivery to the mouse brain of functional beta-galactosidase, human IgG and IgM, and two antibodie

185 Transport of beta-galactosidase, IgG, IgM, and antibodies against amy

186 platform, we could investigate the levels of beta-galactosidase in cells grown under different nutrie

187 eously induce expression of Fgfr2(S252W) and beta-galactosidase in either the neural crest or mesoder

188 m, we were able to visualize the activity of beta-galactosidase in embryos at stages when the customa

189 diverse factors on the performance of enzyme beta-galactosidase in formulations for reduction of leve

190 remodeling in Pw1(nLacZ+/-) mouse expressing beta-galactosidase in PW1(+) cells and in differentiated

191 promoter does not produce elevated levels of beta-galactosidase in response to iron deprivation in th

192 l fusion does not produce elevated levels of beta-galactosidase in response to iron deprivation in th

193 The distribution of neurons expressing beta-galactosidase in the brain and the relative intensi

194 f AxlA, beta-glucosidase, xyloglucanase, and beta-galactosidase in the optimal proportions of 51:5:19

195 ally infect and express transgenes (hGM-CSF, beta-galactosidase) in tumor-associated vascular endothe

196 e signal, Green fluorescent protein (GFP) or beta-galactosidase, indicates transcription and translat

197 set of treated cells also stain positive for beta-galactosidase, indicating senescence.

198 compounds, 4-epi-fagomine (2b) was the best beta-galactosidase inhibitor, and it also prevented LPS-

199 igated using gene targeted mice with nuclear beta-galactosidase inserted into the Islet-1 locus.

200 lactose-free food and controlled release of beta-galactosidase into lactose-intolerant individuals.

201 with a genetic circuit in which synthesis of beta-galactosidase is under control of the arsenite-dere

202 ranoside and a constant amount of the enzyme beta-galactosidase, is produced at frequencies in excess

203 rotein (EBP), a spliced variant of lysosomal beta-galactosidase, is the primary receptor of elastin p

204 (protein G, ovalbumin, bovine serum albumin, beta-galactosidase, lactoferrin) on the EIG with initial

205 beta-Galactosidase (lacZ) has bifunctional activity.

206 Using mice expressing beta-galactosidase (lacZ) under the control of seven rep

207 s can completely account for the increase in beta-galactosidase levels in mutT lacZamber cultures, wi

208 defects, elevation of senescence-associated beta-galactosidase levels, and changes in gene expressio

209 of type IV collagen was investigated, but no beta-galactosidase-like activity capable of collagen mod

210 shape, accumulated the senescence-associated beta-galactosidase marker, and increased P16 protein exp

211 stain positive for the senescence-associated beta-galactosidase marker, suggesting that cells have lo

212 beta-galactosidase-marking studies revealed that, within

213 lactosylceramidase, alpha-galactosidase, and beta-galactosidase) mediating glycosphingolipid hydrolys

214 We examined STOML1 null mutant mice with a beta-galactosidase-neomycin cassette gene-trap reporter

215 y employing Wnt1Cre/R26R mice, which express beta-galactosidase only in neural crest derived neurons,

216 CpsA, specific protein domains were fused to beta-galactosidase or alkaline phosphatase.

217 Similarly, pretreating neutrophils with endo-beta-galactosidase or neuraminidase converted ANCA assay

218 AH rats treated with a control AAV1 carrying beta-galactosidase or saline.

219 parison with rats administered AAV1 carrying beta-galactosidase or saline.

220 Cre activity was assessed by beta-galactosidase or yellow fluorescent protein express

221 ere detected in immune cells of C57BL/6, BRE-beta-galactosidase, or BMP-4(betagal/+) mice.

222 er exhibit an elevated VEGF, localization of beta-galactosidase outside the subventricular zone (SVZ)

223 This shows that the glucose binding site of beta-galactosidase played an important role in lac opero

224 wn by reduced telomerase activity, increased beta-galactosidase-positive cells, upregulation of the s

225 ncreased the number of senescence-associated beta-galactosidase-positive HSCs and decreased alpha-smo

226 rom these mice resulted in the generation of beta-galactosidase-positive liver progenitor cells, demo

227 from lactulose was performed with commercial beta-galactosidase preparations from Aspergillus oryzae,

228 uORF2 is translated in vivo by demonstrating beta-galactosidase production from lacZ coding sequences

229 beta-Galactosidase promotes the isomerization by means o

230 atment with the deglycosylating enzyme, endo-beta-galactosidase, reduced the mass of neutrophil hLAMP

231 As determined by beta-galactosidase release assays, this mutant exhibited

232 of KAR2 and PDI1 mRNAs, and expression of a beta-galactosidase reporter activated by Hac1(i) Phospho

233 w that mice overexpressing human HB-EGF with beta-galactosidase reporter exhibit an elevated VEGF, lo

234 Expression of the bacterial beta-galactosidase reporter gene (lacZ) in the vector us

235 deletion of the intronic CArG region from a beta-galactosidase reporter gene abolished transgene exp

236 the 5'UTR clearly decreased expression of a beta-galactosidase reporter in a proportional manner, a

237 essfully conferred thermoregulation upon the beta-galactosidase reporter in E. coli.

238 The anatomical distribution of a beta-galactosidase reporter indicated that Cx36 was expr

239 blished pCTEN-Cre:R26R mice by crossing R26R beta-galactosidase reporter mice with pCTEN-Cre transgen

240 rg403Gln, (MHC(403/+)) and an Mef2-dependent beta-galactosidase reporter transgene.

241 ough a premature UAG stop codon located in a beta-galactosidase reporter.

242 HAC1 splicing, induction of KAR2, PDI1, and beta-galactosidase reporters, and survival of ER stress,

243 DNA-functionalized beta-galactosidase retains its ability to catalyze the h

244 , and PAI-1, inhibited senescence-associated beta-galactosidase (SA-beta-gal) activity and production

245 by measuring both the senescence associated-beta-galactosidase (SA-beta-Gal) activity and the expres

246 s (ROS) production and senescence-associated beta-galactosidase (SA-beta-gal) activity but an increas

247 Senescence-associated beta-galactosidase (SA-beta-Gal) activity was investigat

248 ration; an increase in senescence-associated beta-galactosidase (SA-beta-Gal) activity, a marker of c

249 acellular reactive oxygen species (iROS), SA-beta-galactosidase (SA-beta-gal) activity, and autofluor

250 as marked by increased senescence-associated beta-galactosidase (SA-beta-Gal) staining and gammaH2AX-

251 ce: NHOK overexpressed senescence-associated beta-galactosidase (SA-beta-Gal), p16INK4A, IL-6, and IL

252 of flat, enlarged and senescence-associated beta-galactosidase (SA-beta-Gal)-positive cells.

253 ponse (DDR) signaling, senescence-associated beta-galactosidase (SA-betagal) activity, increased expr

254 ), and found that only senescence-associated beta-galactosidase (SAbetagal) activity is specifically

255 An anti-beta-galactosidase scFv:MOG fusion protein (scFv GL117:M

256 tices (addition of enzymatic preparation and beta-galactosidase separately and dry ice addition) may

257 ce alignment of CpGAL with other known plant beta-galactosidase showed high amino acid sequence homol

258 activation of DC before adoptive transfer of beta-galactosidase-specific T cells dramatically increas

259 s for senescence activation, as indicated by beta--galactosidase staining.

260 nied by an increase in senescence-associated beta-galactosidase staining and a marked induction of p1

261 cence was evaluated by senescence-associated beta-Galactosidase staining and by Western blot analysis

262 beta-Galactosidase staining enabled by a lacZ cassette t

263 in liver tissue and by senescence-associated beta-galactosidase staining in a culture-based model of

264 KLK4 protein levels in rat enamel and beta-galactosidase staining in LacZ-C57BL/6-Klk4 (+/LacZ

265 beta-Galactosidase staining in PRCP(gt/gt) mice reveals

266 By beta-galactosidase staining, a subpopulation of Cdc42-nu

267 ion of collagen IV in the mesangium and less beta-galactosidase staining, an indicator of cell senesc

268 -F assay, thymidine incorporation assay, and beta-galactosidase staining, respectively.

269 escence, determined by senescence-associated beta-galactosidase staining, was obviously attenuated by

270 By beta-galactosidase staining, we demonstrated that Mig-6

271 n and quantification of senescence-activated beta-galactosidase staining.

272 alyzed in Sdc4(-/-) lacZ-knockin mice, using beta-galactosidase staining.

273 hotoreceptor cell layer showed the strongest beta-galactosidase staining.

274 usprofundi harbors a model polyextremophilic beta-galactosidase that functions in cold, hypersaline c

275 se site based on a substituted enzyme (G794A-beta-galactosidase) that traps allolactose.

276 eurons were labeled with an antibody against beta-galactosidase, the protein product of the lacZ gene

277 th the Cre-loxP system allowed to direct the beta-galactosidase to proximal dendrites, and in particu

278 xpress exoglycosidases, one of which is BgaC beta-galactosidase, to deglycosidate host surface glycol

279 r, with reduced co-localisation of the viral beta-galactosidase transgene with MAdCAM-1+ sinus-lining

280 We found that beta-galactosidase translocation is driven only by the n

281 er-based approach to quantify pep-1-mediated beta-galactosidase translocation.

282 Mig-6/lacZ reporter mouse strain expressing beta-galactosidase under the control of the Mig-6 gene p

283 try or DNA uncoating, since HSV-1 expressing beta-galactosidase under the control of the neurofilamen

284 Here we used RRas2-knockout mice expressing beta-galactosidase under the regulation of the endogenou

285 cence, as evidenced by senescence-associated beta-galactosidase upregulation, decreased self-renewal

286 tose hydrolysis by the immobilized K. lactis beta-galactosidase using genipin as a crosslinker was 87

287 ck down mRNA of a selected chromosomal gene (beta-galactosidase) using an artificial miniCRISPR locus

288 the maximum GOS concentration with K. lactis beta-galactosidase was achieved in 1 and 5h at 40 and 4

289 Initially, beta-galactosidase was employed as a detectable model fo

290 Expression of senescence-associated beta-galactosidase was greatly induced in hepatocytes ex

291 Escherichia coli beta-galactosidase was incubated in the presence of the

292 a single enzyme molecule of Escherichia coli beta-galactosidase was measured using a capillary electr

293 Finally, the expression level of beta-galactosidase was significantly higher when point m

294 in-like growth factor binding protein 7, and beta-galactosidase were able to distinguish the severe n

295 Here we focus on beta-galactosidase, which is overexpressed in primary ov

296 eakdown of some lactose and the provision of beta-galactosidase, which remains active in the gastroin

297 d catalytic ability of the hydrolytic enzyme beta-galactosidase, which serves as the protein core, de

298 -SIGN cells with HHV-8 induces expression of beta-galactosidase, which was used to determine TCID50 l

299 o detect enzyme activity for the reaction of beta-galactosidase with p-aminophenyl-galactopyranoside

300 Kanzi apples had lower activity of beta-galactosidase, with no decline in the extent of bra