ライフサイエンスコーパス: beta-galactosidase

1 or immobilization and controlled released of beta-galactosidase.

2 to enzymatic hydrolisis by Escherichia coli beta-galactosidase.

3 Enzymatic assays confirmed its activity of beta-galactosidase.

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

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

6 x2 gene was replaced by n-LacZ gene encoding beta-galactosidase.

7 a selective artificial protein receptor for beta-galactosidase.

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

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

10 osan nanocomposites bound Aspergillus oryzae beta-galactosidase.

11 interference with the enzymatic activity of beta-galactosidase.

12 and kinetic binding studies with substituted beta-galactosidases.

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

14 ymatic hydrolysis of lactose by supplemental beta-galactosidases.

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

16 We discovered that plant-secreted beta-galactosidase 1 (BGAL1) of Nicotiana benthamiana pr

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

18 the promoter of the pectin-metabolizing gene beta-GALACTOSIDASE 1 (RhBGLA1), and reduced expression o

19 mutated in Niemann Pick disease type A, and beta galactosidase-1, which is mutated in GM1 gangliosid

20 resolution for pyruvate kinase (232 kDa) and beta-galactosidase (466 kDa), extending the limits of is

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

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

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

24 iline chitosan silver nanocomposite adsorbed beta-galactosidase, a multi-fold enhancement in catalyti

25 1 green fluorescent protein (GFP)-AAP2BR and beta-galactosidase-AAP2BR fusion proteins, respectively,

26 ence markers including senescence-associated beta-galactosidase, accumulation of cytosolic p16(INK4A)

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

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

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

30 and a 39% reduction in senescence-associated beta-galactosidase activity (p < 0.01) but no changes in

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

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

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

34 enescence, verified by senescence-associated beta-galactosidase activity and cell cycle markers p16 a

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

36 Analysis of beta-galactosidase activity and controlled release revea

37 the saponins effects on Kluyveromyces lactis beta-galactosidase activity and correlated these changes

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

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

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

41 gh cells showed higher senescence-associated beta-galactosidase activity and increased gene expressio

42 ystem and procedure for the determination of beta-galactosidase activity are proposed.

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

44 beta-Galactosidase activity decreased in the presence of

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

46 uorescent probes for imaging caspase-3/7 and beta-galactosidase activity in live cells.

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

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

49 howed developmental stage- and cell-specific beta-galactosidase activity mimicking the endogenous ame

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

51 of cells positive for senescence-associated beta-galactosidase activity was also evident with chroni

52 beta-Galactosidase activity was detected in osteocytes o

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

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

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

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

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

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

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

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

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

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

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

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

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

66 Cellular senescence was monitored by beta-galactosidase activity.

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

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

69 ed senescence-related proteins p53, p16, and beta-galactosidase activity.

70 4/CDKN2A proteins, and senescence-associated beta-galactosidase activity.

71 ein expression and secretion, DNA damage and beta-galactosidase activity; unfortunately, these traits

72 CC oxidase activity, membrane permeability, <beta>-galactosidase activity and, therefore, less soften

73 st, but also able to protect a model enzyme (beta-galactosidase) against lyophilization and heat chal

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

75 hydrolysis in Arabidopsis: alpha-xylosidase, beta-galactosidase, alpha-fucosidase, soluble beta-gluco

76 beta-Galactosidase also exhibited glycoproteineous prope

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

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

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

80 beta-Galactosidase and beta-N-acetylhexosaminidase were

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

82 cipitation and crosslinking (combi-CLEAs) of beta-galactosidase and glucose isomerase for catalyzing

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

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

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

86 d modified the molecular interaction between beta-galactosidase and o-nitrophenyl-beta-d-galactoside,

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

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

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

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

91 with multiple proteins (e.g. BSA, HSA, GOx, beta-galactosidase) and monomer classes including acryla

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

93 enzymes, namely beta-glucosidase, invertase, beta-galactosidase, and catalase, are encapsulated in ZI

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

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

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

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

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

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

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

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

102 atory gene used as recognition elements with beta-galactosidase as the reporter protein was designed

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

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

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

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

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

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

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

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

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

112 with alpha-l-arabinofuranosidase (AFase) and beta-galactosidase (beta-Gal) activities, resulting in p

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

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

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

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

117 ctosidase beta 1 (GLB1) gene cause lysosomal beta-galactosidase (beta-Gal) deficiency and clinical on

118 ctosidase beta 1 (GLB1) gene cause lysosomal beta-galactosidase (Beta-Gal) deficiency, resulting in a

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

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

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

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

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

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

125 beta-Galactosidase (beta-gal), one of the typical lysoso

126 teins- i) bovine serum albumin (BSA) and ii) beta-galactosidase (beta-gal), was investigated by micro

127 f enzyme activity in mouse models expressing beta-galactosidase (beta-gal).

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

129 particles and free antibodies conjugated to beta-galactosidase (beta-gal).

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

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

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

133 ), enzymes involved in cell wall metabolism (beta-galactosidase, beta-glucosidase, beta-amylase, chit

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

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

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

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

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

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

140 4 (MUM4), to express the cell wall modifying beta-galactosidase (BGAL)-encoding gene MUCILAGE-MODIFIE

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

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

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

144 fects of tannic acid on Kluyveromyces lactis beta-galactosidase catalytic activity and correlate thes

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

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

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

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

149 The hydrolysis of lactose over beta-galactosidase converted 95.77 +/- 0.67% of lactose

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

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

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

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

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

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

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

157 opmental pattern with the LacZ gene encoding beta-galactosidase enzyme activity assay and Cre protein

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

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

160 beta-Galactosidase enzymes are used in the dairy industr

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

162 beta-galactosidase expression was predominantly found in

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

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

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

166 beta-Galactosidase formulations can be added to infant m

167 e utilised in the development and testing of beta-galactosidase formulations.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

192 bioanalytical system allows determination of beta-galactosidase in the wide range of activity (up to

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

194 of senescence such as senescence-associated beta-galactosidase, increased p21 expression, micronucle

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

196 different origins (isoenzymes), detection of beta-galactosidase inhibitor and finally to the determin

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

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

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

200 dent Apoptosis (AIDA)) whereby a single anti-beta-galactosidase intracellular single chain Fv antibod

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

202 beta-Galactosidase is vital to dairy industries because

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

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

205 BdBGAL1, unlike other xyloglucan beta-galactosidases, is able to remove both galactoses f

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

207 beta-Galactosidase (lacZ) has bifunctional activity.

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

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

210 In addition, we found that serum LAMP1 and beta-galactosidase levels were significantly decreased i

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

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

213 d as a platform to immobilize Lens culinaris beta-galactosidase (Lsbgal) which resulted in 93% of imm

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

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

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

217 yaniline chitosan silver nanocomposite bound beta-galactosidase on addition of metal ions as compared

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

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

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

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 f cellular senescence-related genes, such as beta-galactosidase, p21, p53, and gammaH2AX, and mTOR/pS

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

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

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

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

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

229 beta-Galactosidase promotes the isomerization by means o

230 of caspase-3 after binding to the tetrameric beta-galactosidase protein.

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

232 strain expressing a disulfide-bond sensitive beta-galactosidase reported previously.

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

234 Golgicide A (GCA) inhibited HSV-1 entry via beta-galactosidase reporter assay and impaired incoming

235 HV-1 entry and infection, as measured by the beta-galactosidase reporter assay.

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

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

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

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

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

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

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

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

244 of diamagnetic NiL(1) and NiL(2) by light or beta-galactosidase, respectively, converts them into par

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

246 reduced proliferation, senescence-associated beta-galactosidase (SA-beta-gal) activation, and increas

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

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

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

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

251 r senescence marked by senescence-associated beta-galactosidase (SA-beta-gal), p16Ink4a, and p53 in l

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 h "turn-on" ratio upon senescence-associated beta-galactosidase (SABG) activation.

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

257 -resistant acid phosphatase histoenzymology, beta-galactosidase, sclerostin immunochemistry, and term

258 lar dichroism shows that saponin changes the beta-galactosidase secondary structure, favoring its pro

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

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

261 e on xyloglucan, including alpha-xylosidase, beta-galactosidase, soluble and membrane-bound beta-gluc

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

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

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

265 omers showed increased senescence-associated beta-galactosidase staining and increased senescence-ass

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

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

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

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 immunofluorescence and senescence-associated beta-galactosidase staining.

273 to understand the effects of tannins on the beta-galactosidase structure and how they are related to

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 The effect of beta-galactosidase to glucose isomerase activity ratio a

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

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

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

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

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

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

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

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

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

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

293 matic activity of two commercially available beta-galactosidases were investigated.

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

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

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

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

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

299 sted that saponins increased the affinity of beta-galactosidase with the artificial substrate o-nitro

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