1 lular distribution of (64)Cu was measured by
cell fractionation.
2 ion, as determined by immunofluorescence and
cell fractionation.
3 sociated with microsomal membranes following
cell fractionation.
4 sed form of gB could be coisolated following
cell fractionation.
5 ablished both through immunofluorescence and
cell fractionation.
6 by indirect immunofluorescence as well as by
cell fractionation.
7 also confirmed by coimmunoprecipitation and
cell fractionation.
8 eins in Escherichia coli was used along with
cell fractionation.
9 live cell imaging, immunocytochemistry, and
cell fractionation.
10 labelling, domain-specific biotinylation and
cell fractionation.
11 Cell fractionation according to lineage depletion and AL
12 -cell imaging, deconvolution microscopy, and
cell fractionation,
all concurred that exogenous rSPARC
13 found predominantly as a soluble protein by
cell fractionation,
all three proteins were found to loc
14 We show that by
cell fractionation,
almost all MPP10 was found in isolat
15 Microscopic and
cell fractionation analyses of parasites expressing one
16 Immunocytochemical staining and
cell fractionation analysis demonstrated that sentrin mo
17 pitope tag into NIH 3T3 cells and subsequent
cell fractionation analysis shows that the PATE protein
18 A11 in cells by using immunofluorescence and
cell fractionation analysis.
19 2 in the nucleolar fraction as determined by
cell fractionation and by immnocytochemical analysis.
20 Cell fractionation and confocal immunofluorescence micro
21 Cell fractionation and confocal localization of formin I
22 Cell fractionation and confocal microscope studies revea
23 Both
cell fractionation and confocal microscopic analyses of
24 In the present work,
cell fractionation and confocal microscopy studies demon
25 n null mice (Peri-/- MEF), we demonstrate by
cell fractionation and confocal microscopy that up to 50
26 Based on
cell fractionation and confocal microscopy, we find SH2-
27 gating enzyme 9 (Ubc9) in HCC cell nuclei by
cell fractionation and confocal microscopy; physical int
28 Cell fractionation and cytological experiments suggest t
29 degraded with a t1/2 of 2.9 h, were found by
cell fractionation and density-shift experiments to resi
30 Cell fractionation and electron-microscopic immunolabeli
31 Cell fractionation and extractions with MgCl(2) indicate
32 Using
cell fractionation and fluorescence methods, we demonstr
33 h most of the CAD in the cell was cytosolic,
cell fractionation and fluorescence microscopy showed th
34 underlying Tor-dependent signaling, we used
cell fractionation and immunoaffinity chromatography to
35 Cell fractionation and immunoblot analyses using polyclo
36 Cell fractionation and immunoblot analysis confirmed thi
37 A::TnphoA) mutants do not elicit the HR, but
cell fractionation and immunoblot analysis revealed that
38 Cell fractionation and immunoblotting showed mrnp 41 in
39 Cell fractionation and immunoblotting showed that PEB1a
40 their secretion phenotypes were assessed by
cell fractionation and immunochemistry.
41 Using
cell fractionation and immunocytochemical experimental a
42 Cell fractionation and immunocytochemistry indicated tha
43 Cell fractionation and immunocytochemistry show caveolae
44 Cell fractionation and immunocytochemistry studies demon
45 In this work we used
cell fractionation and immunocytochemistry to determine
46 taining RNA are all detected on membranes by
cell fractionation and immunoelectron microscopy.
47 Cell fractionation and immunofluorescence analyses indic
48 n of ERalpha to the nucleus as shown by both
cell fractionation and immunofluorescence microscopic st
49 ght into this process, we applied mechanical
cell fractionation and immunofluorescence microscopy to
50 venous etoposide administration, followed by
cell fractionation and immunofluorescence studies of var
51 By
cell fractionation and immunogold electron microscopy, w
52 Cell fractionation and immunogold labeling show that in
53 as predominantly localized in the nucleus by
cell fractionation and immunostaining.
54 Cell fractionation and in situ hybridization analysis of
55 Furthermore,
cell fractionation and in vitro methylation assays demon
56 Cell fractionation and labeling studies with [(3)H]palmi
57 nt Ras localization to the PM as measured by
cell fractionation and photobleaching.
58 Cell fractionation and PP1 catalytic subunit isolation s
59 Cell fractionation and protease accessibility experiment
60 Cell fractionation and qRT-PCR analysis indicated that L
61 Cell fractionation and quantitative RT-PCR revealed that
62 We have utilized
cell fractionation and ribosome profiling to obtain a ge
63 of FMR1 and the FXR proteins, we carried out
cell fractionation and sedimentation experiments with mo
64 l subcellular localization were evaluated by
cell fractionation and Western blot analysis.
65 Cell fractionation and Western blotting demonstrated tha
66 We determined by use of
cell fractionation and Western blotting that, during in
67 Cell fractionation and western-blot analysis localized t
68 Protease protection,
cell fractionation,
and affinity purification experiment
69 In this report, using immunocytochemistry,
cell fractionation,
and chromatin immunoprecipitation an
70 were assessed by arteriovenous measurements,
cell fractionation,
and immunofluorescence.
71 ing immunogold labeling/electron microscopy,
cell fractionation,
and protein analysis techniques, we
72 vidence using immunofluorescence microscopy,
cell fractionation,
and SNARE protein interaction studie
73 ked Golgi fraction was isolated by classical
cell fractionation,
and the protein complement (the Golg
74 alphas, using immunofluorescence microscopy,
cell fractionation,
and total internal reflection fluore
75 nce localization, sucrose density gradients,
cell fractionation,
and yeast two-hybrid experiments.
76 By
cell fractionation,
ANKRA is found both in the cytosol a
77 We previously reported a
cell fractionation approach that includes the selection
78 Cell fractionation as well as indirect immunofluorescenc
79 In the present study, we found by
cell fractionation assays and confocal microscopy that p
80 NMD substrates classified based on
cell fractionation assays as "nucleus associated" or "cy
81 Cell fractionation assays localized p32 to the P100 frac
82 Developmental 2D Western blots,
cell fractionation assays, and analysis of a missense pr
83 d the associated nascent RNA are prepared by
cell fractionation,
avoiding immunoprecipitation or RNA
84 r intracellular calreticulin released during
cell fractionation because it was expressed on circulati
85 Cell fractionation by sucrose gradient centrifugation in
86 These results suggest
cell fractionation can be used to study the uptake of mo
87 Using transmission electron microscopy,
cell fractionation,
cell wall sorting signal domain swap
88 ng immunohistochemistry/confocal imaging and
cell fractionation/
co-immunoprecipitation, we found that
89 This hypothesis was supported by
cell fractionation,
coimmunoprecipitation, and coimmunol
90 Cell fractionation,
coimmunoprecipitation, and immunogol
91 Cell fractionation combined with quantitative assays was
92 Cell fractionation confirmed the lysosomal localization
93 In addition,
cell fractionation data indicate that Cdc37 is found in
94 Cell fractionation demonstrated a predominant decrease i
95 OptiPrep gradient
cell fractionation demonstrated that BK channels were co
96 lular localization of the kinase activity by
cell fractionation demonstrated that it is enriched in c
97 immunofluorescence, immunogold labeling, and
cell fractionation demonstrated that rat slit diaphragms
98 A
cell fractionation experiment using cisplatin-treated He
99 Cell fractionation experiments also revealed that phosph
100 Strikingly,
cell fractionation experiments and confocal immunofluore
101 Cell fractionation experiments and cryoimmunoelectron mi
102 Cell fractionation experiments confirmed that macroH2A1
103 tron microscopy, using anti-MompA serum, and
cell fractionation experiments confirmed the localizatio
104 N-terminus and site-directed mutagenesis and
cell fractionation experiments confirmed this protein is
105 Cell fractionation experiments demonstrated that LdK39 w
106 Subsequent immunocytochemistry and
cell fractionation experiments fully supported the concl
107 Cell fractionation experiments indicated that the change
108 Mutational analysis and
cell fractionation experiments indicated that the inv(16
109 Cell fractionation experiments on freshly isolated CD4+
110 TAF1 colocalizes with UBF in Hela cells, and
cell fractionation experiments provided further evidence
111 Furthermore,
cell fractionation experiments revealed that significant
112 Confocal microscopy and
cell fractionation experiments revealed that upon LPS st
113 GFP fusion protein localization and
cell fractionation experiments show that this E3 ligase
114 Cell fractionation experiments showed that caspase-3 act
115 Pulse-chase
cell fractionation experiments showed that chitosome pro
116 Cell fractionation experiments showed that ExoT is trans
117 Cell fractionation experiments showed that it is localiz
118 Cell fractionation experiments showed that meningococcal
119 Cell fractionation experiments suggested that Inp53p ass
120 Cell fractionation experiments surprisingly revealed two
121 immunolocalization, immunoprecipitation, and
cell fractionation experiments, here we show association
122 AKT2 was localized to the cytoplasm by
cell fractionation experiments, immunocytochemistry, and
123 In agreement with the results of
cell fractionation experiments, immunofluorescence micro
124 In
cell fractionation experiments, more signal recognition
125 ntermediate was isolated in the periplasm in
cell fractionation experiments.
126 experiments to calculate the effective whole-
cell fractionation factors between water and organic mat
127 Cell fractionation,
fluorescence imaging and immunoelect
128 Subcellular localization using
cell fractionation followed by immunoblot detection, as
129 Cell fractionation followed by Western blot analysis ind
130 ncluding several attempts to isolate them by
cell fractionation from different cell types.
131 fluorescent protein-fused PIMT proteins and
cell fractionation-
immunoblot analysis revealed that apa
132 bes catalyzed by transglutaminase 2 prior to
cell fractionation,
immunoprecipitation, and detection w
133 and function of beta-catenin was analysed by
cell fractionation,
immunoprecipitation, immunoblots, QR
134 test this, we measured V-ATPase assembly by
cell fractionation in HEK293T cells treated with and wit
135 in EAAT4 and GluRdelta2 by protein blot and
cell fractionation in SCA5 autopsy tissue.
136 trafficking in control and BDL livers using
cell fractionation in the context of in vivo pulse-chase
137 Immunofluorescence and
cell fractionation indicate that Bud1p remains associate
138 Cell fractionation indicated specific loss of acidic lip
139 Cell fractionation indicated that Frmpd1 stabilizes AGS3
140 Cell fractionation into a cytoskeleton-unbound and a cyt
141 Cell fractionation localized both raf1CAAX and raf1(257L
142 Using
cell-fractionation methods, we observed that approximate
143 Cell fractionation of Arabidopsis leaves revealed that A
144 Crude
cell fractionation of infected cells using detergent lys
145 Using quantitative confocal microscopy and
cell fractionation of Nef-expressing cells and HIV-1-inf
146 Cell fractionation of SCP-2 overexpressing L-cells and W
147 mY RNAs are largely cytoplasmic in wild-type
cells, fractionation of knockout cells revealed that the
148 However, extraction of viable
cells, fractionation of lineages, and in vitro analysis
149 beta-Catenin signaling was assessed by
cell fractionation or immunoconfocal microscopy to detec
150 Refinement of the
cell fractionation procedure indicated that the completi
151 zed with double-label immunofluorescence and
cell fractionation procedures.
152 ial patterning, we developed a novel ex vivo
cell fractionation/
reconstitution assay.
153 Immunoelectron microscopy and
cell fractionation reveal that both proteins travel thro
154 ccessibility, TX-114 phase partitioning, and
cell fractionation revealed that Msp exists as distinct
155 Cell fractionation revealed that SecADelta11 and SecADel
156 Cell fractionation revealed that variation in quantity o
157 scence assay, surface proteolysis, and novel
cell fractionation schemes revealed that MOSP in TDE exi
158 Cell fractionation showed that adenosine or an ADORA2A o
159 Cell fractionation showed that approximately 80% of the
160 Consistent with these results,
cell fractionation showed that both the GFP-2a fusion an
161 Furthermore, immunofluorescence staining and
cell fractionation showed that erlotinib treatment led t
162 Liver
cell fractionation showed that macrophages and activated
163 Cell fractionation showed that Omega-3 fatty acids induc
164 Cell fractionation showed that the phosphorylated pool o
165 Cell fractionation showed that the viral preintegration
166 Cell fractionation shows that both EGF-Rs and cAbl are f
167 Cell fractionation shows that cyclins A, E, and Cdk2 are
168 on by both immunofluorescence microscopy and
cell fractionation shows that the export of Pma1p from t
169 ows little or no endo H resistance, although
cell fractionation still needs to be optimized for these
170 In addition, in
cell fractionation studies an estimated 25% of Mr 34000
171 Cell fractionation studies and confocal microscopy showe
172 Cell fractionation studies and green fluorescent protein
173 ce its plasma membrane localization based on
cell fractionation studies and immunoelectron microscopy
174 Biochemical
cell fractionation studies as well as confocal images of
175 Cell fractionation studies demonstrate that exogenous Ap
176 Cell fractionation studies demonstrate that PANCR is pri
177 Previous
cell fractionation studies demonstrated that chitin synt
178 Cell fractionation studies demonstrated that expression
179 Cell fractionation studies determined that IL-12 and TNF
180 However, immunofluorescence and
cell fractionation studies identified Bax activation and
181 Cell fractionation studies indicated that NO donors caus
182 Cell fractionation studies localize the 47- and 49-kDa p
183 Cell fractionation studies localize the three additional
184 Furthermore, in
cell fractionation studies of mitotic cells, phospho-PP-
185 Cell fractionation studies of primary bovine articular c
186 Cell fractionation studies of the t(2;5) translocation-c
187 Cell fractionation studies revealed that approximately 9
188 Cell fractionation studies revealed that cytosolic SNAP-
189 Cell fractionation studies revealed that KSR formed a co
190 Cell fractionation studies revealed that membrane-associ
191 Cell fractionation studies revealed that the N terminus
192 rog ECA(CYC) per milligram (dry weight), and
cell fractionation studies revealed that these molecules
193 Immunocytochemical and
cell fractionation studies revealed that TM6SF2 was pres
194 Cell fractionation studies showed that active p35/CDK5 w
195 Biochemical and
cell fractionation studies showed that BfpB is a 58-kDa
196 Triton X-114 phase separation and
cell fractionation studies showed that dominant negative
197 Infected-
cell fractionation studies showed that insoluble fractio
198 Direct
cell fractionation studies showed that latent virus is p
199 erinuclear and cytosolic localization, while
cell fractionation studies showed that most of the p38(J
200 Cell fractionation studies showed that NF90 and its hete
201 Cell fractionation studies showed that only a small amou
202 Cell fractionation studies showed that SPN binds prefere
203 Cell fractionation studies showed that the fluorescent M
204 Immunofluorescence and
cell fractionation studies showed that the major MV memb
205 In vivo cell labeling and
cell fractionation studies showed that the majority of W
206 Cell fractionation studies showed that the NAE amidohydr
207 Biochemical and
cell fractionation studies suggest caveolae contain func
208 sus coimmunoprecipitated (Shc-antibody), and
cell fractionation studies that suggested that the Shc.P
209 Immunocytological and
cell fractionation studies with a specific antibody reve
210 Cell fractionation studies with S. gordonii further corr
211 assessed by chemical cross-linking following
cell fractionation studies with VP40 transfected cells.
212 surprisingly, immunofluorescence microscopy,
cell fractionation studies, and studies with enhanced gr
213 Using confocal microscopy and
cell fractionation studies, butyrate pretreatment of a h
214 Data from recent
cell fractionation studies, however, predominantly those
215 ivo, together with coimmunoprecipitation and
cell fractionation studies, provide compelling evidence
216 In
cell fractionation studies, the 46-kDa protein cofractio
217 udged by two-hybrid, immunofluorescence, and
cell fractionation studies.
218 d supported by early electron microscopy and
cell fractionation studies.
219 in antibody staining, which was confirmed by
cell fractionation studies.
220 nucleoids and/or mitochondrial ribosomes in
cell fractionation studies.
221 eolin-1 by immunofluorescence microscopy and
cell fractionation studies; and (iii) a caveolin-3-deriv
222 Cell-fractionation studies showed that it is the monocyt
223 Immunohistochemistry and
cell-fractionation studies suggested that mutant beta-ca
224 itor treatments either prior to or following
cell fractionation suggested the presence of a cell enve
225 Cell fractionation suggests that the overexpressed prote
226 to the plasma membrane as assessed by either
cell fractionation,
surface biotinylation, or the plasma
227 By
cell fractionation,
surface rTPO fractionated distinctly
228 fraction was substantiated by two different
cell fractionation techniques.
229 microsurgery as well as isolation by common
cell fractionation techniques.
230 We now show by
cell fractionation that folate receptors also must be cl
231 Herein we show, with morphology and
cell fractionation,
that all the components of a mitogen
232 By immunofluorescence and
cell fractionation,
the exocyst subunits were found to s
233 hIP-chip), ChIP-quantitative PCR (qPCR), and
cell fractionation,
the stable association of RBF1 with
234 By
cell fractionation,
these signaling molecules cosediment
235 o microscopy, immunoelectron microscopy, and
cell fractionation to enter transferrin-positive REs wit
236 nd immunogold electron microscopy as well as
cell fractionation to identify the intracellular localiz
237 Cell fractionation,
two-phase partitioning, and detergen
238 tagging (LOPIT), which combines biochemical
cell fractionation using density gradient ultracentrifug
239 Cell fractionation was done to analyze this further.
240 Using confocal microscopy and
cell fractionation,
we demonstrated that up to 40% of en
241 g co-localization with organelle markers and
cell fractionation,
we determined that COMMD1 is located
242 Using ChIP-sequencing data and
cell fractionation,
we have compared the genomic distrib
243 ting the subcellular distribution of Chk1 by
cell fractionation,
we observed that around 20% of it lo
244 Using
cell fractionation,
we show that PLCgamma2-IP(3)-Ca(2+)
245 Also,
cell fractionation/
Western blot studies revealed that a
246 cytochemical findings have been supported by
cell fractionation,
which demonstrated that full-length
247 We coupled
cell fractionation with stable isotope labeling with ami