1 e and dominant-negative mutants of PAK2, and
immunodepletion.
2 s homolog of ATR (Xatr) from egg extracts by
immunodepletion.
3 only protein removed from the extract during
immunodepletion.
4 mmune competence after stress, infection, or
immunodepletion.
5 milar to that for catalytic subunit DNA-PKcs
immunodepletion.
6 oliferation, without the necessity for prior
immunodepletion.
7 ed by infiltrating PMNs and, conversely, PMN
immunodepletion abrogates tumor control.
8 Immunodepletion/
add-back experiments demonstrate that PT
9 Using
immunodepletion/
add-back experiments in Xenopus egg extr
10 Amyloid-beta
immunodepletion alleviated some but not all of the synap
11 XNercc
immunodepletion also slows aster assembly induced by Ran
12 Immunodepletion analyses demonstrated that the 50-kDa pr
13 ern immunoblotting, immunoprecipitation, and
immunodepletion analyses were performed using antibodies
14 Immunodepletion analysis shows that the Mad1-free Mad2 p
15 Maskin
immunodepletion and add-back experiments demonstrate tha
16 epeat addition processivity, as shown by p82
immunodepletion and add-back.
17 action (MLR) were used to assess efficacy of
immunodepletion and confirm donor-specific tolerance and
18 ropinosomes/endosomes is abrogated by septin
immunodepletion and function-blocking antibodies and is
19 Syndecan-1
immunodepletion and further degradation experiments iden
20 Immunodepletion and gene disruption indicate BID is requ
21 Immunodepletion and immunoprecipitation studies indicate
22 Immunodepletion and knockout studies indicated that thro
23 Immunodepletion and okadaic acid inhibition studies demo
24 0 is not sufficient for AP release; however,
immunodepletion and reconstitution experiments establish
25 Immunodepletion and reconstitution with recombinant prot
26 Immunodepletion and reexpression experiments revealed th
27 81-Galpha(q/11) complex was revealed by CD81
immunodepletion and reexpression experiments.
28 C in in vitro rephosphorylation assays using
immunodepletion and rescue with recombinant protein.
29 hese cells by size-exclusion chromatography,
immunodepletion,
and absolute quantification mass spectr
30 ich were abrogated by Tat heat inactivation,
immunodepletion,
and cysteine mutation at position 30.
31 y assessed functional tolerance, efficacy of
immunodepletion,
and donor-specific chimerism.
32 y inactivate Mediator (immunoneutralization,
immunodepletion,
and inhibitory polypeptides), we find t
33 say in combination with immunoprecipitation,
immunodepletion,
and specific inhibition.
34 Using
immunodepletion approach and a rephosphorylation assay i
35 Second, we used purification and
immunodepletion approaches to identify a critical role f
36 f phosphatase inhibitors in combination with
immunodepletion assays identified this activity to be re
37 demonstrated in HeLa nuclear extracts using
immunodepletion assays.
38 Platelet
immunodepletion before TGN markedly exacerbated hematuri
39 Both inhibitor types and myofibroblast
immunodepletion block the emergence of castration-resist
40 o chromatin with similar kinetics, and DUE-B
immunodepletion blocks replication and the loading of Cd
41 l-free system lends itself to use in protein
immunodepletion,
complementation and drug inhibition as
42 al adhesion to airway epithelia, and MUC1-ED
immunodepletion completely abrogated their inhibitory ac
43 as found to contain DNase IIalpha, but after
immunodepletion,
considerable acid-active endonuclease r
44 y and sufficient to displace dCas9, and FACT
immunodepletion converts Cas9's activity from multi-turn
45 Maraviroc (CCR5 antagonist) or CCL5
immunodepletion diminished 95% and 70% of the effect of
46 Whole animal KC, MIP-2, or TNFalpha
immunodepletion each abrogated TPA-induced inflammation,
47 Plasma
immunodepletion experiments and experiments using recomb
48 zation on Cdc2 in the p53 null cells, though
immunodepletion experiments demonstrated that only a sma
49 - or two-step immunoprecipitation assays and
immunodepletion experiments followed by Western blot ana
50 t in extracts of estrogen-treated cells, and
immunodepletion experiments identify this factor as p21(
51 two-hybrid analysis, and immunoprecipitation/
immunodepletion experiments indicate that Tap binds tigh
52 Immunodepletion experiments indicate that the Cdc73-CPSF
53 Immunodepletion experiments indicate that virtually all
54 Co-immunoprecipitation and
immunodepletion experiments indicated that approximately
55 Immunodepletion experiments indicated that EWI-2-CD9/CD8
56 Immunodepletion experiments of mitotic extracts revealed
57 Immunodepletion experiments revealed that c-ErbB-2 prote
58 ytes was shown to be biologically important;
immunodepletion experiments revealed that TNF-alpha was
59 Furthermore,
immunodepletion experiments show that MGL accounts for a
60 Immunodepletion experiments showed that the LP-BER activ
61 Immunodepletion experiments suggest that extension requi
62 Here, we demonstrate by
immunodepletion experiments that 5'-dRP-N(3) excision in
63 Co-immunoprecipitation and
immunodepletion experiments using an antibody to muted c
64 G12
immunodepletion experiments with hydrolyzed gluten showe
65 by immunoblotting, immunoprecipitation, and
immunodepletion experiments.
66 ct, as determined by immunoprecipitation and
immunodepletion experiments.
67 usly we described a reliable method based on
immunodepletion for isolating mesenchymal stem cells (MS
68 Using
immunodepletion from and antibody addition to Xenopus la
69 Emi1
immunodepletion from cycling Xenopus extracts strongly d
70 e systemically administered MSCs purified by
immunodepletion from male bleomycin (BLM)-resistant BALB
71 TAF(I)41
immunodepletion from nuclear extracts dramatically reduc
72 Immunodepletion from the medium of all Abeta species com
73 SRC-1
immunodepletion from type II cell nuclear extracts reduc
74 Immunodepletion from Xenopus egg extracts indicated that
75 omoted cell death that was suppressed by NGF
immunodepletion in a mouse photoreceptor cell line (661w
76 Immunodepletion,
in vitro phosphorylation, and peptide-m
77 embly experiments and an additional 1-3 h if
immunodepletion is performed.
78 adoptive transfer of lymphocytes after host
immunodepletion,
it is possible to mediate objective can
79 in was purified from betaTC6,F7 cells via an
immunodepletion method.
80 receiving: I) no other treatment (n=4), II)
immunodepletion (
n=5), and III) immunodepletion plus a s
81 Here, we show that INU1-induced CLEC-2
immunodepletion occurs through Src-family kinase-depende
82 Immunodepletion of 4.1 disrupted microtubule arrays and
83 otubules into asters depends on 4.1R in that
immunodepletion of 4.1R from the extract resulted in ran
84 Immunodepletion of ACF from rat liver extracts abolished
85 ular endothelial cell migration; conversely,
immunodepletion of Angptl4 reduced PgammaCA-mediated cel
86 Immunodepletion of annexin II from type II cell cytosol
87 d proteins from the target cell, followed by
immunodepletion of antibodies that recognize proteins fr
88 Immunodepletion of antimicrobial factors with staphyloci
89 Furthermore,
immunodepletion of APE1 from active gel filtration fract
90 Furthermore,
immunodepletion of APRIL under conditions that prevent A
91 timulated barbed-end polymerization, whereas
immunodepletion of Arp2 or sequestration of Arp2 using s
92 Immunodepletion of AS160 in tibialis anterior muscle lys
93 l MNC protein is significantly attenuated by
immunodepletion of AUF1, providing new evidence that thi
94 Immunodepletion of Bid from cell extracts eliminated the
95 Immunodepletion of both ATM and ATR abrogated the checkp
96 Immunodepletion of both tPA and lysine-binding proteins
97 Immunodepletion of Bub1 abolishes the spindle checkpoint
98 Here, we show that
immunodepletion of Bub1 from egg extracts blocks the abi
99 Immunodepletion of BubR1 greatly reduces kinetochore bin
100 Immunodepletion of C- but not N-terminal proteoforms nor
101 Furthermore,
immunodepletion of CAK under high-salt conditions, which
102 y, RNA interference, co-immunoprecipitation,
immunodepletion of candidate proteins, and reconstitutio
103 Immunodepletion of caspase-3 from 293 extracts abolished
104 hed cleavage of Bcl-2 and caspase-7, whereas
immunodepletion of caspase-7 had no effect on Bcl-2 clea
105 se) activity, most of which was removed upon
immunodepletion of CD151.
106 Immunodepletion of CD4(+) but not CD8(+) T cells in tumo
107 Immunodepletion of CD8 T cells fully restored melanoma g
108 Immunodepletion of Cdc6 by microinjection of anti-Cdc6 a
109 Immunodepletion of CDK11(p110) from splicing extracts gr
110 Immunodepletion of CDK2/cyclin E in HeLa nuclear extract
111 Surprisingly,
immunodepletion of cellular extracts suggests IKKalpha i
112 Immunodepletion of CENP-C from metaphase egg extract pre
113 Immunodepletion of Claspin from egg extracts abolishes b
114 Immunodepletion of components of the complex - Cul-1, Sk
115 Immunodepletion of condensin inhibited microtubule growt
116 Immunodepletion of conditioned medium with an IDE antibo
117 Immunodepletion of conditioned medium with antibodies to
118 Immunodepletion of conventional PKCs from the cell lysat
119 Immunodepletion of COPI coatomer complex and associated
120 Immunodepletion of CUGBP2 co-precipitates ACF, and these
121 Furthermore,
immunodepletion of cystatin C from the conditioned mediu
122 Immunodepletion of cytoplasmic dynein from the A549 cell
123 Nevertheless,
immunodepletion of cytosol using the anti-P200/myosin II
124 Immunodepletion of DDK from Xenopus egg extracts impairs
125 Immunodepletion of detergent extracts with anti-Vti1p re
126 In vitro,
immunodepletion of DjA1 from interphase cytosol reduced
127 pendent gap filling was nearly eliminated by
immunodepletion of DNA polymerase lambda, but was restor
128 ion of a DNA-PK inhibitor, wortmannin, or by
immunodepletion of DNA-PKcs, supporting a positive role
129 Immunodepletion of Drf1 does not prevent DNA replication
130 Immunodepletion of DSIF from a Drosophila nuclear extrac
131 proximately 60% of the total soluble SS, and
immunodepletion of du1- mutant extracts with this antise
132 Immunodepletion of dynamin proteins also inhibited vesic
133 Finally, we show that
immunodepletion of E2F3 activity inhibits the induction
134 Immunodepletion of EB1 from cytostatic factor-arrested M
135 NA replication and that caffeine, as well as
immunodepletion of either ATM or ATR, abolishes this inh
136 on is blocked by addition of caffeine and by
immunodepletion of either ATR or Claspin.
137 tablishment of CSF arrest in meiosis II, and
immunodepletion of either protein blocked the establishm
138 Immunodepletion of either xFANCA or xFANCD2 from egg ext
139 Immunodepletion of endogenous Aven allowed mitotic entry
140 Immunodepletion of endogenous VHR eliminated the dephosp
141 Immunodepletion of ePAB increases the rate of both ARE-m
142 is specific for TRAP25 allowed quantitative
immunodepletion of essentially all TRAP/Mediator compone
143 Immunodepletion of factor VII from zebrafish plasma sele
144 However,
immunodepletion of FDH activity in RAT1 cells and in mur
145 Immunodepletion of fkn from five RA synovial tissue homo
146 In vivo,
immunodepletion of fkn from six RA SFs significantly inh
147 Immunodepletion of FLNA from nuclear extracts resulted i
148 Immunodepletion of gelsolin, but not Xenopus ADF/cofilin
149 We previously reported that
immunodepletion of Greatwall kinase prevents Xenopus egg
150 Immunodepletion of HeLa lysates by a monoclonal antibody
151 Here we show that
immunodepletion of Hip from reticulocyte lysate or addit
152 Immunodepletion of histone H1 caused the assembly of abe
153 Immunodepletion of hPrp16 from splicing extracts specifi
154 Immunodepletion of Hsc70 and Hsp70 impaired delta releas
155 ermore, the present results demonstrate that
immunodepletion of Hsp27 depletes cas-3.
156 purifies with the sGC-activating effect, and
immunodepletion of Hsp70 from COS-7 cytosol coincided wi
157 Immunodepletion of Hsp90 depletes Apaf-1 and thereby inh
158 Immunodepletion of HSP90-alpha from conditioned medium s
159 Of significance,
immunodepletion of IAP-2 from the hypoxic cytosol restor
160 he rate of cyclin B1 import was decreased by
immunodepletion of importin beta from cytosol.
161 Interference with MAPK activation by
immunodepletion of its activator MEK, or by addition of
162 acrine manner; these effects were blocked by
immunodepletion of Jagged-1 in EC-conditioned medium or
163 Immunodepletion of Jak2 virtually eliminated the ligand-
164 Immunodepletion of Janus kinases from the cell lysate be
165 nations of DNA ends was also decreased after
immunodepletion of Ku from the extract.
166 ed FAK by 70%, and this was accounted for by
immunodepletion of LAR.
167 Immunodepletion of LARP7 also depleted most of the 7SK r
168 shedding enhancer from the findings that (i)
immunodepletion of LasA from the partially purified samp
169 ocyte-derived fibrocyte differentiation, and
immunodepletion of LGALS3BP from MDA-MB 231 conditioned
170 Immunodepletion of LspA proteins from H. ducreyi culture
171 n effect similar to that obtained via direct
immunodepletion of matrix metalloproteinase-1.
172 Immunodepletion of MIP-1alpha from cytotrophoblast condi
173 Immunodepletion of Mos also abolished the transient acti
174 Immunodepletion of Mos from interphase egg extracts was
175 Immunodepletion of Nap1 decreased H1M binding to mitotic
176 Immunodepletion of NC2 beta/Dr1 protein complexes rescue
177 Immunodepletion of NELF also impairs promoter proximal p
178 Immunodepletion of NELF or DSIF from a nuclear extract d
179 Critically, specific
immunodepletion of neutrophils (polymorphonuclear leukoc
180 However, we show that intratumoral
immunodepletion of neutrophils does not abolish the effe
181 Additionally,
immunodepletion of neutrophils in infected mice confirme
182 Immunodepletion of neutrophils or monocytes inhibited th
183 in macrophages isolated from SCID mice after
immunodepletion of NK cells.
184 enocytes, and the rejection was prevented by
immunodepletion of NK1.1(+) or Ly49D(+) NK cells.
185 Immunodepletion of NQO1-null mice liver cytosol and part
186 RCA1 with the GADD45 promoter because either
immunodepletion of Oct-1 and NF-YA proteins or mutations
187 Immunodepletion of OPN from RASMC-conditioned medium inh
188 Immunodepletion of p15 BID prevents cytochrome c release
189 ells but not in proliferating cells; whereas
immunodepletion of p27(kip1) from cdk2-immunoprecipitate
190 or, and zymosan particles and was blocked by
immunodepletion of p42(mapk/erk2) and by specific inhibi
191 Immunodepletion of p75 and p40 from LGG-CM reversed LGG-
192 in rat lens explants, and this is blocked by
immunodepletion of PDGF-D.
193 Furthermore,
immunodepletion of Pin1 from mitotic cell extracts preve
194 Phosphorylation of lamin B was inhibited by
immunodepletion of PKCalpha from activated cytosol and w
195 PKCdelta phosphorylated NLRC4 S533 in vitro,
immunodepletion of PKCdelta from macrophage lysates bloc
196 ntibody, INU1, results in virtually complete
immunodepletion of platelet CLEC-2 in mice, which is, ho
197 Immunodepletion of platelets decreased early perivascula
198 ivity in fibrosarcoma cell culture medium by
immunodepletion of PLF.
199 The addition of kinase-defective Plk or
immunodepletion of Plk disrupts the fragmentation proces
200 Immunodepletion of Plx1 completely inhibited activation
201 2 kinase involved in checkpoint response, as
immunodepletion of Plx1 from checkpoint extracts abolish
202 Immunodepletion of Pnuts from egg extracts revealed its
203 Immunodepletion of polymerase lambda, but not polymerase
204 We show that the specific
immunodepletion of polymorphonuclear leukocyte neutrophi
205 Immunodepletion of PP2A from Xenopus egg extract resulte
206 We found that
immunodepletion of PP2A or inhibition of PP2A by okadaic
207 rived from Xenopus eggs, we demonstrate that
immunodepletion of protein phosphatase 2A (PP2A) from eg
208 hagocytosis of apoptotic lymphoma cells, and
immunodepletion of protein S eliminated the prophagocyti
209 In contrast,
immunodepletion of Raf-1 and B-Raf, two other MEK-activa
210 Immunodepletion of RANTES alone or in combination with m
211 In addition,
immunodepletion of Ref-1 from nuclear extracts demonstra
212 However,
immunodepletion of Ref-1/Ape from nuclear extract preven
213 Immunodepletion of Ref-1/Ape prevented probe association
214 d used to generate polyclonal antibodies for
immunodepletion of respective proteins from LGG-conditio
215 Immunodepletion of SBP2 from the lysates abolished Sec i
216 Simultaneous
immunodepletion of Scc2A and Scc2B from the extracts imp
217 f F box protein SKP2, and is not affected by
immunodepletion of SKP1 or mutations in CUL1 disrupting
218 Immunodepletion of SSX2IP impeded gamma-TuRC loading ont
219 Immunodepletion of STX5 and alpha-SNAP from PMs decrease
220 nced T cell accumulation in tissues, whereas
immunodepletion of T cells protected syndecan-1-null mic
221 ation and altered NPC differentiation, while
immunodepletion of Tat from Tat-containing conditioned m
222 The
immunodepletion of tau had no detectable effect on sever
223 Immunodepletion of TFII-I from nuclear extracts prior to
224 ynaptogenic effects, which were prevented by
immunodepletion of TGF-beta1.
225 Third,
immunodepletion of the 100-kDa subunit of X. laevis CPSF
226 pecific effect reversed by neutralization or
immunodepletion of the AutoAb pool.
227 Immunodepletion of the CDC5L complex from HeLa nuclear e
228 tochores assembled in Xenopus extracts after
immunodepletion of the complex did not contain xRod, xZw
229 ounts of CV2 increased the activity, whereas
immunodepletion of the CV2 fraction with an antibody aga
230 Immunodepletion of the endogenous NUFIP causes a marked
231 Immunodepletion of the large aggregated AT8-positive tau
232 Furthermore,
immunodepletion of the MEF2A-MEF2D complex from control
233 kinase activity as PKC-theta on the basis of
immunodepletion of the moesin kinase activity and copuri
234 Similarly,
immunodepletion of the PA700 from the extract also signi
235 enzymatic degradation of heparan sulfate and
immunodepletion of the syndecan-1 and -4 in wound fluid
236 nt basal transcription by either mutation or
immunodepletion of their function.
237 Immunodepletion of TIA-1 and TIAR from Xenopus translati
238 sactivation by Tat in transfected cells, and
immunodepletion of TIP30 from nuclear extracts abolishes
239 Immunodepletion of tissue-type plasminogen activator (tP
240 Inhibition or
immunodepletion of TOP decreased their degradation and t
241 cells against TRAIL-induced killing, whereas
immunodepletion of TRAILshort with a specific Ab restore
242 Immunodepletion of TRIM2 from cell lysates prepared from
243 Immunodepletion of xBLM from a Xenopus egg extract sever
244 Immunodepletion of Xblm from egg extracts results in acc
245 Immunodepletion of Xcds1 (and/or Xchk1) from egg extract
246 Immunodepletion of xCep57 from egg extracts yields weake
247 Immunodepletion of xDNA2 resulted in a significant reduc
248 ciently resected in Xenopus egg extracts and
immunodepletion of Xenopus DNA2 also strongly inhibited
249 Using
immunodepletion of Xenopus nuclear reconstitution extrac
250 Immunodepletion of Xgrip210 blocks not only the assembly
251 control of the checkpoint protein xMps1, as
immunodepletion of xMps1 prevents binding of Plx1 to kin
252 Immunodepletion of XNercc from egg extracts results in d
253 Immunodepletion of Xnf7 from Xenopus laevis egg extracts
254 Immunodepletion of XRIPalpha from the egg extracts block
255 Moreover, we found that
immunodepletion of ZBP-89 prevented recruitment of ATM t
256 and Thr18 of MLC20 with similar potency; (b)
immunodepletion of ZIP kinase from the cell extracts mar
257 The effects of ALF overexpression and ALF
immunodepletion on a thymidine kinase promoter construct
258 ibe methods to inhibit a specific protein by
immunodepletion or addition of an inhibitor such as a do
259 Immunodepletion or affinity depletion of these fragments
260 When CENP-E function is disrupted by
immunodepletion or antibody addition, extracts fail to a
261 em, DNA end joining was reduced by NF90/NF45
immunodepletion or by RNA digestion to an extent similar
262 Immunodepletion or inhibition of calpain-1 in hypotonica
263 Xorbit
immunodepletion or its inhibition by a dominant-negative
264 A selective chemical inhibitor,
immunodepletion,
or genetic deletion of Fap stabilized r
265 t (n=4), II) immunodepletion (n=5), and III)
immunodepletion plus a single dose of mouse anti-human C
266 This GPVI
immunodepletion predominantly occurs through ectodomain
267 tants of CMV-infected mature moDCs, and CD83
immunodepletion removes the inhibitory effect of these s
268 nduced endothelial cell migration, but IL-18
immunodepletion resulted in a 68 +/- 5% decrease in HMVE
269 aster embryo extracts, either by mutation or
immunodepletion,
resulted in loss of their ability to re
270 Alternative hypotheses to explain the DAO
immunodepletion results (such as poisoning of DAO activi
271 f platelets extensively purified by negative
immunodepletion showed platelets contained IL-1beta, and
272 Immunodepletion studies confirm that these subunits have
273 Chemokine
immunodepletion studies confirmed that tumor-derived MCP
274 Immunoprecipitation and
immunodepletion studies indicate that p130 can compensat
275 Immunodepletion studies of P-4-vaccinated mice indicate
276 Immunoinhibition and
immunodepletion studies showed that the Hsp70 chaperone
277 Immunodepletion studies suggested interleukin 6 (IL6) as
278 Through
immunodepletion studies, we identified vascular endothel
279 By using specific anti-ACAT-1 antibodies in
immunodepletion studies, we previously found that ACAT-1
280 eripheral lymphocyte population after severe
immunodepletion such as that which occurs in HIV-infecte
281 Immunodepletion suggested that the identity of p140 was
282 au uptake despite removing less total tau by
immunodepletion,
suggesting specific interactions with s
283 ared ch-TOGp-specific antibodies and show by
immunodepletion that ch-TOGp is required for microtubule
284 lant patients given Campath-1H (Alemtuzumab)
immunodepletion therapy and long-term rapamycin monother
285 ect on the expression of cyclin E. p27(kip1)-
immunodepletion upregulated cyclin E-dependent kinase ac
286 Immunodepletion using antibodies specific for the exosom
287 Immunodepletion using non-neutralizing antibodies to gp1
288 igen was investigated by immunoprecipitation/
immunodepletion,
using commercial monoclonal antibodies
289 Immunodepletion was performed on brain extract from tau-
290 Immunodepletion with anti-asialo-GM1 or anti-CD4 during
291 Similarly,
immunodepletion with anti-FDH antibody does not remove t
292 te with the decrease in platelet count after
immunodepletion with anti-GPIb or anti-CD41 antibody.
293 Immunodepletion with anti-NF1 antibodies dramatically de
294 the Vti1p that is complexed with Vam3p, and
immunodepletion with anti-Nyv1p removes all the Ykt6p in
295 l the Ykt6p that is in a complex with Vam3p,
immunodepletion with anti-Ykt6p removes all the Vti1p th
296 Immunodepletion with antibodies against SSEA-5 and two a
297 Immunodepletion with antiserum to GATA-2 prevented forma
298 Immunodepletion with H185 antibody resulted in no OC125
299 l cross-linker and removed non-native Env by
immunodepletion with non-neutralizing antibodies.
300 are required for Tat activation as shown by
immunodepletion with specific sera and complementation w