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 XNercc
immunodepletion also slows aster assembly induced by Ran
11 Immunodepletion analyses demonstrated that the 50-kDa pr
12 ern immunoblotting, immunoprecipitation, and
immunodepletion analyses were performed using antibodies
13 Immunodepletion analysis shows that the Mad1-free Mad2 p
14 Maskin
immunodepletion and add-back experiments demonstrate tha
15 epeat addition processivity, as shown by p82
immunodepletion and add-back.
16 action (MLR) were used to assess efficacy of
immunodepletion and confirm donor-specific tolerance and
17 ropinosomes/endosomes is abrogated by septin
immunodepletion and function-blocking antibodies and is
18 Syndecan-1
immunodepletion and further degradation experiments iden
19 Immunodepletion and gene disruption indicate BID is requ
20 Immunodepletion and immunoprecipitation studies indicate
21 Immunodepletion and knockout studies indicated that thro
22 Immunodepletion and okadaic acid inhibition studies demo
23 0 is not sufficient for AP release; however,
immunodepletion and reconstitution experiments establish
24 Immunodepletion and reconstitution with recombinant prot
25 Immunodepletion and reexpression experiments revealed th
26 81-Galpha(q/11) complex was revealed by CD81
immunodepletion and reexpression experiments.
27 C in in vitro rephosphorylation assays using
immunodepletion and rescue with recombinant protein.
28 hese cells by size-exclusion chromatography,
immunodepletion,
and absolute quantification mass spectr
29 ich were abrogated by Tat heat inactivation,
immunodepletion,
and cysteine mutation at position 30.
30 y assessed functional tolerance, efficacy of
immunodepletion,
and donor-specific chimerism.
31 y inactivate Mediator (immunoneutralization,
immunodepletion,
and inhibitory polypeptides), we find t
32 say in combination with immunoprecipitation,
immunodepletion,
and specific inhibition.
33 Using
immunodepletion approach and a rephosphorylation assay i
34 Second, we used purification and
immunodepletion approaches to identify a critical role f
35 f phosphatase inhibitors in combination with
immunodepletion assays identified this activity to be re
36 demonstrated in HeLa nuclear extracts using
immunodepletion assays.
37 Platelet
immunodepletion before TGN markedly exacerbated hematuri
38 Both inhibitor types and myofibroblast
immunodepletion block the emergence of castration-resist
39 o chromatin with similar kinetics, and DUE-B
immunodepletion blocks replication and the loading of Cd
40 l-free system lends itself to use in protein
immunodepletion,
complementation and drug inhibition as
41 al adhesion to airway epithelia, and MUC1-ED
immunodepletion completely abrogated their inhibitory ac
42 as found to contain DNase IIalpha, but after
immunodepletion,
considerable acid-active endonuclease r
43 Maraviroc (CCR5 antagonist) or CCL5
immunodepletion diminished 95% and 70% of the effect of
44 Whole animal KC, MIP-2, or TNFalpha
immunodepletion each abrogated TPA-induced inflammation,
45 Plasma
immunodepletion experiments and experiments using recomb
46 zation on Cdc2 in the p53 null cells, though
immunodepletion experiments demonstrated that only a sma
47 - or two-step immunoprecipitation assays and
immunodepletion experiments followed by Western blot ana
48 t in extracts of estrogen-treated cells, and
immunodepletion experiments identify this factor as p21(
49 two-hybrid analysis, and immunoprecipitation/
immunodepletion experiments indicate that Tap binds tigh
50 Immunodepletion experiments indicate that the Cdc73-CPSF
51 Immunodepletion experiments indicate that virtually all
52 Co-immunoprecipitation and
immunodepletion experiments indicated that approximately
53 Immunodepletion experiments indicated that EWI-2-CD9/CD8
54 Immunodepletion experiments of mitotic extracts revealed
55 Immunodepletion experiments revealed that c-ErbB-2 prote
56 ytes was shown to be biologically important;
immunodepletion experiments revealed that TNF-alpha was
57 Furthermore,
immunodepletion experiments show that MGL accounts for a
58 Immunodepletion experiments showed that the LP-BER activ
59 Immunodepletion experiments suggest that extension requi
60 Here, we demonstrate by
immunodepletion experiments that 5'-dRP-N(3) excision in
61 Co-immunoprecipitation and
immunodepletion experiments using an antibody to muted c
62 G12
immunodepletion experiments with hydrolyzed gluten showe
63 by immunoblotting, immunoprecipitation, and
immunodepletion experiments.
64 ct, as determined by immunoprecipitation and
immunodepletion experiments.
65 usly we described a reliable method based on
immunodepletion for isolating mesenchymal stem cells (MS
66 Using
immunodepletion from and antibody addition to Xenopus la
67 Emi1
immunodepletion from cycling Xenopus extracts strongly d
68 e systemically administered MSCs purified by
immunodepletion from male bleomycin (BLM)-resistant BALB
69 TAF(I)41
immunodepletion from nuclear extracts dramatically reduc
70 Immunodepletion from the medium of all Abeta species com
71 SRC-1
immunodepletion from type II cell nuclear extracts reduc
72 Immunodepletion from Xenopus egg extracts indicated that
73 omoted cell death that was suppressed by NGF
immunodepletion in a mouse photoreceptor cell line (661w
74 Immunodepletion,
in vitro phosphorylation, and peptide-m
75 embly experiments and an additional 1-3 h if
immunodepletion is performed.
76 adoptive transfer of lymphocytes after host
immunodepletion,
it is possible to mediate objective can
77 in was purified from betaTC6,F7 cells via an
immunodepletion method.
78 receiving: I) no other treatment (n=4), II)
immunodepletion (
n=5), and III) immunodepletion plus a s
79 Here, we show that INU1-induced CLEC-2
immunodepletion occurs through Src-family kinase-depende
80 Immunodepletion of 4.1 disrupted microtubule arrays and
81 otubules into asters depends on 4.1R in that
immunodepletion of 4.1R from the extract resulted in ran
82 Immunodepletion of ACF from rat liver extracts abolished
83 Immunodepletion of all detectable Hb from TLF1 does not
84 ular endothelial cell migration; conversely,
immunodepletion of Angptl4 reduced PgammaCA-mediated cel
85 Immunodepletion of annexin II from type II cell cytosol
86 d proteins from the target cell, followed by
immunodepletion of antibodies that recognize proteins fr
87 Immunodepletion of antimicrobial factors with staphyloci
88 Furthermore,
immunodepletion of APE1 from active gel filtration fract
89 Furthermore,
immunodepletion of APRIL under conditions that prevent A
90 timulated barbed-end polymerization, whereas
immunodepletion of Arp2 or sequestration of Arp2 using s
91 Immunodepletion of AS160 in tibialis anterior muscle lys
92 l MNC protein is significantly attenuated by
immunodepletion of AUF1, providing new evidence that thi
93 Immunodepletion of Bid from cell extracts eliminated the
94 Immunodepletion of both ATM and ATR abrogated the checkp
95 Immunodepletion of both tPA and lysine-binding proteins
96 Immunodepletion of Bub1 abolishes the spindle checkpoint
97 Here, we show that
immunodepletion of Bub1 from egg extracts blocks the abi
98 Immunodepletion of BubR1 greatly reduces kinetochore bin
99 Furthermore,
immunodepletion of CAK under high-salt conditions, which
100 y, RNA interference, co-immunoprecipitation,
immunodepletion of candidate proteins, and reconstitutio
101 Immunodepletion of caspase-3 from 293 extracts abolished
102 hed cleavage of Bcl-2 and caspase-7, whereas
immunodepletion of caspase-7 had no effect on Bcl-2 clea
103 se) activity, most of which was removed upon
immunodepletion of CD151.
104 Immunodepletion of CD4(+) but not CD8(+) T cells in tumo
105 Immunodepletion of CD8 T cells fully restored melanoma g
106 Immunodepletion of Cdc6 by microinjection of anti-Cdc6 a
107 Immunodepletion of CDK11(p110) from splicing extracts gr
108 Immunodepletion of CDK2/cyclin E in HeLa nuclear extract
109 Surprisingly,
immunodepletion of cellular extracts suggests IKKalpha i
110 Immunodepletion of CENP-C from metaphase egg extract pre
111 Immunodepletion of Claspin from egg extracts abolishes b
112 Immunodepletion of components of the complex - Cul-1, Sk
113 Immunodepletion of condensin inhibited microtubule growt
114 Immunodepletion of conditioned medium with an IDE antibo
115 Immunodepletion of conditioned medium with antibodies to
116 Immunodepletion of conventional PKCs from the cell lysat
117 Immunodepletion of COPI coatomer complex and associated
118 Immunodepletion of CUGBP2 co-precipitates ACF, and these
119 Furthermore,
immunodepletion of cystatin C from the conditioned mediu
120 Immunodepletion of cytoplasmic dynein from the A549 cell
121 Nevertheless,
immunodepletion of cytosol using the anti-P200/myosin II
122 Immunodepletion of DDK from Xenopus egg extracts impairs
123 Immunodepletion of detergent extracts with anti-Vti1p re
124 pendent gap filling was nearly eliminated by
immunodepletion of DNA polymerase lambda, but was restor
125 ion of a DNA-PK inhibitor, wortmannin, or by
immunodepletion of DNA-PKcs, supporting a positive role
126 Immunodepletion of Drf1 does not prevent DNA replication
127 Immunodepletion of DSIF from a Drosophila nuclear extrac
128 proximately 60% of the total soluble SS, and
immunodepletion of du1- mutant extracts with this antise
129 Immunodepletion of dynamin proteins also inhibited vesic
130 Finally, we show that
immunodepletion of E2F3 activity inhibits the induction
131 Immunodepletion of EB1 from cytostatic factor-arrested M
132 NA replication and that caffeine, as well as
immunodepletion of either ATM or ATR, abolishes this inh
133 on is blocked by addition of caffeine and by
immunodepletion of either ATR or Claspin.
134 tablishment of CSF arrest in meiosis II, and
immunodepletion of either protein blocked the establishm
135 Immunodepletion of either xFANCA or xFANCD2 from egg ext
136 Immunodepletion of endogenous Aven allowed mitotic entry
137 Immunodepletion of endogenous VHR eliminated the dephosp
138 Immunodepletion of ePAB increases the rate of both ARE-m
139 is specific for TRAP25 allowed quantitative
immunodepletion of essentially all TRAP/Mediator compone
140 Immunodepletion of factor VII from zebrafish plasma sele
141 However,
immunodepletion of FDH activity in RAT1 cells and in mur
142 Immunodepletion of fkn from five RA synovial tissue homo
143 In vivo,
immunodepletion of fkn from six RA SFs significantly inh
144 Immunodepletion of FLNA from nuclear extracts resulted i
145 Immunodepletion of gelsolin, but not Xenopus ADF/cofilin
146 We previously reported that
immunodepletion of Greatwall kinase prevents Xenopus egg
147 Immunodepletion of HeLa lysates by a monoclonal antibody
148 Here we show that
immunodepletion of Hip from reticulocyte lysate or addit
149 Immunodepletion of histone H1 caused the assembly of abe
150 Immunodepletion of hPrp16 from splicing extracts specifi
151 Immunodepletion of Hsc70 and Hsp70 impaired delta releas
152 ermore, the present results demonstrate that
immunodepletion of Hsp27 depletes cas-3.
153 purifies with the sGC-activating effect, and
immunodepletion of Hsp70 from COS-7 cytosol coincided wi
154 Immunodepletion of Hsp90 depletes Apaf-1 and thereby inh
155 Immunodepletion of HSP90-alpha from conditioned medium s
156 Of significance,
immunodepletion of IAP-2 from the hypoxic cytosol restor
157 he rate of cyclin B1 import was decreased by
immunodepletion of importin beta from cytosol.
158 KIs prevent CAK from activating the CDK-2 as
immunodepletion of induced CKIs from the inhibitory extr
159 Interference with MAPK activation by
immunodepletion of its activator MEK, or by addition of
160 acrine manner; these effects were blocked by
immunodepletion of Jagged-1 in EC-conditioned medium or
161 Immunodepletion of Jak2 virtually eliminated the ligand-
162 Immunodepletion of Janus kinases from the cell lysate be
163 nations of DNA ends was also decreased after
immunodepletion of Ku from the extract.
164 ed FAK by 70%, and this was accounted for by
immunodepletion of LAR.
165 Immunodepletion of LARP7 also depleted most of the 7SK r
166 shedding enhancer from the findings that (i)
immunodepletion of LasA from the partially purified samp
167 ocyte-derived fibrocyte differentiation, and
immunodepletion of LGALS3BP from MDA-MB 231 conditioned
168 Immunodepletion of LspA proteins from H. ducreyi culture
169 n effect similar to that obtained via direct
immunodepletion of matrix metalloproteinase-1.
170 Immunodepletion of MIP-1alpha from cytotrophoblast condi
171 Immunodepletion of Mos also abolished the transient acti
172 Immunodepletion of Mos from interphase egg extracts was
173 Immunodepletion of Nap1 decreased H1M binding to mitotic
174 Immunodepletion of NC2 beta/Dr1 protein complexes rescue
175 Immunodepletion of NELF also impairs promoter proximal p
176 Immunodepletion of NELF or DSIF from a nuclear extract d
177 Critically, specific
immunodepletion of neutrophils (polymorphonuclear leukoc
178 However, we show that intratumoral
immunodepletion of neutrophils does not abolish the effe
179 Additionally,
immunodepletion of neutrophils in infected mice confirme
180 Immunodepletion of neutrophils or monocytes inhibited th
181 in macrophages isolated from SCID mice after
immunodepletion of NK cells.
182 enocytes, and the rejection was prevented by
immunodepletion of NK1.1(+) or Ly49D(+) NK cells.
183 Immunodepletion of NQO1-null mice liver cytosol and part
184 RCA1 with the GADD45 promoter because either
immunodepletion of Oct-1 and NF-YA proteins or mutations
185 Immunodepletion of OPN from RASMC-conditioned medium inh
186 Immunodepletion of p15 BID prevents cytochrome c release
187 ells but not in proliferating cells; whereas
immunodepletion of p27(kip1) from cdk2-immunoprecipitate
188 or, and zymosan particles and was blocked by
immunodepletion of p42(mapk/erk2) and by specific inhibi
189 Furthermore,
immunodepletion of p67(phox) from adventitial fibroblast
190 Immunodepletion of p75 and p40 from LGG-CM reversed LGG-
191 in rat lens explants, and this is blocked by
immunodepletion of PDGF-D.
192 Furthermore,
immunodepletion of Pin1 from mitotic cell extracts preve
193 Phosphorylation of lamin B was inhibited by
immunodepletion of PKCalpha from activated cytosol and w
194 PKCdelta phosphorylated NLRC4 S533 in vitro,
immunodepletion of PKCdelta from macrophage lysates bloc
195 ntibody, INU1, results in virtually complete
immunodepletion of platelet CLEC-2 in mice, which is, ho
196 Immunodepletion of platelets decreased early perivascula
197 ivity in fibrosarcoma cell culture medium by
immunodepletion of PLF.
198 The addition of kinase-defective Plk or
immunodepletion of Plk disrupts the fragmentation proces
199 Immunodepletion of Plx1 completely inhibited activation
200 2 kinase involved in checkpoint response, as
immunodepletion of Plx1 from checkpoint extracts abolish
201 Immunodepletion of Pnuts from egg extracts revealed its
202 Immunodepletion of polymerase lambda, but not polymerase
203 We show that the specific
immunodepletion of polymorphonuclear leukocyte neutrophi
204 Immunodepletion of PP2A from Xenopus egg extract resulte
205 We found that
immunodepletion of PP2A or inhibition of PP2A by okadaic
206 rived from Xenopus eggs, we demonstrate that
immunodepletion of protein phosphatase 2A (PP2A) from eg
207 hagocytosis of apoptotic lymphoma cells, and
immunodepletion of protein S eliminated the prophagocyti
208 In contrast,
immunodepletion of Raf-1 and B-Raf, two other MEK-activa
209 Immunodepletion of RANTES alone or in combination with m
210 In addition,
immunodepletion of Ref-1 from nuclear extracts demonstra
211 However,
immunodepletion of Ref-1/Ape from nuclear extract preven
212 Immunodepletion of Ref-1/Ape prevented probe association
213 d used to generate polyclonal antibodies for
immunodepletion of respective proteins from LGG-conditio
214 Immunodepletion of SBP2 from the lysates abolished Sec i
215 Simultaneous
immunodepletion of Scc2A and Scc2B from the extracts imp
216 Immunodepletion of Scythe from extracts completely preve
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 nced T cell accumulation in tissues, whereas
immunodepletion of T cells protected syndecan-1-null mic
220 ation and altered NPC differentiation, while
immunodepletion of Tat from Tat-containing conditioned m
221 The
immunodepletion of tau had no detectable effect on sever
222 Immunodepletion of TFII-I from nuclear extracts prior to
223 ynaptogenic effects, which were prevented by
immunodepletion of TGF-beta1.
224 Third,
immunodepletion of the 100-kDa subunit of X. laevis CPSF
225 pecific effect reversed by neutralization or
immunodepletion of the AutoAb pool.
226 Immunodepletion of the CDC5L complex from HeLa nuclear e
227 tochores assembled in Xenopus extracts after
immunodepletion of the complex did not contain xRod, xZw
228 ounts of CV2 increased the activity, whereas
immunodepletion of the CV2 fraction with an antibody aga
229 Immunodepletion of the endogenous NUFIP causes a marked
230 Immunodepletion of the large aggregated AT8-positive tau
231 Furthermore,
immunodepletion of the MEF2A-MEF2D complex from control
232 kinase activity as PKC-theta on the basis of
immunodepletion of the moesin kinase activity and copuri
233 Similarly,
immunodepletion of the PA700 from the extract also signi
234 enzymatic degradation of heparan sulfate and
immunodepletion of the syndecan-1 and -4 in wound fluid
235 nt basal transcription by either mutation or
immunodepletion of their function.
236 Immunodepletion of TIA-1 and TIAR from Xenopus translati
237 sactivation by Tat in transfected cells, and
immunodepletion of TIP30 from nuclear extracts abolishes
238 Immunodepletion of tissue-type plasminogen activator (tP
239 Inhibition or
immunodepletion of TOP decreased their degradation and t
240 cells against TRAIL-induced killing, whereas
immunodepletion of TRAILshort with a specific Ab restore
241 Immunodepletion of TRIM2 from cell lysates prepared from
242 Immunodepletion of xBLM from a Xenopus egg extract sever
243 Immunodepletion of Xblm from egg extracts results in acc
244 Immunodepletion of Xcds1 (and/or Xchk1) from egg extract
245 Immunodepletion of xCep57 from egg extracts yields weake
246 Immunodepletion of xDNA2 resulted in a significant reduc
247 ciently resected in Xenopus egg extracts and
immunodepletion of Xenopus DNA2 also strongly inhibited
248 Using
immunodepletion of Xenopus nuclear reconstitution extrac
249 Immunodepletion of Xgrip210 blocks not only the assembly
250 control of the checkpoint protein xMps1, as
immunodepletion of xMps1 prevents binding of Plx1 to kin
251 Immunodepletion of XNercc from egg extracts results in d
252 Immunodepletion of Xnf7 from Xenopus laevis egg extracts
253 Immunodepletion of XRIPalpha from the egg extracts block
254 Moreover, we found that
immunodepletion of ZBP-89 prevented recruitment of ATM t
255 and Thr18 of MLC20 with similar potency; (b)
immunodepletion of ZIP kinase from the cell extracts mar
256 The effects of ALF overexpression and ALF
immunodepletion on a thymidine kinase promoter construct
257 ibe methods to inhibit a specific protein by
immunodepletion or addition of an inhibitor such as a do
258 Immunodepletion or affinity depletion of these fragments
259 When CENP-E function is disrupted by
immunodepletion or antibody addition, extracts fail to a
260 em, DNA end joining was reduced by NF90/NF45
immunodepletion or by RNA digestion to an extent similar
261 Immunodepletion or inhibition of calpain-1 in hypotonica
262 Xorbit
immunodepletion or its inhibition by a dominant-negative
263 A selective chemical inhibitor,
immunodepletion,
or genetic deletion of Fap stabilized r
264 t (n=4), II) immunodepletion (n=5), and III)
immunodepletion plus a single dose of mouse anti-human C
265 This GPVI
immunodepletion predominantly occurs through ectodomain
266 tants of CMV-infected mature moDCs, and CD83
immunodepletion removes the inhibitory effect of these s
267 nduced endothelial cell migration, but IL-18
immunodepletion resulted in a 68 +/- 5% decrease in HMVE
268 aster embryo extracts, either by mutation or
immunodepletion,
resulted in loss of their ability to re
269 Alternative hypotheses to explain the DAO
immunodepletion results (such as poisoning of DAO activi
270 f platelets extensively purified by negative
immunodepletion showed platelets contained IL-1beta, and
271 Immunodepletion studies confirm that these subunits have
272 Chemokine
immunodepletion studies confirmed that tumor-derived MCP
273 Immunoprecipitation and
immunodepletion studies indicate that p130 can compensat
274 Immunodepletion studies of P-4-vaccinated mice indicate
275 Immunoinhibition and
immunodepletion studies showed that the Hsp70 chaperone
276 Immunodepletion studies suggested interleukin 6 (IL6) as
277 Through
immunodepletion studies, we identified vascular endothel
278 By using specific anti-ACAT-1 antibodies in
immunodepletion studies, we previously found that ACAT-1
279 eripheral lymphocyte population after severe
immunodepletion such as that which occurs in HIV-infecte
280 Immunodepletion suggested that the identity of p140 was
281 au uptake despite removing less total tau by
immunodepletion,
suggesting specific interactions with s
282 ared ch-TOGp-specific antibodies and show by
immunodepletion that ch-TOGp is required for microtubule
283 lant patients given Campath-1H (Alemtuzumab)
immunodepletion therapy and long-term rapamycin monother
284 ect on the expression of cyclin E. p27(kip1)-
immunodepletion upregulated cyclin E-dependent kinase ac
285 Immunodepletion using antibodies specific for the exosom
286 Immunodepletion using non-neutralizing antibodies to gp1
287 igen was investigated by immunoprecipitation/
immunodepletion,
using commercial monoclonal antibodies
288 Immunodepletion was performed on brain extract from tau-
289 Immunodepletion with anti-asialo-GM1 or anti-CD4 during
290 Similarly,
immunodepletion with anti-FDH antibody does not remove t
291 te with the decrease in platelet count after
immunodepletion with anti-GPIb or anti-CD41 antibody.
292 Immunodepletion with anti-NF1 antibodies dramatically de
293 the Vti1p that is complexed with Vam3p, and
immunodepletion with anti-Nyv1p removes all the Ykt6p in
294 l the Ykt6p that is in a complex with Vam3p,
immunodepletion with anti-Ykt6p removes all the Vti1p th
295 Immunodepletion with antibodies against SSEA-5 and two a
296 clitaxel treated cells was reduced following
immunodepletion with antibodies directed against individ
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