1 bly in frog egg extracts from which NuMA was
immunodepleted.
2 tolerance induced in recipients that are not
immunodepleted.
3 Here, we
immunodeplete a single subunit, the Nup107-160 complex,
4 After
immunodepleting alpha-synuclein, we observed a specific
5 Immunodepleting amyloid or tau proteins from the PA103 s
6 ivity from lysates of mAb-treated cells: the
immunodepleted and heated lysates lose the capacity to i
7 iapoptotic effect of ARDS BAL was blocked by
immunodepleting BAL of G-CSF and GM-CSF.
8 intestines, most of the ACAT activity can be
immunodepleted by anti-ACAT-2.
9 ase activity associated with U(L)42 could be
immunodepleted by antibody to cdc2, and (v) U(L)42 trans
10 e-treated HeLa cells because MAC activity is
immunodepleted by Bax antibodies.
11 izing CXCL5 expressed on ECs or when used to
immunodeplete coculture-conditioned medium.
12 We then used
immunodepleted cytosol and GDP dissociation inhibitor-tr
13 Immunodepleting cytosolic PDK1 from an in vitro reaction
14 tially purified Narp and can be specifically
immunodepleted,
demonstrating that Narp is the active pr
15 ract-based system in which Mediator has been
immunodepleted displays a near-absolute dependence on ec
16 MVEC migration beyond the effect detected by
immunodepleting each factor alone.
17 addition of recombinant hSBF protein to the
immunodepleted extract reconstituted stimulated transcri
18 , restored the splicing activity of the Sip1-
immunodepleted extract.
19 constitutes mitotic aster assemblies in 4.1R-
immunodepleted extracts in vitro.
20 nalysis of preinitiation complexes formed in
immunodepleted extracts suggests that CDK9 phosphorylate
21 tion and in vitro transcription assays using
immunodepleted extracts supplemented with recombinant pr
22 less active in restoring gap filling to the
immunodepleted extracts, and polymerase beta was complet
23 In xCep57
immunodepleted extracts, sperm centrosomes nucleate with
24 ucible DNA binding upon addition of Ref-1 to
immunodepleted extracts.
25 Purified MMCP reconstituted activity in
immunodepleted extracts.
26 PFK-M in skeletal muscle because nNOS can be
immunodepleted from cytosolic skeletal muscle extracts u
27 When XDna2 was
immunodepleted from interphase egg extracts, chromosomal
28 ation frequency was found after pol iota was
immunodepleted from nuclear extracts of the cells.
29 prepare control matrix, endogenous Myl3 was
immunodepleted from pooled rat serum.
30 This activity can be
immunodepleted from prostate cancer tissue extracts.
31 Moreover, the alpha7-2 subunit could be
immunodepleted from protein extracts by solid-phase immu
32 ated when yTAF40 and associated proteins are
immunodepleted from solution, indicating that the functi
33 When Bax was
immunodepleted from the cytosolic extracts of p53-expres
34 ract but failed to activate Pak when Akt was
immunodepleted from the extract.
35 reover, glycolate-removing activity could be
immunodepleted from the fractionated extracts by antiser
36 eriments in which Xwee1, Xchk1, or both were
immunodepleted from Xenopus egg extracts suggested that
37 re produced that had the unique property of "
immunodepleting"
GPVI from the murine platelet surface a
38 Conversely,
immunodepleting GSTp from protein extracts attenuated JN
39 TFIIB) and in a complex system, using TFIIB-
immunodepleted HeLa cell nuclear extract (NE).
40 Immunodepleted HeLa S100 transcription extract no longer
41 autoimmune disease scleroderma were used to
immunodeplete human RNase P activity.
42 l anti-ACAT-2 antibodies that quantitatively
immunodepleted human ACAT-2, a 46-kDa protein expressed
43 ies raised against PAPP-A both inhibited and
immunodepleted IGFBP-4 protease activity in human fibrob
44 e complex (IC)-mediated inflammation in mice
immunodepleted in platelets and/or neutrophils or defici
45 that re-addition of exogenous drICE to such
immunodepleted lysates restores apoptotic activity.
46 leotide-treated cells, and was lost from the
immunodepleted lysates.
47 rs, and this toxicity was eliminated through
immunodepleting macrophage/microglia from the culture.
48 nformation-dependent and could be reduced by
immunodepleting Mcc(ia).
49 cells resulted in decreased virus burden in
immunodepleted MCMV-infected syngeneic mice.
50 s on the cell surface, yet all metastases in
immunodepleted mice were MHC class I-positive.
51 sing combinations of genetically altered and
immunodepleted mice, we found evidence for gamma/delta T
52 Purified anti-FksAp immunoglobulin G
immunodepletes nearly all of the GS activity in crude or
53 y were divided into three matched groups and
immunodepleted of albumin, IgG, IgA, haploglobin, antitr
54 Experiments with plasma
immunodepleted of antithrombin or heparin cofactor II co
55 When MV-4-11 cell extracts were
immunodepleted of AUF1, the rate of decay of ARE(bcl-2)
56 Moreover, Kc cell nuclear extracts that were
immunodepleted of B52 lost their ability to splice this
57 Drosophila S-2 cell extracts that were
immunodepleted of dTAFIII105 were substantially reduced
58 Proteoliposomes from extracts
immunodepleted of either Vam3p or Ypt7p could not fuse,
59 CSF extracts
immunodepleted of Emi1 degrade cyclin B, and exit from m
60 ack into a Xenopus egg extract that has been
immunodepleted of endogenous condensin.
61 oocyte-type 5S rRNA genes in nuclear extract
immunodepleted of endogenous TFIIIA.
62 ally by measuring FXIII-A2 in plasma samples
immunodepleted of FXIII-A2B2.
63 In HeLa cell extracts
immunodepleted of hPrp18, the second step of pre-mRNA sp
64 Infection of mice
immunodepleted of IFN-gamma-producing cells or infection
65 rom Xenopus eggs that can be fractionated or
immunodepleted of individual proteins.
66 Mice
immunodepleted of neutrophils before surgery demonstrate
67 In mice
immunodepleted of neutrophils or lacking the leukocyte-s
68 ER activity is much reduced in cell extracts
immunodepleted of p53.
69 Recipients
immunodepleted of PMNs before transplantation demonstrat
70 pRB during G(1)/S but was found in extracts
immunodepleted of pRB in M-phase.
71 Human plasma selectively
immunodepleted of pre-beta(1)-HDL was used to study fact
72 Lens lysates were
immunodepleted of proteasomes using an antibody against
73 on leukocytes, an HL-60 membrane preparation
immunodepleted of PSGL-1 supported rolling of L-selectin
74 ssociation inhibitor), together with cytosol
immunodepleted of Rab5, fusion was virtually absent.
75 lectrophoretic mobility shift assay extracts
immunodepleted of Ref-1 protein demonstrated that the in
76 Xenopus laevis egg extracts
immunodepleted of Rsk lost their capacity to undergo mit
77 SFs from six RA patients
immunodepleted of soluble fkn induced 56% less migration
78 Synovial fluids (SF) were
immunodepleted of sVCAM-1 to identify a role for sVCAM-1
79 himeric mice in which wild-type (WT) marrow,
immunodepleted of T cells and stromal cells, is transpla
80 Strikingly, when tumor-bearing mice were
immunodepleted of T lymphocytes or asialo GM1-positive c
81 duced from normal human plasma (NHP), plasma
immunodepleted of TAFI (TdP), and TdP reconstituted with
82 rified components lacking TAFI or in plasmas
immunodepleted of TAFI.
83 -independent manner in HeLa nuclear extracts
immunodepleted of TBP and major TAFIIs.
84 complex is combined with a S.pombe fraction
immunodepleted of TBP.
85 effects of SC-CM were abolished if SC-CM was
immunodepleted of TGF-beta1 or if the latency-associated
86 Genomic DNA replicated in extracts
immunodepleted of X-Mre11 complex accumulates DSBs as de
87 When Xenopus egg extracts were
immunodepleted of Xenopus Hbo1 (XHbo1), chromatin bindin
88 inor 135-kDa protein in the preparation, can
immunodeplete Pan1p but not PAN activity.
89 Coagulation assays using
immunodepleted plasmas showed that the enhancement of he
90 In the BMP9/10-
immunodepleted postnatal retina-a mouse model of HHT vas
91 opoietic stem cells into nonmyeloablated but
immunodepleted (
preconditioned) recipients can produce a
92 To address these issues, we
immunodepleted precursor GLUT4-rich vesicles and then im
93 PTX treatment of a CFTR-
immunodepleted protein preparation incorporated into bil
94 ium that was injected intragraft with CXCL16-
immunodepleted RA synovial fluid (SF).
95 n amounts were equivalent in mock and Ric-8A-
immunodepleted rabbit reticulocyte lysate (RRL).
96 ngly, when we used anti-RanBP1 antibodies to
immunodeplete RanBP1 from Xenopus egg extracts, we found
97 8, whereas an autoimmune serum that does not
immunodeplete RNase P activity did not react with these
98 11(p110) immune complexes to the CDK11(p110)-
immunodepleted splicing reactions completely restored sp
99 s tested directly by examining the effect of
immunodepleting Ssa1/2p from yeast cytosol and subsequen
100 Anti-p43 antibodies
immunodeplete telomerase RNA and telomerase activity fro
101 Anti-Cbl antibody completely
immunodepleted the CrkL-associated 120kDa phosphotyrosyl
102 Here we
immunodepleted the EJC core component eIF4A3 from HeLa c
103 erum was not specific to DAO, even though it
immunodepleted the majority of DAO activity from root ex
104 overexpressed p9 in Xenopus egg extracts and
immunodepleted the protein from these extracts.
105 tep of pre-mRNA splicing is less affected by
immunodepleting the complex.
106 man fetal neurons, which could be blocked by
immunodepleting the supernatants of granzyme B (GrB).
107 tivity when added to extracts that have been
immunodepleted using anti-CDC5L antibodies.
108 estored replication activity to egg extracts
immunodepleted with anti-DUE-B antibody, suggesting that
109 Islet homogenates
immunodepleted with anti-IAPP-specific antibodies were n
110 -1-specific IgG showed that fibrinogen is co-
immunodepleted with FALP and approximately 17% of total
111 tipartite complex with all these proteins as
immunodepleting with anti-p85 antiserum substantially re
112 Immunodepleting Xkid from egg extracts prevented normal
113 omboplastin-triggered thrombin generation in
immunodepleted zebrafish plasma.