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