1 A
phosphospecific Ab was generated to this region of Pak (
2 f Stat5a (Ser(726)) as determined by a novel
phosphospecific Ab; and 3) Stat5a/b DNA binding to the S
3 A panel of
phosphospecific Abs was used to investigate the phosphor
4 erformed on archived bone marrow (BM) with a
phosphospecific anti-AKT antibody.
5 cally by quantitative immunoblotting using a
phosphospecific anti-RyR antibody.
6 Using
phosphospecific antibodies (Abs) directed to single phos
7 n was evaluated by immunoblot analysis using
phosphospecific antibodies against mitogen-activated pro
8 In this study, using
phosphospecific antibodies against rat IRS-1 phosphoryla
9 Phosphospecific antibodies against T308 and S473 were va
10 ed, in parallel, by biochemical assays using
phosphospecific antibodies against the ppERK and pKv4.2.
11 Phosphospecific antibodies and immunohistochemistry were
12 In this study, we have generated
phosphospecific antibodies and studied the developmental
13 ve detection of protein phosphorylation when
phosphospecific antibodies are not available, and provid
14 generally recommended that immunoblots using
phosphospecific antibodies be performed using bovine ser
15 Finally, these
phosphospecific antibodies demonstrated enhanced stainin
16 Use of
phosphospecific antibodies demonstrated that endogenous
17 These results were confirmed by use of
phosphospecific antibodies directed against phosphoserin
18 Phosphospecific antibodies directed against serine 474 d
19 ibits markedly lower levels of labeling with
phosphospecific antibodies directed against the S453, S5
20 using tandem mass spectrometry and generated
phosphospecific antibodies for each of these sites.
21 Western analysis of the cell extracts using
phosphospecific antibodies for MEK1/2 and ERK1/2 demonst
22 Using
phosphospecific antibodies for six phosphorylation sites
23 characterized a suite of MYPT1 proteins and
phosphospecific antibodies for specificity toward monoph
24 Western blot analysis using
phosphospecific antibodies indicated that 7a protein act
25 Immunoblotting with
phosphospecific antibodies indicated that there was litt
26 orylation of this residue can be detected by
phosphospecific antibodies raised against the correspond
27 All three
phosphospecific antibodies responded similarly to test d
28 Western blot analysis with
phosphospecific antibodies revealed that phosphorylation
29 Immunoblotting with
phosphospecific antibodies shows that activation of Fes
30 Phosphospecific antibodies that recognize sequences surr
31 Using newly developed
phosphospecific antibodies to p300 (pSer(1834)), and sit
32 Phosphospecific antibodies to proteins from the Erk path
33 We raised
phosphospecific antibodies to the four closely spaced si
34 Using
phosphospecific antibodies we showed that extracellular
35 Phosphospecific antibodies were used to identify phospho
36 Using LC-MS/MS and
phosphospecific antibodies, a novel IL-2/IL-15 inducible
37 By using
phosphospecific antibodies, both residues were observed
38 Western blot analysis, using
phosphospecific antibodies, revealed that mitogen-activa
39 w, using mass spectrometry, mutagenesis, and
phosphospecific antibodies, that agonist-regulated phosp
40 We now show, using
phosphospecific antibodies, that glucose and nitrogen ac
41 44, anti-serine/threonine, and anti-tyrosine
phosphospecific antibodies, to determine sCD44 concentra
42 stern blotting and immunohistochemistry with
phosphospecific antibodies, we demonstrate here that per
43 vitro kinase assays, mass spectrometry, and
phosphospecific antibodies, we identify serine 226 in GL
44 easured in cells by probing immunoblots with
phosphospecific antibodies.
45 physiological modulation of rabphilin using
phosphospecific antibodies.
46 kinase kinase 6 (MKK6), were assessed using
phosphospecific antibodies.
47 n can be monitored with C-terminal tail FPR1-
phosphospecific antibodies.
48 pectrometry and confirmed by mutagenesis and
phosphospecific antibodies.
49 g two-dimensional-phosphopeptide mapping and
phosphospecific antibodies.
50 TOF MS analysis, 2D gel electrophoresis, and
phosphospecific antibodies.
51 en greater multiplexing without the need for
phosphospecific antibodies.
52 due, which can subsequently be detected with
phosphospecific antibodies.
53 inases was determined by immunoblotting with
phosphospecific antibodies.
54 analyzed by SDS-PAGE and immunoblotted with
phosphospecific antibodies.
55 In this report we used a polyreactive
phosphospecific antibody (alpha-pDSQ) that recognizes a
56 lation was assessed by immunoblotting with a
phosphospecific antibody (anti-Ser(P)(2448)) and with mT
57 orylation of serine 369 was detected using a
phosphospecific antibody (KOR-P) able to distinguish the
58 Using a new
phosphospecific antibody (pPC2) to this site, we demonst
59 present study, we have taken advantage of a
phosphospecific antibody against Tyr789-phosphorylated R
60 Immunoblotting using a
phosphospecific antibody confirms these sites as Plk3 ph
61 To assess CDKL5 activity, we utilized a
phosphospecific antibody for phosphorylated EB2, a well-
62 We produced a
phosphospecific antibody for this site in CPI-17 and use
63 radiation as low as 0.5 Gy, and binding of a
phosphospecific antibody is detectable after the introdu
64 f ephrin-B signaling was investigated with a
phosphospecific antibody on cryosections and retinal who
65 ts insulin-dependent immunoreactivity with a
phosphospecific antibody raised against the protein kina
66 By combining the use of a
phosphospecific antibody recognizing a substrate motif o
67 m(s) of PKD activation, we developed a novel
phosphospecific antibody recognizing phosphorylated Ser(
68 However, Western blot analysis using a
phosphospecific antibody revealed no increase in insulin
69 Western blotting with a
phosphospecific antibody revealed that BTK rapidly autop
70 Immunoblot analysis with a
phosphospecific antibody showed that RIG-I serine 8 phos
71 ith young in a Western blot analysis using a
phosphospecific antibody that recognizes phosphotyrosine
72 strate consensus sequence RXRXX(pS/pT) and a
phosphospecific antibody that recognizes serine 21/9 of
73 A
phosphospecific antibody that recognizes these sites sho
74 Using a
phosphospecific antibody that specifically recognized SO
75 To confirm these results, we procured a
phosphospecific antibody to a peptide containing phospho
76 Using a
phosphospecific antibody to Syk (Tyr525/Tyr526) that mea
77 We generated a
phosphospecific antibody to Thr(P)-214 in the T-loop of
78 Furthermore, using a
phosphospecific antibody we show that phosphoserine-54 C
79 Using in vitro mapping, a
phosphospecific antibody, co-transfection assays, and un
80 ey NKCC2 phosphorylation, as detected with a
phosphospecific antibody, R5.
81 oth p46 and p55 isoforms of JNK, measured by
phosphospecific antibody, was increased severalfold.
82 Using a
phosphospecific antibody, we demonstrate that TRIP8b pho
83 By generating a
phosphospecific antibody, we demonstrate that tyrosine 9
84 Using a
phosphospecific antibody, we found that Y174 is phosphor
85 Furthermore, using a
phosphospecific antibody, we have elucidated the develop
86 two-dimensional phosphopeptide mapping and a
phosphospecific antibody, we identified tyrosine 813 as
87 Western analysis using a second
phosphospecific antibody, which primarily recognizes PKD
88 a-adrenergic receptor stimulation by using a
phosphospecific antibody.
89 phosphorylation and by immunoblotting with a
phosphospecific antibody.
90 s spectrometry analysis and detection with a
phosphospecific antibody.
91 nduced phosphorylation of MKK3/6 detected by
phosphospecific antiserum but did not affect the poly(IC
92 Using a
phosphospecific antiserum to Lck, we show here that Lck
93 rylate the T-loop of Cdk9, we used a Thr-186-
phosphospecific antiserum to screen a phosphatase expres
94 PLK and phospho-TbCentrin2, identified using
phosphospecific antiserum.
95 Studies with
phosphospecific AR antibodies showed that PP1 inhibition
96 ical, and the molecular mechanisms mediating
phosphospecific binding are poorly understood.
97 paralogues have different characteristics of
phosphospecific binding to threonine-3 of histone H3, pr
98 (T412) in ECT2, which comprises a consensus
phosphospecific-
binding module for the Plk1 polo-box dom
99 Immunoblot analyses using anti-S535
phosphospecific eIF2Bepsilon antibody showed that S535 p
100 Recently,
phosphospecific flow cytometry has emerged as a powerful
101 ource for researchers interested in applying
phosphospecific flow cytometry to complex populations of
102 Here, using
phosphospecific flow cytometry to obtain malignant B-cel
103 In this study, using
phosphospecific flow cytometry, we analyze elements of t
104 d MAPK signaling was measured by whole-blood
phosphospecific flow cytometry.
105 d when the panA gene was disrupted, based on
phosphospecific fluorescent staining of proteins separat
106 ation of the tag, which can be detected with
phosphospecific GSK-3beta antibodies.
107 ced by immunofluorescence focus staining for
phosphospecific histone H2AX.
108 excellent agreement with activity assays and
phosphospecific immunoblotting with the same samples, we
109 Mass spectrometry analysis of
phosphospecific immunoprecipitation reactions revealed n
110 lity shift assay, immunoblot analysis with a
phosphospecific MAP kinase antibody, and an immune compl
111 MITF could be a target of RANKL signaling, a
phosphospecific MITF antibody directed against conserved
112 ct this phosphorylation event, we employed a
phosphospecific monoclonal antibody probe that recognize
113 Phosphospecific motif antibodies offer a new approach to
114 Western blot analysis using
phosphospecific p38 and p44/p42 mitogen-activated protei
115 itation analyses using IkappaBalpha and S536
phosphospecific p65 NF-kappaB Abs demonstrated that alth
116 ochemistry and Western blot analyses using a
phosphospecific PDE5 antibody.
117 ous phosphorylation of PKC substrates with a
phosphospecific PKC substrate Ab (pPKC(s)).
118 s cell and tissue backgrounds, we prepared a
phosphospecific polyclonal antibody designated alphapSer
119 Our
phosphospecific probes also revealed that paired helical
120 catalytic domains have been repurposed as a
phosphospecific RR input sensor, thereby reversing the f
121 gulation of barrier function, we generated a
phosphospecific VASP antibody targeting the Ser157 resid