ライフサイエンスコーパス: protein chip

1 igase carboxyl terminus of HSC70-interacting protein (CHIP).

2 carboxyl terminal of Hsp70/Hsp90 interacting protein (CHIP).

3 tein, carboxyl terminus of Hsc70-interacting protein (CHIP).

4 nd are thus an ideal substrate for selective protein chips.

5 y of the problems previously associated with protein chips.

6 d analysed using 17 different substrates and protein chips.

7 ate with the C terminus of Hsp70 interacting protein (CHIP), a multidomain ubiquitin ligase, to media

8 nstrate that C terminus of HSC70-interacting protein (CHIP), a regulator of protein quality control,

9 sm was carboxy terminus of Hsp70-interacting protein (CHIP), a tau ubiquitin ligase.

10 The carboxyl terminus of Hsp70-interacting protein (CHIP), a ubiquitin ligase/cochaperone, particip

11 Here we show that the LIM-binding protein Chip acts as a cofactor for the Drosophila LIM-H

12 studies, the C terminus of Hsc70-interacting protein (CHIP), an E3 ubiquitin ligase that ubiquitinate

13 tein and the sampled analyte directly on the protein chip and subsequent in situ analysis by MALDI ma

14 two years has established the usefulness of protein chips and made important advances in preparing p

15 -down of the plasma membrane quality control proteins CHIP and Hsc70 partially restored DeltaF508CFTR

16 perones, the C terminus of Hsp70-interacting protein (CHIP) and the Hsp70/Hsp90 organizer protein, we

17 ligase carboxy terminus of Hsp70-interacting protein (CHIP) and the molecular chaperone Hsp90 are imp

18 igase carboxyl terminus of Hsc70-interacting protein (CHIP), and inhibits proteasome function.

19 Protein chips are disposable arrays of microwells in sil

20 scale monitoring of the immune response with protein chips are revealing new participants in the path

21 Protein chips are widely used for high-throughput proteo

22 We constructed a protein chip array (Antigen Discovery, Inc.) by expressi

23 Enzyme-linked immunosorbent assays and/or protein-chip arrays indicated a timeline change of SP to

24 Analysis by protein-chip arrays showed that only the 15-mer beta73Hi

25 d the COOH terminus of the Hsp70-interacting protein (CHIP) as a binding partner.

26 d the carboxyl terminus of Hsc70-interacting protein (CHIP) as an E47 binding protein.

27 in ligase COOH terminus of Hsp70 interacting protein (CHIP) as being connected to this process.

28 terminus of heat shock protein70-interacting protein (CHIP) as we show that Abeta accumulation decrea

29 In this work, an automated protein chip assay (enzyme-linked sandwich immunoassay)

30 Further, using multistacking protein chips, at least 14 chips can be probed simultane

31 t the carboxyl terminus of HSP70-interacting protein (CHIP) binds, ubiquitinates, and promotes the ub

32 ser desorption/ionization (MALDI)-compatible protein chips by ambient ion landing of proteins and suc

33 We further demonstrated that such protein chips can be used to analyze protein activity.

34 RCA-amplified protein chips can now profile up to 150 proteins in vari

35 er of chromatin immunoprecipitated DNA-bound proteins (ChIP-chip) or of DNA adenine methyltransferase

36 sfection with the C-terminal hsp-interacting protein (CHIP) construct, a TPR-containing ubiquitin lig

37 l degradation of Mst1 in a Hsp70 interacting protein (CHIP)-dependent manner.

38 The C terminus of Hsp70 interacting protein (CHIP) E3 ligase functions as a key regulator of

39 ablation of C-terminus of Hsc70-interacting protein (CHIP) E3 ubiquitin-ligase impairs hepatic cytoc

40 may be present in the sequences bound by the protein ChIP'ed.

41 an overcome many of the pitfalls of previous protein chip fabrications.

42 HCC (n = 57) were applied to metal affinity protein chips for protein profiling by SELDI-TOF MS.

43 and successive utilization of the resulting protein chips for the development of bioanalytical assay

44 Diagnostic utility of RCA-amplified protein chips has been shown for multiplexed allergen te

45 uitin ligase C-terminus of Hsc70 interacting protein (CHIP) has been shown in vitro and in vivo to as

46 The C-terminus Hsp70 interacting protein (CHIP) has dual function as both co-chaperone an

47 with multivariate statistical analysis, RCA protein chips have the potential to identify multiplexed

48 8 and UbcH5a-C terminus of Hsc70-interacting protein (CHIP)-Hsc70-Hsp40) complexes, as well as protei

49 biquitin ligase C-terminal Hsp70-interacting protein (CHIP), if freed from chaperones during acute st

50 s between Ap, Bar and the LIM-domain binding protein Chip in tarsus four, and between Al, Lim1 and Ch

51 f the carboxyl terminus of Hsp70-interacting protein (CHIP) in alpha-synuclein aggregation.

52 igase carboxyl terminus of Hsc70-interacting protein (CHIP) in the regulation of MLK3 protein levels.

53 tein, carboxyl terminus of Hsp70-interacting protein (CHIP), in a complex with Hsp90 plays an importa

54 erminus of heat shock protein 70-interacting protein (CHIP), increased SRF activity, as well as beta-

55 t the carboxyl terminus of Hsc70-interacting protein (CHIP) interacts with wild-type Slug (wtSlug).

56 In contrast to nearly all homodimeric proteins, CHIP is asymmetric.

57 C-terminus of Hsc/p70-Interacting Protein (CHIP) is a homodimeric E3 ubiquitin ligase.

58 e carboxyl terminus of the Hsc70-interacting protein (CHIP) is an Hsp70 co-chaperone as well as an E3

59 al Hsp70 (heat shock protein 70)-interacting protein (CHIP) links the two major arms of protein quali

60 n through COOH terminus of Hsp70-interacting protein (CHIP)-mediated ubiquitination.

61 igase of the C terminus of Hsc70-interacting protein (CHIP) on myocytes has been reported.

62 ases, carboxyl terminus of HSC70-interacting protein (CHIP) or DIP1/Mib1, enhanced DAPK degradation,

63 The Drosophila protein Chip potentiates activation by several enhancers

64 The protein chips prepared by this technique are fully compa

65 mic range and easy adaptability of plasmonic protein chips presents new opportunities in proteomic re

66 biquitin ligase C-terminal Hsp70-interacting protein (CHIP) recognizes and marks for degradation not

67 e we present the first study that integrates protein ChIP-seq and Hi-C data to systematically identif

68 nal significance of FoxO1 against other FoxO proteins, ChIP-seq was performed with chromatin from liv

69 u peptide MALDI sequencing; the lectin-based protein chips showed the ability to enrich glycopeptides

70 e samples were preadsorbed on four different protein chip surfaces, and the protein composition was a

71 and when used in conjunction with Ciphergen protein chip technology (also referred to as SELDI-Surfa

72 (ToF; MALDI-ToF) mass spectrometry utilizing protein chip technology and artificial neural networks (

73 res of protein kinases and demonstrates that protein chip technology is useful for high-throughput sc

74 Protein chip technology permits analysis of the expressi

75 We have developed a novel protein chip technology that allows the high-throughput

76 , this method offers an improved approach to protein chip technology that should prove useful for dia

77 We applied Protein Chip technology toward discovery of allograft re

78 s spectrometry in conjunction with Ciphergen protein chip technology we have used relative importance

79 To this end, we have evaluated the use of Protein Chip technology, coupled with bioinformatics ana

80 be used to develop a mass-spectrometry-based protein chip technology.

81 By means of a protein-chip technology, we identified a cluster of prot

82 shock cognate protein 70 (Hsc70)-interacting protein (CHIP) that leads to its ubiquitination/proteaso

83 square design for the sample allocation on a Protein chip, the use of the pairwise Pearson correlatio

84 Despite recent improvements in these protein chips, their applications are still limited for

85 e report two similar strategies to fabricate protein chips through capture onto a solid surface of th

86 ily member Apterous requires the LIM-binding protein Chip to execute patterned outgrowth of the Droso

87 The carboxyl terminus of hsc70-interacting protein (CHIP) ubiquitin ligase was previously associate

88 e report the development and construction of protein chips using derivatized glass and nitrocellulose

89 Three types of protein chips were used in this report to demonstrate th

90 (E3) carboxyl terminus of Hsp70-interacting protein (CHIP) were markedly increased in HG-treated car

91 d ion landing apparatus that can manufacture protein chips with a predefined array of sample position

92 ures with subsequent MALDI analysis, and the protein chips with immobilized antibodies were used for

93 The protein chips with immobilized proteolytic enzymes showe