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Johns Hopkins HealthCare huprot human microarray
Huprot Human Microarray, supplied by Johns Hopkins HealthCare, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/huprot+human+microarray/human+proteome+microarray/pm40339788-68-11-21
Average 90 stars, based on 1 article reviews
huprot human microarray - by Bioz Stars, 2026-09
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Microarray:

Article Title: Chemical proteomics accelerates the target discovery of natural products.
Article Snippet: More than half of the global novel drugs are directly or indirectly derived from natural products (NPs) because of their better selectivity towards proteins.. Traditional medicines perform multiple bioactivities through various NPs binding to drug targets, which highlights the opportunities of target discovery for drug development.. However, detecting the binding relationship between NPs and targets remains challenging.

Article Title: Icariin alleviates uveitis by targeting peroxiredoxin 3 to modulate retinal microglia M1/M2 phenotypic polarization.
Article Snippet: .. The HuProt microarray was obtained from the Johns Hopkins Medical Institutions Protein Microarray Core (CDI Laboratories, Inc).The array experiment was performed by Wayen Biotechnologies (Shanghai, China) according to the following procedure. ..

Article Title: E17241 as a Novel ABCA1 (ATP-Binding Cassette Transporter A1) Upregulator Ameliorates Atherosclerosis in Mice
Article Snippet: .. Protein binding microarray chips comprised of ≈20 000 individual human GST (glutathione S-transferase)- and His-tagged full-length proteins were obtained from the Johns Hopkins Medical Institutions Protein Microarray Core (CDI Laboratories, Inc). .. Microarray proteomic analyses were performed according to the procedure detailed below, and the data were processed24 by Wayen Biotechnologies Inc (Shanghai, China).

Article Title: Deciphering the autoreactome: Massively parallelized methods for autoantibody detection in humans.
Article Snippet: Autoantibodies have a substantial impact on human health ranging from autoimmune diseases to cancer diagnostics.. Knowledge of the antigens recognized can allow for more accurate diagnostics, a better understanding of pathogeneses and thus improved prevention, as well as laying the foundation for the development of new therapies.. A critical step to acquire this knowledge is to detect the exact self-antigens targeted by autoantibodies out of the pool of 20,000 human proteins against which reactivities could be observed.

Article Title: The cytomegalovirus protein US31 induces inflammation through mono-macrophages in systemic lupus erythematosus by promoting NF-κB2 activation.
Article Snippet: .. Protein array screening of US31-binding proteins The Johns Hopkins Medical Institutions Protein Microarray Core produced the protein binding microarray chips with 19394 individual human GST-and His6tagged full-length proteins. .. Recombinant US31 purified from BL21/pET21a-US31 (1.5 μg/μl) was labeled using an Alexa-Flour-647 microscale protein labeling kit (A30009, Molecular Probes/Invitrogen).

Article Title: Targeting HINT1 to improve synaptic plasticity: toward loganin as a new antidepressant strategy.
Article Snippet: Histidine triad nucleotide-binding protein 1 (HINT1) is related to depression.. However, the underlying mechanisms and whether HINT1 is a therapeutic target for depression remain unclear.. In this study, we report that loganin, an antidepressant candidate from our previous research, directly targets HINT1 to alleviate depressive-like behaviors.

Protein Binding:

Article Title: E17241 as a Novel ABCA1 (ATP-Binding Cassette Transporter A1) Upregulator Ameliorates Atherosclerosis in Mice
Article Snippet: .. Protein binding microarray chips comprised of ≈20 000 individual human GST (glutathione S-transferase)- and His-tagged full-length proteins were obtained from the Johns Hopkins Medical Institutions Protein Microarray Core (CDI Laboratories, Inc). .. Microarray proteomic analyses were performed according to the procedure detailed below, and the data were processed24 by Wayen Biotechnologies Inc (Shanghai, China).

Article Title: The cytomegalovirus protein US31 induces inflammation through mono-macrophages in systemic lupus erythematosus by promoting NF-κB2 activation.
Article Snippet: .. Protein array screening of US31-binding proteins The Johns Hopkins Medical Institutions Protein Microarray Core produced the protein binding microarray chips with 19394 individual human GST-and His6tagged full-length proteins. .. Recombinant US31 purified from BL21/pET21a-US31 (1.5 μg/μl) was labeled using an Alexa-Flour-647 microscale protein labeling kit (A30009, Molecular Probes/Invitrogen).

Diagnostic Assay:

Article Title: Identification of Novel Biomarkers for Behcet Disease Diagnosis Using Human Proteome Microarray Approach
Article Snippet: .. This study was approved by the Ethics Committee of Peking Union Medical College Hospital. table ft1 table-wrap mode="anchored" t5 caption a7 Diagnostic symptom Positive number/ total(positive rate) Other symptom Positive number/ total(positive rate) Oral ulcers 110/113(97.3%) Untreated new-onset BD 59/113(52.2%) Genital ulcers 81/113(71.7%) Arthritis 22/107(20.6%) Eye lesions 28/113(24.78%) Epididymitis 8/105(7.6%) Skin lesions 68/113(60.18%) Gastrointestinal lesions 23/109(21.1%) Positive pathergy test 31/73(42.47%) Central nervous symptoms 15/112(13.4%) Vascular lesions 21/105(20.0%) Cardiac lesions 7/101(6.9%) Respiratory lesions 2/104(1.9%) Open in a separate window caption a8 The Clinical symptoms information of the BD patients Construction and Quality Control Test of HuProt Arrays The HuProt arrays, comprised of∼20,000 unique full-length proteins were constructed in Dr. Zhu's laboratory at Johns Hopkins University School of Medicine. .. Briefly, human ORFs cloned into a yeast expression vector (pEGH-A) were induced to produce N-terminally tagged GST fusions in Saccharomyces cerevisiae under control of the galactose-inducible GAL1 promoter.

Control:

Article Title: Identification of Novel Biomarkers for Behcet Disease Diagnosis Using Human Proteome Microarray Approach
Article Snippet: .. This study was approved by the Ethics Committee of Peking Union Medical College Hospital. table ft1 table-wrap mode="anchored" t5 caption a7 Diagnostic symptom Positive number/ total(positive rate) Other symptom Positive number/ total(positive rate) Oral ulcers 110/113(97.3%) Untreated new-onset BD 59/113(52.2%) Genital ulcers 81/113(71.7%) Arthritis 22/107(20.6%) Eye lesions 28/113(24.78%) Epididymitis 8/105(7.6%) Skin lesions 68/113(60.18%) Gastrointestinal lesions 23/109(21.1%) Positive pathergy test 31/73(42.47%) Central nervous symptoms 15/112(13.4%) Vascular lesions 21/105(20.0%) Cardiac lesions 7/101(6.9%) Respiratory lesions 2/104(1.9%) Open in a separate window caption a8 The Clinical symptoms information of the BD patients Construction and Quality Control Test of HuProt Arrays The HuProt arrays, comprised of∼20,000 unique full-length proteins were constructed in Dr. Zhu's laboratory at Johns Hopkins University School of Medicine. .. Briefly, human ORFs cloned into a yeast expression vector (pEGH-A) were induced to produce N-terminally tagged GST fusions in Saccharomyces cerevisiae under control of the galactose-inducible GAL1 promoter.

Construct:

Article Title: Identification of Novel Biomarkers for Behcet Disease Diagnosis Using Human Proteome Microarray Approach
Article Snippet: .. This study was approved by the Ethics Committee of Peking Union Medical College Hospital. table ft1 table-wrap mode="anchored" t5 caption a7 Diagnostic symptom Positive number/ total(positive rate) Other symptom Positive number/ total(positive rate) Oral ulcers 110/113(97.3%) Untreated new-onset BD 59/113(52.2%) Genital ulcers 81/113(71.7%) Arthritis 22/107(20.6%) Eye lesions 28/113(24.78%) Epididymitis 8/105(7.6%) Skin lesions 68/113(60.18%) Gastrointestinal lesions 23/109(21.1%) Positive pathergy test 31/73(42.47%) Central nervous symptoms 15/112(13.4%) Vascular lesions 21/105(20.0%) Cardiac lesions 7/101(6.9%) Respiratory lesions 2/104(1.9%) Open in a separate window caption a8 The Clinical symptoms information of the BD patients Construction and Quality Control Test of HuProt Arrays The HuProt arrays, comprised of∼20,000 unique full-length proteins were constructed in Dr. Zhu's laboratory at Johns Hopkins University School of Medicine. .. Briefly, human ORFs cloned into a yeast expression vector (pEGH-A) were induced to produce N-terminally tagged GST fusions in Saccharomyces cerevisiae under control of the galactose-inducible GAL1 promoter.

Protein Array:

Article Title: The cytomegalovirus protein US31 induces inflammation through mono-macrophages in systemic lupus erythematosus by promoting NF-κB2 activation.
Article Snippet: .. Protein array screening of US31-binding proteins The Johns Hopkins Medical Institutions Protein Microarray Core produced the protein binding microarray chips with 19394 individual human GST-and His6tagged full-length proteins. .. Recombinant US31 purified from BL21/pET21a-US31 (1.5 μg/μl) was labeled using an Alexa-Flour-647 microscale protein labeling kit (A30009, Molecular Probes/Invitrogen).

Produced:

Article Title: The cytomegalovirus protein US31 induces inflammation through mono-macrophages in systemic lupus erythematosus by promoting NF-κB2 activation.
Article Snippet: .. Protein array screening of US31-binding proteins The Johns Hopkins Medical Institutions Protein Microarray Core produced the protein binding microarray chips with 19394 individual human GST-and His6tagged full-length proteins. .. Recombinant US31 purified from BL21/pET21a-US31 (1.5 μg/μl) was labeled using an Alexa-Flour-647 microscale protein labeling kit (A30009, Molecular Probes/Invitrogen).



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a The schematic diagram of human proteome <t>microarray,</t> which contains over 20,000 individual proteins printed in duplicate, to identify binding partners of high-dose and low-dose dexamethasone, respectively. b , c Human proteome microarray analysis reveals the proteins (in blue) which bind to both low and high-dose dexamethasone, and proteins (in green) which selectively bind to high-dose dexamethasone. d Principle of DARTS assay for the isolation of proteins protected from degradation by dexamethasone. e Dexamethasone protects two groups of protein bands (highlighted in black rectangle) from degradation in DARTS using whole cell lysate from dexamethasone-treated Raw264.7 cells coupled with Coomassie blue staining. f Molecular weight (MW) plot of putative high-dose dexamethasone-binding proteins identified by human proteome microarray analysis. g The protective effects of serial doses of dexamethasone on Tau and GR from digestion by protease are evaluated by DARTS coupled with immunoblotting. GAPDH is resistant to protease under the condition and serves as a loading indicator. Representative image is shown ( n = 3). h Quantification of Tau and GR stability treated with serial dosages of dexamethasone assayed by DARTS ( n = 3). i The interaction between dexamethasone and Tau, assayed by solid phase binding. 10 mM Tau was coated to the plate, and a serial dilution of biotin-labeled dexamethasone was added, followed by incubation with HRP-labeled Streptavidin and its substrate ( n = 3). Inset shows the Scatchard plot analysis for K D value calculation. j – p One-step kinetic SPR assay for binding of Tau to different GCs, as indicated. q qRT-PCR analysis of Tau mRNA levels in different tissues, as indicated ( n = 3). r Double-immunoflurorescence staining of femur section using antibodies against Tau (green) and TRAP, osteocalcin (OCN) and sclerostin (SOST) (red). DAPI stains nuclei. Arrows indicate positive staining cells. Scale bar = 20 µm. BM, bone marrow. Data are means ± SD in h , i , q .
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Image Search Results


a The schematic diagram of human proteome microarray, which contains over 20,000 individual proteins printed in duplicate, to identify binding partners of high-dose and low-dose dexamethasone, respectively. b , c Human proteome microarray analysis reveals the proteins (in blue) which bind to both low and high-dose dexamethasone, and proteins (in green) which selectively bind to high-dose dexamethasone. d Principle of DARTS assay for the isolation of proteins protected from degradation by dexamethasone. e Dexamethasone protects two groups of protein bands (highlighted in black rectangle) from degradation in DARTS using whole cell lysate from dexamethasone-treated Raw264.7 cells coupled with Coomassie blue staining. f Molecular weight (MW) plot of putative high-dose dexamethasone-binding proteins identified by human proteome microarray analysis. g The protective effects of serial doses of dexamethasone on Tau and GR from digestion by protease are evaluated by DARTS coupled with immunoblotting. GAPDH is resistant to protease under the condition and serves as a loading indicator. Representative image is shown ( n = 3). h Quantification of Tau and GR stability treated with serial dosages of dexamethasone assayed by DARTS ( n = 3). i The interaction between dexamethasone and Tau, assayed by solid phase binding. 10 mM Tau was coated to the plate, and a serial dilution of biotin-labeled dexamethasone was added, followed by incubation with HRP-labeled Streptavidin and its substrate ( n = 3). Inset shows the Scatchard plot analysis for K D value calculation. j – p One-step kinetic SPR assay for binding of Tau to different GCs, as indicated. q qRT-PCR analysis of Tau mRNA levels in different tissues, as indicated ( n = 3). r Double-immunoflurorescence staining of femur section using antibodies against Tau (green) and TRAP, osteocalcin (OCN) and sclerostin (SOST) (red). DAPI stains nuclei. Arrows indicate positive staining cells. Scale bar = 20 µm. BM, bone marrow. Data are means ± SD in h , i , q .

Journal: Cell Research

Article Title: Tau is a receptor with low affinity for glucocorticoids and is required for glucocorticoid-induced bone loss

doi: 10.1038/s41422-024-01016-0

Figure Lengend Snippet: a The schematic diagram of human proteome microarray, which contains over 20,000 individual proteins printed in duplicate, to identify binding partners of high-dose and low-dose dexamethasone, respectively. b , c Human proteome microarray analysis reveals the proteins (in blue) which bind to both low and high-dose dexamethasone, and proteins (in green) which selectively bind to high-dose dexamethasone. d Principle of DARTS assay for the isolation of proteins protected from degradation by dexamethasone. e Dexamethasone protects two groups of protein bands (highlighted in black rectangle) from degradation in DARTS using whole cell lysate from dexamethasone-treated Raw264.7 cells coupled with Coomassie blue staining. f Molecular weight (MW) plot of putative high-dose dexamethasone-binding proteins identified by human proteome microarray analysis. g The protective effects of serial doses of dexamethasone on Tau and GR from digestion by protease are evaluated by DARTS coupled with immunoblotting. GAPDH is resistant to protease under the condition and serves as a loading indicator. Representative image is shown ( n = 3). h Quantification of Tau and GR stability treated with serial dosages of dexamethasone assayed by DARTS ( n = 3). i The interaction between dexamethasone and Tau, assayed by solid phase binding. 10 mM Tau was coated to the plate, and a serial dilution of biotin-labeled dexamethasone was added, followed by incubation with HRP-labeled Streptavidin and its substrate ( n = 3). Inset shows the Scatchard plot analysis for K D value calculation. j – p One-step kinetic SPR assay for binding of Tau to different GCs, as indicated. q qRT-PCR analysis of Tau mRNA levels in different tissues, as indicated ( n = 3). r Double-immunoflurorescence staining of femur section using antibodies against Tau (green) and TRAP, osteocalcin (OCN) and sclerostin (SOST) (red). DAPI stains nuclei. Arrows indicate positive staining cells. Scale bar = 20 µm. BM, bone marrow. Data are means ± SD in h , i , q .

Article Snippet: HuProt human proteome microarray version 4.0 (HuProt TM , CDI Laboratories), which is composed of ~ 20,000 human FL proteins with N-terminal glutathione S-transferase tag was used to isolate dexamethasone-binding proteins.

Techniques: Microarray, Binding Assay, Isolation, Staining, Molecular Weight, Western Blot, Serial Dilution, Labeling, Incubation, SPR Assay, Quantitative RT-PCR

a Distribution of PAK6 candidate interactors according to their Z-score retrieved from a Human Proteome Microarray probed with recombinant full-length human PAK6. b A GO:BP analysis using gProfiler g:GOSt ( https://biit.cs.ut.ee/gprofiler/gost ) was performed for PAK6 candidate interactors with Z score >2.5 (left) and for PAK6 interactors annotated in PPI web-based tools PINOT, HIPPIE and MIST (PHM) (right). GO:BP terms with 2000 (array) and 1000 (PHM) term size were grouped into semantic categories. c Venn diagrams showing overlaps between the primary cilium proteome (GO:0005929, 640 genes) and the experimental (array) PAK6 interactome (left) or the literature-based (PHM) PAK6 interactome (right). d Protein network of overlapping PAK6 interactors with the primary cilium proteome (c) (including PAK6) obtained with STRING ( https://string-db.org/cgi/input?sessionId=b1S4T5BW27rz&input_page_show_search=on ); number of nodes: 11, number of edges: 11, average node degree: 2, average local clustering coefficient: 0.591, expected number of edges: 3, PPI enrichment P -value: 0.000502. Blue nodes are ciliary proteins present in the experimental PAK6 interactome (array) and grey nodes are those found in the literature-based PAK6 interactome. The interaction between LRRK2 and PAK6 identified in this study (blue) has been inserted manually.

Journal: Cell Death & Disease

Article Title: PAK6 rescues pathogenic LRRK2-mediated ciliogenesis and centrosomal cohesion defects in a mutation-specific manner

doi: 10.1038/s41419-024-07124-4

Figure Lengend Snippet: a Distribution of PAK6 candidate interactors according to their Z-score retrieved from a Human Proteome Microarray probed with recombinant full-length human PAK6. b A GO:BP analysis using gProfiler g:GOSt ( https://biit.cs.ut.ee/gprofiler/gost ) was performed for PAK6 candidate interactors with Z score >2.5 (left) and for PAK6 interactors annotated in PPI web-based tools PINOT, HIPPIE and MIST (PHM) (right). GO:BP terms with 2000 (array) and 1000 (PHM) term size were grouped into semantic categories. c Venn diagrams showing overlaps between the primary cilium proteome (GO:0005929, 640 genes) and the experimental (array) PAK6 interactome (left) or the literature-based (PHM) PAK6 interactome (right). d Protein network of overlapping PAK6 interactors with the primary cilium proteome (c) (including PAK6) obtained with STRING ( https://string-db.org/cgi/input?sessionId=b1S4T5BW27rz&input_page_show_search=on ); number of nodes: 11, number of edges: 11, average node degree: 2, average local clustering coefficient: 0.591, expected number of edges: 3, PPI enrichment P -value: 0.000502. Blue nodes are ciliary proteins present in the experimental PAK6 interactome (array) and grey nodes are those found in the literature-based PAK6 interactome. The interaction between LRRK2 and PAK6 identified in this study (blue) has been inserted manually.

Article Snippet: HuProt TM Human Proteome Microarray v4.0 was purchased from Cambridge Protein Arrays (Babraham Research Campus, Cambridge, UK) and employed to screen PAK6 interactor candidates following manufacturer’s instructions.

Techniques: Microarray, Recombinant