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Johns Hopkins HealthCare human glass 12k cdna chip
Expression of IL-6 in TSU-Pr1 cells. TSU-Pr1 cells stably transfected with pp32 anti-sense express higher levels of IL-6 message as compared to parental TSU-Pr1 cells and vector-only control by RT-PCR analysis, which validates the <t>cDNA</t> microarray analysis (see Figure 6).
Human Glass 12k Cdna Chip, 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
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human glass 12k cdna chip - by Bioz Stars, 2026-10
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1) Product Images from "pp32 Reduction Induces Differentiation of TSU-Pr1 Cells"

Article Title: pp32 Reduction Induces Differentiation of TSU-Pr1 Cells

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Expression of IL-6 in TSU-Pr1 cells. TSU-Pr1 cells stably transfected with pp32 anti-sense express higher levels of IL-6 message as compared to parental TSU-Pr1 cells and vector-only control by RT-PCR analysis, which validates the cDNA microarray analysis (see Figure 6).
Figure Legend Snippet: Expression of IL-6 in TSU-Pr1 cells. TSU-Pr1 cells stably transfected with pp32 anti-sense express higher levels of IL-6 message as compared to parental TSU-Pr1 cells and vector-only control by RT-PCR analysis, which validates the cDNA microarray analysis (see Figure 6).

Techniques Used: Expressing, Stable Transfection, Transfection, Plasmid Preparation, Control, Reverse Transcription Polymerase Chain Reaction, Microarray

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Microarray:

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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
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Article Title: The cytomegalovirus protein US31 induces inflammation through mono-macrophages in systemic lupus erythematosus by promoting NF-κB2 activation.
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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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Image Search Results


The layout of the DNA microarray method module; each detection panel includes 4 detection modules, which can detect two specimens at the same time. Modules 1 and 3 are used to detect mutations in the rpoB gene, and modules 2 and 4 are used to detect mutations in the katG gene and inhA promoter. QC quality control probe; EC external control probe; BC blank control; NC negative control probe; IC internal control probe; WT wild-type.

Journal: Scientific Reports

Article Title: Analysis of the application of a gene chip method for detecting Mycobacterium tuberculosis drug resistance in clinical specimens: a retrospective study

doi: 10.1038/s41598-021-97559-y

Figure Lengend Snippet: The layout of the DNA microarray method module; each detection panel includes 4 detection modules, which can detect two specimens at the same time. Modules 1 and 3 are used to detect mutations in the rpoB gene, and modules 2 and 4 are used to detect mutations in the katG gene and inhA promoter. QC quality control probe; EC external control probe; BC blank control; NC negative control probe; IC internal control probe; WT wild-type.

Article Snippet: The CapitalBio DNA microarray chip method is used to qualitatively detect nucleic acids in samples of Mtb isolates from clinical TB patients.

Techniques: Microarray, Negative Control

The drug susceptibility test was used as a standard method to evaluate the efficacy of the  DNA microarray  for detecting RIF and INH resistance and MDR-TB.

Journal: Scientific Reports

Article Title: Analysis of the application of a gene chip method for detecting Mycobacterium tuberculosis drug resistance in clinical specimens: a retrospective study

doi: 10.1038/s41598-021-97559-y

Figure Lengend Snippet: The drug susceptibility test was used as a standard method to evaluate the efficacy of the DNA microarray for detecting RIF and INH resistance and MDR-TB.

Article Snippet: The CapitalBio DNA microarray chip method is used to qualitatively detect nucleic acids in samples of Mtb isolates from clinical TB patients.

Techniques: Microarray

Comparison of the diagnostic efficacy of the  DNA microarray  method when sputum smear grades were ≤ 1 + and ≥ 2 +

Journal: Scientific Reports

Article Title: Analysis of the application of a gene chip method for detecting Mycobacterium tuberculosis drug resistance in clinical specimens: a retrospective study

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Figure Lengend Snippet: Comparison of the diagnostic efficacy of the DNA microarray method when sputum smear grades were ≤ 1 + and ≥ 2 +

Article Snippet: The CapitalBio DNA microarray chip method is used to qualitatively detect nucleic acids in samples of Mtb isolates from clinical TB patients.

Techniques: Diagnostic Assay, Microarray

Specimen processing procedure: A total of 5,911 sputum smear-positive specimens were collected. After experimental processing, 4148 specimens that were positive with the DNA microarray method and DST were finally included in the study. NTM, nontuberculous mycobacteria ; DST, drug sensitivity test.

Journal: Scientific Reports

Article Title: Analysis of the application of a gene chip method for detecting Mycobacterium tuberculosis drug resistance in clinical specimens: a retrospective study

doi: 10.1038/s41598-021-97559-y

Figure Lengend Snippet: Specimen processing procedure: A total of 5,911 sputum smear-positive specimens were collected. After experimental processing, 4148 specimens that were positive with the DNA microarray method and DST were finally included in the study. NTM, nontuberculous mycobacteria ; DST, drug sensitivity test.

Article Snippet: The CapitalBio DNA microarray chip method is used to qualitatively detect nucleic acids in samples of Mtb isolates from clinical TB patients.

Techniques: Microarray

Pattern diagrams of several common drug-resistant gene mutations detected by the DNA microarray method. The white box is the detection site of the wild-type codon, and the red box is the site of the detected mutant codon. ( a ) rpoB gene Leu511Pro (CTG → CCG); ( b ) rpoB gene Asp516Tyr (GAC → TAC); ( c ) rpoB gene His526Tyr (CAC → TAC); ( d ) rpoB gene Ser531Trp (TCG → TGG); ( e ) rpoB gene Ser531Leu (TCG → TTG); ( f ) katG gene Ser315Thr (AGC → ACC); ( g ) katG gene Ser315Asn (AGC → AAC); ( h ) inhA gene promoter-15 (C → T).

Journal: Scientific Reports

Article Title: Analysis of the application of a gene chip method for detecting Mycobacterium tuberculosis drug resistance in clinical specimens: a retrospective study

doi: 10.1038/s41598-021-97559-y

Figure Lengend Snippet: Pattern diagrams of several common drug-resistant gene mutations detected by the DNA microarray method. The white box is the detection site of the wild-type codon, and the red box is the site of the detected mutant codon. ( a ) rpoB gene Leu511Pro (CTG → CCG); ( b ) rpoB gene Asp516Tyr (GAC → TAC); ( c ) rpoB gene His526Tyr (CAC → TAC); ( d ) rpoB gene Ser531Trp (TCG → TGG); ( e ) rpoB gene Ser531Leu (TCG → TTG); ( f ) katG gene Ser315Thr (AGC → ACC); ( g ) katG gene Ser315Asn (AGC → AAC); ( h ) inhA gene promoter-15 (C → T).

Article Snippet: The CapitalBio DNA microarray chip method is used to qualitatively detect nucleic acids in samples of Mtb isolates from clinical TB patients.

Techniques: Microarray, Mutagenesis

Non-tuberculous species identified from 2013 to 2018 in a tertiary hospital in Beijing, China

Journal: BMC Microbiology

Article Title: Prevalence of nontuberculous mycobacteria in a tertiary hospital in Beijing, China, January 2013 to December 2018

doi: 10.1186/s12866-020-01840-5

Figure Lengend Snippet: Non-tuberculous species identified from 2013 to 2018 in a tertiary hospital in Beijing, China

Article Snippet: DNA microarray chip method (Mycobacterial Species Identification Array Kit, CapitalBio Technology Inc., Beijing, China) can accurately distinguish between M. avium and M. intracellulae , which have quite similar phenotypes.

Techniques:

Specimen types among which NTM were identified in this study

Journal: BMC Microbiology

Article Title: Prevalence of nontuberculous mycobacteria in a tertiary hospital in Beijing, China, January 2013 to December 2018

doi: 10.1186/s12866-020-01840-5

Figure Lengend Snippet: Specimen types among which NTM were identified in this study

Article Snippet: DNA microarray chip method (Mycobacterial Species Identification Array Kit, CapitalBio Technology Inc., Beijing, China) can accurately distinguish between M. avium and M. intracellulae , which have quite similar phenotypes.

Techniques: