dna microarray scanner c Search Results


95
Sartorius AG surescan dna microarray scanner
. The 3’ and the 5’ target recognition arms bind to the multiplex PCR products of the β-lactamase genes. During the binding process, the padlock probes are circularized and subsequently ligated. The maximum distance of the padlock probe binding region to the 3’ or 5’-ends of the PCR product should not exceed 200 base pairs. Since the padlock probes gets concatenated with the PCR product upon the ligation reaction, longer distances cause an inhibition of subsequent RCAs. The C2CA sequence is needed for the circle-to-circle amplification and comprises an AluI restriction site for monomerization of the amplification products. The barcode sequence is derived from the 16S rRNA gene. This allowed us to halve the number of <t>microarray</t> probes because the C2CA products and 16S rRNA gene PCR products are detected on the same microarray probe but in different fluorescence channels.
Surescan Dna Microarray Scanner, supplied by Sartorius AG, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/surescan dna microarray scanner/product/Sartorius AG
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90
MWG-Biotech ag affymetrix 428 scanner
. The 3’ and the 5’ target recognition arms bind to the multiplex PCR products of the β-lactamase genes. During the binding process, the padlock probes are circularized and subsequently ligated. The maximum distance of the padlock probe binding region to the 3’ or 5’-ends of the PCR product should not exceed 200 base pairs. Since the padlock probes gets concatenated with the PCR product upon the ligation reaction, longer distances cause an inhibition of subsequent RCAs. The C2CA sequence is needed for the circle-to-circle amplification and comprises an AluI restriction site for monomerization of the amplification products. The barcode sequence is derived from the 16S rRNA gene. This allowed us to halve the number of <t>microarray</t> probes because the C2CA products and 16S rRNA gene PCR products are detected on the same microarray probe but in different fluorescence channels.
Affymetrix 428 Scanner, supplied by MWG-Biotech ag, 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/result/affymetrix 428 scanner/product/MWG-Biotech ag
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90
Clondiag GmbH atr03 at dna microarray transmission scanner
. The 3’ and the 5’ target recognition arms bind to the multiplex PCR products of the β-lactamase genes. During the binding process, the padlock probes are circularized and subsequently ligated. The maximum distance of the padlock probe binding region to the 3’ or 5’-ends of the PCR product should not exceed 200 base pairs. Since the padlock probes gets concatenated with the PCR product upon the ligation reaction, longer distances cause an inhibition of subsequent RCAs. The C2CA sequence is needed for the circle-to-circle amplification and comprises an AluI restriction site for monomerization of the amplification products. The barcode sequence is derived from the 16S rRNA gene. This allowed us to halve the number of <t>microarray</t> probes because the C2CA products and 16S rRNA gene PCR products are detected on the same microarray probe but in different fluorescence channels.
Atr03 At Dna Microarray Transmission Scanner, supplied by Clondiag GmbH, 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/result/atr03 at dna microarray transmission scanner/product/Clondiag GmbH
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90
Lumonics Inc dna chip scanner scanarray lite
. The 3’ and the 5’ target recognition arms bind to the multiplex PCR products of the β-lactamase genes. During the binding process, the padlock probes are circularized and subsequently ligated. The maximum distance of the padlock probe binding region to the 3’ or 5’-ends of the PCR product should not exceed 200 base pairs. Since the padlock probes gets concatenated with the PCR product upon the ligation reaction, longer distances cause an inhibition of subsequent RCAs. The C2CA sequence is needed for the circle-to-circle amplification and comprises an AluI restriction site for monomerization of the amplification products. The barcode sequence is derived from the 16S rRNA gene. This allowed us to halve the number of <t>microarray</t> probes because the C2CA products and 16S rRNA gene PCR products are detected on the same microarray probe but in different fluorescence channels.
Dna Chip Scanner Scanarray Lite, supplied by Lumonics Inc, 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/result/dna chip scanner scanarray lite/product/Lumonics Inc
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99
Thermo Fisher mgu74av2 dna chip scanning
. The 3’ and the 5’ target recognition arms bind to the multiplex PCR products of the β-lactamase genes. During the binding process, the padlock probes are circularized and subsequently ligated. The maximum distance of the padlock probe binding region to the 3’ or 5’-ends of the PCR product should not exceed 200 base pairs. Since the padlock probes gets concatenated with the PCR product upon the ligation reaction, longer distances cause an inhibition of subsequent RCAs. The C2CA sequence is needed for the circle-to-circle amplification and comprises an AluI restriction site for monomerization of the amplification products. The barcode sequence is derived from the 16S rRNA gene. This allowed us to halve the number of <t>microarray</t> probes because the C2CA products and 16S rRNA gene PCR products are detected on the same microarray probe but in different fluorescence channels.
Mgu74av2 Dna Chip Scanning, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
Innopsys Inc dna microarray scanner
. The 3’ and the 5’ target recognition arms bind to the multiplex PCR products of the β-lactamase genes. During the binding process, the padlock probes are circularized and subsequently ligated. The maximum distance of the padlock probe binding region to the 3’ or 5’-ends of the PCR product should not exceed 200 base pairs. Since the padlock probes gets concatenated with the PCR product upon the ligation reaction, longer distances cause an inhibition of subsequent RCAs. The C2CA sequence is needed for the circle-to-circle amplification and comprises an AluI restriction site for monomerization of the amplification products. The barcode sequence is derived from the 16S rRNA gene. This allowed us to halve the number of <t>microarray</t> probes because the C2CA products and 16S rRNA gene PCR products are detected on the same microarray probe but in different fluorescence channels.
Dna Microarray Scanner, supplied by Innopsys Inc, 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/result/dna microarray scanner/product/Innopsys Inc
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90
Genomic Solutions Inc dna microarray scanner genetac uc4×4
. The 3’ and the 5’ target recognition arms bind to the multiplex PCR products of the β-lactamase genes. During the binding process, the padlock probes are circularized and subsequently ligated. The maximum distance of the padlock probe binding region to the 3’ or 5’-ends of the PCR product should not exceed 200 base pairs. Since the padlock probes gets concatenated with the PCR product upon the ligation reaction, longer distances cause an inhibition of subsequent RCAs. The C2CA sequence is needed for the circle-to-circle amplification and comprises an AluI restriction site for monomerization of the amplification products. The barcode sequence is derived from the 16S rRNA gene. This allowed us to halve the number of <t>microarray</t> probes because the C2CA products and 16S rRNA gene PCR products are detected on the same microarray probe but in different fluorescence channels.
Dna Microarray Scanner Genetac Uc4×4, supplied by Genomic Solutions Inc, 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/result/dna microarray scanner genetac uc4×4/product/Genomic Solutions Inc
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94
Danaher Inc two color microarray scanner
Differential expression of leupaxin, DKK1, and DKK3 by palmoplantar (PP) and by nonpalmoplantar (NP) fibroblasts. Representative differences in gene expression patterns of leupaxin, DKK1, and DKK3 between palmoplantar fibroblasts and nonpalmoplantar fibroblasts as measured by <t>microarray</t> (top; quantitative results are summarized in and ). (middle) RT-PCR confirms the expression patterns of leupaxin, DKK1, and DKK3 in palmoplantar and in nonpalmoplantar fibroblasts. These data are representative of five independent experiments. (bottom) Real-time PCR to quantitate the expression of leupaxin, DKK1, and DKK3 after normalization of the target gene to GAPDH. Data are reported as means ± SD.
Two Color Microarray Scanner, supplied by Danaher Inc, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/two color microarray scanner/product/Danaher Inc
Average 94 stars, based on 1 article reviews
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90
FUJIFILM dna microarray scanner fla-8000
Differential expression of leupaxin, DKK1, and DKK3 by palmoplantar (PP) and by nonpalmoplantar (NP) fibroblasts. Representative differences in gene expression patterns of leupaxin, DKK1, and DKK3 between palmoplantar fibroblasts and nonpalmoplantar fibroblasts as measured by <t>microarray</t> (top; quantitative results are summarized in and ). (middle) RT-PCR confirms the expression patterns of leupaxin, DKK1, and DKK3 in palmoplantar and in nonpalmoplantar fibroblasts. These data are representative of five independent experiments. (bottom) Real-time PCR to quantitate the expression of leupaxin, DKK1, and DKK3 after normalization of the target gene to GAPDH. Data are reported as means ± SD.
Dna Microarray Scanner Fla 8000, supplied by FUJIFILM, 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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90
Goodgene Inc dna chip scanner
Differential expression of leupaxin, DKK1, and DKK3 by palmoplantar (PP) and by nonpalmoplantar (NP) fibroblasts. Representative differences in gene expression patterns of leupaxin, DKK1, and DKK3 between palmoplantar fibroblasts and nonpalmoplantar fibroblasts as measured by <t>microarray</t> (top; quantitative results are summarized in and ). (middle) RT-PCR confirms the expression patterns of leupaxin, DKK1, and DKK3 in palmoplantar and in nonpalmoplantar fibroblasts. These data are representative of five independent experiments. (bottom) Real-time PCR to quantitate the expression of leupaxin, DKK1, and DKK3 after normalization of the target gene to GAPDH. Data are reported as means ± SD.
Dna Chip Scanner, supplied by Goodgene Inc, 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/result/dna chip scanner/product/Goodgene Inc
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GSI Lumonics Inc dna chip scanner scanarray lite
Histology results according to cytology, <t> HPV </t> <t> DNA chip </t> results, <xref ref-type= a and HC2 results" width="250" height="auto" />
Dna Chip Scanner Scanarray Lite, supplied by GSI Lumonics Inc, 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/result/dna chip scanner scanarray lite/product/GSI Lumonics Inc
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Applied Precision Inc modified dna array scanner
Histology results according to cytology, <t> HPV </t> <t> DNA chip </t> results, <xref ref-type= a and HC2 results" width="250" height="auto" />
Modified Dna Array Scanner, supplied by Applied Precision Inc, 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/result/modified dna array scanner/product/Applied Precision Inc
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Image Search Results


. The 3’ and the 5’ target recognition arms bind to the multiplex PCR products of the β-lactamase genes. During the binding process, the padlock probes are circularized and subsequently ligated. The maximum distance of the padlock probe binding region to the 3’ or 5’-ends of the PCR product should not exceed 200 base pairs. Since the padlock probes gets concatenated with the PCR product upon the ligation reaction, longer distances cause an inhibition of subsequent RCAs. The C2CA sequence is needed for the circle-to-circle amplification and comprises an AluI restriction site for monomerization of the amplification products. The barcode sequence is derived from the 16S rRNA gene. This allowed us to halve the number of microarray probes because the C2CA products and 16S rRNA gene PCR products are detected on the same microarray probe but in different fluorescence channels.

Journal: Bio-protocol

Article Title: Detection of Pathogens and Ampicillin-resistance Genes Using Multiplex Padlock Probes

doi: 10.21769/BioProtoc.2504

Figure Lengend Snippet: . The 3’ and the 5’ target recognition arms bind to the multiplex PCR products of the β-lactamase genes. During the binding process, the padlock probes are circularized and subsequently ligated. The maximum distance of the padlock probe binding region to the 3’ or 5’-ends of the PCR product should not exceed 200 base pairs. Since the padlock probes gets concatenated with the PCR product upon the ligation reaction, longer distances cause an inhibition of subsequent RCAs. The C2CA sequence is needed for the circle-to-circle amplification and comprises an AluI restriction site for monomerization of the amplification products. The barcode sequence is derived from the 16S rRNA gene. This allowed us to halve the number of microarray probes because the C2CA products and 16S rRNA gene PCR products are detected on the same microarray probe but in different fluorescence channels.

Article Snippet: Pipettes ( e.g ., Sartorius, catalog numbers: 728020, 728050, 728060 and 728070) Microbiological incubator shaker ( e.g ., IKA, model: KS 4000 i control) Tabletop centrifuge for 1.5 ml tubes ( e.g ., Eppendorf, model: 5424) Roche MagNA Lyser Instrument (Basel, Switzerland) Thermomixer comfort (Eppendorf, Hamburg, Germany) Epoch Microplate spectrophotometer (Biotek, Winooski, VT, USA) Biosan DNA/RNA UV-cleaner box (Warren, MI, USA) (recommended, see Note 4) Thermal cycler ( e.g ., Thermo Fisher Scientific, Applied Biosystems, model: GeneAmp TM PCR System 2700) (Paisley, UK) Heraeus Megafuge 40R with a TX-750 rotor (Thermo Fisher Scientific, Thermo Scientific TM , model: Heraeus TM Megafuge TM 40R, catalog number: 75004518; TX-750 rotor: Thermo Fisher Scientific, Thermo Scientific TM , catalog number: 75003180) and inserts for plates (Thermo Fisher Scientific, Thermo Scientific TM , catalog number: 75003617) and Falcon tubes (Thermo Fisher Scientific, Thermo Scientific TM , catalog number: 75003608) Slide humidity incubation box ( e.g ., LabScientific, catalog number: HIC-3) GeneMachines Omnigrid 100 contact arrayer (Madison, WI, USA) International Microarray Pin Stealth 3 SMP3 (Telechem, catalog number: SMP3) Agilent SureScan DNA Microarray Scanner (Santa Clara, CA, USA) Autoclave Sartorius arium pro UV ultrapure water system (Sartorius, model: arium ® pro)

Techniques: Multiplex Assay, Binding Assay, Ligation, Inhibition, Sequencing, Amplification, Derivative Assay, Microarray, Fluorescence

For the species identification, the 16S rRNA gene is amplified using universal 16S primers (A1). Subsequently, the PCR products are labeled using a linear PCR and Cy5-modified cytosines (A2). In parallel, β-lactamase genes are pre-amplified in a 33-plex PCR (B1). Then, the padlock probes are hybridized (B2) and ligated (B3) using the β-lactamase PCR products as template and amplified in a first rolling circle amplification (RCA) (B4). The RCA products comprise a C2CA sequence and corresponding 16S rRNA barcode sequences. In a next reaction, the RCA products are monomerized (B5) using a restriction enzyme and circularized (B6) to serve as a new template for a second RCA (B7). These C2CA products are labelled in a linear PCR reaction using Atto532-modified cytosines (B8). Finally, the labelled amplification products from the 16S rRNA gene PCR and from the multiplex padlock assay are pooled together and hybridized to a microarray detecting the products at two different fluorescence wavelengths (C).

Journal: Bio-protocol

Article Title: Detection of Pathogens and Ampicillin-resistance Genes Using Multiplex Padlock Probes

doi: 10.21769/BioProtoc.2504

Figure Lengend Snippet: For the species identification, the 16S rRNA gene is amplified using universal 16S primers (A1). Subsequently, the PCR products are labeled using a linear PCR and Cy5-modified cytosines (A2). In parallel, β-lactamase genes are pre-amplified in a 33-plex PCR (B1). Then, the padlock probes are hybridized (B2) and ligated (B3) using the β-lactamase PCR products as template and amplified in a first rolling circle amplification (RCA) (B4). The RCA products comprise a C2CA sequence and corresponding 16S rRNA barcode sequences. In a next reaction, the RCA products are monomerized (B5) using a restriction enzyme and circularized (B6) to serve as a new template for a second RCA (B7). These C2CA products are labelled in a linear PCR reaction using Atto532-modified cytosines (B8). Finally, the labelled amplification products from the 16S rRNA gene PCR and from the multiplex padlock assay are pooled together and hybridized to a microarray detecting the products at two different fluorescence wavelengths (C).

Article Snippet: Pipettes ( e.g ., Sartorius, catalog numbers: 728020, 728050, 728060 and 728070) Microbiological incubator shaker ( e.g ., IKA, model: KS 4000 i control) Tabletop centrifuge for 1.5 ml tubes ( e.g ., Eppendorf, model: 5424) Roche MagNA Lyser Instrument (Basel, Switzerland) Thermomixer comfort (Eppendorf, Hamburg, Germany) Epoch Microplate spectrophotometer (Biotek, Winooski, VT, USA) Biosan DNA/RNA UV-cleaner box (Warren, MI, USA) (recommended, see Note 4) Thermal cycler ( e.g ., Thermo Fisher Scientific, Applied Biosystems, model: GeneAmp TM PCR System 2700) (Paisley, UK) Heraeus Megafuge 40R with a TX-750 rotor (Thermo Fisher Scientific, Thermo Scientific TM , model: Heraeus TM Megafuge TM 40R, catalog number: 75004518; TX-750 rotor: Thermo Fisher Scientific, Thermo Scientific TM , catalog number: 75003180) and inserts for plates (Thermo Fisher Scientific, Thermo Scientific TM , catalog number: 75003617) and Falcon tubes (Thermo Fisher Scientific, Thermo Scientific TM , catalog number: 75003608) Slide humidity incubation box ( e.g ., LabScientific, catalog number: HIC-3) GeneMachines Omnigrid 100 contact arrayer (Madison, WI, USA) International Microarray Pin Stealth 3 SMP3 (Telechem, catalog number: SMP3) Agilent SureScan DNA Microarray Scanner (Santa Clara, CA, USA) Autoclave Sartorius arium pro UV ultrapure water system (Sartorius, model: arium ® pro)

Techniques: Amplification, Labeling, Modification, Sequencing, Multiplex Assay, Microarray, Fluorescence

Differential expression of leupaxin, DKK1, and DKK3 by palmoplantar (PP) and by nonpalmoplantar (NP) fibroblasts. Representative differences in gene expression patterns of leupaxin, DKK1, and DKK3 between palmoplantar fibroblasts and nonpalmoplantar fibroblasts as measured by microarray (top; quantitative results are summarized in and ). (middle) RT-PCR confirms the expression patterns of leupaxin, DKK1, and DKK3 in palmoplantar and in nonpalmoplantar fibroblasts. These data are representative of five independent experiments. (bottom) Real-time PCR to quantitate the expression of leupaxin, DKK1, and DKK3 after normalization of the target gene to GAPDH. Data are reported as means ± SD.

Journal: The Journal of Cell Biology

Article Title: Mesenchymal–epithelial interactions in the skin

doi: 10.1083/jcb.200311122

Figure Lengend Snippet: Differential expression of leupaxin, DKK1, and DKK3 by palmoplantar (PP) and by nonpalmoplantar (NP) fibroblasts. Representative differences in gene expression patterns of leupaxin, DKK1, and DKK3 between palmoplantar fibroblasts and nonpalmoplantar fibroblasts as measured by microarray (top; quantitative results are summarized in and ). (middle) RT-PCR confirms the expression patterns of leupaxin, DKK1, and DKK3 in palmoplantar and in nonpalmoplantar fibroblasts. These data are representative of five independent experiments. (bottom) Real-time PCR to quantitate the expression of leupaxin, DKK1, and DKK3 after normalization of the target gene to GAPDH. Data are reported as means ± SD.

Article Snippet: Scanning of the two fluorescent intensities of the cDNA chip was performed by a standard two-color microarray scanner (model GenePix 4000A DNA; Axon Instruments, Inc.).

Techniques: Quantitative Proteomics, Gene Expression, Microarray, Reverse Transcription Polymerase Chain Reaction, Expressing, Real-time Polymerase Chain Reaction

Histology results according to cytology,  HPV   DNA chip  results, <xref ref-type= a and HC2 results" width="100%" height="100%">

Journal: Journal of Pathology and Translational Medicine

Article Title: Clinical Significance of an HPV DNA Chip Test with Emphasis on HPV-16 and/or HPV-18 Detection in Korean Gynecological Patients

doi: 10.4132/jptm.2016.05.09

Figure Lengend Snippet: Histology results according to cytology, HPV DNA chip results, a and HC2 results

Article Snippet: The hybridized HPV DNA was visualized using a DNA chip scanner (ScanArray LITE, GSI Lumonics Inc., Bedford, MA, USA).

Techniques:

Age-adjusted odds ratio for ≥HSIL histology in each  HPV  group

Journal: Journal of Pathology and Translational Medicine

Article Title: Clinical Significance of an HPV DNA Chip Test with Emphasis on HPV-16 and/or HPV-18 Detection in Korean Gynecological Patients

doi: 10.4132/jptm.2016.05.09

Figure Lengend Snippet: Age-adjusted odds ratio for ≥HSIL histology in each HPV group

Article Snippet: The hybridized HPV DNA was visualized using a DNA chip scanner (ScanArray LITE, GSI Lumonics Inc., Bedford, MA, USA).

Techniques:

Comparison between  HPV   DNA chip  results <xref ref-type= a and HC2 results" width="100%" height="100%">

Journal: Journal of Pathology and Translational Medicine

Article Title: Clinical Significance of an HPV DNA Chip Test with Emphasis on HPV-16 and/or HPV-18 Detection in Korean Gynecological Patients

doi: 10.4132/jptm.2016.05.09

Figure Lengend Snippet: Comparison between HPV DNA chip results a and HC2 results

Article Snippet: The hybridized HPV DNA was visualized using a DNA chip scanner (ScanArray LITE, GSI Lumonics Inc., Bedford, MA, USA).

Techniques: Comparison

Clinical performance of cytology,  HPV   DNA chip  test, and HC2 test

Journal: Journal of Pathology and Translational Medicine

Article Title: Clinical Significance of an HPV DNA Chip Test with Emphasis on HPV-16 and/or HPV-18 Detection in Korean Gynecological Patients

doi: 10.4132/jptm.2016.05.09

Figure Lengend Snippet: Clinical performance of cytology, HPV DNA chip test, and HC2 test

Article Snippet: The hybridized HPV DNA was visualized using a DNA chip scanner (ScanArray LITE, GSI Lumonics Inc., Bedford, MA, USA).

Techniques:

Age-adjusted odds ratio for ≥HSIL histology in each  HPV  group exhibiting “NILM” and “ASC or AGC” cytology

Journal: Journal of Pathology and Translational Medicine

Article Title: Clinical Significance of an HPV DNA Chip Test with Emphasis on HPV-16 and/or HPV-18 Detection in Korean Gynecological Patients

doi: 10.4132/jptm.2016.05.09

Figure Lengend Snippet: Age-adjusted odds ratio for ≥HSIL histology in each HPV group exhibiting “NILM” and “ASC or AGC” cytology

Article Snippet: The hybridized HPV DNA was visualized using a DNA chip scanner (ScanArray LITE, GSI Lumonics Inc., Bedford, MA, USA).

Techniques: