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Unitma Co Ltd tissue micro arrayer® device quick-raytm
Tissue Micro Arrayer® Device Quick Raytm, supplied by Unitma Co Ltd, 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/arraymate+device/tissue+microarray+system+quick+ray+ut06/pmc08665204-118-34-39
Average 90 stars, based on 1 article reviews
tissue micro arrayer® device quick-raytm - by Bioz Stars, 2026-10
90/100 stars

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other:

Article Title: Molecular subtypes and quantitative analysis of PD-L1 and tumor-associated immune cells in uterine carcinosarcoma.
Article Snippet: The Quick-Ray UT06 (UNITMA, Seoul, Korea) was used to construct TMAs from formalinfixed paraffin-embedded (FFPE) blocks with a single 2 mm core.

Article Title: Expression of Insulin-like growth factor 2 mRNA-binding protein 3 and its diagnostic value in breast cancer
Article Snippet: To summarize, the Quick-Ray ® UT-06 tissue microarray system and the Quick-Ray premade recipient block (UB-06) wax model, both produced by Unitma Co., Ltd. in Seoul, Korea, were utilized for the preparation of tissue specimens measuring 1 mm in diameter.

Article Title: Prognostic Significance of RBM3 Expression in Epithelial Ovarian Cancer: A Tissue Microarray-Based Study.
Article Snippet: A pair of 2 mm tissue cores was extracted from each donor block and transferred to a recipient block using the Quick-Ray Manual Tissue Microarrayer (Unitma, Seoul, Republic of Korea).

Immunohistochemical staining:

Article Title: The Monocarboxylate Transporters MCT1 and MCT4 Are Highly Expressed in Glioblastoma and Crucially Implicated in the Pathobiology.
Article Snippet: Monocarboxylate transporters (MCTs) are crucially implicated in cancer cell metabolism by transporting lactate/H+ ions and thus regulating the pH of the microenvironment.. We assessed MCT1 and MCT4 expression in 98 cases of adulttype hemispheric Glioblastomas (GBMs) (IDH wildtype), along with 51 cases of IDHmutant astrocytic and oligodendroglial tumors (grade 2–4) for comparison.. U87MG and LN229 cell lines were used for in vitro analysis.

Staining:

Article Title: The Monocarboxylate Transporters MCT1 and MCT4 Are Highly Expressed in Glioblastoma and Crucially Implicated in the Pathobiology.
Article Snippet: Monocarboxylate transporters (MCTs) are crucially implicated in cancer cell metabolism by transporting lactate/H+ ions and thus regulating the pH of the microenvironment.. We assessed MCT1 and MCT4 expression in 98 cases of adulttype hemispheric Glioblastomas (GBMs) (IDH wildtype), along with 51 cases of IDHmutant astrocytic and oligodendroglial tumors (grade 2–4) for comparison.. U87MG and LN229 cell lines were used for in vitro analysis.

Construct:

Article Title: The Monocarboxylate Transporters MCT1 and MCT4 Are Highly Expressed in Glioblastoma and Crucially Implicated in the Pathobiology.
Article Snippet: Monocarboxylate transporters (MCTs) are crucially implicated in cancer cell metabolism by transporting lactate/H+ ions and thus regulating the pH of the microenvironment.. We assessed MCT1 and MCT4 expression in 98 cases of adulttype hemispheric Glioblastomas (GBMs) (IDH wildtype), along with 51 cases of IDHmutant astrocytic and oligodendroglial tumors (grade 2–4) for comparison.. U87MG and LN229 cell lines were used for in vitro analysis.

Article Title: Spatial profiling reveals unique immune microenvironment in premenopausal triple-negative breast cancer associated with therapy response.
Article Snippet: .. TMA was constructed using the Quick Ray manual tissue microarrayer from Unitma Co.Ltd., Seoul, Korea as mentioned in previous publication [13]. ..

Article Title: Enhanced IL36RN Expression and Its Association With Immune Microenvironment Predicts Poor Prognosis in Gastric Cancer.
Article Snippet: .. Tissue microarrays (TMA) were constructed using the manual Tissue Microarrayer System Quick Ray (UT06, UNITMA, Korea). ..

Microarray:

Article Title: The Monocarboxylate Transporters MCT1 and MCT4 Are Highly Expressed in Glioblastoma and Crucially Implicated in the Pathobiology.
Article Snippet: Monocarboxylate transporters (MCTs) are crucially implicated in cancer cell metabolism by transporting lactate/H+ ions and thus regulating the pH of the microenvironment.. We assessed MCT1 and MCT4 expression in 98 cases of adulttype hemispheric Glioblastomas (GBMs) (IDH wildtype), along with 51 cases of IDHmutant astrocytic and oligodendroglial tumors (grade 2–4) for comparison.. U87MG and LN229 cell lines were used for in vitro analysis.

Blocking Assay:

Article Title: Expression rates of p16, p53 in head and neck cutaneous squamous cell carcinoma based on human-papillomavirus positivity
Article Snippet: .. The corresponding areas of each paraffin block were then sectioned twice using a 2 mm-diameter cylinder and transferred to a recipient paraffin block using a tissue microarrayer (Unitma, Seoul, Korea). .. Immunohistochemical (IHC) staining of individual 4-μm thick slide sections derived from tissue microarray blocks was performed using the Ventana Bench Mark XT automated staining system (Ventana Medical Systems, Tucson, AZ, United States), according to the manufacturer’s protocol.



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(a) Linear Multiplex Amplification starting from clonal RNA free genomic DNA, extracted DNA is internally labeled with biotin (Label [L]) and amplified in a linear multiplex PCR reaction; (b) Hybridization: the biotin labeled, single-stranded DNA product hybridizes specifically under stringent conditions to the corresponding probes. The resulting duplex is detected using a horse-radish peroxidase (Enzyme [E]) – streptavidin conjugate, which converts the substrate (Seramun green [S]) into a colored local precipitate. (c) Detection: the <t>ArrayMate™</t> Reader (or ArrayTube™ Reader ATR 03) enables the visualization and subsequent automated analysis of the array image. The presence of a dark precipitated spot indicates successful hybridization; (d) Analysis: the assay specific software analysis script, supplied with the ArrayMate™ Reader (or ArrayTube™ Reader ATR 03), measures the signal intensity of each probe and determines with an assay specific algorithm which genes/alleles are present in the sample. (e) Genotype analysis: the PatternMatching software supplied with the ArrayMate™ Reader (or ArrayTube™ Reader ATR 03) is comparing the resulting pattern with a local database including 132 reference serovars previously sero- and genotyped, finally a report is given to which serovar the sample strain belongs with regard to the Kauffman-White Scheme.
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(a) Linear Multiplex Amplification starting from clonal RNA free genomic DNA, extracted DNA is internally labeled with biotin (Label [L]) and amplified in a linear multiplex PCR reaction; (b) Hybridization: the biotin labeled, single-stranded DNA product hybridizes specifically under stringent conditions to the corresponding probes. The resulting duplex is detected using a horse-radish peroxidase (Enzyme [E]) – streptavidin conjugate, which converts the substrate (Seramun green [S]) into a colored local precipitate. (c) Detection: the <t>ArrayMate™</t> Reader (or ArrayTube™ Reader ATR 03) enables the visualization and subsequent automated analysis of the array image. The presence of a dark precipitated spot indicates successful hybridization; (d) Analysis: the assay specific software analysis script, supplied with the ArrayMate™ Reader (or ArrayTube™ Reader ATR 03), measures the signal intensity of each probe and determines with an assay specific algorithm which genes/alleles are present in the sample. (e) Genotype analysis: the PatternMatching software supplied with the ArrayMate™ Reader (or ArrayTube™ Reader ATR 03) is comparing the resulting pattern with a local database including 132 reference serovars previously sero- and genotyped, finally a report is given to which serovar the sample strain belongs with regard to the Kauffman-White Scheme.
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(a) Linear Multiplex Amplification starting from clonal RNA free genomic DNA, extracted DNA is internally labeled with biotin (Label [L]) and amplified in a linear multiplex PCR reaction; (b) Hybridization: the biotin labeled, single-stranded DNA product hybridizes specifically under stringent conditions to the corresponding probes. The resulting duplex is detected using a horse-radish peroxidase (Enzyme [E]) – streptavidin conjugate, which converts the substrate (Seramun green [S]) into a colored local precipitate. (c) Detection: the ArrayMate™ Reader (or ArrayTube™ Reader ATR 03) enables the visualization and subsequent automated analysis of the array image. The presence of a dark precipitated spot indicates successful hybridization; (d) Analysis: the assay specific software analysis script, supplied with the ArrayMate™ Reader (or ArrayTube™ Reader ATR 03), measures the signal intensity of each probe and determines with an assay specific algorithm which genes/alleles are present in the sample. (e) Genotype analysis: the PatternMatching software supplied with the ArrayMate™ Reader (or ArrayTube™ Reader ATR 03) is comparing the resulting pattern with a local database including 132 reference serovars previously sero- and genotyped, finally a report is given to which serovar the sample strain belongs with regard to the Kauffman-White Scheme.

Journal: PLoS ONE

Article Title: Fast DNA Serotyping and Antimicrobial Resistance Gene Determination of Salmonella enterica with an Oligonucleotide Microarray-Based Assay

doi: 10.1371/journal.pone.0046489

Figure Lengend Snippet: (a) Linear Multiplex Amplification starting from clonal RNA free genomic DNA, extracted DNA is internally labeled with biotin (Label [L]) and amplified in a linear multiplex PCR reaction; (b) Hybridization: the biotin labeled, single-stranded DNA product hybridizes specifically under stringent conditions to the corresponding probes. The resulting duplex is detected using a horse-radish peroxidase (Enzyme [E]) – streptavidin conjugate, which converts the substrate (Seramun green [S]) into a colored local precipitate. (c) Detection: the ArrayMate™ Reader (or ArrayTube™ Reader ATR 03) enables the visualization and subsequent automated analysis of the array image. The presence of a dark precipitated spot indicates successful hybridization; (d) Analysis: the assay specific software analysis script, supplied with the ArrayMate™ Reader (or ArrayTube™ Reader ATR 03), measures the signal intensity of each probe and determines with an assay specific algorithm which genes/alleles are present in the sample. (e) Genotype analysis: the PatternMatching software supplied with the ArrayMate™ Reader (or ArrayTube™ Reader ATR 03) is comparing the resulting pattern with a local database including 132 reference serovars previously sero- and genotyped, finally a report is given to which serovar the sample strain belongs with regard to the Kauffman-White Scheme.

Article Snippet: The visualization was achieved by adding 100 µl of peroxidase substrate D1 to the ArrayStrips, and signals were detected with the ArrayMate device (Alere Technologies, Jena, Germany) ( ).

Techniques: Multiplex Assay, Amplification, Labeling, Hybridization, Software