180 k (amadid Search Results


180k oligo-array  (Agilent technologies)
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Agilent technologies 180k oligo-array
180k Oligo Array, supplied by Agilent technologies, 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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sureprint g3 human cgh microarray kit, 4×180k, amadid: 022060  (Agilent technologies)
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Agilent technologies sureprint g3 human cgh microarray kit, 4×180k, amadid: 022060
Sureprint G3 Human Cgh Microarray Kit, 4×180k, Amadid: 022060, supplied by Agilent technologies, 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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custom-designed microarrays  (Agilent technologies)
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Agilent technologies custom-designed microarrays
Custom Designed Microarrays, supplied by Agilent technologies, 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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snp array 180k  (Agilent technologies)
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Agilent technologies snp array 180k
Snp Array 180k, supplied by Agilent technologies, 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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c4×180k (amadid 022060-agilent cytogenomics edition 3.0  (Agilent technologies)
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Agilent technologies c4×180k (amadid 022060-agilent cytogenomics edition 3.0
C4×180k (Amadid 022060 Agilent Cytogenomics Edition 3.0, supplied by Agilent technologies, 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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c4×180k (amadid 022060-agilent cytogenomics edition 3.0 - by Bioz Stars, 2026-04
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180 k oligo-array  (Agilent technologies)
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Agilent technologies 180 k oligo-array
180 K Oligo Array, supplied by Agilent technologies, 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/180 k oligo-array/product/Agilent technologies
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180k array cgh  (Agilent technologies)
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Agilent technologies 180k array cgh
(A) QF‐PCR of fetus showing triallelic trisomy pattern for the STR marker D21S1411 (21q22.3) (red box); (B) additional STR marker, D21S1412 (21q22.2), showing triallelic trisomy pattern; (C) <t>180K</t> microarray showing a duplication approximately 4.98 Mb of parts of chromosome bands 21q22.2 and q22.3; (D) FISH on fetal material showing a submicroscopic insertion of chromosome band 21q22.2q22.3 in the long arm of chromosome 16; and (E) FISH on the patient's partner showing a balanced interchromosomal insertion: 46,XY.ish ins(16;21)(q22;q22.2q22.3).
180k Array Cgh, supplied by Agilent technologies, 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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180k array cgh - by Bioz Stars, 2026-04
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cgh 4×180k mouse slides  (Agilent technologies)
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Agilent technologies cgh 4×180k mouse slides
Generation and validation of the new Ts66Yah mouse model. (A) Representation of the deletion produced in Ts65Dn using CRISPR/Cas9 and two pairs of gRNAs. (B) Sequence electropherogram and PCR amplification products from the genotyping of Ts66Yah mice. (C) Genomic sequence of the new junction found in the deleted minichromosome of Ts66Yah mice. Blue font shows PCR primer localizations. (D) One metaphase spread showing the presence of an additional minichromosome (arrow) in Ts66Yah fibroblasts. (E) Comparative genomic hybridization (log2) of genomic DNA from Ts66Yah mice versus wild type <t>(180K</t> probes) compared to Ts65Dn mice (two 100K probes). (F) Comparison of the Ts66Yah and Ts65Dn minichromosomes. Orange and red colors show the sequence of Mmu17 and Mmu16, respectively. Numbers with letters represent the Giemsa banding.
Cgh 4×180k Mouse Slides, supplied by Agilent technologies, 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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array comparative genomic hybridisation (array-cgh 180k)  (Oxford Gene Technology)
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Oxford Gene Technology array comparative genomic hybridisation (array-cgh 180k)
Generation and validation of the new Ts66Yah mouse model. (A) Representation of the deletion produced in Ts65Dn using CRISPR/Cas9 and two pairs of gRNAs. (B) Sequence electropherogram and PCR amplification products from the genotyping of Ts66Yah mice. (C) Genomic sequence of the new junction found in the deleted minichromosome of Ts66Yah mice. Blue font shows PCR primer localizations. (D) One metaphase spread showing the presence of an additional minichromosome (arrow) in Ts66Yah fibroblasts. (E) Comparative genomic hybridization (log2) of genomic DNA from Ts66Yah mice versus wild type <t>(180K</t> probes) compared to Ts65Dn mice (two 100K probes). (F) Comparison of the Ts66Yah and Ts65Dn minichromosomes. Orange and red colors show the sequence of Mmu17 and Mmu16, respectively. Numbers with letters represent the Giemsa banding.
Array Comparative Genomic Hybridisation (Array Cgh 180k), supplied by Oxford Gene Technology, 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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Average 90 stars, based on 1 article reviews
array comparative genomic hybridisation (array-cgh 180k) - by Bioz Stars, 2026-04
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custom 4 × 180k microarray  (Agilent technologies)
90
Agilent technologies custom 4 × 180k microarray
Generation and validation of the new Ts66Yah mouse model. (A) Representation of the deletion produced in Ts65Dn using CRISPR/Cas9 and two pairs of gRNAs. (B) Sequence electropherogram and PCR amplification products from the genotyping of Ts66Yah mice. (C) Genomic sequence of the new junction found in the deleted minichromosome of Ts66Yah mice. Blue font shows PCR primer localizations. (D) One metaphase spread showing the presence of an additional minichromosome (arrow) in Ts66Yah fibroblasts. (E) Comparative genomic hybridization (log2) of genomic DNA from Ts66Yah mice versus wild type <t>(180K</t> probes) compared to Ts65Dn mice (two 100K probes). (F) Comparison of the Ts66Yah and Ts65Dn minichromosomes. Orange and red colors show the sequence of Mmu17 and Mmu16, respectively. Numbers with letters represent the Giemsa banding.
Custom 4 × 180k Microarray, supplied by Agilent technologies, 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/custom 4 × 180k microarray/product/Agilent technologies
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custom 4 × 180k microarray - by Bioz Stars, 2026-04
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4×180k microarray format  (Agilent technologies)
90
Agilent technologies 4×180k microarray format
Generation and validation of the new Ts66Yah mouse model. (A) Representation of the deletion produced in Ts65Dn using CRISPR/Cas9 and two pairs of gRNAs. (B) Sequence electropherogram and PCR amplification products from the genotyping of Ts66Yah mice. (C) Genomic sequence of the new junction found in the deleted minichromosome of Ts66Yah mice. Blue font shows PCR primer localizations. (D) One metaphase spread showing the presence of an additional minichromosome (arrow) in Ts66Yah fibroblasts. (E) Comparative genomic hybridization (log2) of genomic DNA from Ts66Yah mice versus wild type <t>(180K</t> probes) compared to Ts65Dn mice (two 100K probes). (F) Comparison of the Ts66Yah and Ts65Dn minichromosomes. Orange and red colors show the sequence of Mmu17 and Mmu16, respectively. Numbers with letters represent the Giemsa banding.
4×180k Microarray Format, supplied by Agilent technologies, 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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180k oligonucleotide platform (amadid 026570)  (Agilent technologies)
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Agilent technologies 180k oligonucleotide platform (amadid 026570)
Generation and validation of the new Ts66Yah mouse model. (A) Representation of the deletion produced in Ts65Dn using CRISPR/Cas9 and two pairs of gRNAs. (B) Sequence electropherogram and PCR amplification products from the genotyping of Ts66Yah mice. (C) Genomic sequence of the new junction found in the deleted minichromosome of Ts66Yah mice. Blue font shows PCR primer localizations. (D) One metaphase spread showing the presence of an additional minichromosome (arrow) in Ts66Yah fibroblasts. (E) Comparative genomic hybridization (log2) of genomic DNA from Ts66Yah mice versus wild type <t>(180K</t> probes) compared to Ts65Dn mice (two 100K probes). (F) Comparison of the Ts66Yah and Ts65Dn minichromosomes. Orange and red colors show the sequence of Mmu17 and Mmu16, respectively. Numbers with letters represent the Giemsa banding.
180k Oligonucleotide Platform (Amadid 026570), supplied by Agilent technologies, 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/180k oligonucleotide platform (amadid 026570)/product/Agilent technologies
Average 90 stars, based on 1 article reviews
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Image Search Results


(A) QF‐PCR of fetus showing triallelic trisomy pattern for the STR marker D21S1411 (21q22.3) (red box); (B) additional STR marker, D21S1412 (21q22.2), showing triallelic trisomy pattern; (C) 180K microarray showing a duplication approximately 4.98 Mb of parts of chromosome bands 21q22.2 and q22.3; (D) FISH on fetal material showing a submicroscopic insertion of chromosome band 21q22.2q22.3 in the long arm of chromosome 16; and (E) FISH on the patient's partner showing a balanced interchromosomal insertion: 46,XY.ish ins(16;21)(q22;q22.2q22.3).

Journal: Clinical Case Reports

Article Title: A prenatal case of partial trisomy 21 (q22.2q22.3), resulting from a paternal insertion translocation ins(16;21) and uncovered by QF‐PCR, and characterized by array CGH and FISH

doi: 10.1002/ccr3.1563

Figure Lengend Snippet: (A) QF‐PCR of fetus showing triallelic trisomy pattern for the STR marker D21S1411 (21q22.3) (red box); (B) additional STR marker, D21S1412 (21q22.2), showing triallelic trisomy pattern; (C) 180K microarray showing a duplication approximately 4.98 Mb of parts of chromosome bands 21q22.2 and q22.3; (D) FISH on fetal material showing a submicroscopic insertion of chromosome band 21q22.2q22.3 in the long arm of chromosome 16; and (E) FISH on the patient's partner showing a balanced interchromosomal insertion: 46,XY.ish ins(16;21)(q22;q22.2q22.3).

Article Snippet: Additional targeted 180K array CGH (Agilent Technologies, Santa Clara, USA; Amadid 023363) showed a duplication of approximately 4.98 Mb of parts of chromosome bands 21q22.2 and q22.3 (ISCN: arr[hg18] 21q22.2q22.3(39,119,758‐44,102,267)x3) (Fig. C).

Techniques: Marker, Microarray

Generation and validation of the new Ts66Yah mouse model. (A) Representation of the deletion produced in Ts65Dn using CRISPR/Cas9 and two pairs of gRNAs. (B) Sequence electropherogram and PCR amplification products from the genotyping of Ts66Yah mice. (C) Genomic sequence of the new junction found in the deleted minichromosome of Ts66Yah mice. Blue font shows PCR primer localizations. (D) One metaphase spread showing the presence of an additional minichromosome (arrow) in Ts66Yah fibroblasts. (E) Comparative genomic hybridization (log2) of genomic DNA from Ts66Yah mice versus wild type (180K probes) compared to Ts65Dn mice (two 100K probes). (F) Comparison of the Ts66Yah and Ts65Dn minichromosomes. Orange and red colors show the sequence of Mmu17 and Mmu16, respectively. Numbers with letters represent the Giemsa banding.

Journal: Disease Models & Mechanisms

Article Title: Ts66Yah, a mouse model of Down syndrome with improved construct and face validity

doi: 10.1242/dmm.049721

Figure Lengend Snippet: Generation and validation of the new Ts66Yah mouse model. (A) Representation of the deletion produced in Ts65Dn using CRISPR/Cas9 and two pairs of gRNAs. (B) Sequence electropherogram and PCR amplification products from the genotyping of Ts66Yah mice. (C) Genomic sequence of the new junction found in the deleted minichromosome of Ts66Yah mice. Blue font shows PCR primer localizations. (D) One metaphase spread showing the presence of an additional minichromosome (arrow) in Ts66Yah fibroblasts. (E) Comparative genomic hybridization (log2) of genomic DNA from Ts66Yah mice versus wild type (180K probes) compared to Ts65Dn mice (two 100K probes). (F) Comparison of the Ts66Yah and Ts65Dn minichromosomes. Orange and red colors show the sequence of Mmu17 and Mmu16, respectively. Numbers with letters represent the Giemsa banding.

Article Snippet: After labeling, the DNAs were hybridized on CGH 4×180K mouse slides (AMADID 027411, Agilent Technologies).

Techniques: Produced, CRISPR, Sequencing, Amplification, Hybridization