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Agilent(Hewlett-Packard...
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| Part No. |
MR-0050.008
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| OCR Text |
...assay for the identification of snvs associated with alport syndrome (as) *only 192 mid combinations available. research application ? identification of snvs in the col4a3 , col4a4 and col4a5 genes genes col4a3, col4a4, col4a5 genomic... |
| Description |
ALPORT MASTR
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| File Size |
116.89K /
2 Page |
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Agilent(Hewlett-Packard...
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| Part No. |
MR-0160.024
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| OCR Text |
... ? for detection of mutations (snvs and small indels) in tp53 in ffpe-derived dna ? for detection of mutations (snvs and small indels) in tp53 in blood-derived dna ? for detection of mutations (snvs and small indels) in tp53 in f... |
| Description |
TP53 MASTR
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| File Size |
98.13K /
2 Page |
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Agilent(Hewlett-Packard...
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| Part No. |
MR-0171.024
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| OCR Text |
...s assay allows the analysis of snvs, indels and cnvs in one single sequencing run. *only 192 mid combinations available. research application ? for the detection of variants (snvs and cnvs), in 3 selected genes associated with stargardt ... |
| Description |
STARGARDT MASTR
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| File Size |
391.94K /
2 Page |
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Agilent(Hewlett-Packard...
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| Part No. |
MR-0182.024
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| OCR Text |
snvs and indels in nras , kras and braf genes associated with various types of cancer. the flexible research assay can analyze the most frequent mutations (plex 1 only) and for the entire coding regions of nras , kras and braf . a... |
| Description |
SOMATIC 1 MASTR Plus
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| File Size |
129.21K /
2 Page |
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Agilent(Hewlett-Packard...
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| Part No. |
MR-0200.024
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| OCR Text |
...panel for the identification of snvs in the hotspots of 26 frequently mutated genes in solid tumors. this ngs assay is designed with input from selected inca centers in france. assay characteristics genes with hotspots included akt erbb2... |
| Description |
Tumor Hotspot MASTR Plus
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| File Size |
953.68K /
4 Page |
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Agilent(Hewlett-Packard...
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| Part No. |
MR-0120.008
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| OCR Text |
snvs and cnvs in the dmd gene associated with muscular dystrophies research application detection of dmd variants associated with ? duchenne muscular dystrophy (dmd) ? becker muscular dystrophy (bmd) ? x-linked dilated cardiomyopa... |
| Description |
DMD MASTR
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| File Size |
106.80K /
2 Page |
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Agilent(Hewlett-Packard...
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| Part No. |
MR-0110.008
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| OCR Text |
...assay for the identification of snvs and cnvs associated with marfan syndrome. *only 192 mid combinations available. research application ? identification of snvs and cnvs in the fbn1 gene genes fbn1 genomic region analyzed 21.1 kb nu... |
| Description |
MARFAN MASTR
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| File Size |
116.69K /
2 Page |
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Agilent(Hewlett-Packard...
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| Part No. |
MR-0130.024 EGFR18-21MASTR
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| OCR Text |
...detection of germline variants, snvs, in exons 18-21 of egfr in ffpe-derived dna. genes full coding region of exons 18-21 of egfr genomic region analyzed 0.6 kb number of amplicons 4 amplicon length 100-180 bp number of plexes 1 design... |
| Description |
For detection of germline variants, snvs, in exons 18-21 of EGFR in FFPE-derived DNA
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| File Size |
107.92K /
2 Page |
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Agilent(Hewlett-Packard...
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| Part No. |
MR-0130.024
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| OCR Text |
snvs, in exons 18-21 of egfr in ffpe-derived dna the egfr 18-21 mastr is a molecular research panel for the identification of variants in exons 18 to 21 of the egfr gene, which codes for the epidermal growth factor receptor (egfr). ... |
| Description |
EGFR 18-21 MASTR
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| File Size |
738.09K /
2 Page |
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it Online |
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