siRNA / miRNA gene silencing Human siRNA negative control

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Get tips on using SNP Type™ 96.96 Genotyping Reagent Kit with Control Line Fluid—10 IFCs to perform Cell line authentication Human prostatic cancer cell line DU145

Products Fluidigm SNP Type™ 96.96 Genotyping Reagent Kit with Control Line Fluid—10 IFCs

Get tips on using SNP Type™ 96.96 Genotyping Reagent Kit with Control Line Fluid—10 IFCs to perform Cell line authentication Human prostatic cancer cell line PC3

Products Fluidigm SNP Type™ 96.96 Genotyping Reagent Kit with Control Line Fluid—10 IFCs

Get tips on using Lipofectamine® 2000 Transfection Reagent to perform siRNA / RNAi /miRNA transfection Human Cells - HeLa Lipofectamine

Products Thermo Fisher Scientific Lipofectamine® 2000 Transfection Reagent

Get tips on using Lipofectamine® 2000 Transfection Reagent to perform siRNA / RNAi /miRNA transfection Human Cells - HESC Lipofectamine

Products Thermo Fisher Scientific Lipofectamine® 2000 Transfection Reagent

DNA DNA isolation / purification Bacteria Gram negative Klebsiella

DNA DNA isolation / purification Bacteria Gram negative Rhodopseudomonas

Cellular assays Cell Isolation Double-negative T Cell Isolation

Get tips on using Anti-TATA binding protein TBP antibody [58C9] - Loading Control (ab61411) to perform Western blotting TBP

Products Abcam Anti-TATA binding protein TBP antibody [58C9] - Loading Control (ab61411)

DNA isolation and purification is the first critical step in sample preparation that helps ensure optimal performance of downstream assays like PCR, microarrays, and sequencing. Failure in yielding high-quality DNA would be the major reason that DNA doesn't work for the downstream application. To circumvent this, one should follow the recommended storage conditions to minimize DNA degradation by nucleases and shouldn't overload the purification system.

DNA DNA isolation / purification Bacteria Gram negative E.coli

DNA isolation and purification is the first critical step in sample preparation that helps ensure optimal performance of downstream assays like PCR, microarrays, and sequencing. Failure in yielding high-quality DNA would be the major reason that DNA doesn't work for the downstream application. To circumvent this, one should follow the recommended storage conditions to minimize DNA degradation by nucleases and shouldn't overload the purification system.

DNA DNA isolation / purification Bacteria Gram negative Legionella

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