rna-isolation-purification-cells-immortalized-bxpc-3

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Wound healing assay can be challenging due to inconsistencies and variations while making a wound on the confluent cell monolayer, consequently leads to wounds of varying sizes and widths. Moreover, this assay causes damage to the cells that are at the edge of the wound, which can prevent cell migration into the wound site and healing. The best solution is to use the standard wound healing assay kits using either combs or inserts to make a defined wound field or gap and prevent the well-to-well variation in these assays.

Cellular assays Wound healing assay cell type human gHMVEC (glioma human microvascular endothelial cells)

Get tips on using SENSE mRNA-Seq Library Prep Kit V2 to perform RNA sequencing Human - Glioblastoma stem-like cells (GSCs)

Products Lexogen SENSE mRNA-Seq Library Prep Kit V2

Cell culture media 3D Cell Culture Media Human breast cancer MCF-7 cells-Mammospheres

Cell culture media 3D Cell Culture Media Mouse primary breast cancer ephitelial cells-Mammospheres

Cellular assays DNA Damage Assay Human bronchial epithelial cells (hBE)

Cellular assays DNA Damage Assay Human bronchial epithelial cells (hBE)

Cellular assays DNA Damage Assay Human bronchial epithelial cells (hBE)

Get tips on using In Situ Cell Death Detection Kit, Fluorescein to perform TUNEL assay cell type - PC-3 human prostate cancer

Products Sigma-Aldrich In Situ Cell Death Detection Kit, Fluorescein

DNA microarrays enable researchers to monitor the expression of thousands of genes simultaneously. However, the sensitivity, accuracy, specificity, and reproducibility are major challenges for this technology. Cross-hybridization, combination with splice variants, is a prime source for the discrepancies in differential gene expression calls among various microarray platforms. Removing (either from production or downstream bioinformatic analysis) and/or redesigning the microarray probes prone to cross-hybridization is a reasonable strategy to increase the hybridization specificity and hence, the accuracy of the microarray measurements.

DNA Microarray Gene expression arrays Human endometrial stromal cells Biotin

DNA microarrays enable researchers to monitor the expression of thousands of genes simultaneously. However, the sensitivity, accuracy, specificity, and reproducibility are major challenges for this technology. Cross-hybridization, combination with splice variants, is a prime source for the discrepancies in differential gene expression calls among various microarray platforms. Removing (either from production or downstream bioinformatic analysis) and/or redesigning the microarray probes prone to cross-hybridization is a reasonable strategy to increase the hybridization specificity and hence, the accuracy of the microarray measurements.

DNA Microarray Gene expression arrays Human whole blood cells Biotin

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