B16F10 In Vitro RNA Expression Analysis Assay (Real-time PCR)
CAT#: ITS-1022-YF88
Target Cell Organism: Mouse
Target Cell Alternative Name: B16-F10
Target Cell Name: B16F10
Assay Type: Gene and Protein Expression Assays
Assay Overview
This assay is to provide B16F10-based In Vitro RNA Expression Analysis Assay (Real-time PCR) to accelerate our client's oncology projects. The assay will be customized according to the specific requirements. Please contact our scientists to discuss more details.
Target Cell Name
B16F10
Target Cell Organism
Mouse
Target Cell Background
B16F10 cell line (from Mus musculus C57BL/6J strain) is a convenient and widely used experimental model of highly metastatic melanoma to study cytotoxicity, migration, metastatic spread and tissue invasion. B16-F10 is a cell line exhibiting a morphology of spindle-shaped and epithelial-like cells that was isolated from skin tissue of a mouse with melanoma. Use these cells in your skin cancer research.
Target Cell Alternative Name
B16-F10
Related Diseases
Melanoma
Research Area
Oncology
Assay Name
In Vitro RNA Expression Analysis Assay (Real-time PCR)
Short Description
B16F10-cell based In Vitro RNA Expression Analysis Assay (Real-time PCR)
Assay Description
Real-time PCR is the most commonly used platform to evaluate mRNA or miRNA expression after conversion of mRNA or miRNA into cDNA. Amplification of a target gene is evaluated by quantifying th fluorescence signal generated using DNA intercalating dyes (SYBER green) or gene-specific probes. This technique can also be used to screen gene mutations, DNA modifications and confirm results obtained from northern blotting or microarray. Additionally, real-time PCR is the most suitable tool for gene expression analysis for RNA samples with low yields compared to hybridization techniques.
Assay Type
Gene and Protein Expression Assays
Assay Type Details
Following transcription, primary transcript RNA is converted into mature RNA by post-transcriptional modifications. Post-transcriptional modification includes three major steps namely the addition of a 5'cap, addition of a 3'polyadenylation tail and RNA splicing. Stability of RNA has been considered as very important for gene expression and proteins at the post-transcriptional level.