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Analysis of LITAF Gene (Mutation) by RT-qPCR (CAT#: STEM-MT-2475-LGZ)

Introduction

Official Full Name: lipopolysaccharide induced TNF factor<br />Also known as: PIG7; SIMPLE; TP53I7<br />Lipopolysaccharide is a potent stimulator of monocytes and macrophages, causing the secretion of tumor necrosis factor-α (TNF-α) and other inflammatory mediators. The gene encodes lipopolysaccharide-induced tnf-alpha factor, which is a dna-binding protein and can mediate the expression of tnf-alpha by directly binding to the promoter region of tnf-alpha gene. The transcription of this gene is induced by the tumor suppressor p53 and is related to the p53-induced apoptosis pathway. Mutations in this gene cause Charcot-Marie-Tooth disease type 1C (CMT1C) and may be involved in the carcinogenesis of extramammary Paget's disease (EMPD). Multiple alternatively spliced transcript variants have been found for this gene.




Principle

Quantitative reverse transcription PCR (RT-qPCR) is an experimental method applied to PCR experiments using RNA as the starting material. In this method, total or messenger RNA (mRNA) is first transcribed into complementary DNA (cDNA) by reverse transcriptase. Subsequently, qPCR reaction was performed using cDNA as template.

Applications

Gene mutation analysis.

Procedure

1. Sample processing and preparation of PCR reaction system.
2. Add the amplification template, cover the PCR reaction cover, mix well, centrifuge at low speed instantaneously, and transfer to the PCR instrument.
3. Set the program for PCR amplification.
4. Data analysis.

Materials

Sample: depends on the customer's analysis requirements