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Analysis of BAG4 Gene (Mutation) by RT-qPCR (CAT#: STEM-MT-1892-LGZ)

Introduction

Official Full Name: BAG cochaperone 4<br />Also known as: SODD; BAG-4<br />The protein encoded by this gene is a member of the bag1-related protein family. BAG1 is an anti-apoptotic protein that functions by interacting with a variety of apoptosis and growth-related proteins, including BCL-2, raf protein kinase, steroid hormone receptors, growth factor receptors, and heat shock protein 70kda family members . The protein contains a BAG domain near the C-terminus, which can bind and inhibit the chaperone activity of Hsc70/Hsp70. The protein was found to associate with the death domains of tumor necrosis factor receptor type 1 (TNF-R1) and death receptor 3 (DR3), thereby negatively regulating downstream cell death signaling. The regulatory role of this protein in cell death was demonstrated in epithelial cells, which undergo apoptosis when integrin-mediated matrix contacts are lost. Alternative splicing transcript variants encoding different isoforms have been identified.




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