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Analysis of RGS4 Gene (Mutation) by RT-qPCR (CAT#: STEM-MT-0624-LGZ)

Introduction

Official Full Name: regulator of G protein signaling 4
Also known as: RGP4; SCZD9
Members of the regulator of G protein signaling (RGS) family are GTPase-activating protein (gap) regulatory molecules of the G α subunit of heterotrimeric G proteins. RGS proteins are capable of inactivating G protein subunits of the Gi α, Go α, and Gq α subtypes. They convert the G protein to the inactive GDP-bound form. Regulators of G protein signaling 4 belong to this family. All RGS proteins share a conserved 120 amino acid sequence known as the RGS domain. Regulator of G protein signaling 4 protein shares 37% identity with RGS1 and 97% identity with rat Rgs4. This protein negatively regulates signaling upstream or at the level of heterotrimeric G proteins and localizes in the cytoplasm. Alternative splicing transcript variants of this gene 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
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