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Analysis of IRAG1 Gene (Mutation) by RT-qPCR (CAT#: STEM-MT-2261-LGZ)

Introduction

Official Full Name: inositol 1,4,5-triphosphate receptor associated 1
Also known as: IRAG; JAW1L; MRVI1
The gene is similar to a putative mouse tumor suppressor gene (Mrvi1) that is frequently disrupted by mouse AIDS-related virus (MRV). The encoded protein is present in the endoplasmic reticulum membrane and is similar to Jaw1, a lymphocyte-restricted protein whose expression is downregulated during lymphocyte differentiation. This protein is a substrate of cGMP-dependent kinase-1 (PKG1) and acts as a regulator of IP3-induced calcium release. Mouse studies have shown that the integration of MRV in Mrvi1 induces myeloid leukemia by altering the expression of a gene important for myeloid cell growth and/or differentiation and thus may serve as a myeloid leukemia tumor suppressor gene. Several alternatively spliced transcript variants encoding different isoforms of this gene have been identified and use alternative translation initiation sites, including non-aug (CUG) initiation sites.




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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