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Analysis of NPR1 Gene (Mutation) by RT-qPCR (CAT#: STEM-MT-0502-LGZ)

Introduction

Official Full Name: natriuretic peptide receptor 1
Also known as: ANPa; NPRA; ANPRA; GUC2A; GUCY2A
Guanidyl cyclases that catalyze GTP to cGMP are divided into soluble and membrane forms (Garbers and Lowe,). The membrane guanylyl cyclases, often termed guanylyl cyclases A through F, form a family of cell-surface receptors with a similar topographic structure: an extracellular ligand-binding domain, a single membrane-spanning domain, and an intracellular region that con tains a protein kinase -like domain and a cyclase catalytic domain. GC-A and GC-B act as natriuretic peptide receptors; they are also known as atrial natriuretic peptide receptors A (NPR1) and B (NPR2); MIM 108961). See also NPR3 (MIM 108962), which encodes a protein with only a ligand-binding transmembrane and a 37 amino acid cytoplasmic domain. NPR1 is a membrane-bound guanylate cyclase that acts as a receptor for atrial and brain natriuretic peptides (ANP (MIM 108780) and BNP (MIM 600295).




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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