Analysis of BCL10 Gene (Mutation) by RT-qPCR (CAT#: STEM-MT-0115-LGZ)

Introduction

Also known as: CLAP; mE10; CIPER; IMD37; c-E10; CARMEN
This gene was translocated in a case of mucosa-associated lymphoid tissue (MALT) lymphoma. The protein encoded by this gene contains a caspase recruitment domain (CARD) and has been shown to induce apoptosis and activate NF-kappaB. This protein has been reported to interact with other CARD domain-containing proteins, including CARD9, 10, 11, and 14, which are considered upstream regulators of NF-kappaB signaling. The protein was found to form a complex with MALT1, a protein encoded by another gene known to be translocated in MALT lymphoma. MALT1 and this protein are thought to cooperate in the activation of NF-kappaB, and dysregulation of either of them may lead to the same pathological process leading to malignancy. Alternative splicing results in multiple transcript variants.

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Principle Applications Procedure Materials Notes Related Products

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

Immunodeficiency 37, Mesothelioma, malignant, Germ cell tumor of testis, Lymphoma, non-Hodgkin, familial, Mucosa-associated lymphoma

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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