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Description

The Genebio EML4 Dual Color Break Apart Probe is designed to detect rearrangements involving the chromosomal region 2p21 harboring the EML4 gene. Inversions in the short arm of chromosome 2 [inv(2)(p21p23)] have been frequently detected in non-small cell lung cancer and lead to the formation of EML4-ALK fusion transcripts. A few reports also identified these fusion transcripts in breast, gastric, and colorectal cancers.

What is the purpose of the Genebio EML4 Dual Color Break Apart Probe?

The Genebio EML4 Dual Color Break Apart Probe serves a vital purpose in the field of genetic research and diagnostics. This innovative probe is specifically designed to detect and identify gene rearrangements involving the EML4 (echinoderm microtubule-associated protein-like 4) gene.

The EML4 gene is known to play a significant role in the development of certain types of cancer, particularly non-small cell lung cancer (CLC). In some cases, a rearrangement occurs within the EML4 gene, resulting in the fusion of a portion of the EML4 gene with another gene called ALK (anaplastic lymphoma kinase). This EML4-ALK fusion gene is implicated in the development and progression of NSCLC.

The purpose of the Genebio EML4 Dual Color Break Apart Probe is to accurately and efficiently detect these gene rearrangements and identify the presence of the EML4-ALK fusion gene. The probe utilizes a dual-color scheme, where one color is used to detect the intact EML4 gene, while the other color is employed to identify the rearranged EML4 gene.

By using this probe, researchers and clinicians can gain valuable insights into the genetic makeup of tumors and make informed decisions regarding patient treatment options. Identification of the EML4-ALK fusion gene can help determine if a patient is a suitable candidate for targeted therapy with ALK inhibitors, which have shown promising results in the treatment of NSCLC patients with this specific gene rearrangement.

The Genebio EML4 Dual Color Break Apart Probe is highly sensitive and specific, allowing for the accurate detection of even low levels of the EML4-ALK fusion gene. This is crucial in ensuring that patients who may benefit from targeted therapy are not overlooked.

In addition to its diagnostic capabilities, the Genebio EML4 Dual Color Break Apart Probe can also be used in research settings to further understand the role of this gene rearrangement in cancer development and progression. By studying the EML4-ALK fusion gene, researchers can uncover potential therapeutic targets and develop new treatments for NSCLC.

The dual-color scheme of the probe is particularly advantageous as it allows for easy visualization and interpretation of the results. The intact EML4 gene appears as one color, while the rearranged EML4 gene appears as another color. This clear distinction minimizes the chances of misinterpretation and enhances the accuracy of the test.

How does the Genebio EML4 Dual Color Break Apart Probe work?

The Genebio EML4 Dual Color Break Apart Probe is a powerful tool used in genetic research to detect specific gene rearrangements. Specifically, this probe is designed to identify and analyze the EML4 gene, which is known to be involved in certain types of cancer, particularly non-small cell lung cancer.

The probe works based on the principle of fluorescence in situ hybridization (FISH). FISH is a technique that allows researchers to visualize and map the genetic material within cells. In the case of the EML4 Dual Color Break Apart Probe, it enables the identification of rearrangements in the EML4 gene.

The probe consists of two different fluorescently labeled DNA probes. One probe is labeled with a green fluorophore, and the other probe is labeled with a red fluorophore. These probes are designed to specifically bind to complementary sequences within the EML4 gene.

In normal cells, the EML4 gene is intact and not rearranged. When the two probes bind to the EML4 gene, they are in close proximity to each other, resulting in the emission of a yellow color when observed under a fluorescence microscope.

However, in cells with EML4 gene rearrangements, the gene is split into two parts. This separation causes the green-labeled probe and the red-labeled probe to be separated as well. As a result, when observed under a fluorescence microscope, the two separate parts of the gene will emit either a green or red color, indicating the presence of a gene rearrangement.

To use the Genebio EML4 Dual Color Break Apart Probe, researchers first prepare a sample containing cells of interest. The cells are fixed onto a slide and then treated with reagents to prepare them for hybridization with the probe.

The probe is then applied to the sample and allowed to hybridize, or bind, to the target DNA sequences within the EML4 gene. After a washing step to remove any unbound probe, the sample is examined under a fluorescence microscope.

Under the microscope, the intact EML4 gene will appear as a yellow signal, indicating that the green and red probes are in close proximity. This indicates that the gene is not rearranged.

In contrast, if a gene rearrangement has occurred, the separated parts of the EML4 gene will emit either a green or red signal, depending on which part of the gene they belong to. This clear distinction between colors allows for easy visualization and interpretation of the results.

The Genebio EML4 Dual Color Break Apart Probe is a valuable tool in genetic research and diagnostics. Its ability to accurately detect gene rearrangements involving the EML4 gene, particularly the EML4-ALK fusion gene, provides important information for patient treatment decisions and further understanding of cancer development and progression. With its high sensitivity and specificity, the probe ensures that patients who may benefit from targeted therapy are not overlooked.

What are the specific genes targeted by the Genebio EML4 Dual Color Break Apart Probe?

The Genebio EML4 Dual Color Break Apart Probe is designed to target specific genes involved in a specific genetic abnormality called the EML4-ALK fusion. This fusion occurs in a subset of lung cancer patients and is characterized by the fusion of the EML4 (echinoderm microtubule-associated protein-like 4) gene with the ALK (anaplastic lymphoma kinase) gene.

The EML4-ALK fusion results in the production of a unique protein that promotes the growth and survival of cancer cells. By targeting this specific fusion gene, the Genebio EML4 Dual Color Break Apart Probe allows researchers to detect and analyze the presence of this fusion in patient samples.

The probe utilizes a dual-color fluorescent labeling system to visualize the EML4-ALK fusion. The probe is designed to bind to specific regions of the EML4 gene and can detect the rearrangement of the gene caused by the fusion with the ALK gene. This rearrangement is visualized as a break apart signal, where the two halves of the EML4 gene are separated.

The specific genes targeted by the Genebio EML4 Dual Color Break Apart Probe are the regions within the EML4 gene that undergo rearrangement due to the fusion with the ALK gene. These regions may vary depending on the specific variant of the EML4-ALK fusion present in the patient samples.

Can the Genebio EML4 Dual Color Break Apart Probe be used for other applications besides gene break apart analysis?

Exploring the Versatility of Genebio EML4 Dual Color Break Apart Probe

Introduction: Genebio EML4 Dual Color Break Apart Probe is a cutting-edge tool widely used for gene break apart analysis. This solution offers precise insights into gene rearrangements associated with various diseases. However, this blog post aims to shed light on the versatility of this probe beyond its primary application. We will explore alternative applications where the Genebio EML4 Dual Color Break Apart Probe can be employed, expanding its potential for research and diagnostics.

1. Identification of Gene Fusion Events: Apart from gene break apart analysis, the Genebio EML4 Dual Color Break Apart Probe can be effectively utilized for the identification of gene fusion events. This technique can assist in studying the formation of novel fusion genes, which can provide valuable information about the pathogenesis of diseases such as cancer. It enables researchers to identify and characterize fusion events, facilitating targeted therapeutic approaches.

2. Assessment of Chromosomal Aberrations: The versatility of the Genebio EML4 Dual Color Break Apart Probe extends to the assessment of chromosomal aberrations. By detecting chromosomal rearrangements, such as translocations or inversions, this probe enables researchers to gain insights into genomic instability and its association with diseases. Identification of these aberrations aids in understanding disease mechanisms and can potentially serve as diagnostic markers.

3. Investigation of Genomic Rearrangements: The Genebio EML4 Dual Color Break Apart Probe can be used to investigate genomic rearrangements beyond gene break apart analysis. It can provide valuable information about structural variations in the genome, such as deletions, duplications, or inversions. This can aid in understanding the genetic basis of diseases and identifying potential therapeutic targets. Additionally, studying genomic rearrangements can provide insights into evolutionary processes and population genetics.

4. Characterization of Gene Expression Patterns: In addition to its role in detecting gene rearrangements, the Genebio EML4 Dual Color Break Apart Probe can also be used to study gene expression patterns. By targeting specific genes or gene regions, researchers can analyze their expression levels and patterns in different cell types or under various conditions. This can contribute to our understanding of gene regulation and the molecular mechanisms underlying diseases.

5. Evaluation of Drug Resistance Mechanisms: The versatility of the Genebio EML4 Dual Color Break Apart Probe extends to the evaluation of drug resistance mechanisms. By analyzing gene rearrangements or fusions associated with drug resistance, researchers can identify potential biomarkers that can predict treatment response and guide personalized therapies. This can help in the development of more effective treatment strategies and improve patient outcomes.

Are there any specific equipment or instruments required to use the Genebio EML4 Dual Color Break Apart Probe?

Exploring Genebio EML4 Dual Color Break Apart Probe: Essential Equipment and Instruments

Introduction: For nature enthusiasts delving into the fascinating world of genetic research, the Genebio EML4 Dual Color Break Apart Probe offers a valuable tool for studying genetic abnormalities. To utilize this probe effectively, certain equipment and instruments are required to ensure accurate and reliable results. In this blog post, we will discuss the specific requirements for utilizing the Genebio EML4 Dual Color Break Apart Probe.

1. Fluorescence Microscope: A fluorescence microscope is an essential piece of equipment for visualizing the results obtained from the Genebio EML4 Dual Color Break Apart Probe. This microscope is used to observe the fluorescence signals emitted by the labeled DNA probes, allowing for the detection and analysis of gene rearrangements.

2. Imaging System: To capture and document the fluorescence signals produced by the EML4 Dual Color Break Apart Probe, an imaging system is necessary. This system typically comprises a high-resolution camera, software, and a computer. It enables researchers to analyze and quantify the fluorescence signals efficiently.

3. Hybridization System: To perform the hybridization process effectively, a hybridization system is required. This system ensures proper temperature control and stability during the hybridization process. The Genebio EML4 Dual Color Break Apart Probe may require specific hybridization conditions, and a reliable hybridization system will facilitate optimal results.

4. Incubator: An incubator is needed to maintain a controlled environment for the hybridization process. It provides a stable temperature, humidity, and CO2 levels, ensuring optimal conditions for the DNA probes to hybridize with their target sequences. This helps to enhance the sensitivity and specificity of the assay.

5. Centrifuge: A centrifuge is essential for various steps involved in the preparation of samples for the Genebio EML4 Dual Color Break Apart Probe assay. It is used for DNA extraction, purification, and concentration, ensuring high-quality DNA samples for accurate and reliable results.

6. PCR Machine: A PCR (Polymerase Chain Reaction) machine is necessary for amplifying the DNA samples before performing the hybridization assay with the Genebio EML4 Dual Color Break Apart Probe. This step helps to increase the signal intensity and improve the sensitivity of the assay.

7. Labeled DNA Probes: The Genebio EML4 Dual Color Break Apart Probe utilizes specific DNA probes that are labeled with fluorophores. These labeled probes enable the visualization and detection of gene rearrangements. The probes should be stored properly and handled with care to maintain their stability and functionality.

8. Consumables: Various consumables are required for the Genebio EML4 Dual Color Break Apart Probe assay, including microcentrifuge tubes, pipette tips, PCR tubes, and reagents. These consumables should be of high quality to prevent contamination and ensure accurate results.

9. Safety Equipment: As with any laboratory work, safety equipment is necessary when working with the Genebio EML4 Dual Color Break Apart Probe. This includes lab coats, gloves, safety goggles, and proper disposal containers for biohazardous waste. Following safety protocols is crucial to protect oneself and maintain a safe working environment.

Are there any alternative probes or methods available for gene break apart analysis?

Exploring Alternative Probes and Methods for Gene Break Apart Analysis

Introduction: Gene break apart analysis plays a crucial role in various research fields, such as cancer genetics and molecular diagnostics. While traditional probe-based methods have been widely used, advancements in technology have paved the way for alternative approaches. In this blog post, we will delve into alternative probes and methods available for gene break apart analysis, providing nature enthusiasts with a comprehensive overview of the latest options in this field.

1. Fluorescence In Situ Hybridization (FISH) Probes: FISH probes have been a stalwart in gene break apart analysis due to their high sensitivity and specificity. However, alternative FISH probes, such as next-generation FISH probes, have emerged, offering enhanced resolution, reduced probe preparation time, and improved signal intensity. These advanced FISH probes utilize multicolor fluorescence and innovative labeling techniques to enable better visualization of gene break apart events.

2. Reverse Transcription-Polymerase Chain Reaction (RT-PCR): RT-PCR is another valuable alternative method for gene break apart analysis. This technique involves the conversion of RNA into complementary DNA (cDNA) followed by PCR amplification. By targeting specific gene regions, RT-PCR allows for the identification of gene fusion events and breakpoints. Additionally, real-time RT-PCR can quantify gene expression levels, offering further insights into the genetic alterations present.

3. Next-Generation Sequencing (NGS) Techniques: NGS has revolutionized the field of gene analysis, including gene break apart analysis. This high-throughput sequencing method allows for the simultaneous analysis of multiple genes, providing a comprehensive view of genetic alterations. NGS techniques, such as RNA-Seq and DNA-Seq, can identify gene fusion events, breakpoints, and other structural variations with high accuracy and sensitivity. Furthermore, NGS can also provide information on gene expression levels, mutation profiles, and other genomic features, making it a versatile tool for gene analysis.

4. Digital PCR (dPCR): Digital PCR is a quantitative method that allows for the precise measurement of DNA or RNA molecules in a sample. This technique partitions the sample into thousands of individual reactions, enabling the detection and quantification of rare genetic events, such as gene break apart events. With its high sensitivity and precision, dPCR can provide accurate and reliable results, making it a valuable alternative for gene break apart analysis.

5. Multiplex Ligation-dependent Probe Amplification (MLPA): MLPA is a multiplex PCR-based technique that allows for the detection of copy number variations, including gene rearrangements. By using multiple probes specific to different target sequences, MLPA can identify gene break apart events and quantify the relative abundance of different gene fusion variants. This method offers a cost-effective and efficient alternative for gene break apart analysis, particularly in cases where targeted analysis of specific genes is required.