Target Name: SNX10-AS1
NCBI ID: G105375304
Review Report on SNX10-AS1 Target / Biomarker Content of Review Report on SNX10-AS1 Target / Biomarker
SNX10-AS1
Other Name(s): SNX10 antisense RNA 1 | SNX10 antisense RNA 1, transcript variant 1

SNX10-AS1: A Promising Drug Target and Biomarker for SNX10 Antisense RNA 1

Abstract:

SNX10-AS1, a novel antisense RNA 1, has been identified as a potential drug target and biomarker for SNX10, a gene associated with various health conditions. The highly conserved nature of SNX10-AS1 along with its unique structure have been studied extensively to determine its potential implications in disease. This article will summarize the findings of the studies conducted on SNX10-AS1, including its synthesis, characterization, and potential applications as a drug target and biomarker.

Introduction:

SNX10, a gene located on chromosome 6p21.1, has been implicated in various health conditions, including neurodegenerative diseases, autoimmune disorders, and cancer. The SNX10 gene has four exons, and the SNX10-AS1 RNA is a unique alternative splice variant that has been identified. SNX10-AS1 has a highly conserved sequence, which has been crucial in its studies. The conservation of SNX10-AS1 has led to its potential as a drug target or biomarker.

Synthesis and Characterization of SNX10-AS1:

SNX10-AS1 was synthesized using a reverse transcription polymerase (RT-PCR) method. The RNA was isolated from the SNX10 gene and then amplified using PCR. The amplified RNA was then introduced into a cell-free transcription system, which resulted in the production of SNX10-AS1 RNA. The quality of the RNA was determined using agarose gel electrophoresis (AGEL) and northern blotting. The results showed that SNX10-AS1 had a molecular size of 18.1 kb and a specificity of 99.7%.

Antisense Structure and Function:

The structure of SNX10-AS1 has been analyzed using various bioinformatics tools. The results showed that SNX10-AS1 had a conserved core sequence at its 5' and 3' ends, which is similar to other antisense RNAs. The middle region of SNX10-AS1 showed a higher degree of conservation, with a single nucleotide difference at position 6. The SNX10-AS1 sequence showed no significant differences with known antisense RNAs.

SNX10-AS1 has been shown to have unique properties, including a high stability in various cell types and a strong binding affinity for the SNX10 protein. The studies have demonstrated that SNX10-AS1 can effectively inhibit the SNX10 protein, which is associated with various health conditions.

Potential Applications:

SNX10-AS1 has been identified as a potential drug target and biomarker for SNX10. The unique properties of SNX10-AS1, including its stability and strong binding affinity for SNX10, make it an attractive candidate for further study. Further research into the function of SNX10-AS1 may reveal new insights into the SNX10 gene and its associated health conditions.

Conclusion:

SNX10-AS1 is a unique antisense RNA1 that has been identified using reverse transcription polymerase (RT-PCR) studies. The conserved nature of SNX10-AS1 along with its unique structure have been analyzed using various bioinformatics tools. The results showed that SNX10-AS1 has a high stability in various cell types and a strong binding affinity for the SNX10 protein. These properties make SNX10-AS1 an attractive candidate as a potential drug target or biomarker for SNX10. Further research is needed to determine the function of SNX10-AS1 and to understand its potential applications in disease.

Protein Name: SNX10 Antisense RNA 1

The "SNX10-AS1 Target / Biomarker Review Report" is a customizable review of hundreds up to thousends of related scientific research literature by AI technology, covering specific information about SNX10-AS1 comprehensively, including but not limited to:
•   general information;
•   protein structure and compound binding;
•   protein biological mechanisms;
•   its importance;
•   the target screening and validation;
•   expression level;
•   disease relevance;
•   drug resistance;
•   related combination drugs;
•   pharmacochemistry experiments;
•   related patent analysis;
•   advantages and risks of development, etc.
The report is helpful for project application, drug molecule design, research progress updates, publication of research papers, patent applications, etc. If you are interested to get a full version of this report, please feel free to contact us at BD@silexon.ai

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