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RABL2B Knockout Cell Lines

Gene: RABL2B

Official Full Name: RAB, member of RAS oncogene family like 2Bprovided by HGNC

Gene Summary: The RABL2B protein is a member of the RAB gene family which belongs to the RAS GTPase superfamily. RABL2B is located within a subtelomeric region of 22q13.3. Multiple alternatively spliced transcript variants encoding several different isoforms have been found for this gene. [provided by RefSeq, Aug 2008]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO31155 RABL2B Knockout cell line (HeLa) Human RABL2B 1:3~1:6 Negative Online Inquiry
KO31156 RABL2B Knockout cell line (HCT 116) Human RABL2B 1:2~1:4 Negative Online Inquiry
KO31157 RABL2B Knockout cell line (HEK293) Human RABL2B 1:3~1:6 Negative Online Inquiry
KO31158 RABL2B Knockout cell line (A549) Human RABL2B 1:3~1:4 Negative Online Inquiry

Background

RABL2B Gene Knockout Cell Lines are specialized cellular models that have been genetically modified to disrupt the expression of the RABL2B gene, which is involved in an array of cellular processes, including cell growth, proliferation, and differentiation. Knocking out this gene allows for the study of its functional roles in various biological contexts and disease mechanisms.

The primary function of these cell lines is to enable researchers to investigate the consequences of RABL2B disruption on cellular behavior and signaling pathways. By employing techniques such as CRISPR/Cas9 gene editing, the RABL2B Gene Knockout Cell Lines provide a reliable system for analyzing the resultant phenotypic changes that may correlate with disease states, particularly in oncological or developmental biology contexts. This mechanistic insight is vital for elucidating the roles that RABL2B may play in cellular pathology.

In terms of scientific importance and applications, these cell lines are invaluable in translational research and drug development. Researchers utilize RABL2B knockouts to model diseases such as cancer, where aberrations in cellular signaling can lead to uncontrolled proliferation. Additionally, the RABL2B Gene Knockout system supports high-throughput screening platforms, making it an essential tool for the identification of novel therapeutic agents.

Compared to alternative models, RABL2B Gene Knockout Cell Lines offer a significant advantage through their precise genetic alterations and reproducibility in experiments, allowing for more accurate assessments of gene function than traditional methods like RNA interference. Their use can also lead to the identification of new biomarkers for diseases associated with RABL2B dysregulation.

Overall, RABL2B Gene Knockout Cell Lines represent a cutting-edge resource for researchers and clinicians interested in understanding gene function and disease mechanisms. Their capacity to provide critical insights contributes to the advancement of therapeutic strategies, enhancing the potential for impactful scientific discoveries. Our company specializes in providing high-quality genetically modified cell lines and is committed to supporting the research community with reliable and innovative biological products tailored to facilitate groundbreaking studies.

Please note that all services are for research use only. Not intended for any clinical use.

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