Gene: BCAT2
Official Full Name: branched chain amino acid transaminase 2provided by HGNC
Gene Summary: This gene encodes a branched chain aminotransferase found in mitochondria. The encoded protein forms a dimer that catalyzes the first step in the production of the branched chain amino acids leucine, isoleucine, and valine. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO38840 | BCAT2 Knockout cell line (HeLa) | Human | BCAT2 | 1:3~1:6 | Negative | Online Inquiry |
KO38841 | BCAT2 Knockout cell line (HCT 116) | Human | BCAT2 | 1:2~1:4 | Negative | Online Inquiry |
KO38842 | BCAT2 Knockout cell line (HEK293) | Human | BCAT2 | 1:3~1:6 | Negative | Online Inquiry |
KO38843 | BCAT2 Knockout cell line (A549) | Human | BCAT2 | 1:3~1:4 | Negative | Online Inquiry |
BCAT2 Gene Knockout Cell Lines are precisely engineered cellular models designed to produce a deficiency in the branched-chain amino acid transaminase 2 (BCAT2) gene. This gene plays a critical role in the metabolism of branched-chain amino acids (BCAAs) such as leucine, isoleucine, and valine, which are essential for various metabolic pathways in cells. By utilizing CRISPR-Cas9 gene editing technology, these knockout cell lines provide invaluable resources for studying the functional implications of BCAT2 deficiency on cellular metabolism, signaling pathways, and overall cell health.
The primary mechanism of action in these cell lines involves the targeted disruption of the BCAT2 gene, resulting in the abrogation of its transaminase activities that catalyze amino acid transfers. This creates a biological model that is essential for understanding how BCAT2 deficiency impacts various physiological processes, including protein synthesis, energy production, and neuroprotective mechanisms. This is especially relevant in research related to metabolic disorders, neurological diseases, and conditions associated with altered BCAA levels.
The scientific importance of BCAT2 Gene Knockout Cell Lines extends into both research and clinical settings, as they can be utilized to explore the roles of BCAAs in health and disease. These models offer researchers a platform to investigate the underlying mechanisms of diseases like Maple Syrup Urine Disease and to evaluate potential therapeutic strategies targeting BCAA metabolism.
Compared to alternative models, such as wild-type or non-edited cells, the BCAT2 knockout lines provide a distinct advantage by offering a consistent and reproducible system to study BCAT2's role without interference from normal gene expression. Additionally, these cell lines facilitate the screening of drug compounds aimed at restoring metabolic balance, contributing to more effective therapeutic interventions.
For researchers and clinicians working in the fields of metabolism, neurology, and endocrinology, investing in BCAT2 Gene Knockout Cell Lines represents a significant step toward innovative discoveries and advancements in treatment methodologies. The expertise of our company in gene editing and cell line development ensures that these products are of the highest quality, designed to meet the rigorous demands of scientific investigation. Our commitment to advancing biological research is evident in our continuous development of next-generation cell lines that empower the scientific community.
Please note that all services are for research use only. Not intended for any clinical use.
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