Gene: FANCA
Official Full Name: FA complementation group Aprovided by HGNC
Gene Summary: The Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2). The previously defined group FANCH is the same as FANCA. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and defective DNA repair. The members of the Fanconi anemia complementation group do not share sequence similarity; they are related by their assembly into a common nuclear protein complex. This gene encodes the protein for complementation group A. Alternative splicing results in multiple transcript variants encoding different isoforms. Mutations in this gene are the most common cause of Fanconi anemia. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
GP00542 | FANCA gRNA1-gRNA2 KO plasmid | FANCA | $850 | |||
KO17708 | FANCA Knockout cell line (HeLa) | Human | FANCA | 1:3~1:6 | Negative | Online Inquiry |
KO17709 | FANCA Knockout cell line (HCT 116) | Human | FANCA | 1:2~1:4 | Negative | Online Inquiry |
KO17710 | FANCA Knockout cell line (HEK293) | Human | FANCA | 1:3~1:6 | Negative | Online Inquiry |
KO17711 | FANCA Knockout cell line (A549) | Human | FANCA | 1:3~1:4 | Negative | Online Inquiry |
FANCA Gene Knockout Cell Lines are specialized biological tools created to aid in the study of Fanconi anemia, a genetic disorder characterized by increased susceptibility to cancer and various bone marrow failures due to defects in DNA repair mechanisms. These cell lines are meticulously engineered to have the FANCA gene, which is critical for the repair of DNA interstrand crosslinks, disrupted or entirely inactivated. The knockout of this gene allows researchers to investigate the biological pathways affected by its absence, thereby enhancing the understanding of the molecular processes underlying Fanconi anemia and related cancers.
The key functions of the FANCA Gene Knockout Cell Lines stem from their ability to model the phenotypic consequences of FANCA deficiency. By using CRISPR-Cas9 technology or other gene-editing modalities to create these knockout lines, scientists can study the role of FANCA in DNA repair, cell cycle regulation, and cellular response to genotoxic stress. These models also facilitate the testing of therapeutic interventions aimed at restoring function or compensating for the loss of FANCA activity, making them invaluable in both basic and translational research.
Scientifically, these cell lines serve a dual purpose: they not only advance our fundamental understanding of Fanconi anemia but also open avenues for the development of novel therapies. In clinical settings, they provide a platform for drug screening and toxicity testing, particularly for agents that target DNA repair pathways. Their relevance extends beyond Fanconi anemia, as insights gained from these models can be applied to other cancers characterized by similar DNA repair deficiencies.
Compared to existing models, our FANCA Gene Knockout Cell Lines offer unique advantages, including high reproducibility and genetic stability, making them more reliable for experimental replication. Additionally, they are optimized for enhanced growth conditions, leading to increased yields for downstream applications such as high-throughput screening.
For researchers, clinicians, and pharmaceutical developers, the FANCA Gene Knockout Cell Lines are indispensable resources that contribute significantly to the exploration of genetic disorders and cancer biology. They bridge the gap between fundamental research and practical applications, ensuring that findings can be translated into meaningful therapeutic strategies.
Our company's expertise in genetic engineering and commitment to providing high-quality biological products ensure that these cell lines are developed with the utmost precision and care, supporting groundbreaking research and innovative therapies in genomics and oncology.
Please note that all services are for research use only. Not intended for any clinical use.
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