Gene: SYCE1L
Official Full Name: synaptonemal complex central element protein 1 likeprovided by HGNC
Gene Summary: Predicted to be involved in synaptonemal complex assembly. Located in intermediate filament cytoskeleton. [provided by Alliance of Genome Resources, Apr 2025]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO13617 | SYCE1L Knockout cell line (HeLa) | Human | SYCE1L | 1:3~1:6 | Negative | Online Inquiry |
KO13618 | SYCE1L Knockout cell line (HCT 116) | Human | SYCE1L | 1:2~1:4 | Negative | Online Inquiry |
KO13619 | SYCE1L Knockout cell line (HEK293) | Human | SYCE1L | 1:3~1:6 | Negative | Online Inquiry |
KO13620 | SYCE1L Knockout cell line (A549) | Human | SYCE1L | 1:3~1:4 | Negative | Online Inquiry |
SYCE1L Gene Knockout Cell Lines are engineered cellular models that have had the SYCE1L gene specifically disrupted, enabling researchers to investigate the role of this gene in various biological processes. The SYCE1L gene is implicated in the formation and maintenance of the synaptonemal complex, which is crucial for homologous chromosome pairing and recombination during meiosis. By utilizing these knockout cell lines, scientists can explore the downstream effects of SYCE1L deficiency on cellular functions, gene expression patterns, and developmental outcomes.
These knockout lines are constructed using precise gene-editing technologies such as CRISPR/Cas9, allowing for accurate and efficient modification of the target gene. Once the gene is knocked out, various assays can be conducted to elucidate the functional consequences of the deletion, whether it involves studying meiotic progression, investigating potential fertility implications, or exploring the role of SYCE1L in associated pathways.
The scientific importance of SYCE1L Gene Knockout Cell Lines extends across multiple fields, including cell biology, genetics, reproductive health, and cancer research. In clinical settings, these models can provide valuable insights that may contribute to the development of therapeutic strategies for dealing with infertility or genetic disorders related to meiotic failure.
Compared to alternative methods of studying gene function, such as transient knockdown approaches, the SYCE1L Gene Knockout Cell Lines offer a stable and consistent model that allows for long-term studies. They also facilitate high-throughput screening applications, making them an enabling tool for drug discovery and functional genomics.
For researchers and clinicians seeking innovative solutions to explore genetic functions and mechanisms, these knockout cell lines are an indispensable resource. Our extensive expertise in genotyping, cell line development, and molecular biology underpins the quality of the SYCE1L Gene Knockout Cell Lines, ensuring that users have access to reliable and cutting-edge tools necessary for advancing their research. Your inquiry into the dynamics of genetic expression and its implications can be transformed with these advanced models, leading to significant breakthroughs in the understanding of gene function and related diseases.
Please note that all services are for research use only. Not intended for any clinical use.
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