Gene: FKBP8
Official Full Name: FKBP prolyl isomerase 8provided by HGNC
Gene Summary: The protein encoded by this gene is a member of the immunophilin protein family, which play a role in immunoregulation and basic cellular processes involving protein folding and trafficking. Unlike the other members of the family, this encoded protein does not seem to have PPIase/rotamase activity. It may have a role in neurons associated with memory function. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO28971 | FKBP8 Knockout cell line (HeLa) | Human | FKBP8 | 1:3~1:6 | Negative | Online Inquiry |
KO28972 | FKBP8 Knockout cell line (HCT 116) | Human | FKBP8 | 1:2~1:4 | Negative | Online Inquiry |
KO28973 | FKBP8 Knockout cell line (HEK293) | Human | FKBP8 | 1:3~1:6 | Negative | Online Inquiry |
KO28974 | FKBP8 Knockout cell line (A549) | Human | FKBP8 | 1:3~1:4 | Negative | Online Inquiry |
FKBP8 Gene Knockout Cell Lines are expertly engineered cellular models designed to facilitate research into the biological functions and pathways associated with the FKBP8 gene. This gene encodes a member of the FK506-binding protein family, which plays crucial roles in protein folding, intracellular transport, and cellular stress responses. By utilizing CRISPR-Cas9 gene editing technology, these knockout cell lines effectively eliminate FKBP8 gene expression, providing a valuable tool for understanding its physiological relevance and involvement in various cellular processes, such as apoptosis, signal transduction, and cellular differentiation.
The primary function of FKBP8 Gene Knockout Cell Lines serves to provide researchers with a precise in vitro environment to investigate the implications of FKBP8 deficiency. By observing changes in cell behavior, researchers can elucidate the downstream effects of FKBP8 on cell cycle regulation, immune responses, and disease mechanisms. These cell lines are particularly valuable for studies involving cancer, neurodegenerative disorders, and metabolic syndromes, where FKBP8 has been implicated in molecular pathways contributing to disease pathology.
One of the significant advantages of our FKBP8 Gene Knockout Cell Lines is their robust genetic validation and reproducibility, ensuring consistent results across experiments compared to traditional methods, such as siRNA or chemical inhibitors. Unlike other knockout models, these specific cell lines allow for the thorough exploration of available cellular interactions and compensatory mechanisms, enabling researchers to gain a comprehensive understanding of FKBP8 functionality in various biological contexts.
Additionally, these cell lines are crafted to suit diverse research needs, supporting high-throughput screening applications, drug discovery initiatives, and in-depth mechanistic studies. By using our FKBP8 Gene Knockout Cell Lines, researchers and clinicians can make groundbreaking advancements in understanding pathophysiological conditions associated with FKBP8, potentially leading to novel therapeutic approaches.
Our company specializes in the development of meticulously characterized biological products that cater to the evolving needs of the scientific community. With a commitment to quality and precision, we ensure that our FKBP8 Gene Knockout Cell Lines empower researchers in their quest to uncover new biological insights and enhance overall scientific knowledge.
Please note that all services are for research use only. Not intended for any clinical use.
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