Gene: TAP1
Official Full Name: transporter 1, ATP binding cassette subfamily B memberprovided by HGNC
Gene Summary: The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MDR/TAP subfamily. Members of the MDR/TAP subfamily are involved in multidrug resistance. The protein encoded by this gene is involved in the pumping of degraded cytosolic peptides across the endoplasmic reticulum into the membrane-bound compartment where class I molecules assemble. Mutations in this gene may be associated with ankylosing spondylitis, insulin-dependent diabetes mellitus, and celiac disease. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2014]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO35130 | TAP1 Knockout cell line (HeLa) | Human | TAP1 | 1:3~1:6 | Negative | Online Inquiry |
KO35131 | TAP1 Knockout cell line (HCT 116) | Human | TAP1 | 1:2~1:4 | Negative | Online Inquiry |
KO35132 | TAP1 Knockout cell line (HEK293) | Human | TAP1 | 1:3~1:6 | Negative | Online Inquiry |
KO35133 | TAP1 Knockout cell line (A549) | Human | TAP1 | 1:3~1:4 | Negative | Online Inquiry |
TAP1 Gene Knockout Cell Lines are precisely engineered cellular models that have undergone targeted genetic modification to disrupt the TAP1 (Transporter associated with Antigen Processing 1) gene. This gene plays a crucial role in the transport of peptides from the cytosol into the endoplasmic reticulum, where they can be loaded onto MHC class I molecules for presentation to CD8+ T cells. The absence of the TAP1 gene significantly alters antigen presentation pathways, allowing researchers to study immune responses, T cell recognition, and interactions with pathogens or cancer cells in a controlled environment.
These cell lines function by utilizing CRISPR-Cas9 technology or other gene editing techniques to ensure precise knockout of the TAP1 gene. This mechanism enables the creation of a robust system that can elucidate the role of TAP1 in immune evasion, intracellular signaling, and potential therapeutic interventions. Researchers can generate insights into how tumors evade immune detection by modifying peptide presentation or how viral infections can exploit these pathways.
The scientific importance of TAP1 Gene Knockout Cell Lines is evident in their expansive applications in basic research and clinical settings. They serve as vital tools for immunologists studying T cell activation and tumor immunology, drug developers aiming to enhance cancer immunotherapy, and vaccine researchers investigating ways to improve antigen presentation and immune response. By providing clear insights into the workings of the immune system, these cell lines facilitate advancements in personalized medicine and immunotherapy strategies.
Compared to traditional wild-type cell lines, TAP1 Gene Knockout Cell Lines offer unique advantages such as enhanced reproducibility in experimental results, the ability to model specific immune scenarios, and the potential for discovering new therapeutic targets. The strategic use of these knockout models not only cuts down on variables that complicate experiments but also allows researchers to advance their understanding of TAP1-mediated processes with high specificity.
For researchers, clinicians, and biopharmaceutical companies seeking to innovate in immunology or cancer research, TAP1 Gene Knockout Cell Lines provide an invaluable resource. Their precise genetic modification and well-characterized background render them exceptional tools for advancing scientific discovery and therapeutic development.
Our company specializes in providing high-quality, genetically modified cell lines that meet the rigorous standards of the scientific community. With expertise in genetic engineering and an extensive track record, we are committed to supporting research that shapes the future of biomedical science.
Please note that all services are for research use only. Not intended for any clinical use.
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