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SLC17A7 Knockout Cell Lines

Gene: SLC17A7

Official Full Name: solute carrier family 17 member 7provided by HGNC

Gene Summary: The protein encoded by this gene is a vesicle-bound, sodium-dependent phosphate transporter that is specifically expressed in the neuron-rich regions of the brain. It is preferentially associated with the membranes of synaptic vesicles and functions in glutamate transport. The protein shares 82% identity with the differentiation-associated Na-dependent inorganic phosphate cotransporter and they appear to form a distinct class within the Na+/Pi cotransporter family. [provided by RefSeq, Jul 2008]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO14085 SLC17A7 Knockout cell line (HCT 116) Human SLC17A7 1:2~1:4 Negative Online Inquiry
KO14086 SLC17A7 Knockout cell line (HEK293) Human SLC17A7 1:3~1:6 Negative Online Inquiry

Background

SLC17A7 Gene Knockout Cell Lines are specifically engineered cellular models that possess a complete disruption of the solute carrier family 17 member 7 (SLC17A7) gene, known to encode the vesicular glutamate transporter 1 (VGLUT1). This knockout facilitates the study of excitatory neurotransmission, synaptic plasticity, and related pathophysiological conditions within the central nervous system. These cell lines serve as invaluable tools for investigating the functional implications of SLC17A7 in neuronal signaling, providing insight into the molecular underpinnings of neurological disorders such as epilepsy, schizophrenia, and mood disorders.

The primary mechanism by which the SLC17A7 knockout functions is through the absence of VGLUT1, a critical protein responsible for packaging glutamate into synaptic vesicles. This alteration leads to an accumulation of extracellular glutamate, providing a platform for researchers to assess altered synaptic dynamics, receptor activity, and downstream signaling pathways in a controlled environment. By utilizing these knockout models, scientists can elucidate the role of glutamate signaling in both physiological and pathological contexts.

In a research or clinical setting, the importance of SLC17A7 Gene Knockout Cell Lines cannot be overstated. They are critical for drug discovery, allowing for the screening of compounds that modulate excitatory neurotransmission, and for the identification of novel therapeutic targets in glutamate-related diseases. Each knockout line offers an unrivaled opportunity to manipulate genetic variables, making it easier to draw conclusions about the role of specific genes and proteins.

What sets our SLC17A7 Gene Knockout Cell Lines apart from alternatives is their rigorously validated genetic modification and the availability of detailed phenotypic characterization. Unlike less specific models, our cell lines undergo extensive quality assessments to ensure consistent performance and reproducibility in experiments, enhancing the reliability of research outcomes.

Researchers and clinicians alike will find significant value in incorporating these cell lines into their studies. The SLC17A7 Gene Knockout Cell Lines not only provide a pathway for advancing scientific understanding of neurobiology but also support innovative therapeutic development.

Our company, with years of expertise in genetic engineering and cell line development, is dedicated to offering high-quality biological products that push the boundaries of scientific inquiry. By providing advanced tools like the SLC17A7 Gene Knockout Cell Lines, we empower the research community to tackle complex challenges in neuroscience and beyond.

Please note that all services are for research use only. Not intended for any clinical use.

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