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SLC37A1 Knockout Cell Lines

Gene: SLC37A1

Official Full Name: solute carrier family 37 member 1provided by HGNC

Gene Summary: The protein encoded by this gene localizes to the endoplasmic reticulum (ER) membrane. This protein translocates glucose-6-phosphate from the cytoplasm into the lumen of the ER for hydrolysis into glucose by another ER membrane protein. This gene is a member of the solute carrier 37 gene family. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO21862 SLC37A1 Knockout cell line (HeLa) Human SLC37A1 1:3~1:6 Negative Online Inquiry
KO21863 SLC37A1 Knockout cell line (HCT 116) Human SLC37A1 1:2~1:4 Negative Online Inquiry
KO21864 SLC37A1 Knockout cell line (HEK293) Human SLC37A1 1:3~1:6 Negative Online Inquiry
KO21865 SLC37A1 Knockout cell line (A549) Human SLC37A1 1:3~1:4 Negative Online Inquiry

Background

SLC37A1 Gene Knockout Cell Lines represent a cutting-edge tool for researchers investigating cellular metabolism and transporter functions, specifically focusing on the solute carrier family 37 member 1 (SLC37A1) gene. These engineered cell lines have been meticulously developed through CRISPR/Cas9 gene editing technology, resulting in the permanent disruption of SLC37A1 expression. This gene encodes a crucial glucose-6-phosphate transporter involved in gluconeogenesis and glycogenesis, making its knockout pivotal for studying the metabolic pathways influenced by glucose homeostasis.

The primary function of the SLC37A1 knockout cell lines is to provide a robust model for elucidating the role of SLC37A1 in cellular processes. This includes investigating its impact on insulin signaling, metabolic diseases such as diabetes, and the broader implications on cellular energy balance. The complete absence of SLC37A1 permits researchers to explore compensatory mechanisms and alternative transport pathways, offering crucial insights that could lead to the development of therapeutic strategies for metabolic disorders.

In terms of scientific significance, these knockout models have wide-ranging applications, from fundamental cell biology research to translational studies aimed at developing novel treatment modalities. They facilitate a deeper understanding of the physiology behind glucose metabolism and the pathophysiology of diseases linked to SLC37A1 dysfunction, making them invaluable in both academic research and clinical investigations.

When compared to alternative gene editing tools or wild-type cell lines, SLC37A1 knockout cell lines stand out due to their specificity and reliability. The precision of CRISPR technology ensures minimal off-target effects, allowing for accurate experimental outcomes that are reproducible. Moreover, these cell lines are readily available, saving researchers valuable time in generating custom models and ensuring immediate accessibility for urgent experiments.

For researchers and clinicians dedicated to advancing our understanding of metabolic regulation, SLC37A1 Gene Knockout Cell Lines present a crucial resource that bridges basic research and clinical applications. By purchasing from us, you're engaging with a company that prides itself on excellence in genetic engineering and cell line development, backed by a team of experts committed to supporting your research endeavors with high-quality biological products.

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

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