Gene: ALAS1
Official Full Name: 5'-aminolevulinate synthase 1provided by HGNC
Gene Summary: This gene encodes the mitochondrial enzyme which is catalyzes the rate-limiting step in heme (iron-protoporphyrin) biosynthesis. The enzyme encoded by this gene is the housekeeping enzyme; a separate gene encodes a form of the enzyme that is specific for erythroid tissue. The level of the mature encoded protein is regulated by heme: high levels of heme down-regulate the mature enzyme in mitochondria while low heme levels up-regulate. A pseudogene of this gene is located on chromosome 12. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jan 2015]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO39058 | ALAS1 Knockout cell line (HeLa) | Human | ALAS1 | 1:3~1:6 | Negative | Online Inquiry |
KO39059 | ALAS1 Knockout cell line (HCT 116) | Human | ALAS1 | 1:2~1:4 | Negative | Online Inquiry |
KO39060 | ALAS1 Knockout cell line (HEK293) | Human | ALAS1 | 1:3~1:6 | Negative | Online Inquiry |
KO39061 | ALAS1 Knockout cell line (A549) | Human | ALAS1 | 1:3~1:4 | Negative | Online Inquiry |
ALAS1 Gene Knockout Cell Lines are specialized cellular models in which the ALAS1 gene, responsible for coding the enzyme aminolevulinate synthase 1, has been selectively disrupted. These models are pivotal for studying heme biosynthesis, allowing researchers to delve into the metabolic pathways critical for various cellular functions, including oxygen transport and electron transfer. By eliminating ALAS1 expression, these cell lines facilitate the examination of downstream effects and biological consequences associated with disrupted heme production, which is particularly relevant in the context of hematological disorders and certain metabolic diseases.
The key mechanism underlying these knockout cell lines involves CRISPR-Cas9 genome editing technology, which enables precise insertion or deletion of target genes. By ensuring the complete knockout of ALAS1, researchers can accurately assess the role of this enzyme and its impact on cellular functions and viability. This robust model can be utilized to explore the pharmacological effects of potential therapeutic agents aimed at correcting metabolic dysfunctions linked to heme deficiency.
In terms of scientific importance, ALAS1 Gene Knockout Cell Lines serve as invaluable tools for pharmacological testing and the elucidation of pathophysiological mechanisms in diseases such as porphyrias and other anemias. Their application in both research and clinical settings can speed up the drug discovery process, enhance the understanding of metabolic pathways, and support the development of novel treatment strategies.
Compared to traditional models, these cell lines offer unparalleled specificity and reproducibility. Existing alternatives often rely on wild-type models that may introduce confounding variables due to normal expression levels of the target gene. The ALAS1 knockout model provides a pure context to study the absence of its enzymatic function without the variability introduced by residual amounts of functional protein.
Researchers and clinicians will find ALAS1 Gene Knockout Cell Lines valuable due to their ability to provide deep insights into the mechanisms of heme-related diseases, ultimately aiding in the development of targeted therapies. As you seek to expand your research or clinical offerings, consider leveraging our expertise in producing highly specialized biological models. Our commitment to quality and precision ensures that you receive robust and reliable cell lines, tailored to meet the demands of your scientific inquiries.
Please note that all services are for research use only. Not intended for any clinical use.
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