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ALAD Knockout Cell Lines

Gene: ALAD

Official Full Name: aminolevulinate dehydrataseprovided by HGNC

Gene Summary: The ALAD enzyme is composed of 8 identical subunits and catalyzes the condensation of 2 molecules of delta-aminolevulinate to form porphobilinogen (a precursor of heme, cytochromes and other hemoproteins). ALAD catalyzes the second step in the porphyrin and heme biosynthetic pathway; zinc is essential for enzymatic activity. ALAD enzymatic activity is inhibited by lead and a defect in the ALAD structural gene can cause increased sensitivity to lead poisoning and acute hepatic porphyria. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2015]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO02932 ALAD Knockout cell line (HeLa) Human ALAD 1:3~1:6 Negative Online Inquiry
KO02933 ALAD Knockout cell line (HCT 116) Human ALAD 1:2~1:4 Negative Online Inquiry
KO02934 ALAD Knockout cell line (HEK293) Human ALAD 1:3~1:6 Negative Online Inquiry
KO02935 ALAD Knockout cell line (A549) Human ALAD 1:3~1:4 Negative Online Inquiry

Background

ALAD Gene Knockout Cell Lines are advanced biological tools specifically designed to facilitate the study of the Aminolevulinic Acid Dehydratase (ALAD) gene, which plays a crucial role in the heme biosynthesis pathway. These cell lines have been engineered using CRISPR/Cas9 technology, resulting in knockout variants that completely lack functional ALAD expression. This targeted approach enables researchers to investigate the effects of ALAD absence on cellular metabolism, oxidative stress response, and associated physiological processes.

The primary function of the ALAD Gene Knockout Cell Lines is to serve as a model for elucidating the biological consequences of ALAD disruption. By studying these cell lines, researchers can dissect the molecular mechanisms linking ALAD to a variety of diseases, including porphyria and certain types of anemia. Additionally, these knockout models can provide insights into the therapeutic potential of targeting heme biosynthesis in diverse pathological contexts.

Scientifically, the ALAD Gene Knockout Cell Lines hold significant importance in both basic and translational research. Their applications extend to drug discovery, particularly in oncology and hematology, where understanding the role of metabolic pathways is critical for developing effective therapeutics. Comparative studies with wild-type cell lines also allow researchers to identify potential compensatory mechanisms that may arise from the genetic alteration.

One of the unique selling points of ALAD Gene Knockout Cell Lines is their precision and reproducibility, enabled by robust CRISPR/Cas9 technology. Unlike conventional methods such as pharmacological inhibitors or RNA interference, these knockout lines provide a reliable genetic model that represents a true absence of the ALAD gene. Furthermore, our well-characterized cell lines can save researchers valuable time in experimental design and validation, fostering more efficient and impactful research outcomes.

For researchers and clinicians focusing on gene function, metabolic pathways, and disease mechanisms, ALAD Gene Knockout Cell Lines present an invaluable resource. By employing these cell lines, users can gain deeper insights into ALAD-related processes, facilitating innovations that bridge the gap between basic science and clinical applications.

Our company specializes in developing high-quality genetic models that empower scientific discovery. With a commitment to advancing research tools and a solid background in molecular biology, we strive to support the scientific community with superior products like the ALAD Gene Knockout Cell Lines.

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

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