Gene: MMAB
Official Full Name: metabolism of cobalamin associated Bprovided by HGNC
Gene Summary: This gene encodes a protein that catalyzes the final step in the conversion of vitamin B(12) into adenosylcobalamin (AdoCbl), a vitamin B12-containing coenzyme for methylmalonyl-CoA mutase. Mutations in the gene are the cause of vitamin B12-dependent methylmalonic aciduria linked to the cblB complementation group. Alternatively spliced transcript variants have been found. [provided by RefSeq, Apr 2011]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO20508 | MMAB Knockout cell line (HeLa) | Human | MMAB | 1:3~1:6 | Negative | Online Inquiry |
KO20509 | MMAB Knockout cell line (HCT 116) | Human | MMAB | 1:2~1:4 | Negative | Online Inquiry |
KO20510 | MMAB Knockout cell line (HEK293) | Human | MMAB | 1:3~1:6 | Negative | Online Inquiry |
KO20511 | MMAB Knockout cell line (A549) | Human | MMAB | 1:3~1:4 | Negative | Online Inquiry |
MMAB Gene Knockout Cell Lines represent a breakthrough in biochemical research, specifically designed for the study of the methionine adenosyltransferase (MAT) pathway and its associated metabolic processes. This product provides a specialized, genetically modified cell line in which the MMAB gene has been systematically inactivated through a rigorous CRISPR/Cas9 gene-editing technique. As a result, these knockout cell lines allow researchers to explore the phenotypic and molecular consequences of the loss of MMAB function, which is pivotal in the biosynthesis of adenosylmethionine and various metabolic disorders linked to vitamin B12 metabolism.
The key functioning mechanism of MMAB Gene Knockout Cell Lines lies in their ability to facilitate the examination of metabolic alterations under conditions of MMAB deficiency. Researchers can observe how the absence of this gene affects cellular pathways, enzymatic activities, and downstream metabolic products, providing insight into the implications of MMAB in developing therapies for metabolic diseases and understanding altered biochemical states.
The scientific significance of these knockout cell lines is substantial, given that metabolic dysfunctions associated with MMAB mutations are implicated in conditions such as methylmalonic acidemia. Utilizing MMAB Gene Knockout Cell Lines in research helps to clarify the mechanisms driving these disorders, paving the way for advanced diagnostics and therapeutic strategies.
One unique selling point of MMAB Gene Knockout Cell Lines is their high specificity and reproducibility compared to other genetically modified lines on the market. These cell lines offer precise gene-targeting capabilities with verified knockout efficiency, reducing the likelihood of off-target effects and enhancing the reliability of experimental results.
For researchers and clinicians, the value of MMAB Gene Knockout Cell Lines extends beyond basic research; they serve as vital tools in drug discovery, metabolic research, and the development of personalized medicine approaches. The availability of validated models that accurately reflect human genetics is essential for advancing our understanding of metabolic conditions and evaluating potential therapeutics.
Leveraging years of expertise in genetic engineering and cell line development, our company is committed to providing high-quality biological products that accelerate research and foster innovation in the life sciences. With MMAB Gene Knockout Cell Lines, we empower scientists to make significant strides in understanding and treating metabolic diseases.
Please note that all services are for research use only. Not intended for any clinical use.
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