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- Table of Contents
Facts about Microsomal glutathione S-transferase 1.
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Human | |
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Gene Name: | MGST1 |
Uniprot: | P10620 |
Entrez: | 4257 |
Belongs to: |
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MAPEG family |
glutathione S-transferase 12; GST12EC 2.5.1.18; MGC14525; MGST; MGST-I; microsomal glutathione S-transferase 1; Microsomal GST-1; Microsomal GST-I
Mass (kDA):
17.599 kDA
Human | |
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Location: | 12p12.3 |
Sequence: | 12; NC_000012.12 (16347142..16377192) |
Highly expressed in liver.
Microsome. Mitochondrion outer membrane; Peripheral membrane protein. Endoplasmic reticulum membrane; Multi-pass membrane protein.
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MGST1 is an important enzyme involved in redox-homeostatic mechanisms. Increased ROS lead to the oxidative stress-induced senescence of young mesangial cells. MGST1 downregulation is linked to aging and disease in various systems, including human and animal physiology. MiR-34a has also been linked to aging and disease, including cancer and chronic obstructive pulmonary disease. It also targets SIRT1/6, which plays a role in senescence and redox-homeostatic mechanisms in the redox-homeostatic systems.
The gene PCBD1 encodes a protein called pterin-4 alpha-carbinolamine dehydratase, which recycles a component of the cell called tetrahydrobiopterin. This compound plays an important role in the metabolism of amino acids, including phenylalanine, by converting it into tyrosine. This protein is also involved in neurotransmitters that send signals between nerve cells. It is important for protein building and is also involved in the process of detoxification.
MGST1 is a gene on chromosome 12 that encodes a protein that is involved in redox control and detoxification. In humans, it is essential for preventing hepatitis B virus infection. It also acts as a key regulator of the NF-kB signaling pathway. Its target is HBV, but other viruses such as HIV also infect the liver.
MGST1 is a gene that has a role in hematopoiesis. In mice, MGST1 was expressed at high levels, and knockdown by lentiviral shRNA dramatically reduced the number of differentiated hematopoietic cells. Knockdown of MGST1 decreased mitochondrial metabolism and induced the induction of glycolytic enzymes, which are intimately coupled with HSPC dynamics. This gene is essential for hematopoiesis and embryonic development in vertebrates, and is therefore crucial for hematopoietic stem cell differentiation.
This gene is expressed in almost all recognizable nuclei of the pancreas. It is expressed in pancreatic duct cells, and can be detected as early as E13.5. Hnf1b and MGST1 are inserted into the Cre recombinase gene through a process called transgenic expression. It has been shown that the CreER gene, which encodes MGST1, recapitulates the expression of Hnf1b.
A study performed on M-ADSCs found that these cells showed a reduction in discrete degree on induction day three, indicating synchronization. Transcriptomes were not significantly different on day nine compared to day thirteen, but several key genes related to liver specialization were upregulated. HNF1b, MGST1 marker and AFP were detected in 92.1% and 93.3% of induced cells, respectively, and at day 13 these cells reached a peak of 99.8% and 99.9%, respectively.
PMID: 3372534 by Dejong J.L., et al. Gene expression of rat and human microsomal glutathione S- transferases.
PMID: 8812420 by Kelner M.J., et al. Structural organization of the human microsomal glutathione S- transferase gene (GST12).