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S-methyl-5′-thioadenosine phosphorylase human
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50 μG
642,00 €
642,00 €
Voraussichtliches Versanddatum26. Mai 2025
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Größe auswählen
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50 μG
642,00 €
About This Item
642,00 €
Voraussichtliches Versanddatum26. Mai 2025
Empfohlene Produkte
Rekombinant
expressed in E. coli
Qualitätsniveau
Assay
≥80% (SDS-PAGE)
Form
solution
Relevante Krankheit(en)
cancer
Versandbedingung
dry ice
Lagertemp.
−70°C
Anwendung
S-methyl-5′-thioadenosine phosphorylase human (MTAP) is an enzyme used in cancer research that is deficient in many types of cancer. Decreased MTAP expression may be used as a potential indicator of disease progression of gastrointestinal stromal tumors [1]. MTAP may be a used to develop potential therapeutic strategies for hepatocellular carcinoma (HCC) since MTAP inactivation has been linked to HCC development and invasiveness [2].
Biochem./physiol. Wirkung
Physikalische Eigenschaften
N-terminal GST-tagged 57 kDa protein containing amino acids 2-end.
Physikalische Form
Supplied as a solution in 25 mM Tris-HCl, pH 8.0,100 mM NaCl, 0.05% Tween®-20, 10% glycerol,and 3 mM DTT.
Rechtliche Hinweise
TWEEN is a registered trademark of Croda International PLC
Lagerklassenschlüssel
12 - Non Combustible Liquids
WGK
WGK 1
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
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Marina Kvaskoff et al.
Twin research and human genetics : the official journal of the International Society for Twin Studies, 14(5), 422-432 (2011-10-04)
An evolving hypothesis postulates that melanomas may arise through 'nevus-associated' and 'chronic sun exposure' pathways. We explored this hypothesis by examining associations between nevus-associated loci and melanoma risk across strata of body site and histological subtype. We genotyped 1028 invasive
Olga Camacho-Vanegas et al.
American journal of human genetics, 90(4), 614-627 (2012-04-03)
Diaphyseal medullary stenosis with malignant fibrous histiocytoma (DMS-MFH) is an autosomal-dominant syndrome characterized by bone dysplasia, myopathy, and bone cancer. We previously mapped the DMS-MFH tumor-suppressing-gene locus to chromosomal region 9p21-22 but failed to identify mutations in known genes in
Promoter-hypermethylation is causing functional relevant downregulation of methylthioadenosine phosphorylase (MTAP) expression in hepatocellular carcinoma
Claus Hellerbrand, Marcus Muhlbauer, et al.
Molecular Pharmacology, 52, 64-72 (2006)
Zarah Glad Zimling et al.
Histopathology, 60(6B), E96-105 (2012-03-08)
Malignant pleural mesothelioma (MPM) often causes diagnostic difficulties for pathologists. We assessed whether loss of methylthioadenosine phosphorylase (MTAP), a key enzyme in the intracellular recycling of adenosine triphosphate (ATP) often deleted in MPM, could be detected with immunohistochemistry (IHC) and
Tony W H Li et al.
Carcinogenesis, 33(2), 427-435 (2011-12-14)
Chronic inflammation is an underlying risk factor for colon cancer. Tumor necrosis factor alpha (TNF-α) plays a critical role in the development of inflammation-induced colon cancer in a mouse model. S-adenosylmethionine (SAMe) and its metabolite methylthioadenosine (MTA) can inhibit lipopolysaccharide-induced
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